Stem Cell (petition)

The first link doesn't load and the second link has been truncated and therefore does not work.
 
no, the only way forward is to give people an idea about what they are actually giving money for :p
 
typical my only way forward is to make people aware of my Ataxia.

No, you just chose to do that. If you want help, just like everything else in this world, you need to explain properly what it's for. You come across as having a bad attitude towards the people you have just asked for help.

Try again.
 
Something along these lines
[url]http://en.wikipedia.org/wiki/Ataxia[/url] said:
Ataxia (from Greek α- [used as a negative prefix] + -τάξις [order], meaning "lack of order") is a neurological sign and symptom consisting of gross lack of coordination of muscle movements. Ataxia is a non-specific clinical manifestation implying dysfunction of parts of the nervous system that coordinate movement, such as the cerebellum. Several possible causes exist for these patterns of neurological dysfunction. The term "dystaxia" is rarely used as a synonym.

[url]http://vimeo.com/2333247[/url] said:
Brian traveled to China over the summer of 2008 to receive a second round of adult stem cell therapy for the treatment of symptoms associated with Ataxia. A muscle wasting neurological disorder, Brian's SCA1 saw marked improvement a second time around.

Adult stem cells are not a cure - but may offer quality-of-life improvements to patients with few or no alternatives. Hospitals in China now treat a wide range of spinal cord injuries, neurodegenerative conditions and are rapidly tackling cardiovascular conditions as well.

While we have hope that adult stem cell therapies will be available in many other countries in the near future, many conditions are currently treated through providers in China. Follow patients and read experiences at StemCellsChina.com.

More info at http://www.stemcellschina.com/ When it's up


And then a paragraph of what the 18k will be fore..
 
i know Brian hes been to China twice why dont the British copy the Chinese.

I have no idea as I know nothing about the subject, I doubt any of us know anything about it apart from you. That's why you need to explain to us what it is and what's going on. I just googled and that came up.
 
need more publicity. my nans got it, pretty bad :(


its the worlds nastiest disease I have Ataxia SC1, I'm screwed but 6 Umbilical cord Stem Cell injections could fix me, Brian McNeal from Scotland has been twice hes OK, i'm willing to pay for any treatment, but i have to go to China, I'm trying to be treated over here, i need the strength of a petition to do it.
also my sister has it./
 
Is there a uk charity for this? Do you know why the uk doesn't do it?

First things first if there is no charity is to register a charity and right to mps, nhs etc and find out why the uk doesn't do it.
 
This thread strikes me as unnecessarily confusing. I skimmed through, then read the whole thing, twice. Suggest delete thread, and start again with an explanation of why you want money, some sort of credentials, and ways to donate (PayPal?)?
 
This thread strikes me as unnecessarily confusing. I skimmed through, then read the whole thing, twice. Suggest delete thread, and start again with an explanation of why you want money, some sort of credentials, and ways to donate (PayPal?)?

I need 18K to go to China but that's not what I'm after, our doctors refuse to treat me, i think a petition would be hard to refuse and id rather give my money to the UK.
 
I need 18K to go to China but that's not what I'm after, our doctors refuse to treat me, i think a petition would be hard to refuse and id rather give my money to the UK.

It depends why they don't treat. Is it because of uk laws on stem cells? lack of research? hasn't passed the strict medical trials? remember china hasn't got these laws in placed so is much easier to get "experimental" treatment.
 
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