I work for the charity on behalf of SEC Fundraising and it's an incredible journey, you get to hear lots of stories about people's experiences in hospital and how our charity has helped them. I will try my upmost to keep the vital funding coming in to help get the centre built for MND patients like Ian and his family
I live in Australia and I have just been diagnosed with motor neurone disease, I know that there is no cure for it and I know that I am going to die possibly in the next 2 years. But I would like to talk to anyone who has mnd ,for there prospective, so if anyone knows of any online forums could you please leave the details here. Thank you 😊
I work for the charity on behalf of SEC Fundraising and it's an incredible journey, you get to hear lots of stories about people's experiences in hospital and how our charity has helped them. I will try my upmost to keep the vital funding coming in to help get the centre built for MND patients like Ian and his family
What a gorgeos brave man with a gorgeous brave family.
Lovely family.
I live in Australia and I have just been diagnosed with motor neurone disease, I know that there is no cure for it and I know that I am going to die possibly in the next 2 years. But I would like to talk to anyone who has mnd ,for there prospective, so if anyone knows of any online forums could you please leave the details here. Thank you 😊
Hi sorry you have this illness. If you google MND forum or ALS forum there are several available.
One of MND po