Stem cell treatment for MS for Judy
Spende geschützt
What happened:
Around 1988 I had high exposures to solvents used in printer ink where I taught in Japan as the printer was kept in a small windowless room. Unbeknownst to me or anyone at the school the air in the printer room was toxic. I stayed in the room to finish each long print run, and a few days later an arm or leg or both would become temporarily paralyzed, each time returning to normal after 3 weeks. I had no idea why this was happening. This continued for the next six years. I then moved to
Brazil and the UK to teach and found out I had a severe allergy to solvents. From then on, I conscientiously avoided breathing or being near printer ink / solvents. However, I didn't believe I had MS until years went by, went through menopause, and lost protective hormones. I then started feeling slight MS body symptoms and telephoned my neurologist cousin who explained in his experience it would likely to be
" downhill from here". I then arranged to go to the U.S. for a limited stem cell treatment which was successful in mitigating some symptoms.
Recommended treatment:
Studies I've read recommend having stem cell treatment every few years because as my cousin indicated, MS isn’t curable through allopathic medicine, only able to be managed. Now at this point where my condition is gradually deteriorating I need to have extensive MS stem cell treatment as soon as possible to halt and if possible reverse the decline. This treatment is available with Swiss Medica at one of their three treatment centres in Europe. For more info please follow the link to read and scroll down to the video:
http://www.mstreatment-europe.com/ms-new-treatment.html
How soon I need the funds and how they will help me:
As soon as reasonably possible as my MS has become progressive. Although this is a relatively new treatment there is evidence of anything from a 50% -90% improvement in many patients. My chances are good as I have already benefited to some extent from my first stem cell treatment. As soon as the progression is slowed down the better it will be for me so I can then lead a more normal, productive, creative life where I can do many more practical everyday things.
The urgency of my situation:
I need to start the treatment soon as it is becoming physically more and more difficult for me to travel comfortably.
Starting the enhanced treatment as soon as possible will also be of great benefit to my family.
Around 1988 I had high exposures to solvents used in printer ink where I taught in Japan as the printer was kept in a small windowless room. Unbeknownst to me or anyone at the school the air in the printer room was toxic. I stayed in the room to finish each long print run, and a few days later an arm or leg or both would become temporarily paralyzed, each time returning to normal after 3 weeks. I had no idea why this was happening. This continued for the next six years. I then moved to
Brazil and the UK to teach and found out I had a severe allergy to solvents. From then on, I conscientiously avoided breathing or being near printer ink / solvents. However, I didn't believe I had MS until years went by, went through menopause, and lost protective hormones. I then started feeling slight MS body symptoms and telephoned my neurologist cousin who explained in his experience it would likely to be
" downhill from here". I then arranged to go to the U.S. for a limited stem cell treatment which was successful in mitigating some symptoms.
Recommended treatment:
Studies I've read recommend having stem cell treatment every few years because as my cousin indicated, MS isn’t curable through allopathic medicine, only able to be managed. Now at this point where my condition is gradually deteriorating I need to have extensive MS stem cell treatment as soon as possible to halt and if possible reverse the decline. This treatment is available with Swiss Medica at one of their three treatment centres in Europe. For more info please follow the link to read and scroll down to the video:
http://www.mstreatment-europe.com/ms-new-treatment.html
How soon I need the funds and how they will help me:
As soon as reasonably possible as my MS has become progressive. Although this is a relatively new treatment there is evidence of anything from a 50% -90% improvement in many patients. My chances are good as I have already benefited to some extent from my first stem cell treatment. As soon as the progression is slowed down the better it will be for me so I can then lead a more normal, productive, creative life where I can do many more practical everyday things.
The urgency of my situation:
I need to start the treatment soon as it is becoming physically more and more difficult for me to travel comfortably.
Starting the enhanced treatment as soon as possible will also be of great benefit to my family.
Organisator
Judy Epstein
Organisator