Bettina would like to live, please donate for a treatment with Spinraza

The 31-year-old, however, suffers from a rare neuromuscular disorder (SMA) , which are characterised by loss of lower motor neurons and progressive muscle wasting,
Bettina is already in a very critical condition.
For Bettina to live on, she urgently needs a treatment withh Spinraza.

But Bettina’s health insurance does not want to pay for it, because this medicine is too expensive

Website
Donate for Bettina

Bettina on FaceBook
https://www.facebook.com/bettinawillleben

#Treatment #Spinraza #Hope #life quality

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En kommentar till “Bettina would like to live, please donate for a treatment with Spinraza”

  1. Good news comes from Bettina. She has reached her goal

    In only 16 days we have all done the impossible together. What hardly anyone believed in: To raise 600,000 francs with an online campaign for Bettina to enable her to have her first year of treatment with the drug Spinraza. And to initiate a discussion at the political level as well. Instead of the originally planned 3 months, the campaign comes to an end after only 16 days. We are overwhelmed and thank YOU ALL for your huge solidarity and the media for their support, without which this success would not have been possible. Bettina will now live – because YOU have helped her.

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