Okay, hold onto your "hats" because if this one does not upset you, floor you, and make you want to run like hell away from insurance companies and medical care, then you are much stronger than I am...
I have been awaiting a call from the "infusion" clinic all week long. My Rheumatologist and I decided it was time to stop the Humira, which seems to not be working for me. He had two choices for me, both of which are infusions. One of them, I would have to have an infusion once a month, which meant a trip to Dallas every month. The other, Rituxan, that I have two infusions to begin it, two weeks apart, THEN I can go anywhere from 4 TO usually 6 MONTHS before I need another two week treatment!!! Well, you can imagine my decision! Of course going a couple of times a year versus a monthly trip to Dallas was music to my ears, and pocket book. He also agreed that the Rituxan seemed to be a better fit under the circumstances of the fast degeneration we are seeing in my joints . So last week, I believe a week ago this past Wednesday, he began the paperwork. In fact, I went for a new bone scan and blood work while I was there at the University where he practices, and by the time I finished those, the infusion department was calling to tell me they were already working on getting me approved through insurance and so forth. So, I thought WOW they are on the ball with things. So, I felt like this would be done very soon. I really never gave much thought to my part of the "co-pay". I knew it would be considered more on an "outpatient" either hospital or stand alone treatment center, so my part should not be but about $100.00, possibly $200.00 depending on how they coded the center itself. Even though we have been out a butt load of money lately, I knew we could swing that. Anyway, I did not hear anything last week, but I knew that Humana usually drags their feet on prior authorization stuff so thus I figured it would be this past Monday or Tuesday before I heard anything. Well, over the weekend on Saturday, I went to my Mom's for a short while. When I returned my husband said that a woman from "Humana" (Right Source Pharmacy is how the call came up on caller ID) called and said that I was "approved" for the Rituxan! So we were just elated! We though wow, quick, and for the insurance to call on a weekend, that was a small miracle. So, Monday I waited all day for a call, and nothing. I called the infusion center late in the afternoon on Monday, and was told that they "may" have that paperwork, but it would not have had time to be processed and my "treatment" plan worked out etc. So, I thought okay I will hear the next day. Well, Tuesday came, nothing, Wednesday came, and I even got a letter from Humana saying I was "approved" for the medication. I was starting to get antsy by then, so Thursday afternoon late, I called the infusion center again. I was then told (by someone else) that YES, my insurance approval was in, BUT they were still working on the treatment plans and I should hear shortly, Well, we were "miffed" about it, mainly because they had acted SO QUICKLY right from the beginning, calling me before I could even leave the facility the week before and now it was like, well we will get to you when we can kind of an attitude. AS all of you know, and have read, my last couple of weeks, and more like couple of months have been just about more than a human should have to ever deal with. Everything that can have happened, should not have happened, etc.. DID or DID NOT happen for me. Between dentists (several appointments including two teeth pulled), glasses for us both, the entire realm of our PCP NO LONGER wanting to have my husband as a patient, having my hips and elbows injected, and finding out I have much more degeneration than just a couple of years ago, and the list goes on...I was just impatient as heck. So, yesterday, amidst waiting on a call about one of my own medications that I will be out of over the weekend, and my doctors office has usually called it in well before now, and the infusion clinic, and some other stuff (it is even down to the fact that we ordered Mom's glasses from the same place we did ours, and when they got to final inspection something was wrong, and they had to make them over again..which we are thrilled they caught the problem, but again it delayed her getting them)... that my nerves have had about all I can take. Behind the "scenes" of doctors, being sick, the pain.... etc... I helped my Mom order a new "settee", a new glider recliner, got her on a new phone service that is WAY cheaper than AT and T is charging her for LOCAL SERVICE ONLY, and just a whole barrage of things for her, and our own daily stuff. So, my plate has been full, running over, and just needing to be all thrown out and re-ordered (LOL).. even though some of it is "good stress", it is still stress...
So, late yesterday afternoon (after the phone RINGING ALL DAY LONG FROM JIM'S CLIENT) I had just about given up on a call. I was NOT hearing from the infusion center, I was NOT hearing if my medication got mailed out, and we both were just puzzled about all of it. Okay, the phone is FINALLY from the infusion center. So, we got excited! I began with an introduction from "Lynn", and as she started off, I could tell in her voice, she was "hesitant" about discussing benefits etc.. The first part of that conversation started with well, we have spoken with your insurance company, and your part to pay is $4,500.00!!!!!!! YES!! You are not seeing things! She did day FOUR THOUSAND FIVE HUNDRED DOLLARS!! And quickly she began saying BUT we have a CHARITY PROGRAM YOU MAY QUALIFY FOR ON THE BALANCE! Well, all I heard was that astronomical figure and here I was thinking $200.00 at THE MOST!! So, I started asking questions, like YOU ARE IN NETWORK with HUMANA RIGHT???? She told me yes several times. Now by then I was in tears, and I still have some of the laryngitis, thus I told her I would let my husband finish the conversation with her. By this time I was sobbing uncontrollably with my puppies on the sofa. Here was one FINAL HOPE with MEDICATION to possibly SLOW DOWN the horrid symptoms of RA, Lupus and possibly now they feel I "may" have MS, and my insurance has totally lost their minds., and there was NO WAY, NO HOW, I could EVER AFFORD that! I am already still reeling over the cost of a damned root canal and crown! Jim was still talking with her about this charity application, and continuing to question her about my insurance. It just was NOT RIGHT! All I should owe if they are IN NETWORK was a 100. or 200. co-pay! Hell I have had inpatients stays, major surgeries, was in the hospital 6 WEEK! and none of that cost anywhere near that figure. Inc fact for the most part I paid very little with the exception of an inpatient room charge on a couple of occasions. So nothing made sense. Jim was being send via email this "charity" application, and in the process he asked her if they would PLEASE HAVE ONE OF THEIR SUPERVISORS CALL HUMANA and RE-VERIFY benefits!??? She said of course, and Jim also got on the phone and call Humana also. He is so lucky, he got through quickly and even got transferred up the "food chain" to several people that were "higher up" and had more knowledge and more "pull". In fact they even put one of their "reps" online to go over my benefits again and see what the hell was wrong. Well, I KNEW, then they were trying to put the medication under PART D DRUG PLAN, rather than as an OUTPATIENT VISIT TO THE INFUSION CENTER! I knew that had to be "co-pay" in regard to "dough nut hole" crap with my Part D, drug plan by the conversation he was having with this guy. Well, in the meantime, after a very long talk with him, and I am saying benefits were verified WRONG, they are trying to say it is like me going to the "pharmacy" and picking up some "prescription" medication that costs thousands of dollars, then of course I would owe a co-pay etc.... and so forth, meet "deductibles" and so on. The phone rings again as we are talking about all of it, and I am saying NO WAY, NO HOW, and I WILL NOT TAKE CHARITY! I will just go back on less expensive injection at home. It is Lynn, the first lady that called me. I walk outside and Jim is saying, say that again?? He said, well we can "deal with" that. And he is smiling at me... I am so totally distraught by now, I did not even care. Well, come to find out, I WAS RIGHT! HUMANA verified benefits UNDER PART D, NOT PART B and that was totally WRONG! I do and will only OWE 100.00 !!!!!! They totally did not give any information correctly to the infusion center, and I guess the infusion center (even though they said that kind of out of pocket they do not see often) never questioned why so high??? Humana was basing everything on like I said I went in and got the Medication itself from the pharmacy.... and NOT as an outpatient "treatment".... By the way, Humana got their butts reamed by the Infusion center supervisor, and I have not called them yet, but believe me they are going to get an ear full...this has happened more than once this year with myself and my Mom... SO TO MAKE A LONG STORY a little shorter. the fact is I ONLY OWE 100.00 "CO-PAY" & I am set up to have my 1st infusion TUESDAY! So, I am already deciding what to take with me, since it is about a 6 or more hour process... :):) My main question and moral to this is HOW does someone elderly without anyone to help them DEAL WITH THIS??? If no one was around to help my Mom, like I do fighting them tooth and nail all the time, she would be paying lots of money out of pocket that she does not owe. She tried to do it with the surgery center last year. They filed with a wrong code, Humana paid it wrong, and they tried to charge Mom over 600.00 that she DID NOT OWE! It took me A YEAR to get them both straightened out... with an apology finally from the head guy at the surgery center... So, this frightens me on so many levels... I feel for those who "do not know" better.. and also HOW AND THE HELL IS ANYONE SUPPOSED TO AFFORD THOSE KINDS OF ASTRONOMICAL TYPE OF CHARGES... IT IS INSANITY!!!!! It is a wonder I did not have a heart attack... I am so very, very thankful that God was walking with me through it all... That is MY STORY and I pray I do not have to EVER GO THROUGH THAT AGAIN!
_____________________________________________________________
Next post to go with the one above...
I
can say that I am GLAD that I DO KNOW it well enough to KNOW THEY WERE
WRONG! I guess if I have any type of thing the Lord has given me, is the
"sense" enough to know when someone is being ripped off, used, abused,
and taken advantage of. I have helped
my Mom, and several others with things that without my help, they may
have paid a great deal out of pocket that they DID NOT OWE! So I am very
thankful that I have been given that "talent" if you want to call it
that. It burns me up to no end to watch someone take advantage of
someone else. Or someone do something or not do something right just
because they are lazy, inconsiderate, OR like a good for instance just
today with me, someone feels the "need" to exert their "power" over
another to show they can.. I have ONE medication that comes from a
pharmacy in Dallas. Always has, always will. That is how that doctor
wants it, and he had them ship it "priority" mail to me. But, I still
have to call about 5 days early, I usually do it about 4, unless a
holiday is in there, or sometimes I know he is only in the office on
Friday half a day. So, that is what happened this time. I called my
script in Tuesday afternoon. I am due to RUN OUT by SUNDAY. So, because
he is only in the office a half day on Fridays and he also does
surgeries now sometimes on Wednesdays. I wanted to make sure I did it
just early enough that I would not run out and be left hanging. Well,
the "usual" woman that takes care of all scripts must be out for some
reason. Because she usually gets it out the same day, or always the next
day, I get a call from that pharmacy, they send me the meds, which
unless something happens, and it has before, I get them the next day.
