Guest guest Posted January 23, 2009 Report Share Posted January 23, 2009 GMA had the President of the Reeves foundation on this morning. I cried my eyes out. Finally someone may get help for something. I am keeping my fingers crossed that this will work. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2009 Report Share Posted January 23, 2009 Tears of joy for me and all of us I am sure! It's about time and it will work! Take care Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2009 Report Share Posted January 23, 2009 , I know how you feel; this is a long time coming and maybe now with a new administration we will start expanding quicker on stem cell research. Jackie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2009 Report Share Posted January 24, 2009 , I would join you if only I could cross my fingers! I'll just hope with you that they find something to reverse the symptoms or cure the disease before my 3 kids start to show symptoms. I was 40 before I had any symptoms and they are about there now. 5 yrs of Vit C has given me some more strength and muscles in my hands and forearms and some muscles in my legs and feet, but no improvement in the foot drop yet. I hope to live long enough for the Vit C to reverse the footdrop or a cure is found to reverse it quicker. I think we are all encouraged by the recent findings. Sue Quote Link to comment Share on other sites More sharing options...
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