The NAA10 Patient Support Group is set up and run entirely by parents. It is funded entirely by voluntary donations and fundraising activities as we don’t receive any government funding. We rely on contributions of donors and efforts of voluntary fundraisers as a fundamental source in order to develop our patient group and support families.
We want to support and develop our website and social media channels, develop patient leaflets, contribute to further research and to vitally continue to raise awareness of NAA10 given how ultra rare it is.
There are many different ways in which you can help us with our fundraising efforts.
Please help support us by donating or raising on our behalf. We would be delighted to support you if you have any ideas to help us raise money for our NAA10 Patient Support Group.