Well I called and just left a brief message asking the other lady if she
did get my request (you have to call their refill hotline to ask for
refills) and make sure that the hotline did her the message. Well, this
other "hair brained" witch must be doing the scripts for some reason.
Maybe the usual woman is out this week etc. So, this other "butt" calls
me back yesterday about noon and says "yes, I am calling it in today..
you were a day or two early... well no I was not, it has to be mailed...
but I kept my mouth shut... well I know how she is... she loves to
"play" MS. Authority... she WAITED (and I knew she would, I just felt it
in my bones ) until LATE LAST EVENING. to call it in. so the pharmacy
did NOT get it in time to MAIL IT YESTERDAY. SO, NOW, I call them and
they are "getting it ready" and it will go out today!!!! Well that is
cutting it TOO CLOSE!!! SHE should have DONE HER JOB CORRECTLY and
called that script in early yesterday. She had it for two days, and
could have already done it. It was only about 4 or 5 days before it was
to run out... but she is that kind of person, if she thinks she can MAKE
HERSELF LOOK LIKE SHE IS SOME KIND OF AUTHORITY, then she does it and
guess who suffers??? The Patients!! There was NO reason to HOLD it up,
other than being a jack ass. The normal woman would have called it in on
Wednesday, I would have them no later than today... no harm, no foul...
now if something happens, I may not have it tomorrow... hopefully the
mail will go as it should and I will receive the package tomorrow... but
SHE wanted to make herself LOOK like she was IN CHARGE!!! Those are the
kinds of people that just burn me up!!! They DO NOT give a damned about
anyone but themselves. She could care less if she harms or hurts
someone else as long as she "got" her way... and that was just to be
ridiculous!!! I see it time after time... and not just myself... I watch
people bless their hearts get run over like a tractor trailer by
garbage like that... and they just "take it" because they do not know
NOT TO! People do that with their doctors. We were "taught" that doctors
are "Gods" ..What they said was the BIble and we MUST abide by it...
BULL, if you go to a doctor and you are not satisfied with their
practices, or you feel like they are not taking care of you as they
should, then GET ANOTHER ONE!!! Do NOT think they are PERFECT! We now
tend to know better, but many people still and my Mom is one of them,
think what that doctor says is gospel,., it happened with her heart...
the "1st" test they ran on her heart back in January showed "extreme
mitral prolapse" BUT MOM was NOT having the SYMPTOMS that really showed
it being to the point of being SERIOUS! The doctor was already talking
about taking her to Dallas, doing a procedure, then doing open heart
surgery etc... and it MAY COME TO THAT LATER BUT... I sat down and said,
can we not do something else first, before we jump off into major heart
surgery??? So, due to her NOT taking her meds that morning of the first
test, and having a great deal more fluid on her than usual, the doctor
thought that could be contributing to it "appearing" worse than it was.
Well, the doctor put her on a larger diuretic pill, and asked her to
drink some "less" fluids, especially the 3 days before the next test...
and when they did another test... it was NOT severe, and in fact it was
not even bad enough to go for another special test in Dallas! So, there
are times if you do not say something, or someone does not say or do
something, you may go through something totally not necessary.... and I
guess somewhere in my "genes" is something that makes me want to
"protect" those that are taken advantage of, in any way, abuse, of any
kind... and of those out there that are like a pack of wolves, just
waiting for some poor soul to come along they can "pounce" on..
__________________________________________________________
Third to go with 1st two....
The "benefits" and entitlements we "should"
get that honestly, we the people paid in for all the years we worked
seem to have gone for everything but OUR entitlements! That "robbing"
Peter to pay "Paul" ...
thus now when we are having people work many more years, and then
retire at later times, they also collect more of their entitlements like
Medicare and Social Security for more years. I guess no one thought
about that when people lived to be only in their 60's or so. Now we have
MANY elderly that are still driving their cars and taking care of
themselves into their 80's plus! Thus we are going to need more money to
pay our their benefits, and then we have children that soon will be in
the work force headed for either "put your own money aside for
retirement" or get older and have nothing. It has not been that long
ago, that my Dad retired. After 45 years at the same place, he got a
retirement and between that and his Social Security, they did okay. But,
that was also when interest rates were high and they made a good deal
of money on investments. Now that same money is making NOTHING! I see
what tiny amounts Mom's little bit of nest egg makes and there no way
one she could "live off what little interest" that money makes now. IT
is insanity. It seems I use that word a lot lately... but it is this
entire nation, our entire world has just dropped down to dog eat dog,
and GREED is the name of the game. I am truly "ashamed" of humans and
some of the horrible stunts they pull. So, I get the entire thing about
trying to get "benefits" you are due to even work for you. And now I
read that our UPS corporation is cutting their employees families
completely out of the health insurance! I don't even think they are
going to "offer" the benefits if you pay out of pocket for them! And UPS
is NO SMALL corporation! I also cannot fathom that "cities", huge
cities in the US can go "bankrupt"???? How does a city spend so much
money when taxes are paid by citizens and all kinds of "revenue" is
made, go "belly up?" What does that tell us about our nation? heck our
World? WE have "nations" in the same shape! Their "money" is not worth
the paper it is written on... same way with homes here. How can you take
a home that was just valued at 300,000. a couple of years ago, and it
only be worth 100,000.00 today!???? Where the hell did all of that come
from??? Property "used" to be the "best" investment you could make. We
were told it "always holds its value"... well I am here to tell you NOT
ANYMORE! I don't think there is one item in this world that truly will
hold its "value"... everything is volatile... nothing is "steady"... we
live in a world much like a volcano... we never know when it will
explode or worse implode all around itself...
Ah, and I am quite sure... and am NOT quite... through....
"Through my heart's work of writing, I share with you my complex journey a top the mountain, sliding down, crawling up, & living through the realms of Autoimmune Arthritic Illnesses. Taming "The Wolf" Thru each Day... One Step at a Time … Together We Are Learning to Survive. Please follow along, to New Beginnings - looking Thru the Window Pane of Pain in life where we shall find our journey leading us to - New Perspectives
Friday, August 23, 2013
Thursday, August 22, 2013
Giving a "Voice" to All of the Frustration of Being Chronically Ill Human Being...
I believe the very first thing I want to point out is in the "title" of this blog post. That is the two words, "Human Being". None of us are robots, although as of late, many act like it. None of us are beyond mistakes, stresses, illness, economic woes, job losses, kid issues, family problems, and an entire gamut of "what could" and does happen to "good" people. When I say "good" people, I am speaking of us main stream normal everyday folks, that try our best to do our jobs, take care of our bills, raise a family, and be a "stand up" kind of person, who wants what is best for all. We don't begrudge others a nice life, a good vehicle, health for them and their families, and the ability have have what is considered a "quality of Life" we feel is truly worth living.
All of that sounds very simple. Life.. used to be "simple". I know what some will say to my next statement, "life seemed a great deal more simple, when we did not have but a one room school house, raised our own food and animals, got our milk directly from the source, had the "ice" man delivery the "ice" block for your ice box, had a radio NOT a TV, not the internet, not fast cars, cell phones, video games, and back when kids went outside to play. When kids played then, even in my life, I went out to "use" my imagination to occupy time. I was an only child, thus I spent Summers outside, with my dollar, my little table, making up all kinds of different things that kept me out in fresh air, active, and not sitting in front of a television for 12 or more hours a day. I can see now "hind sight being what it is...20-20" many things that are contributing factors to all of our "hardships", our downfalls, our chronic illnesses, whether emotional, mental or physical that we want to shove under the rug, run to the doctor, take a quick pill, much like running through the "drive-thru" for coffee, we are too lazy to park, get out of the car, and go into a place to get coffee anymore.. our excuse?? We are TOO busy! Well, if you are TOO busy to go inside and buy your lunch, get a donut, pick up a six pack of beer (now that you can even drive thru for freaking beer), then I say you are TOO DAMNED BUSY!
All of the above seems to not have much to do with what the title of this post is, nor does it seem any of it relevant to chronic illness and chronic pain. But, it is all relevant. Our entire lives have evolved, in good ways, I will not say that all we have accomplished is "bad". But, we have also "engineered" ourselves right out of jobs, "automated" our lives into a never stopping conveyor belt of high prices, lower quality items, food that is "tainted", medications that are "tainted", people that are not willing to get up off their butts and do their jobs. If they can't sit behind a desk and be "boss", then they think the job is "beneath" them. Boy, you cannot tell me you do not know those like that. I have met several in my life time so far, and it gets worse everyday.
We will not accept that WE HUMANS HAVE RUINED OUR WATER, AIR, AND LAND!!! WE have MELTED THE POLAR CAPS. WE have CAUSED CANCERS, HEART ATTACKS, AND STRESS THAT SEND PEOPLE RUNNING TO THE NUT HOUSE! Or "self-medicating"... how many do you know that weekly, daily use alcohol, food, TV, video games, being on line in a social media place, possibly other drugs that are not "legal", sex, shopping, spending more money than they make... and the list goes on and on... of ADDICTIONS! We totally rely on so many addictions, whether to food, spending, or alcohol to "prop" ourselves up daily so we can do it all over again in this rat race we call life.
We will bitch, moan, whine, and stomp our feet, of things we do NOT believe are RIGHT! BUT, take action?? IF you can gripe about it, then you can DO SOMETHING! Write an email, a letter, make a phone call, attend a rally... do something other than give these things "lip service". I can tell you right now WORDS with NO ACTIONS, gets you NOTHING BUT FURTHER UPSET AND STRESS! It only leads to more frustration, more depression, more attitude of giving up and throwing in the dish towel of life. So, why are we so in "fear" of voicing how we feel???
