Liam Naughton

Liam's page

Fundraising for ME Association
£1,187
raised of £1,000 target
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Event: Brighton Half Marathon 2023, on 26 February 2023
Biomedical research into M.E.is seriously underfunded. We need to do more if we are to learn how and why this cruel illness starts - how to test for it or treat it, or better still, how to cure it.

Story

Thanks for taking the time to visit my JustGiving page.

I will be running the Brighton Half Marathon on Sunday 26th February in support of the Ramsay Research Fund, the research arm of the M.E (myalgic encephalomyelitis) Association. 

M.E affects someone very close to me and I've seen first hand how debilitating and often misunderstood this condition can be. Post Covid-19 many more people have been diagnosed with ME and whilst research is finally taking place at a rapid pace, research needs further funding to finally find effective treatments or even a cure. 

Some further info about M.E and the research fund. Thank you!

M.E. (myalgic encephalomyelitis) or Chronic Fatigue Syndrome, blights the lives of 250,000 people in UK today. It changes lives drastically, often disrupting education or making employment impossible. People may be housebound or confined to bed for many months or years. There is no known cure.   

The Ramsay Research Fund supports vital research into the causes and treatment of ME/CFS, to help find answers and to give thousands of people hope.   

Biomedical research into the underlying physical cause of ME/CFS, and into effective forms of treatment, receives no government or outside funding and is thus seriously underfunded.   ME/CFS is such a complex illness that research into it is rather like piecing together a complex multi-dimensional jigsaw puzzle. Whilst some progress IS being made, we need to do more, MUCH MORE, if we are to understand this cruel illness.

The Ramsay Research Fund is named after the late Dr Melvin Ramsay - the pioneering consultant who first brought M.E. to the attention of the medical profession. It is a 'restricted' fund, so all money that you give is used for research - not administration, not support, just research. 

Medical research is expensive and it can be a long and slow process, but we believe it offers the best hope. That's why we’re are asking for your help. We want to do more to exploit the better understanding we now have about M.E. and then build on any discoveries to help change lives for the better.   

One day we WILL find the cause of ME/CFS  

One day we WILL have an effective treatment and cure.  

And with your help, that day will come sooner.   

Click here to learn more about the progress that we are making."



About the campaign

Biomedical research into M.E.is seriously underfunded. We need to do more if we are to learn how and why this cruel illness starts - how to test for it or treat it, or better still, how to cure it.

About the charity

ME Association

Verified by JustGiving

RCN 801279
The ME Association campaigns hard to get ME recognised as a severe neurological illness. Our helpline provides essential information and support to adults and children who have ME/CFS, and to their families and carers. We also fund biomedical research into the physical nature and causes of ME/CFS.

Donation summary

Total raised
£1,186.61
+ £218.00 Gift Aid
Online donations
£1,186.61
Offline donations
£0.00

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