Well, I am just going to be straight forward…there is no
NIH (National Institute for Health) in Parker’s near future. Although his doctor made every effort to get
him in and even though she talked to the lead doc there, it seems that because of the 17
week long government shutdown, they are now very backlogged. They are only taking
kids that fit criteria for one of their studies. She did ask the doc to ask other docs if
anyone would be interest in a “very unique” kiddo; so he is posting on their JA
doc groups.
Parker was quite upset with this news; we
are, however, please that Parker’s health has had some improvements. His lungs have improved and pulmonology is
happy that capacity is increasing. And
he has not had any other internal organ involvement in quite some time. For this, we are incredibly thankful. He is still in incredible pain; having skin
issues off and on (minor vasculitis, rashes); fevers come and go but are not as
high; and he has some joint swelling, but ankles are not as constantly huge as
they use to be. We do feel that the
Rilonacept has slowed the progression of this disease. And we are pleased with this drug in
combination with prograf and his hizentra weekly infusions; it seems to be a
pretty decent combo for him. Of course, we
wish it was even better, but we are pretty pleased with the progress because it
has kept him out of the hospital and he has had less illness. This is a huge blessing.
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Parker is now seeing a local pain management doctor (this
is doctor number 13…jeeze louise). He is
totally on the same page as us and wants to work on getting Parker off the
narcotics and use other routes to help with pain. He did two rounds of tests with him and it
looks like he is a candidate for nerve ablation. We are seriously considering this for his
back. For the first time, in about 5
years, Parker had zero pain in the area the tests were done and it held for
about 4.5 hours. He told this doctor
through tears, "thank you for the best Christmas present ever". Of course, the doc and I got all teary with
him. We are also going to discuss his
ankles further because his rheumy is wondering if botox injections in his
ankles would help. Through PT, he has
had much improvement but his range of motion is still quite limited due to the destruction
that has already occurred in his ankles and she feels botox might help.
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So in closing, we are so very proud of our two boys. Logan continues to push through dual
enrollment and loves his college classes.
And Parker is juggling massive amounts of medical appointments…Yesterday,
he went to PT even though he felt miserable (a little concerned he might be sick)…
On the way home from PT, I think Parker summed it up best when he said “I am
who I am, and I am really strong!”
Parker and Logan, you inspire me! Happy New Year!Love and Prayers, Cathy Stone
ReplyDeleteRochelle- Logan's eyes look just like Grant's with episcleritis- it is a vascular issue, and it usually tells us a flare is on the way. We have been lucky in that when we see it, we can tweak meds, and normally avoid one. Silver lining, right?
ReplyDeleteHi, I have a few questions about how you deal with and learn about JA issues. If you could, please email me at mtrucillo(at)recallcenter(dot)com when you see this. Thanks!
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