What makes us rant and rave "online", but come up to the person, or place, or thing that is upsetting you, and lips are closed, mouth shut, and a "pleasant" face put on... in other words DO NOT rock the BOAT!!! Why??? FEAR???? Have WE as a society that is supposed to be the MOST DEMOCRATIC (I get to where I despise that word... we need a "new" word for those that can give "voice" to their opinions and thoughts, without feeling like you have to "apologize" for what you have done or said. As long as you are NOT HARMING YOUR NEIGHBOR, or causing misery for someone else, you SHOULD BE ABLE TO STAND UP AND SAY HOW YOU FEEL! You should not feel as if your friends, family, doctors, other professionals, anyone is going to "stop" seeing you, not take care of you, no longer "fill" your medications... just because you may not "see" something the same way that another does. WHY are we SO ASHAMED of our own thoughts and feelings.?
We live in enough fear of terrorists, of bombs, of those that shoot people for no reason, of the insanity that happens here daily... we are fighting wild fires,, droughts, and ALL OF THE MOTHER NATURE EVENTS that if we look back in history, MAN CREATED HIS OWN DEMISE. We have ignored our Earth way too long. We have ignored polluting it, of using it up, of covering it up with concrete; then all we can do is "finger point" to who did it? ALL of us! Each and everyone of us are contributors to our own realms of waste, pollution, of the demise of the medical profession, of the demise of our own government. We can bitch all we want to, but WE PUT THEM IN OFFICE! If it is broke, FIX IT! Sometimes the well just runs dry and you have to freaking drill for a new one. And this "well" for our government is dry and getting drier daily.
Ignorance is NOT bliss! It is just plain ignorance. And "denying" all of what is happening, is just sticking your head in the sand and watching for the other shoe to drop on it.
Now onto the "REAL REASON" I am writing this morning... As you can tell, if you are following me here, or on Facebook, my life, as well as my family's life has been in a freaking turmoil now for more than weeks, let's try months. Since January of this year, thank goodness for my spouse, and my Mom, and all of those out there that are "rooting" for my side of the ball game.
I began with what seemed like the "flu". Made sense. After all it was "flu" season. Yet, each day, rather than get better, I seemed to be worse. I began to have pain, and it got worse with each passing day. I developed worse fatigue, muscle aches, deep down in the bone pain, in my legs, my feet, my ankles, hips, and lower back. I was so extremely fatigued, that for weeks, I was literally not able to even drag myself around my drive way to walk, water my flowers, hell I could not even sit at my computer. I went to my regular doctor, my pain doctor, to a neurologist, in fact 3 of them... and had every kind of blood test, EMG, NCS, CT Scans... all coming up with "something" small, that may have "contributed" to the pain, etc... nothing that should cause such massive pain, massive fatigue, and make me feel like I had been just ran over by a bus once or twice. We even questioned my pain pump and went so far as to have the medication completely removed flushed and put new medication back in.
this was already mid-February. We did not know where else to go. I had a couple of doctors that gave me a "new diagnosis". One of which was "myasthenia gravis", and they even suspected Multiple Sclerosis, of which had been suspected on several occasions. This went on until about the first of March. Then one morning, I woke up, and all of the "symptoms" seemed somewhat "better"... each day thereafter it seemed to have a bit better feeling. We never put our finger on the reason why. so in essence I think myself, mu spouse, the doctors "chalked" it up to the "Lupus" and a very bad flare... and the RA, of which the meds were not working as well as they should be... plus I probably did have the flu, and all of it caused that "perfect storm" of illness that raged through my body. What I never did really think about, is in the meantime my pain doctor had "upped" my pain medication when all of the stuff began, and he left it like that. So, possibly I was of course better, other symptoms were going away, but the "pain" could have been somewhat masked over by the increase (change) of pain medication. I got "better", yet I really never got "well". I had other health issues come up, a "myoglobin" issue, that would be a contributor to muscle pain, the RA of course, of which the Humira was definitely not working as it should have been, plus several other things like finding out I had radiculopathy issues, and my lower lumbar spine had definitely done some deterioration in midst all of. Any and all of those things could be combined with my Chronic Lupus/RA issues, to be the culprit of my ongoing new type of pain/illness issues.
Well, the boat seemed to rock a little and put me back in whatever I want to "think" is kind of "normal" for my life. Yet, that was NOT to last long. Come about Mother's Day. I recall it being close to then because I and my Mom were planning to go to the Casino to spend the night. On that Friday before I began to just feel lousy. Again fatigue set in and almost simultaneously, the pain I had so hoped would not return was back with a vengeance. I was definitely in no shape to make even a 2 hour trip to have a good time for Mother's Day, so we decided to postpone and go the following weekend. Well, by then things were already worse. Again, the severe and deep bone pain, in my hips. legs, feet ankles wrists... it was all back once more. This time I went straight to my PCP, getting prednisone injections and a 14 day step down of it, and having them do what they could to "stop" again what we thought was a very bad flare. From there I have battled everything from several of my teeth needing to be pulled all of a sudden, to several cavities, to the double vision I have been fighting for over a year (not one doctor, even the best "neuro-opthamologist") ever figured out why my vision is double., to the excruciating pain I was and this time again it required not only an increase of my oral "break through" meds, BUT an increase of the medication that is in my pain pump. I have spent week and weeks, almost crawling at times around my house, not feeling like even baking something. I have been to my orthopedic surgeon who injected both hips and both elbows that were giving me heck. He feels that my thumbs are too deteriorated to even put medication in, and my hips, and elbows also show signs of further deterioration, which could cause the pain in my legs, hips, lower back, feet and so forth. I am continuing the battle with my own health issues, then week before last I got not only just slapped in the face with, but knocked down with a "suddenly very Odd" "certified letter" from our own Primary Care Doctor. Now this man is wonderful. He diagnosed my Lupus. He had been the doctor who found much of what was going on with me and had been working to "fix" what he could, and sent me to other doctors to do other things to help me feel as well as I possibly could, under my chronic health issues.
This "letter" came while I happened to be at my Mom's and my husband got it. In fact it was for my husband. When I got home, I stepped out to speak with him on our front porch and I could tell by the look on his face, something was very wrong. I had not been gone long, so of course, I was "in a panic" wondering if something happened to one of the dogs, or he had gotten a phone call with bad news. When he began to tell me about this letter, a certified letter he received in the mail, I asked him what he had won? Then I abruptly saw and heard that this was no joke, that this was a serious situation, and after he finished, I had to read the letter and see with my own eyes what he had told me.
It was very formally addressed to him, as if a "stranger" had written it. Yet, this certainly was not a "stranger" at all. This was OUR FAMILY PHYSICIAN that had been our doctor now for at least 6 years. For me, a little longer, because I went to him first. In fact I was probably one of his first 15 patients. He had not been in practice very long at all when I felt like I had found the "perfect march" as far as a family practitioner. Not only did he have an incredible "bedside manner", he is intelligent, he was way educated much more than the usual family doctor, because he tested me and found out things about my health issues that not one doctor in 40 plus years had been able to find.
My Mom was also looking for a new PCP. Her previous one was old, and going out of business basically, so I suggested my new one to her also. She went and also was very pleased. He seemed to be right on top of the latest and greatest. At first, he did it all. There was not any of this referring you to 15 doctors. He tested, found out what was wrong, and with "your" help as an "educated" patient (another big plus in my book, he loved educated patients), he would treat you himself, if possible without sending you all over the country. Again, a small town, with very few PCP in it all the years I was here, this doctor was like an angel sent from above. Things rocked along, and my husband began having issues with his lower back. He does not have insurance. Thus he would be a "cash" pay patient for awhile, until we could afford some kind of policy. But, this new doctor seemed to be much more concerned about "patients" than money, and he charged a very nominal charge to see my husband, he also tried to keep tests, scans, and expensive things out of the picture unless absolutely necessary. So, when my husbands back began to give him more problems other than just the usual three or four times a year, this doctor did a few Xrays, determined the situation was probably something he was born with, and as the years went by, arthritis, and a narrowing of the spinal canal was putting pressure on the main nerves in the lower spine, thus causing horrid pain off and on. Again, we were very impressed. He tried several different types of medications, also treated him for blood pressure issues later, and High cholestral problems, and we were ticking right along, no problems. In fact I had highly recommended him to anyone that happens to be in need of a family doctor.
Well, there was a couple of issues that we had to deal with off and on. One, was the "office manager". He was just an ass, to put it bluntly. He always looked down his nose at everyone. He thought he knew it all, and even though he I am sure is "good" at his job... he is NOT good with people at all. I had more than once complained about his attitude and that I did NOT want to be treated as if I am pond scum. I was certainly not bad about being an overly needy patient, and I tried to refrain from asking for too many "favors". In fact, I really never asked for anything other than a few forms to be filled out in order to get my husbands medication filled for free or for much cheaper than the pharmacies.
This doctor diagnosed my Lupus and RA. He was the one that started me on medications for them, and took care of me, while I tried to find a Rheumatologist with some kind of sense for sure. To this moment, I nor Jim, nor anyone can figure out what the hell went on, and what caused this "sudden" issue, when it is plain as the nose on anyone's face that there was an Error, on the part of their office to NOT tell the Lab to DO THE BLOOD TEST A CERTAIN WAY OR, the LAB did NOT run it the way they were told. Either that, or there is SOMETHING, SOMEONE, is NOT telling me! I know what I see. I know what happens when I am around and there to witness it. But, if I am totally left in the dark about an issue, or something not right, then I cannot make an informed "reason" as to why something like this happens.
