As I watched the Night New last night, and once again, the "fight" over Health Care, continues to cause many, many of us terrible stress. Either we are ill, or have children or other family members ill, or cannot afford the outrageous and constantly rising costs of healthcare and health insurance.
Believe me, after the hip fractures last December, then the cervical neck surgery this past April and the RIDICULOUS CHARGES FROM MY DOCTORS, FOR A CERVICAL BONE STIM DEVICE, TO the the rest of the charges from an ambulance, to the radiologists, the anesthesialogists, to medications, and more, it is like that governments just soon us to "die" rather than "burden" the nation with our chronic health problems.
But, look at "John McCain"... you can bet the government is making sure he has the very, very best care, and all of what he needs to hopefully survive the tumor they found. Which of course I hope so also. I "no matter what "party" I lean towards" would not want anyone in our governments bodies to be ill and pass away.
But, those Congress men and women, and all of our governmental people get the best care the rest of their lives. Even after they are no longer involved and "retire" they still are well taken care of, with pensions, healthcare and benefits.
Which I am not putting down, BUT WHAT ABOUT ALL OF US THAT ARE HERE SUPPORTING THEM? Their own constituents that are the ones that "vote" them in? I am sorry but our President is just not the right person for the job. Not when it comes to many things, he just does not know or understand how to handle. And this constant "tweeting" of major information I feel is somewhat ridiculous. Not ALL that goes on, due to many reasons, needs to be "tweeted" over the world!!!!!
Here is my post from Facebook, as to what I went through last week with doctors and now more health issues that I am fighting with...
I'm totally exhausted! Yesterday having 2 doctors appts in Dallas, that
were scheduled one for early morning and the other mid afternoon in two
totally different locations, about got to me this morning. But, my son
and I did have a great time together. I was glad he went. We got to talk
about lots of things, as well as he got to see my Rheumatologist and my
Pain Dr. whom he had not met either. I wanted him to witness himself
what fantastic doctors I have, and he immediately saw that my
Rheumatologist was truly a "God-send" as well as my Pain Doctor also.
But, now my Rheumatologist wants me to see another "specialist" which I
did not even know existed, which is a Metabolic Mineral and Bone
Specialist, mainly due to the Osteoporosis, in which he was extremely
concerned due to those that have "fractures of the hip" especially due
to osteoporosis, have a 20% HIGHER mortality rate than those without one
and without osteoporosis, plus just having the RA and Lupus, already
leads me into a higher possibility of not "living as long" as others
without it. This doctor also may have other options to "treat" the
osteoporosis, and may provide answers about why I'm having the "chilled
totally drenching night sweats, since this could be related to an
"insulin" problem with my metabolic systems, which can be a
"parathyroid" which is NOT related to regular "Thyroid conditions" and
other issues that may lead us to find out more about chronic health
illnesses, that maybe what I could be having and don't know it. So, I
have to have another bone density scan next week on Tuesday, then
schedule an appt with the specialist at at SW Med Center in Dallas.
I
have to have the scan and results to take with me, so I am waiting
before I schedule the appt. Hopefully it will be soon, so we can find
out what could be going on, which as he also said, I am a very
"complicated" patient, which ALL of my doctors say, so we shall see.
Then I had my pain ump refilled, and I guess i should have "insisted" he
up my meds. I am in so much pain again today, I am about in tears.
Also
he thinks my finger problems, are eczema, so he called in some oinment
for those increased my Sulfasalazine, by 500 mg more twice daily, and if
we don't see results in 2 months then we probably will move on to
Acterma for the RA... the Enbrel may not be dong it's job, if by 2 more
months I am not much better. So, again a med change... probably....
anyway, lots going on, and I hurt like hell... but I've got to get out
briefly for a couple of things, then I hope to have myself on the sofa.
We have yet another horribly hot day with "heat warnings, again... for
about the 5th day.... I will probably not post much more today, just
wanted to let you know a bit about my appts yesterday...