Sunday Sept 27,2009
We are in Mexico and ready for the first day tomorrow. Hotel is great and we look forward to our new mesenchymal stem cells! People are so welcoming here is Mexico.
Rich

We are getting a lot of new members with energy which is really encouraging. On Monday, I am submitting the names of those that have volunteered to fly to Washington DC to meet with Senator Harkin in an effort to get the FDA out of the practice of medicine and allow doctors to be able to administer safe stem cell therapy to their patients here in the U.S. Dr. Centeno, founder of ICMS, wants the Senator to understand first hand the number of people that should be allowed to have stem cell therapy...

Hello my name is Inga. I am a mother of little beautiful girl. She is just six months old and has optic nerve hypoplasia. The only way i could help her is to take her to China. Where doctors maybe could give my girl a sight to see moms and dads faces, sky, flowers, sun, toys...
It's so sad when your the one and only baby can't see those things and enjoy the life as any other baby. I pray to God everyday to help us.
I need help, as i want to take her to China we need money and i would...

Hi all, Sept. 26, 2009
I am heading to Mexico tomorrow with my wife, a friend, Lisa, who has SPMS and her husband! We are going to a clinic 2 miles over the border from San Diego. We will be picked up at the airport by the clinic and taken over the border to a 4-star hotel that is included in the treatment fee.
I am a 54 year old and I have Primary Progressive MS. I was diagnosed in June 06 as RRMS and have tried Avonex and Tysabri and have failed on both. I have also participated...

The blogging capability on the forum is a great way to keep track of updates from members. I hope that all members will use the blog area even if it is just to provide a link to their own site.

There is also Community now available on the blue bar where Blogs is found. Check that out as well. It's where Members can now be found.