Now I do know a couple of "facts". First of all, this business about the government, the DEA, the entire realm of mess in Florida with pain clinics and seedy "quack" pain doctors etc.. has definitely put "fear" into lots of people, along with made a "Good medication" when USED CORRECTLY!, Look like a monster! But, as I said "used CORRECTLY"... IT IS LIKE anything else, if you "abuse" it, then it is Bad for you... or bad for whatever... Then you give "too much power" to some people in a place such as someone over the "legalities" of meds without any governing power over them to oversee what is done, is NOT harming some, and you get a freaked up pile of mess, that THE LEGITIMATE PATIENTS suffer needlessly from! There is NO reason, not one that any person that is truly a Chronic Pain Patient, that has NEVER abused anything, that has lived by their "pain contract", that has "passed" "tests" of whatever, all this time, or been treated like things are totally fine, only to be delivered a ridiculous letter, without any type of warning, without one sit down in front of you and explain WHY this is happening! IF anything is wrong with this, THAT POINT is what is MOST WRONG! WHY NOT have a CONVERSATION AND EXPLAIN this to a PATIENT, rather than take the "unprofessional" and just plain rude way, and not speak to them, not answer their emails, not answer a phone call, not ask them to come in and have a visit, nothing... and then you are also seeing their families??? Now how is that going to go? Like I said above, this situation puts me in such a horrid crack... I am stuck between first of all NOT KNOWING for SURE what is going on, only what I see and know... it puts me in a place of course of being upset, embarrassed, and thinking why should I see them if I could get the same treatment. Down the line a few months, and they stop refilling my medications? And I am not talking about pain medications, I am speaking of medications for my Lupus, my blood pressure, heart and so forth. If this doctor is leaving, or is "mad" at my family, or has something with us that he does not want to treat my family, then he should be professional enough, to just speak up face to face, and tell us what the hell the deal is! If I or my husband, or my Mom, have offended someone, or hell knowing this town, God only knows what kind of stupid "rumor" he has been told... because believe me this town is known for its lying, gossiping, half truths. People do NOT get the entire story, so they "make UP" what they want to... in which sometimes people's lives get frigged up due to a flat out lie being told. Before you open up your mouth when it involves anyone's "reputation" or their "good name", you had better give it deep thought, and then really understand what you could cause. If you are going to "stir up harsh feelings" or cause someone to be "smeared" and you are not sure what you are talking about, it is better to just keep your mouth shut, rather than say something you will harm someone with by being nosy. Small town are noted for that crap. One reason why I did NOT want to move back here... the small town mentality, the gossip, the "whispering" behind your back... those things I just cannot stomach. Since I have been trying now for 3 days to "finish" this and post it, I'm going to say it is "finished" enough to post & if I have further thoughts, I will just add it on and let you know there is a new "piece" under it...
All of that sounds very simple. Life.. used to be "simple". I know what some will say to my next statement, "life seemed a great deal more simple, when we did not have but a one room school house, raised our own food and animals, got our milk directly from the source, had the "ice" man delivery the "ice" block for your ice box, had a radio NOT a TV, not the internet, not fast cars, cell phones, video games, and back when kids went outside to play. When kids played then, even in my life, I went out to "use" my imagination to occupy time. I was an only child, thus I spent Summers outside, with my dollar, my little table, making up all kinds of different things that kept me out in fresh air, active, and not sitting in front of a television for 12 or more hours a day. I can see now "hind sight being what it is...20-20" many things that are contributing factors to all of our "hardships", our downfalls, our chronic illnesses, whether emotional, mental or physical that we want to shove under the rug, run to the doctor, take a quick pill, much like running through the "drive-thru" for coffee, we are too lazy to park, get out of the car, and go into a place to get coffee anymore.. our excuse?? We are TOO busy! Well, if you are TOO busy to go inside and buy your lunch, get a donut, pick up a six pack of beer (now that you can even drive thru for freaking beer), then I say you are TOO DAMNED BUSY!
All of the above seems to not have much to do with what the title of this post is, nor does it seem any of it relevant to chronic illness and chronic pain. But, it is all relevant. Our entire lives have evolved, in good ways, I will not say that all we have accomplished is "bad". But, we have also "engineered" ourselves right out of jobs, "automated" our lives into a never stopping conveyor belt of high prices, lower quality items, food that is "tainted", medications that are "tainted", people that are not willing to get up off their butts and do their jobs. If they can't sit behind a desk and be "boss", then they think the job is "beneath" them. Boy, you cannot tell me you do not know those like that. I have met several in my life time so far, and it gets worse everyday.
We will not accept that WE HUMANS HAVE RUINED OUR WATER, AIR, AND LAND!!! WE have MELTED THE POLAR CAPS. WE have CAUSED CANCERS, HEART ATTACKS, AND STRESS THAT SEND PEOPLE RUNNING TO THE NUT HOUSE! Or "self-medicating"... how many do you know that weekly, daily use alcohol, food, TV, video games, being on line in a social media place, possibly other drugs that are not "legal", sex, shopping, spending more money than they make... and the list goes on and on... of ADDICTIONS! We totally rely on so many addictions, whether to food, spending, or alcohol to "prop" ourselves up daily so we can do it all over again in this rat race we call life.
We will bitch, moan, whine, and stomp our feet, of things we do NOT believe are RIGHT! BUT, take action?? IF you can gripe about it, then you can DO SOMETHING! Write an email, a letter, make a phone call, attend a rally... do something other than give these things "lip service". I can tell you right now WORDS with NO ACTIONS, gets you NOTHING BUT FURTHER UPSET AND STRESS! It only leads to more frustration, more depression, more attitude of giving up and throwing in the dish towel of life. So, why are we so in "fear" of voicing how we feel???
What makes us rant and rave "online", but come up to the person, or place, or thing that is upsetting you, and lips are closed, mouth shut, and a "pleasant" face put on... in other words DO NOT rock the BOAT!!! Why??? FEAR???? Have WE as a society that is supposed to be the MOST DEMOCRATIC (I get to where I despise that word... we need a "new" word for those that can give "voice" to their opinions and thoughts, without feeling like you have to "apologize" for what you have done or said. As long as you are NOT HARMING YOUR NEIGHBOR, or causing misery for someone else, you SHOULD BE ABLE TO STAND UP AND SAY HOW YOU FEEL! You should not feel as if your friends, family, doctors, other professionals, anyone is going to "stop" seeing you, not take care of you, no longer "fill" your medications... just because you may not "see" something the same way that another does. WHY are we SO ASHAMED of our own thoughts and feelings.?
We live in enough fear of terrorists, of bombs, of those that shoot people for no reason, of the insanity that happens here daily... we are fighting wild fires,, droughts, and ALL OF THE MOTHER NATURE EVENTS that if we look back in history, MAN CREATED HIS OWN DEMISE. We have ignored our Earth way too long. We have ignored polluting it, of using it up, of covering it up with concrete; then all we can do is "finger point" to who did it? ALL of us! Each and everyone of us are contributors to our own realms of waste, pollution, of the demise of the medical profession, of the demise of our own government. We can bitch all we want to, but WE PUT THEM IN OFFICE! If it is broke, FIX IT! Sometimes the well just runs dry and you have to freaking drill for a new one. And this "well" for our government is dry and getting drier daily.
Ignorance is NOT bliss! It is just plain ignorance. And "denying" all of what is happening, is just sticking your head in the sand and watching for the other shoe to drop on it.
Now onto the "REAL REASON" I am writing this morning... As you can tell, if you are following me here, or on Facebook, my life, as well as my family's life has been in a freaking turmoil now for more than weeks, let's try months. Since January of this year, thank goodness for my spouse, and my Mom, and all of those out there that are "rooting" for my side of the ball game.
I began with what seemed like the "flu". Made sense. After all it was "flu" season. Yet, each day, rather than get better, I seemed to be worse. I began to have pain, and it got worse with each passing day. I developed worse fatigue, muscle aches, deep down in the bone pain, in my legs, my feet, my ankles, hips, and lower back. I was so extremely fatigued, that for weeks, I was literally not able to even drag myself around my drive way to walk, water my flowers, hell I could not even sit at my computer. I went to my regular doctor, my pain doctor, to a neurologist, in fact 3 of them... and had every kind of blood test, EMG, NCS, CT Scans... all coming up with "something" small, that may have "contributed" to the pain, etc... nothing that should cause such massive pain, massive fatigue, and make me feel like I had been just ran over by a bus once or twice. We even questioned my pain pump and went so far as to have the medication completely removed flushed and put new medication back in.
this was already mid-February. We did not know where else to go. I had a couple of doctors that gave me a "new diagnosis". One of which was "myasthenia gravis", and they even suspected Multiple Sclerosis, of which had been suspected on several occasions. This went on until about the first of March. Then one morning, I woke up, and all of the "symptoms" seemed somewhat "better"... each day thereafter it seemed to have a bit better feeling. We never put our finger on the reason why. so in essence I think myself, mu spouse, the doctors "chalked" it up to the "Lupus" and a very bad flare... and the RA, of which the meds were not working as well as they should be... plus I probably did have the flu, and all of it caused that "perfect storm" of illness that raged through my body. What I never did really think about, is in the meantime my pain doctor had "upped" my pain medication when all of the stuff began, and he left it like that. So, possibly I was of course better, other symptoms were going away, but the "pain" could have been somewhat masked over by the increase (change) of pain medication. I got "better", yet I really never got "well". I had other health issues come up, a "myoglobin" issue, that would be a contributor to muscle pain, the RA of course, of which the Humira was definitely not working as it should have been, plus several other things like finding out I had radiculopathy issues, and my lower lumbar spine had definitely done some deterioration in midst all of. Any and all of those things could be combined with my Chronic Lupus/RA issues, to be the culprit of my ongoing new type of pain/illness issues.
Well, the boat seemed to rock a little and put me back in whatever I want to "think" is kind of "normal" for my life. Yet, that was NOT to last long. Come about Mother's Day. I recall it being close to then because I and my Mom were planning to go to the Casino to spend the night. On that Friday before I began to just feel lousy. Again fatigue set in and almost simultaneously, the pain I had so hoped would not return was back with a vengeance. I was definitely in no shape to make even a 2 hour trip to have a good time for Mother's Day, so we decided to postpone and go the following weekend. Well, by then things were already worse. Again, the severe and deep bone pain, in my hips. legs, feet ankles wrists... it was all back once more. This time I went straight to my PCP, getting prednisone injections and a 14 day step down of it, and having them do what they could to "stop" again what we thought was a very bad flare. From there I have battled everything from several of my teeth needing to be pulled all of a sudden, to several cavities, to the double vision I have been fighting for over a year (not one doctor, even the best "neuro-opthamologist") ever figured out why my vision is double., to the excruciating pain I was and this time again it required not only an increase of my oral "break through" meds, BUT an increase of the medication that is in my pain pump. I have spent week and weeks, almost crawling at times around my house, not feeling like even baking something. I have been to my orthopedic surgeon who injected both hips and both elbows that were giving me heck. He feels that my thumbs are too deteriorated to even put medication in, and my hips, and elbows also show signs of further deterioration, which could cause the pain in my legs, hips, lower back, feet and so forth. I am continuing the battle with my own health issues, then week before last I got not only just slapped in the face with, but knocked down with a "suddenly very Odd" "certified letter" from our own Primary Care Doctor. Now this man is wonderful. He diagnosed my Lupus. He had been the doctor who found much of what was going on with me and had been working to "fix" what he could, and sent me to other doctors to do other things to help me feel as well as I possibly could, under my chronic health issues.
