This is the end of a very sad and
somewhat stressful week. We buried Gabe's and our next-door neighbors
son. Granted all we had to do was attend the funerals and do small
chats survivors but still that is a lot of stress. This week I found
out also, that because my insurance started over again in July (July
1 begets the new insurance year meaning that I have to paydown the
co-pays or whatever). I knew this was going to happen but the
application of having to paydown everything again is mind-boggling
and stressing when you figure that also includes my physical therapy.
So each visit right now in the new insurance year my responsibility
would be $35. I know $35 not seem like a lot but it is when having to
deal with homecare attendants, catheters and all the other crap that
I am buying support disability I just couldn't do it in. Add on top
of that that pesky pleader I have in my ass, hemorrhoid that bleeds
is beginning to bleed worse and worse. Where this bleeding is not
necessarily painful is certainly disconcerting and means some sort of
medical intervention which means some out of pocket pay.
As I mentioned my new insurance year
started July 1. I've been doing therapy, physical therapy for the
past five or six months. I have been fortunate in that I've gone way
beyond the 12 visits my PEHP offered thanks to SB 400.SB 400 Is a
piece of Utah legislation which helps people who cannot pay for their
physical therapy and other things. Essentially free therapy and I was
getting it. That stopped July 1 and I will not be eligible until I
meet by deductible so when my therapist told me that on Tuesday I
quietly, inside my head, freaked out. Really really think I can do is
to quit my physical therapy which I did. My therapist had told that I
was still making progress in my therapy goals but was getting close
to the plateau or for justification to work with me to the
insurance/SB 400 funds. I Must confess I have become used to getting
physical therapy. Not only has been getting the therapy's been nice
but enjoy the interaction with the staff has been sent to. We really
begin to get the illusion a family and belonging but nothing like
having the dollars run out to sever those ties quickly. So before
Kristen to tell me to stop coming I concluded by therapy visits
yesterday. Kristen was quick to say that I had not reached the
plateau yet but she also understood the financial strain that
out-of-pocket pay causes a family like ours. So now I am without
physical therapy. I will continue to attend Wellness can take
advantage of equipment and professional trainers and even some of the
other folks who are at wellness. Now I don't know what will happen
next month when supposedly Medicare will kick in and I should have
double coverage. I'm going to have to do lots of catch up.
Because of the Medicare opportunity
coming up we decided to postpone the visit with daily MD for later
this month but found the closest opportunity to see daily now is the
end of September. This greatly influenced Dianne who I think sunk
into depression for the rest of the day and was kind spooky for me to
because I think something else begin to happen with the old stenosis.
I'm beginning to bleed profusely from the rectum is just another
thing to begin the wear on me another thing I can't really consider
until August 1 and Medicare.
For whatever reason I'm having some
issues sleeping not going to sleep but waking up when I catheterize
during the night just can't get back to sleep.. Some nights are worse
than others in Asia make it to the day just fine but I sort of things
some of this is indicative of the stress is going on my life right
now. But just to be sure I still quite in love with my life and my
wife and my family. I think this depression is just situational And
passing.
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