Fat Stem Cell Treatment: Dramatic Results in MS Patients
April 24, 2009
Comments
9 Responses to “Fat Stem Cell Treatment: Dramatic Results in MS Patients”
Got something to say? **Please Note** - Comments may be edited for clarity or obscenity, and all comments are published at the discretion of ChattahBox.com - Comments are the opinions of the individuals leaving them, and not of ChattahBox.com or its partners. - Please do not spam or submit comments that use copyright materials, hearsay or are based on reports where the supposed fact or quote is not a matter of public knowledge are also not permitted.
I have primary progressive MS, diagnosed 5-08. I am 62 years old. I live in MO. Is there a place in stem study for my type of MS?
I have chronic progressive MS. I am interested in knowing if there is somewhere I can go to be considered for a stem cell study I live in Florida but will travel anywhere required. Diagnosed in 1979. I am 70 years old.
[...] Lynne Perrinon April 24th, 2009 3:59 pm I have primary progressive MS, diagnosed 5-08….Read the Full Story VN:F [1.2.0_562]please [...]
i have progressive ms I have been on copaxone, rebiff and tysabri none worked but they were thinking of putting me on chemo but now decided to try the rebiff again which I dred because my arms and legs and all the other part of my body can’t take the shjots any more, plus I’m a diabetic sodouble the shots. Any how I was writing to you to see if you have any type of stem cell trials that would be open I live in Michigan but can ravel any where Thank you in advance Karen winkler
I have the same question. Does stem cell treatment help primary progressive ms ?
I have PPMS. I live in Canada but would travel anywhere to receive some sort of stem cell treatment.
My wife, Becky, suffers from PPMS. Diagnosed about 5 years ago at age 49. She takes Copaxone shots daily along with spasticity, pain and fluid pills. She also takes something to help her stay awake. Her doctor is a neuro specialist and travels conducting seminars on MS and Becky thinks the world of him. He is hesitant to allow her to try alternative treatments. However with PPMS time is of the essence. Becky is losing use of her legs and has gained weight i.e., now up to 280 pounds. I have quit my job to become her primary caregiver. We live with my daughter and her family. My son-in-law is in the Army and last week was sent to Afganistan for a year.
I have high hopes in Stem Cell research. I’m hopeful that time won’t run out on Becky. We can travel anywhere should she be selected for a clinical trial in Stem Cell treatments. Please advise as to your thoughts.
I have the same question Karen Winkler had 7th of may 2009. I am 43 years old ..and i live in Germany–had tried a lot and nothing with real sucsess
Do you work zogether with someone in Europe–or Germany ??
Maybe its possible to give me a connectet adress or email
thanks a lot for all
wish you all the best
yours Beate caterina
I AM 43 YEARS OLD WAS DIAGNOSED IN MARCH, 2010 WITH PPMS I AM NOW IN A WHEELCHAIR. I HAVE BEEN READING ABOUT STEM CELLS HELPING. I LIVE IN BIMINGHAM, ALABAMA WHERE CAN I GO THAT STEM CELL RESEARCH IS AVAILABLE? I AM WILL.ING TO GO ANYWHERE AND DO ANYTHING TO WALK AGAIN. PLEASE HELP ME!