Well, after weighing all of the opportunities, I have reached the decision to try autologous stem cell which is called a "blastomere stem cell". This seems to be as good of an option as the UC Stem cells, since I have found no research tied to CMT. I am scheduled for treatment on October 2, 2008.
I want to thank all of you, as reading your post has incouraged me to move forward, even though our diseases are not related. I especially want to thank Barbara for all of her help. Hope your recent treatment served you well.
I'll update when I get back. Hopefully another CMT victim might stumble across my post and it will help them.
Thanks to All,
jpfarm
I want to thank all of you, as reading your post has incouraged me to move forward, even though our diseases are not related. I especially want to thank Barbara for all of her help. Hope your recent treatment served you well.
I'll update when I get back. Hopefully another CMT victim might stumble across my post and it will help them.
Thanks to All,
jpfarm