This "letter" came while I happened to be at my Mom's and my husband got it. In fact it was for my husband. When I got home, I stepped out to speak with him on our front porch and I could tell by the look on his face, something was very wrong. I had not been gone long, so of course, I was "in a panic" wondering if something happened to one of the dogs, or he had gotten a phone call with bad news. When he began to tell me about this letter, a certified letter he received in the mail, I asked him what he had won? Then I abruptly saw and heard that this was no joke, that this was a serious situation, and after he finished, I had to read the letter and see with my own eyes what he had told me.
It was very formally addressed to him, as if a "stranger" had written it. Yet, this certainly was not a "stranger" at all. This was OUR FAMILY PHYSICIAN that had been our doctor now for at least 6 years. For me, a little longer, because I went to him first. In fact I was probably one of his first 15 patients. He had not been in practice very long at all when I felt like I had found the "perfect march" as far as a family practitioner. Not only did he have an incredible "bedside manner", he is intelligent, he was way educated much more than the usual family doctor, because he tested me and found out things about my health issues that not one doctor in 40 plus years had been able to find.
My Mom was also looking for a new PCP. Her previous one was old, and going out of business basically, so I suggested my new one to her also. She went and also was very pleased. He seemed to be right on top of the latest and greatest. At first, he did it all. There was not any of this referring you to 15 doctors. He tested, found out what was wrong, and with "your" help as an "educated" patient (another big plus in my book, he loved educated patients), he would treat you himself, if possible without sending you all over the country. Again, a small town, with very few PCP in it all the years I was here, this doctor was like an angel sent from above. Things rocked along, and my husband began having issues with his lower back. He does not have insurance. Thus he would be a "cash" pay patient for awhile, until we could afford some kind of policy. But, this new doctor seemed to be much more concerned about "patients" than money, and he charged a very nominal charge to see my husband, he also tried to keep tests, scans, and expensive things out of the picture unless absolutely necessary. So, when my husbands back began to give him more problems other than just the usual three or four times a year, this doctor did a few Xrays, determined the situation was probably something he was born with, and as the years went by, arthritis, and a narrowing of the spinal canal was putting pressure on the main nerves in the lower spine, thus causing horrid pain off and on. Again, we were very impressed. He tried several different types of medications, also treated him for blood pressure issues later, and High cholestral problems, and we were ticking right along, no problems. In fact I had highly recommended him to anyone that happens to be in need of a family doctor.
Well, there was a couple of issues that we had to deal with off and on. One, was the "office manager". He was just an ass, to put it bluntly. He always looked down his nose at everyone. He thought he knew it all, and even though he I am sure is "good" at his job... he is NOT good with people at all. I had more than once complained about his attitude and that I did NOT want to be treated as if I am pond scum. I was certainly not bad about being an overly needy patient, and I tried to refrain from asking for too many "favors". In fact, I really never asked for anything other than a few forms to be filled out in order to get my husbands medication filled for free or for much cheaper than the pharmacies.
This doctor diagnosed my Lupus and RA. He was the one that started me on medications for them, and took care of me, while I tried to find a Rheumatologist with some kind of sense for sure. To this moment, I nor Jim, nor anyone can figure out what the hell went on, and what caused this "sudden" issue, when it is plain as the nose on anyone's face that there was an Error, on the part of their office to NOT tell the Lab to DO THE BLOOD TEST A CERTAIN WAY OR, the LAB did NOT run it the way they were told. Either that, or there is SOMETHING, SOMEONE, is NOT telling me! I know what I see. I know what happens when I am around and there to witness it. But, if I am totally left in the dark about an issue, or something not right, then I cannot make an informed "reason" as to why something like this happens.
Now I do know a couple of "facts". First of all, this business about the government, the DEA, the entire realm of mess in Florida with pain clinics and seedy "quack" pain doctors etc.. has definitely put "fear" into lots of people, along with made a "Good medication" when USED CORRECTLY!, Look like a monster! But, as I said "used CORRECTLY"... IT IS LIKE anything else, if you "abuse" it, then it is Bad for you... or bad for whatever... Then you give "too much power" to some people in a place such as someone over the "legalities" of meds without any governing power over them to oversee what is done, is NOT harming some, and you get a freaked up pile of mess, that THE LEGITIMATE PATIENTS suffer needlessly from! There is NO reason, not one that any person that is truly a Chronic Pain Patient, that has NEVER abused anything, that has lived by their "pain contract", that has "passed" "tests" of whatever, all this time, or been treated like things are totally fine, only to be delivered a ridiculous letter, without any type of warning, without one sit down in front of you and explain WHY this is happening! IF anything is wrong with this, THAT POINT is what is MOST WRONG! WHY NOT have a CONVERSATION AND EXPLAIN this to a PATIENT, rather than take the "unprofessional" and just plain rude way, and not speak to them, not answer their emails, not answer a phone call, not ask them to come in and have a visit, nothing... and then you are also seeing their families??? Now how is that going to go? Like I said above, this situation puts me in such a horrid crack... I am stuck between first of all NOT KNOWING for SURE what is going on, only what I see and know... it puts me in a place of course of being upset, embarrassed, and thinking why should I see them if I could get the same treatment. Down the line a few months, and they stop refilling my medications? And I am not talking about pain medications, I am speaking of medications for my Lupus, my blood pressure, heart and so forth. If this doctor is leaving, or is "mad" at my family, or has something with us that he does not want to treat my family, then he should be professional enough, to just speak up face to face, and tell us what the hell the deal is! If I or my husband, or my Mom, have offended someone, or hell knowing this town, God only knows what kind of stupid "rumor" he has been told... because believe me this town is known for its lying, gossiping, half truths. People do NOT get the entire story, so they "make UP" what they want to... in which sometimes people's lives get frigged up due to a flat out lie being told. Before you open up your mouth when it involves anyone's "reputation" or their "good name", you had better give it deep thought, and then really understand what you could cause. If you are going to "stir up harsh feelings" or cause someone to be "smeared" and you are not sure what you are talking about, it is better to just keep your mouth shut, rather than say something you will harm someone with by being nosy. Small town are noted for that crap. One reason why I did NOT want to move back here... the small town mentality, the gossip, the "whispering" behind your back... those things I just cannot stomach. Since I have been trying now for 3 days to "finish" this and post it, I'm going to say it is "finished" enough to post & if I have further thoughts, I will just add it on and let you know there is a new "piece" under it...
Tuesday, August 20, 2013
Quality of Life - EVERYONE Deserves It!
I am
still so completely puzzled as to why all of a sudden with no warning,
all of this nightmare comes down on patients? Of course we have known
about Florida and all of the "fake clinics", "fake pharmacies... and
even the issue with WG I guess being fined for not watching more closely
about medications and who is getting them. But that STILL does NOT
explain WHY long-term, contract following, knowing
the medical records and health records well, having all the proof in
the world that a patient is definitely "in horrid chronic pain"..
doctors would be under so much pressure they absolutely STOP even
talking to their patients. Honestly, this makes things WORSE not better
at all! MOST patients if sat down and explained to that a doctor must
stop seeing them for the pain issues, but they will continue their meds
for a month, or help them at least step down a little on the meds until
they can get a physician, and tell people WHY in the heck it is
happening, you will get MORE FLIES with HONEY than with VINEGAR!! You
are talking about PEOPLE'S VERY CORE LIVES HERE!!! People in communities
that know everyone, and everyone seems to know everyone else's
business. And if you destroy their "reputation" by making it appear this
person is some kind of pusher etc... how do you expect that family,
that person to walk into their local stores? How are they supposed to
"work" and help make a living, if the pain is so bad they cannot? Who is
going to pay the bills? Who is going to be a "care taker" of someone
they have at home with many severe chronic health issues? PAIN often is
SILENT as far a just "seeing" a person out in public. Pain patients DO
NOT GO OUT when the pain is TOO BAD!!! THEY STAY BEHIND CLOSED DOORS
TRYING TO COPE! ONLY when a person "feels better", is having a "good
day" and the Illness (not just pain BUT OTHER SYMPTOMS WITH ALONG WITH
IT) are not as "obvious"... which makes things worse. If you "do not
look" ill, people assume you are "well'...I ask what does a chronically
ill patient supposed to "look like" in public??? Of course we have good
days, with less symptoms, and we cherish those days. We CAN possibly
make it to buy a few groceries, or pick up our medications. We can walk
around our yards, enjoying outside, we can go see a friend, or go out to
eat... but those days are rare and precious! So, think about when you
see someone you KNOW i chronically ill... I bet there are times YOU DO
NOT see them for days, weeks, even months.... IT is just not pain, it is
severe fatigue, severe stomach problems, severe headaches, brain fog,
fevers, not being able to be around "sick" people. other medications
that may make you feel lousy, hundreds of other issues besides "pain"
that keeps us "hidden" until we have a "feel somewhat human" day
again... The days that you go you do not even feel like taking a
shower.. the thought of just even putting your legs in just wears you
out, the days that you are on the verge of wanting to scream, sit in the
floor and cry, you beg God or anyone to help you, the double vision,
the scars from many surgeries, you can't be in the sun, you can't run,
you can't do things "normal" people do, you do not feel like putting
makeup on, or fixing your hair, or even seeing anyone. Your pale, your
unable to think, you can't even find words to describe what you are
trying to say, you drop things constantly, you can't remember where you
parked, or what your pin number is, or what stores's debit system works
which way. You have to make a list, to remind you of your lists of
lists, you have sticky notes all over the house to "remind" you of
everything. You battle all of the many demons of going to doctors,
taking a handful of pills (not pain but others) daily just to make sure
you don't get thrush, an infection, that your heart works right, that
your anxiety does not get the best of you, that your muscles do not
spasm so bad you can stand it, that the joints that are "not" replaced
yet try and work right... ALL things "chronically ill" deal with. Then
you have those with kidney failure, lung issues, heart issues, and if
you have had a HEART ATTACK then dealing with TOO MUCH PAIN for TOO LONG
can bring on ANOTHER MI! I was speaking with my Mom the other day, and
she talked about an article she read where a woman had been in so much
pain, for so long, and she was just not able to get anyone to help her,
that she jumped off a building. EVERYONE has their own "breaking
point"... Some have strong thresholds, other their thresholds for pain,
anxiety, and stress are much lower... and when you put a person that is
trying their best to deal with chronic illness and do the "right thing"
in order to have some type of quality of life, and you JERK AWAY the
very thing that gives them QUALITY OF LIFE, what do you think they are
going to do? There is going to be an epidemic of other health issues,
the stress and strain on chronically ill patients bodies is already over
the top. Then you bring in more stressors of life, like not being able
to get their proper meds, and that is enough to make them now want to
deal with it anymore... it is harsh, but it is the truth... as I said
everyone has their BREAKING POINT... So, this "battle" is not just about
medications for pain, it is about the very core of giving quality of
life to everyone.. And taking away something people honestly need to get
that much needed quality is just unfathomable at the very least...
