It is hard to believe that it has been 1 year this past week that I met you and your team and received my stem cell therapy. Time really does fly. I wanted to give you a short update...
I am still off of all my MS meds, feel great and have not had a relapse since 2 months before I came down there. In prior years summer’s, I spent very little time outside because I couldn’t stand the heat and the sun shining on my skin hurt. But not his summer! I was outside doing yard work, walking around and was able to sit on the deck and enjoy the sunny weather. I could tolerate the heat and the sun didn’t hurt. It was really nice. I still have to watch that I don’t over do my activities outside because I can get really tired and fatigued if I over do it. My balance is good and so is my coordination. However, with the weather being cold, I feel a bit more spastic in my movements. I am hoping that since it came on with the colder weather that it will also leave with the warmer weather.
My neurologist has been very surprised with my progress and just can’t seem to understand how well I have done. He still is not in favor of the stem cell therapy but happy with my progress. He was pleasantly surprised that my MRI in October 2011 showed no active inflammation in my brain or spinal cord and everything that showed up was old. All in all, I am very happy with the therapy and tell everyone I see of the great work that you and Stem Cells for Hope do.
God Bess!
I am still off of all my MS meds, feel great and have not had a relapse since 2 months before I came down there. In prior years summer’s, I spent very little time outside because I couldn’t stand the heat and the sun shining on my skin hurt. But not his summer! I was outside doing yard work, walking around and was able to sit on the deck and enjoy the sunny weather. I could tolerate the heat and the sun didn’t hurt. It was really nice. I still have to watch that I don’t over do my activities outside because I can get really tired and fatigued if I over do it. My balance is good and so is my coordination. However, with the weather being cold, I feel a bit more spastic in my movements. I am hoping that since it came on with the colder weather that it will also leave with the warmer weather.
My neurologist has been very surprised with my progress and just can’t seem to understand how well I have done. He still is not in favor of the stem cell therapy but happy with my progress. He was pleasantly surprised that my MRI in October 2011 showed no active inflammation in my brain or spinal cord and everything that showed up was old. All in all, I am very happy with the therapy and tell everyone I see of the great work that you and Stem Cells for Hope do.
God Bess!
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