Families of SMA in Iceland

Safnast hafa 450.500 kr.

FSMA in Iceland is a group of relatives and individuals who held the disease SMA (Spinal Muscular atrophy) in Iceland. The group's mission is to represent their interests as subjects held SMA, as well as their families. The group's purpose is also to promote the cure for the disease as soon as possible. The purpose of the company is also sharing information related diseases, both to those directly related to the disease as well as to the public.
The charity's website is fsma.is

Status
Contributions: 136
Donation count
Total amount
51
127.000 kr.
78
300.500 kr.
7
23.000 kr.

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