Monday, August 19, 2013
Showing My Own Support of the "International Foundation for Autoimmune Arthritis" and the co-founder Tiffany Westrich
http://www.ifautoimmunearthritis.org/Home_Page.html
Please visit the URL above! This is just a wonderful Foundation that is helping by leaps and bounds in the World of Autoimmune Arthritis. The co-founder Tiffany Westrich is just an angel sent to all of us for sure. I want to help all I can to get the site and all of the information about them out to everyone. When you have a moment, visit their brand new website that is above. You can also join them on Facebook to keep up with ALL of their latest ways they are making a difference in the realms of autoimmune arthritis.
Rhia
Please visit the URL above! This is just a wonderful Foundation that is helping by leaps and bounds in the World of Autoimmune Arthritis. The co-founder Tiffany Westrich is just an angel sent to all of us for sure. I want to help all I can to get the site and all of the information about them out to everyone. When you have a moment, visit their brand new website that is above. You can also join them on Facebook to keep up with ALL of their latest ways they are making a difference in the realms of autoimmune arthritis.
Rhia
It Continues to Get WORSE for Legitimate Pain Patients!
http://hometestingblog.testcountry.com/?p=25926
This article is just one more example of how the "few" out there doing WRONG can make legitimate people's lives a living hell. I have seen more stories over the weekend of the very circumstance we are dealing with. IT continues to baffle the hell out of me though, as to WHY a family doctor, who has KNOWN you family for 5 or 6 YEARS... would just NOT SPEAK! No explanation, nothing... not a phone call, nothing but a "form" letter, that he probably did not even sign or read, just sent out like you were some stranger off the street. It is insanity! I know "they" as doctors have their own "reasons" as to why they handle things like they do. I have already went over all of that in my head. BUT!!! IT STILL does NOT make it RIGHT! AND it is the most unprofessional way to handle a patient I have ever seen. Now, due to him being my personal doctor and my Mom's, plus several others I know here in town, WE ALL feel very UNCOMFORTABLE GOING to him... yet after you are an ESTABLISHED patient... that has such a very long medical history with so many complications as I do, thinking about even trying to get another doctor to UNDERSTAND all of my ILLNESSES and treatments... is crazy! Sure they can, but who in their right mind wants to take what "is working", and try to make such a huge change???
If I were a patient that had the "usual" visits. Flu, normal things you go for, blood pressure, physicals, and the occasional stuff, going to a new physician is not that difficult. BUT, when you have SCORES OF symptoms, due to SEVERAL CHRONIC illnesses, trying to "train" (for lack of a better term) a new doctor is a job! It would take a new PCP months and months to even READ MY RECORDS! Much less understand ALL that my current PCP does for me... So, that is another huge issue.... This could be so different if it would have been handled properly. Now I am left in a lurch not really knowing how to handle it all. EVERYONE in that office has acted STRANGE EVEN before the letter went out... to my entire family... and we "felt" something wrong, but did not know what.... and how can I look him in the eye (I am supposed to see him for a follow up on Lupus next week) and in fact have blood work done tomorrow there at the office. If I don't have the myoglobin checked he probably won't refill my muscle relaxers.. see so it runs into huge issues with my own health.
Here is another article that appeared this weekend.... same thing
http://americannewsreport.com/nationalpainreport/my-story-pain-clinics-are-money-mills-8821277.html
This article is just one more example of how the "few" out there doing WRONG can make legitimate people's lives a living hell. I have seen more stories over the weekend of the very circumstance we are dealing with. IT continues to baffle the hell out of me though, as to WHY a family doctor, who has KNOWN you family for 5 or 6 YEARS... would just NOT SPEAK! No explanation, nothing... not a phone call, nothing but a "form" letter, that he probably did not even sign or read, just sent out like you were some stranger off the street. It is insanity! I know "they" as doctors have their own "reasons" as to why they handle things like they do. I have already went over all of that in my head. BUT!!! IT STILL does NOT make it RIGHT! AND it is the most unprofessional way to handle a patient I have ever seen. Now, due to him being my personal doctor and my Mom's, plus several others I know here in town, WE ALL feel very UNCOMFORTABLE GOING to him... yet after you are an ESTABLISHED patient... that has such a very long medical history with so many complications as I do, thinking about even trying to get another doctor to UNDERSTAND all of my ILLNESSES and treatments... is crazy! Sure they can, but who in their right mind wants to take what "is working", and try to make such a huge change???
If I were a patient that had the "usual" visits. Flu, normal things you go for, blood pressure, physicals, and the occasional stuff, going to a new physician is not that difficult. BUT, when you have SCORES OF symptoms, due to SEVERAL CHRONIC illnesses, trying to "train" (for lack of a better term) a new doctor is a job! It would take a new PCP months and months to even READ MY RECORDS! Much less understand ALL that my current PCP does for me... So, that is another huge issue.... This could be so different if it would have been handled properly. Now I am left in a lurch not really knowing how to handle it all. EVERYONE in that office has acted STRANGE EVEN before the letter went out... to my entire family... and we "felt" something wrong, but did not know what.... and how can I look him in the eye (I am supposed to see him for a follow up on Lupus next week) and in fact have blood work done tomorrow there at the office. If I don't have the myoglobin checked he probably won't refill my muscle relaxers.. see so it runs into huge issues with my own health.
Here is another article that appeared this weekend.... same thing
http://americannewsreport.com/nationalpainreport/my-story-pain-clinics-are-money-mills-8821277.html
Wednesday, August 14, 2013
Updating how the "Wolf" can "eat you alive" when it wants to....
I am not sure whether to laugh, cry, scream, be quiet, fade away, burn brightly or.... to just fall off the mountain top... and say to hell with it all. I guess I CAN FATHOM that others have just as MANY STUPID "Life" issues as myself and my family do. I have open eyes and an open heart to so many that are out here suffering in one way, the other... or several! Health issues, money issues, raising kids, jobs or lack of them, the rage, the horror, the outlandish behavior of other so-called "humans"... all frightening as have ever been. Mother Nature has put a "hurtin' on so many across our own nation, and furthermore across the world, even just trying to "digest" all of that is almost impossible. Droughts, fires, severe flooding, pests of all kinds, tornado's, hurricane's, high winds, hail the size of baseballs... I mean everywhere you turn, either some home is falling in a "sink hole", or things are so bone dry, all you see is dust. Then you look at another state, and they are so totally enveloped in floods that cars are floating down main street USA! How insane is that? Then the fires... it is just so difficult to watch, thousands upon thousands of acres of land burn up, and people lose everything, even their lives. Then we have the latest of a barrage of "transportation" evils. Trains, planes, huge buses full of people, all wrecking, reeking havoc for hundreds across the world. It seems every day you turn on the news, or read it online to see once again, yet another bus, train, plane, or even a 50 car pileup has completely blocked off major highways everywhere. That is just a "few" of our MANY, MANY dire straits of issues that as plan American folks, and Plain World people that we deal with daily. The pain, the suffering, lack of clean water, of food, of places to live, of money, of medications (how the HELL can WE as the "great" nation we are supposed to be running OUT OF SOME MEDICATIONS???? I am sorry but that sounds absolutely ludicrous. Look HOW MANY Pharmaceutical companies we have, and a pharmacy on EVERY CORNER even on all 4 corners in many towns, yet we CANNOT KEEP A INVENTORY OF MEDICATIONS WE NEED???? NO, more like if they cannot MAKE A FORTUNE ON IT, they "CUT" OFF THE SUPPLY... in other words , GREED!!!!! This is not including the RIDICULOUS RED TAPE MESS, our Insurance companies, hospitals, clinics and doctors are in... along "in bed" with the pharmaceutical companies, that bunch in Congress, that have their own agenda and the "lobbyists" that contribute to fuel the GREED of this nation! Every time I think about HOW SOME FOOL BEHIND A DESK can TELL ME WHAT I NEED MEDICALLY AND DO NOT NEED MEDICALLY OVER MY OWN PHYSICIAN it BURNS ME TO NO END!!! What the hell do we have physicians for, if some pencil pushing, not caring if you die, person, that does NOT even know a medical term or what the name of a medication or procedure is, much less what it is for, tell US and our DOCTORS what to do??? IT is one sad damned day in America, that is what it is!!!! OF course, then you have the entire other side, of those doctors, hospitals, and so forth that are just as screwed up as the people behind those desks. Never in my 53 years here have I ever seen a bunch of incompetent jack asses trying to half do a job that they have no clue about. I am not A GENIUS BUT!!! I can tell you that myself, along with MANY, MANY of US know more about the world of MEDICINE AND HEALTH, more than some of the nurses, and others that are supposed to be "taking care" of us!!! Talk about scary!!! It is down right a nightmare if you think about it.... Now, I am NOT one normally to be down and out about everything, but this past 8 plus weeks for myself and my family along with a few of my good friends have SUFFERED WAY TOO MUCH... and yes I QUESTION WHY???? I try NOT to question things, and to realize life is what it is going to be. We have SOME CONTROL, but many times we have very LITTLE OR NO CONTROL, when it comes to life and it's good, ugly, nice, down right hellish, and indifferent. I have literally spent HOURS AND HOURS ARGUING WITH People because THEY DO NOT DO THEIR JOBS! Sending myself, or my Mom bills that they DO NOT file RIGHT WITH THE INSURANCE COMPANIES, then EXPECT US TO PAY! That is bull! File it right, you WILL GET PAID! But, I do not think there has been ONE CLAIM THIS YEAR, THAT HAS BEEN FILED PROPERLY! Every doctors office, the hospital, the pharmacy, you name it, has filed something wrong, then tries to collect from us!!! If they would just do their jobs RIGHT, then it would take SO MUCH STRESS OFF OF US!!! IF I WANT TO FILE MY OWN INSURANCE THEN PAY ME AND I WILL DO IT RIGHT THE FIRST TIME!!!
