Hang in there Sharon and Jack! I myself have MS and have had it for about 2 years now. The worse thing is my neurologist told me I had MS for about 5 to 6 years and never knew it. If you need anything just ask me. I will try to provide some answers
I feel the same. He will be quite fine with all the best treatments where the rest of us will deal with what is best for the real people in the world who ALSO have this disease!
Sharon, research the work done by St. Pete Dr. Mary Newport. (for her husband with Alzheimers). Coconut oil found to improve Alzheimers, Parkinsons, MS and other neurodegenertive diseases as well as Type I and Type ll Diabetes.
MS is not a death sentence. Quit weeping and wailing---and that goes for the breathless media clamoring over this "tragedy". Maybe they can raise some money and awareness for non-millionaire victims that could use all of our support.
Sharon, I understand and feel your pain I admire your courage, to live such an ordeal is very hard, my thoughts go to you and to your son, hope is still there. "au revoir"
No matter what you may think of Sharon Osbourne, the main focus of all of this should be her son Jack and sending him well wishes of good health and love and support.
The posting of advertisements, profanity, or personal attacks is prohibited. By using this Web site you agree to accept our Terms of Service. Click here to read the Rules of Engagement.
Reply to Comment The posting of advertisements, profanity, or personal attacks is prohibited. By using this Web site you agree to accept our Terms of Service. Click here to read the Rules of Engagement.
http://www.tampabay.com/news/aging/article879333.ece
The best is Cold Pressed Virgin Coconut Oil - not off the grocery shelf.
Good source: TropicalTraditions.com
#404425
PwMS get excited when someone famous is dx. BUT so far has not made any difference
Sharon, I understand and feel your pain I admire your courage, to live such an ordeal is very hard, my thoughts go to you and to your son, hope is still there.
"au revoir"
unlike so many of us with MS there will be no worries about how to afford a treatment etc.
I am truely hoping that they get involved in either stem cell research or with re-mylanting