ive been accepted on waiting list. edss 7, ppms
l have noticed on the UK HSCT facebook group - that some people raise the cost by online funding. Not sure how it works but it seems a good idea. lf enough people pledge a small amount it will soon mount up. Also, one chap was fortunate to find that his critical health insurance paid up - and he was able to fund his treatment.
l wish you all the best -
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I hope your bold move pays off and the waiting list is not too long.
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thank you i will try fundraising
This man Eric Thomson went to Mexico a few months ago. He was diagnosed with PPMS 5 years ago and used a wheelchair. He has had great success with it. He is also not the only one. See the video of him walking again in this video.
Good Luck Joy. They are doing it on the NHS for PPMS if you have an active lesion
Moyna
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Best of luck Joy!
Pat xx
Wishing you the very best of luck Joy.
Nina x
Good luck
XXX Don
Good luck x
Wishing you all the best hope it proves to be a big success.i think this is the nearest thing we have to a ‘cure’ and i admire people willing to give it a go.
J x
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Good luck for you !
… But four years on MS is a very short time. I´m sure that there is not so much damage to repair …
regards
UWE
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