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It’s about time we found a drug that works.

Dani


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Yes, the trial is a big commitment – with 400-mile round trips, electrocardiograms, breathing tests, blood tests, urine tests, questionnaires, interviews, not to mention those lumbar punctures.

But I didn’t hesitate about joining. It has to be done – because it’s my family’s only hope.

Professor McDermott is targeting my faulty gene, SOD1, with a new drug. It stops the protein from damaging the neurons, which is what’s causing my type of MND.

Some people would be terrified at a big needle going directly into the spine, I know. But I don’t think about it.

I’m doing this for my family, to protect them from the horror of MND. I’m not going to just sit here and be miserable – I’ll do anything to beat this disease. Please join me today by making a donation.

"MND has hit Dani’s family hard – so she’s doing her bit to protect them. She’s amazing. Seeing the sacrifices that she makes, I desperately want the trial to be a success."

Professor Chris McDermott, lead researcher on the SOD1 clinical trial

Research can only happen with support from people like you.

Make a donation

Meet the other unsung heroes

John Albon

"I won't just wither away and die.”

 

Meet John
John Dring

"I'll do this for as long as I have left.”

 

Meet John

For further information and support contact our MND Connect helpline

mndconnect 0808 802 6262