I do question the entire process of "why BAD things have to happen to the "best" folks???? It makes no sense to me these days. The greedy, the ones that could care less about their fellow man, that treat others like trash, that live their lives in a gutter so to speak, seem to "breeze" by... Only to have those of us who, DO GIVE a damned about others, we try and treat people with kindness and compassion, we do NOT live our lives as if we were the only people on the planet, we work, pay our bills, and do all of the "right" things, seem to be hit the hardest with illness, pain, suffering, stressful life situations, and we do NOT DESERVE IT! A dear friend of mine is going through a horrible time fighting the big "C" word again. Bless her heart, she already did that at a very young age, back when we were just youngsters, and she won the battle. NOW, here she is years later, battling the monster again. She is the kindest, sweetest, compassionate, gentle soul, that takes care of her family in every way... and she just does NOT deserve to go through this again... no way, no how.... yet here she is having to once again walk through the hot coals of chemotherapy, and yet still trying to put on a happy face and work! It breaks my heart honestly. I also had a girl I have known since I also was in High School that I saw about 3 weeks ago. Her family and my family were close during those years when we were kids. Our Dad's worked together, we went on weekend trips to the lake together, they hunted deer together... and now her Mom is going blind from macular degeneration... and if that is not bad enough, the woman, who is several years younger than me, has Parkinson's! We are talking about someone in their mid-40's!!!! What makes that even worse, and I did not know it until I saw here a couple of weeks ago, she lost her husband last year to an aneurysm, as they were driving down the highway, he died right there beside her in the passenger seat!!!! Talk about wondering why?? Her Dad already has Alzheimer's, and honestly I think he may be so bad he is either in a nursing home, or he may have passed away, but I was so taken aback by all of the other things she told me, that I felt uneasy even asking. Even though this is a small town, sometimes since I don't get out all the much, I miss out own things going on to others.
Pieces of me feel like they are just "floating away" these days. I feel as if the very "substance" of my own heart and soul that I have walked in, with faith as much as I can, has just taken another road, journeyed away from me... and pieces of that are also my "voice" that has always given me the "right words" to write... it is like that "voice" has been silenced by too much of life's horrible drama. I so looked forward to possibly putting out my 3rd book in a year or so, but now I question whether that will EVER COME TO PASS AT ALL. I truly felt that I had SOMETHING TO GIVE TO OTHERS, through MY WORDS FROM MY HEART, yet somewhere down the line, "my" plans have been altered... so I am just not myself these days... I feel as if I am SOME OTHER person... I do not even recognize myself anymore... not so much in a "physical" sense, but in a sense of "the core center of who I was"... that seems to have "left the building" as that old adage goes.... much like "Elvis"... who I was, seems to not be who I am now... I can "blame" it on illness, pain, drama, life's little nightmares that can change your entire outlook in the blink of an eye".... some good, yet for me, I see it as not good at all... where it that writer, that "creative" entity... I miss her... I miss "Me"... I spend more time trying to "get well" that I spend being "well"....
I have FINALLY my Rheumatologist's Appointment this morning!!! HOOORAY!!! I pray he can help, and he usually does. I have missed not seeing him in over 6 months, so I cannot tell you how LONG MY LIST IS FOR HIM!!! There is LOTS AND LOTS OF FLOOD WATERS that have flown under my bridge since he saw me last. I DID email him some of my issues, and some information last week. I felt the MORE he knows BEFORE I get there, the more fruitful our appointment will be. Alas, I just hope we do have enough time to discuss all that is happening. I believe from an email I received back from him last week, I will be going on an infusion of Rituxan rather than the Humira. Or I gather I will stop the Humira, and only take the Rituxan. I pray it helps to reduce all of this pain, swelling, and mainly damage that is happening from the RA!!! Then I have lots of other things like those two other osteoporosis medications I found out about last week, I want to discuss. If I can take them, and have a chance of doing anything to remotely halt my bones from growing any weaker than they already are, then injections it is. I already take them anyway, so I might as well as 2 more in, that is if it is right now me. Of course there is all of the other pain stuff, joint stuff, and the list is endless to kind of go over... but if we can get at least the RA meds changed over to something else, and get me on those osteoporosis meds... plus I am sure he will have some answers on other things for me... I will be happy...
Then tomorrow, I go to the "foot" doctor... she is taking a look at my big toes, ankles etc... and we are going to see if I need "tarsus tunnel" surgery in my big toes... from the tests it appears that night help so we shall see... From there Friday, I go to have a CT scan on both hips... yes, that one will cost out of butt... they now charge a fortune even with insurance for the damned things... but since my hips seems to be so sore, and giving me hell even after the injections a couple of weeks ago, it could be they are causing lots of the issues I have with my lower back, legs and hips.
AND if things are not bad enough!!! I FOUND OUT MONDAY, that this TOP FRONT TOOTH, THAT GOT busted off half in two in the 4 wheeler accident when I was about 25, is now loose, and has enough decay, that it is no LONGER PATCHABLE!!! My dentist had to tell me I am going to be looking at a ROOT CANAL AND CROWN! I almost DIED, FAINTED, PASSED OUT, AND FREAKED, when I called for A PRICE FOR THOSE!!!!! How the HELL DOES ANYONE AFFORD A ROOT CANAL AND CROWN!!!?????? Lord have mercy, that is like buying a damned car!!! I do not know what I will do on that one... the "cheapest" I found was about $1,600.00 FOR BOTH! I called even "Monarch Dental" and hell they wanted something like well over $2,300.00 OR MORE FOR THE TWO OF THEM!!! Hell I thought they were supposed to be "discounted"... It is insanity... but I have NO PLACE to have a "partial plate" to Hook onto, due to my bad teeth that have just been pulled in back due to the Sjogren's... and I was told if I had them all pulled, the Sjogren's would also cause me grief with a plate... due to the dry mouth... so it is damned if I do, and damned if I don't... I am just baffled over that one...
Well, I shall just stop for now... lots of other stuff I could go into, but I want to get some other stuff done today, since I will be once again in and out the rest of the week with tests and doctors... damned I am over sick of it all... Hugs to all... thank you everyone for your compassion, kindness and friendship.... Hugs, Rhia
I do question the entire process of "why BAD things have to happen to the "best" folks???? It makes no sense to me these days. The greedy, the ones that could care less about their fellow man, that treat others like trash, that live their lives in a gutter so to speak, seem to "breeze" by... Only to have those of us who, DO GIVE a damned about others, we try and treat people with kindness and compassion, we do NOT live our lives as if we were the only people on the planet, we work, pay our bills, and do all of the "right" things, seem to be hit the hardest with illness, pain, suffering, stressful life situations, and we do NOT DESERVE IT! A dear friend of mine is going through a horrible time fighting the big "C" word again. Bless her heart, she already did that at a very young age, back when we were just youngsters, and she won the battle. NOW, here she is years later, battling the monster again. She is the kindest, sweetest, compassionate, gentle soul, that takes care of her family in every way... and she just does NOT deserve to go through this again... no way, no how.... yet here she is having to once again walk through the hot coals of chemotherapy, and yet still trying to put on a happy face and work! It breaks my heart honestly. I also had a girl I have known since I also was in High School that I saw about 3 weeks ago. Her family and my family were close during those years when we were kids. Our Dad's worked together, we went on weekend trips to the lake together, they hunted deer together... and now her Mom is going blind from macular degeneration... and if that is not bad enough, the woman, who is several years younger than me, has Parkinson's! We are talking about someone in their mid-40's!!!! What makes that even worse, and I did not know it until I saw here a couple of weeks ago, she lost her husband last year to an aneurysm, as they were driving down the highway, he died right there beside her in the passenger seat!!!! Talk about wondering why?? Her Dad already has Alzheimer's, and honestly I think he may be so bad he is either in a nursing home, or he may have passed away, but I was so taken aback by all of the other things she told me, that I felt uneasy even asking. Even though this is a small town, sometimes since I don't get out all the much, I miss out own things going on to others.
Pieces of me feel like they are just "floating away" these days. I feel as if the very "substance" of my own heart and soul that I have walked in, with faith as much as I can, has just taken another road, journeyed away from me... and pieces of that are also my "voice" that has always given me the "right words" to write... it is like that "voice" has been silenced by too much of life's horrible drama. I so looked forward to possibly putting out my 3rd book in a year or so, but now I question whether that will EVER COME TO PASS AT ALL. I truly felt that I had SOMETHING TO GIVE TO OTHERS, through MY WORDS FROM MY HEART, yet somewhere down the line, "my" plans have been altered... so I am just not myself these days... I feel as if I am SOME OTHER person... I do not even recognize myself anymore... not so much in a "physical" sense, but in a sense of "the core center of who I was"... that seems to have "left the building" as that old adage goes.... much like "Elvis"... who I was, seems to not be who I am now... I can "blame" it on illness, pain, drama, life's little nightmares that can change your entire outlook in the blink of an eye".... some good, yet for me, I see it as not good at all... where it that writer, that "creative" entity... I miss her... I miss "Me"... I spend more time trying to "get well" that I spend being "well"....
