Alisha Whittam

Alisha's The BIG Sleep 2014 page

Fundraising for IiME
£135
raised of £100 target
by 12 supporters
Donations cannot currently be made to this page
Event: The BIG Sleep 2014, from 11 May 2014 to 17 May 2014
IiME

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RCN 1153730
We fund biomedical research into ME to create a strategy for cure/treatment

Story

Thanks for taking the time to visit my JustGiving page.

http://www.thebigsleepforme.com/

As you may know I have ME or to give it it's full name Myalgic Encephalomyelitis

ME is a illness that not a lot of people understand . I can guarantee you that only 2 people in my whole family understand what this illness has done to me and how it effects our lives, which is my amazing husband Graham and our wonderful daughter Rebecca.

 

please have a read of the information I have copied from the ME Associations website.

 

The typical features of ME/CFS

 


Commonly, a previously fit and active person finds their illness triggered by an infection. Less common triggers include toxins, organophosphate pesticides, vaccinations, major trauma or stress (e.g. a road traffic accident), pregnancy and surgical operations.

In some cases there is no obvious precipitating event and the person reports a gradual decline in health over a period of months or even years.

The predominant symptom of ME/CFS is usually severe fatigue and malaise following mental or physical activity. The full extent of this exhaustion often becomes apparent only 24 to 48 hours after the activity (assuming, of course, the person was not already in a ‘recovery period’ from a previous activity).

The other main symptoms are:

  • Muscle symptoms include exercise intolerance and post-exertional malaise (i.e. feeling shattered the day after undue physical activity), pain/myalgia (present in around 75% of people) and fasciculations (visible twitching of the muscles which sometimes includes blepharospasm/eyelid twitching).
  • Brain and Central Nervous System symptoms include cognitive dysfunction (problems with short-term memory, concentration and maintaining attention), clumsiness, disequilibrium likened to ‘walking on rubber’, and word finding abilities. Problems with control of the autonomic nervous system results in palpitations, sweating episodes and symptoms associated with low blood pressure/postural hypotension (e.g. fainting).
  • Symptoms which suggest on-going abnormalities in immune system function include sore throats, enlarged glands, joint pains, headaches, problems with temperature control and intermittent flu-like feelings.
  • Other symptoms which frequently occur in ME/CFS include sleep disturbances (often increased requirements at the onset followed by an inability to maintain a full night’s sleep), alcohol intolerance (a very characteristic feature, particularly in the early period of illness) and irritable bowel symptomatology.
  • Some people also develop emotional lability or mood swings and features of clinical depression as time goes on.
  • Besides these more obvious and wide-spread symptoms there are also myriad “minor” ones. Not everyone experiences all of them and often they are not mentioned when patients describe their illness; however there is often very visible relief when they find others, too, have similar experiences.

ME/CFS symptoms tend to fluctuate in severity throughout the course of a day and people often report that they have both ‘good days’ and ‘bad days’, although the term ‘good’ is often used in a relative sense. The illness nearly always results in a severe reduction in a person’s ability to cope with all aspects of normal daily living (i.e. social and sporting activities, employment, household tasks). Relapses or exacerbations are often precipitated by infections, excessive physical or mental stress, general anaesthetics and surgical operations, and extremes of temperature.

I  want to raise awareness and money for research into ME , so that the next time somebody I or one of you loves , walks into a dr with symptoms of ME that they don't have to endure the prejudices and poking that I or my fellow sufferers have had to .

Please help even £1 can make a huge difference x x 

 

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About the charity

IiME

Verified by JustGiving

RCN 1153730
Invest in ME Research has, as its objective, to change how myalgic encephalomyelitis (ME) is perceived, treated and researched. We do this by raising funding for biomedical research and improving education about the disease. We are currently facilittaing high-quality biomedical research in UK/Europe

Donation summary

Total raised
£135.00
+ £22.50 Gift Aid
Online donations
£135.00
Offline donations
£0.00

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