Morgaen Warner

Morgaen's SkyDive For ALS/MND/Lou Gehrig's Disease

Fundraising for Motor Neurone Disease Association
£894
raised of £1,000 target
by 48 supporters
Donations cannot currently be made to this page
We fund care, campaigning and research to achieve a world free from MND

Story

Motor Neurone Disease is evil, pure & simple.

Imagine every muscle in your body eventually shutting itself off until you are no longer able to speak or feed yourself but you can still think & feel, hear & see.

Imagine having an itch but you could never move any part of you to be able to scratch it.
This is MND.
This is pure horror for anyone affected by it, whether they have it themselves, or they care for someone who has it.

I am doing this for my friend, Ruth who lost her husband, Neil. And for their son, Tim who lost his father.
And for one of my oldest friends, Brian who has been diagnosed with ALS (A form of MND).
As well as for every other sufferer or carer I've met along the way since Neil was diagnosed.

Anything you can spare will help research the causes & cures. It will also help alleviate the stress & strain that comes with living with MND.
Thanks for listening.

About the charity

The MND Association focuses on improving access to care, research and campaigning for those living with or affected by MND in England, Wales and Northern Ireland. If you or a loved one need practical or emotional support, call our Connect Helpline on 0808 802 6262, Mon to Fri between 10am and 4pm.

Donation summary

Total raised
£893.02
+ £82.75 Gift Aid
Online donations
£893.02
Offline donations
£0.00

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