8 months post hsct stem cell transplant

I am always sick as my immune system grows new antibodies. However ,it is getting less and today I don’t feel like I have a cold. It has been an up-and-down roller-coaster of my multiple sclerosis being better, than my multiple sclerosis being worse, and back and forth over and over again. But that’s exactly what’s supposed to happen. My bladder and bowels finally do work. That alone is a miracle. You guys have always worn underwear but trust me wearing depends sucks all the time. But now I get to wear that wonderful breathable cotton underwear. In December it will be my 1 year and I’m sure I will see even better results after one year. That is one I can get my MMR and chicken pox vaccines. For now I just have to be patient and wait for my white blood cells to divide and grow stronger. I am having a new life party in October in Binghamton and I looking forward to that. I am at the start of a new life. It’s kind of weird I always knew I died of complications due to multiple sclerosis. Now I have no idea how I’m going to die. And I think that’s the way it’s supposed to be. Because it sure makes me feel better. I am on a lot of steroids and still getting some chemotherapy but a very low dose and the steroids do make me a little bit crazy so I’m trying to only stay on my blog site. If you’re ever in the Binghamton area stop by my party Beautiful Dreamer. However I know some of you live in India and turkey and I certainly don’t expect you can make it. 🙂 I can’t wait for the day that I can tell you I’m walking with a cane. I will get there soon. Thanks to all who raised money to get me stem cells. Now I just have to wait. Patience is a virtue.one I dislike very much.

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