My name is Jaci, and we were the lucky family that got to meet Vicki, Tom & Ryan when they came to DC in January. We just visited Dr. Smith again yesterday at NIH, Emily goes in next Wed. for her routine EUA, Dr. Smith wants to do a biopsy as well, so she can study the cells in her eyes more closely. She is also going to give us a referral to see Dr. Winer the endo dr. as well. Emily has been doing great, we really have had an uneventful year, compared to others. (knock on wood). Emily just turned 9 last Friday too! For those that don't know us, Emily was diagnosed with APECED 5 years ago, after showing symptoms for 9 months before then, and no one could figure out what was going on, after sending us to different doctors. Luckily, once we moved to this area, it all was figured out. My husband is in the army, so we see drs. at Walter Reed,
which have been great, we see several endocrinologists there. Emily has hypoparathyroidism, hypothryoidism, photophobia, vitilago, ??...ok, and I know I am forgetting some other things too, obviously not to prevelant though.
looking forward to meeting more of you in this group.
Vicki, I still need to send you those pictures from when you were here, I will look thru my computer and try to send them now, so I don't forget.
Happy Easter!!
Jaci :-)
----- Original Message ---- From: Vicki Robson <vrobson1@...> To: apeced@yahoogroups.com Sent: Saturday, March 10, 2007 3:07:09 PM Subject: Re: [apeced] Re: Hi
HI Linda,
The IVIG sounds great. Thanks for telling me about it. I will search IVIG and Apced, so I can tell his endo all about it. You are so lucky to have Dr. Maclaren nearby. He sounds wonderful! I really wish we had a proactive endo who was knowledgeable about APCED. You would think with our large Medical Center here in Houston, we would! I am questioning Ryan's endo's treatment since we visited the NIH, and Dr. Winer changed his medication and dosages, and the diagnosis of osteoporosis. I am so glad Tara is doing better, and hope the IVIG will help her gain her weight back. Ryan has gained weight since being over medicated on prednisone. He was always tall and thin,(6'2"), but now is about 15-20 lbs overweight. I do believe Ryan was tired quite often while on the Imuran, and I remember he had several eye infections as well. He decided to take this semester off from school to do his microsoft
certications instead. He is also working with his dad at our business and is getting a great deal of experience being their Tech Guy, and creating websites for clients. He hopes to return to school next semester. I understand when you say Tara has an amazing spirit of optimisim. Ryan seems to have the same. Take care, and talk to you soon, Vicki --- lsquittman <lsquittman@optonlin e.net> wrote:
> Hi Vicki, > Tara's liver function tests were occasionally > elevated but this is the > first time they have been elevated for so many > months. The IVIG > cleared up most of her problems last time for two > years but it took > two rounds of infusions. She is not having constant > watery diarrhea > and is absorbing her medication but she is painfully > thin and Dr. > Maclaren feels it will stop
the diarrhea altogether > and she will be > able to gain weight. It should also help the liver > function return to > normal boosted by the Imuran. And it provides > immunity against > infection. If you do a search -IVIG and APECED or > APS1 you will see > that other people with APS 1 and autoimmune problems > have benefitted > from this treatment. Can't hurt. > Was Ryan unusually tired when he was on the Imuran? > That seems to be a > major problem and Tara has frequent stomach aches > which she never had > with the malabsorption. > The thing that keeps me going is all the research > being done, the fact > that she finally has a doctor who is proactive and > really knows what > to do and Tara's amazing spirit of optimism. > I wish Ryan all the best. How are his studies > going? > Best wishes, > Linda > >
> > >
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