Since the thread is gone.....just thought I'd start a new one because I want to report how things have been post treatment for me.
I'd love to hear from the others too....there were so many people who were a part of that original thread and to hear how they are at this time would be wonderful.
My stem cell infusion took place in Greece on November 26, 2009. I've heard that they no longer perform it there, but in Switzerland. I'd love to hear from folks who have gone to Switzerland for the infusion!
Over the initial months after treatment, I experienced a decrease in fatigue, heat insensitivity, and vertigo. It's been 1-1/2 years since then and some of the improvements are still evident. The fatigue and heat sensitivity have been slowly creeping back but the vertigo remains gone.
I would go back for another treatment if money weren't an issue. I've also been told there was a significant cost increase of the second treatment.
There remain aspects of Slavin's treatment that I am disappointed in but having had the relief of some sx was and is a blessing. Some reported that their progression stopped; however, mine has marched on without pause.
If any of the previous stem cell infusion patients are still a part of this forum, it would be so nice to reconnect!!!
Each day as it's given....
Trish
I'd love to hear from the others too....there were so many people who were a part of that original thread and to hear how they are at this time would be wonderful.
My stem cell infusion took place in Greece on November 26, 2009. I've heard that they no longer perform it there, but in Switzerland. I'd love to hear from folks who have gone to Switzerland for the infusion!
Over the initial months after treatment, I experienced a decrease in fatigue, heat insensitivity, and vertigo. It's been 1-1/2 years since then and some of the improvements are still evident. The fatigue and heat sensitivity have been slowly creeping back but the vertigo remains gone.
I would go back for another treatment if money weren't an issue. I've also been told there was a significant cost increase of the second treatment.
There remain aspects of Slavin's treatment that I am disappointed in but having had the relief of some sx was and is a blessing. Some reported that their progression stopped; however, mine has marched on without pause.
If any of the previous stem cell infusion patients are still a part of this forum, it would be so nice to reconnect!!!
Each day as it's given....
Trish
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