I'm a 44 year old male living in Connecticut. I was first diagnosed with ITP at age 22 back in 2001. My count was 1000 when I went into the hospital.
I was hospitalized for about a month (2 weeks in California and then 2 weeks in my home state of NY). They did the standard treatments at the time (Prednisone, IVIG, WinRho, Vincristine) but my count barely moved from 1000.
Once I got a splenectomy, my count returned to normal and has been fine for 22 years. I've generally been able to live a normal live, although the trauma of having ITP is something that you never get over.
In early March, I had to travel for work and ended up catching Covid for the first time. I was fully vaccinated so the illness itself was pretty mild. I tested positive on March 6, and on March 29, I noticed some petechiae on my forehead just before going to work. As I said, it had been 22 years with no incident, but as soon as I saw them, my heart sank. By lunch, I noticed more petechiae on my arms and chest, and went to the ER.
My count was 2000. I was admitted on March 29 and immediately given IVIG and dexamethasone. After two infusions of IVIG and daily dexamethasone, my count was up to 43,000 by Saturday and I was discharged with a daily prescription for 60 mg of Prednisone.
Unfortunately, when I got my bloodwork done the following Tuesday, my count was back down to 8000, and then next day it was 1000, so I was re-admitted on April 5, and I've been in the hospital ever since.
They re-tried IVIG and dexamethasone but it didn't move my count this time. I've been on 60 mg of Prednisone every day, and have had 2 NPlate injections (April 10 and April 17), but my count so far hovers around 3000-4000. I have some minor petechiae but no major bleeding from the nose or mouth/gums.
They've also done a bone marrow biopsy and it appears my system is producing platelets well but my immune system is destroying them.
I'm having my first rituximab infusion tomorrow and will continue with NPlate. I expect to be in the hospital for at least another week or two.
I'm just very concerned because now that I've had a splenectomy, I don't know what will happen if other treatment options don't work. Has anyone else gone through something similar?