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Recent Entries

Post 111 - By: Nikkole Grissom - Post Date: 8/11/2010
Dr. George is my Hero....I own my life to him
Post 112 - By: Michele - Post Date: 8/1/2010
What a wonderful website and your explanation of TTP-HUS was so easy to understand. I will certainly be giving it to our pediatricians. Our son was 15 months old(now 5) when he was in ICU with TTP. Since then we have moved and doctor after doctor is not comfortable giving our son his immunizations. He had no renal involvement. He had Plasma Pheresis for five days, a platelet transfusion and two blood transfusions. Do you have any documentation of problems after discharge that might be linked to having TTP? My son has severe constipation since the hospital stay, as well as, white spots(like vitiligo) and patches on skin. He is still easily tired and looks pale at different moments. We understand that a relapse is unlikely but, as you know from your studies, you are always on the look out. We were told IF it would happen, it would happen within 8 years but it would be highly unlikely to have another episode. He was at Miami Children's Hospital.
Post 113 - By: Patricia Pogue - Post Date: 7/20/2010
Very informative and useful information
Post 114 - By: Amanda M - Post Date: 7/19/2010
I am 25 and was diagnosed with TTP in Dec 04, relapsed in Aug 05'. I had 4 rounds of weekly rituximab. I was okay for 4 years then relapsed again May 09' two days after the birth of my daughter. I also had Preeaclampsia and HELLP. I then relapsed again in Nov 09. Then I had 4 weekly treatments of the rituximab. It is a difficult disease to keep relapsing, but we muct keep our heads up! I also wanted to say that in my experience I feel the rituximab helps to keep me in remission. Thank You Amanda Boston MA
Post 115 - By: Barbara - Post Date: 7/18/2010
My 63 year old sister passed away this Last Wed from TTP. She had been in ICU for only one week - she received 6 plasma pheresis treatments , steroids, & anti biotics -her platelets went up from 10,000 to 40,000 after the first few plasmapheresis treatments then went down to 7000 so the doctor decided to stop the plasmapheresis to give her a chemo therapy drug called bituxapin or something like that. After that The next day she started going down hill very rapidly platelets down to 5000. THis is a horrible disease = she had several small strokes at first- and for a while was recovering = but had a another major stroke while in the hosptial. She was very frightened and lost her vision - Being that this disease is rare - the doctor had to get recommendations from the U of A on what to do..... The family is still in shock that we lost her so quickly. I wish all families going through this horrible disease much luck and strength.

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