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Senior Member
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TYSABRI PROGRESS SO FAR:
Here are my updated graphs regarding some of my Tysabri data. (1) Walking Endurnace: Improved slightly since the start of Tysabri. (2) Vertigo: Reduced markedly. (3) Hours Before Fatigue: Vast improvement. (4) Ankle Movement: Improved slightly since the start of Tysabri. Limiting Data Factors: (a) Excessive heat in So Cal. (b) Limited exercise (c) Periodic UTI's Conclusion: (1) No exacerbations while using Tysabri. (2) Periodic UTI's (3) Has not stopped overall MS progression, but rather delayed it. Clinical Observations: While the data thus far indicate that I am stable, and I do feel great, the reality is that I have progressed to SPMS based on over two decades of medical observation by my medical team. That is not as bad as it may sound since I have had MS for a long time. HERE IS THE "KICKER": Although I have progressed to SPMS, I do not notice it per se as I have habituated to it and feel (and function) much as I did when I had RRMS. Would Tysabri have prevented this if I could have used it ten years ago? Probably not. This is just the natural, biological course of human entropy. What has medication done for me? I think that other than draining my wallet (six figures soon), it may have made the progression much less of an issue, as I am fully functional and productive. It is like having a chronic cold, with just a few coughing episodes...wherein you know it will eventually lead to pneumonia but there is a delay in the time that you get there...and you know it. Thus far, I have concluded a few things about my MS: A - My MS is a tolerable condition. ![]() B - MS just IS, like so many other things in life... C - MS has made me appreciate the most simplistic of things! ![]() -Vic |
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