It has been a few months since my last update. There has been no real Neurological improvement since December. I can definitely state I am stronger, due to Physical Therapy. We say, “If I am not crawling out afterwards, either he, or me, didn’t do our job!” I am beginning to get a handle on […]
Well, today I had my last Rituximab infusion. This is usually proceeded by Benadryl and it is added again somewhere during the infusion. Benadryl, affects me by making me somewhat listless. I get home and sleep for a few hours, ergo I am awake. This is a milestone for me. I am of the […]
I have been reluctant to add an update due to very little change physically. In talking with friends and family, they seem to think that is not true. I have made small improvements they notice, not seeing me every day, that I simply don’t notice. Also there have been a number of visitors come to […]
I have been going through the expected roller coaster ride after having HSCT. I am definitely no worse as in the degeneration has halted. For those that haven’t quite understood. The is the main purpose of HSCT for us people of the Primary Progressive Multiple Sclerosis (PPMS) persuasion. I know a lot of people are […]
http://www.telegraph.co.uk/science/2016/06/09/multiple-sclerosis-patients-walking-working-and-skiing-after-gro/ My Lifelong Sister friend found this article.
These are the words of my Learned Friend and fellow MS recoverer. He has been one of the leading voices in our striving to get the word out about HSCT and to let people know the pitfalls and life altering aspects of the procedure. I felt I would be remiss if I didn’t add this, […]
Good Day Folks, Today was my second Rituximab Infusion. I had no problem with the infusion itself. My energy level afterwards was nil however. The wife, who took me and brought me home, was worried because I was tired and slept a lot. I felt fine otherwise. I feel fine now 12hrs later. But I […]