I have FINALLY my Rheumatologist's Appointment this morning!!! HOOORAY!!! I pray he can help, and he usually does. I have missed not seeing him in over 6 months, so I cannot tell you how LONG MY LIST IS FOR HIM!!! There is LOTS AND LOTS OF FLOOD WATERS that have flown under my bridge since he saw me last. I DID email him some of my issues, and some information last week. I felt the MORE he knows BEFORE I get there, the more fruitful our appointment will be. Alas, I just hope we do have enough time to discuss all that is happening. I believe from an email I received back from him last week, I will be going on an infusion of Rituxan rather than the Humira. Or I gather I will stop the Humira, and only take the Rituxan. I pray it helps to reduce all of this pain, swelling, and mainly damage that is happening from the RA!!! Then I have lots of other things like those two other osteoporosis medications I found out about last week, I want to discuss. If I can take them, and have a chance of doing anything to remotely halt my bones from growing any weaker than they already are, then injections it is. I already take them anyway, so I might as well as 2 more in, that is if it is right now me. Of course there is all of the other pain stuff, joint stuff, and the list is endless to kind of go over... but if we can get at least the RA meds changed over to something else, and get me on those osteoporosis meds... plus I am sure he will have some answers on other things for me... I will be happy...
Then tomorrow, I go to the "foot" doctor... she is taking a look at my big toes, ankles etc... and we are going to see if I need "tarsus tunnel" surgery in my big toes... from the tests it appears that night help so we shall see... From there Friday, I go to have a CT scan on both hips... yes, that one will cost out of butt... they now charge a fortune even with insurance for the damned things... but since my hips seems to be so sore, and giving me hell even after the injections a couple of weeks ago, it could be they are causing lots of the issues I have with my lower back, legs and hips.
AND if things are not bad enough!!! I FOUND OUT MONDAY, that this TOP FRONT TOOTH, THAT GOT busted off half in two in the 4 wheeler accident when I was about 25, is now loose, and has enough decay, that it is no LONGER PATCHABLE!!! My dentist had to tell me I am going to be looking at a ROOT CANAL AND CROWN! I almost DIED, FAINTED, PASSED OUT, AND FREAKED, when I called for A PRICE FOR THOSE!!!!! How the HELL DOES ANYONE AFFORD A ROOT CANAL AND CROWN!!!?????? Lord have mercy, that is like buying a damned car!!! I do not know what I will do on that one... the "cheapest" I found was about $1,600.00 FOR BOTH! I called even "Monarch Dental" and hell they wanted something like well over $2,300.00 OR MORE FOR THE TWO OF THEM!!! Hell I thought they were supposed to be "discounted"... It is insanity... but I have NO PLACE to have a "partial plate" to Hook onto, due to my bad teeth that have just been pulled in back due to the Sjogren's... and I was told if I had them all pulled, the Sjogren's would also cause me grief with a plate... due to the dry mouth... so it is damned if I do, and damned if I don't... I am just baffled over that one...
Well, I shall just stop for now... lots of other stuff I could go into, but I want to get some other stuff done today, since I will be once again in and out the rest of the week with tests and doctors... damned I am over sick of it all... Hugs to all... thank you everyone for your compassion, kindness and friendship.... Hugs, Rhia
Monday, August 12, 2013
When a "good" situation goes HORRIBLY wrong - finishes up from FB posting....
It is from his personal doctor, who he has been seeing now for over 5 YEARS... maybe more... almost since we got to TX.. and we got here in 2005... well, basically, due to THEIR ISSUE, WITH NOT DOING A PROPER TYPE OF LAB WORK!, they arbitrarily decided to send him a KISS OFF LETTER... BASICALLY... in other words... because the "lab work" was DONE IMPROPERLY, rather than checking it out TO FIND OUT WHY IT WAS "NOT RIGHT"... THEY send him a letter, saying "I WON'T SEE YOU ANYMORE"... NOR PRESCRIBE YOUR MEDICATIONS YOU NEED! Now WHY in the HELL would ANY PHYSICIAN with ANY GOOD RELATIONSHIP with a LONG TERM VERY WELL KNOWN PATIENT, THAT has been there forever... and DOES TO THE LETTER whatever this doctor asks.... AND PAYS CASH.. he has NO INSURANCE... just decide NOT TO TALK TO YOU..Not to have you come into the office, JUST HAVE SOME CERTIFIED FORM LETTER SENT TO YOU ON A FRIDAY, so the OFFICE IS CLOSED... and ALLOW A PATIENT TO NOT ONLY BE TORE UP, DISMAYED, PUZZLED, AND ASKING WHAT THE HELL IS GOING ON???? It is BEYOND ME! It is INSANITY!! I do KNOW... THAT THERE IS SOMEONE IN THE OFFICE, THAT DOES NOT care for "us".... and I also know they can be in a position to CAUSE MAJOR ISSUES, due to the position that they play at that doctors office... and it would NOT surprise me IF THEY DID NOT HAVE SOMETHING TO DO WITH ALL OF THIS... Need less to say, IT HAS CAUSED Jim MORE GRIEF TO THE PLACE HE HAS ME HORRIBLY WORRIED... he is BEING ACCUSED TO SOMETHING THAT IS NOT ANYTHING BUT A HORRID LIE!!! AND A JOKE... but IT HAS BEEN TO THE PLACE OF BEING SO UPSET on TOP OF MY OWN ISSUES WITH HEALTH, that I fear I am going to have another HEART ATTACK!!! I am beyond with words upset over all of this... I FEAR EVEN POSTING THIS... because I KNOW THIS TOWN TOO WELL!!!!! (and we are talking about medications that Jim needs... blood pressure, cholesterol, (Anti-depressants, his stomach meds and the meds he takes for his lower back, that without he cannot work!) After all of the research I did online, I found out, that WE PAID FOR THE RIGHT TEST! and these results have been in now for 2 WEEKS... yet we just get this stupid letter this past FRIDAY! WHAT IS UP WITH THAT?????? We have copied documentation from several sources, he has written a long letter about this entire ordeal, attached with the "lab work" done wrong (and it even says it was NOT done as it should have been), and taken it to this office today)... Please continue to pray for us... this is just not good at all.... We KNOW what WE ARE DOING IS RIGHT... but a doctor can make or break you... if they want... or someone else in their office with the "right" or "wrong" power... can make your life a living hell....
Saturday, August 10, 2013
Grand Showing over the next couple of Nights! The Perseids Are Back!!!
The Perseid's are back! They are supposed to be spectacular, and peak on Sunday and Monday with 100 or more an hour! Thought I would share some information for those of you who are night owls and might enjoy the "show"....
http://www.nasa.gov/connect/chat/perseids_2013.html#.UgXc8FOUXgBPerseids Meteor Showers
http://earthsky.org/astronomy-essentials/earthskys-meteor-shower-guide
http://www.nasa.gov/connect/chat/perseids_2013.html#.UgXc8FOUXgBPerseids Meteor Showers
http://earthsky.org/astronomy-essentials/earthskys-meteor-shower-guide
45 Tips for Life (saw this in FB and wanted to share)
I saw this in FB just a little while ago in one of my groups, and it just seemed to "fit" after the week from hell I, along with several have had... thought it might help you also get through a rough patch of the "stickers" of life... :)
45 Tips For Life
1. Life isn't fair, but it's still good.
2. When in doubt, just take the next small step.
3. Life is too short – enjoy it.
4. Your job won't take care of you when you are sick.
Your friends and family will.
5. Pay off your credit cards every month.
6. You don't have to win every argument.
Stay true to yourself.
7. Cry with someone.
It's more healing than crying alone.
8. It's OK to get angry with God. He can take it.
9. Save for retirement starting with your first paycheck.
10. When it comes to chocolate, resistance is futile.
11. Make peace with your past
so it won't screw up the present.
12. It's OK to let your children see you cry.
13. Don't compare your life to others.
You have no idea what their journey is all about.
14. If a relationship has to be a secret,
you shouldn't be in it.
15. Everything can change in the blink of an eye
But don't worry; God never blinks.
16.. Take a deep breath.
It calms the mind.
17. Get rid of anything that isn't useful.
Clutter weighs you down in many ways.
18. Whatever doesn't kill you really
does make you stronger.
19. It's never too late to be happy.
But it’s all up to you and no one else.
20. When it comes to going after what you love in life,
don't take no for an answer.
21. Burn the candles, use the nice sheets,
wear the fancy lingerie. Don't
save it for a special occasion.
Today is special.
Over prepare, then go with the flow.
23. Be eccentric now.
Don't wait for old age to wear purple.
24. The most important sex organ is the brain.
25. No one is in charge of your happiness but you.
26. Frame every so-called disaster with these words
'In five years, will this matter?'
27. Always choose life.
28. Forgive but don’t forget.
29. What other people think of you
is none of your business.
30. Time heals almost everything.
Give time time.
31. However good or bad a situation is,
it will change.
32. Don't take yourself so seriously.
No one else does.
33. Believe in miracles.
34. God loves you because of who God is,
not because of anything you did or didn't do.
35. Don't audit life.
Show up and make the most of it now.
36. Growing old beats the alternative --
dying young.
37. Your children get only one childhood.
38. All that truly matters in the end is that you loved.
39. Get outside every day.
Miracles are waiting everywhere.
40. If we all threw our problems in a pile
and saw everyone else's, we'd
grab ours back.
41. Envy is a waste of time.
Accept what you already have not what you need.
42. The best is yet to come...
43. No matter how you feel,
get up, dress up and show up.
44. Yield.
45. Life isn't tied with a bow,
but it's still a gift."
Friday, August 9, 2013
Dealing with the Realms of Brain Fog
http://www.lupus.org/webmodules/webarticlesnet/templates/new_magazineback.aspx?articleid=3011&zoneid=67&utm_source=Newsletter+8-6-13&utm_campaign=Newsletter+8-6&utm_medium=email
The link above is about "cognitive issues" when it comes to Lupus and learning to cope with them... thought this was a great article, and may help to explain all of the "brain fog" and so forth we endure....
The link above is about "cognitive issues" when it comes to Lupus and learning to cope with them... thought this was a great article, and may help to explain all of the "brain fog" and so forth we endure....
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