We are a charity primarily focused on helping patients and their families with ME (Myalgic...Read more
kymkat2 hours ago
I started choking on a crumb sunday night,before long it felt like my throat felt like it had closed,it was like breathing through a pin pri...
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Recognising the people who make a difference to you
Featured by HealthUnlocked
Chronic fatigue syndrome and Jaw pain
asni027 days ago
Hi there, I haven't been diagnosed with ME yet. Once, I went to see GP with a flare up and she told me that I may have ME. She actually prin...
Sedentary Hobbies Inspiration needed!
Plen22 days ago
Since I develop PVF I've had to quit exercising and find new hobbies. I've discovered my love of jigsaw again. What other seden...
3 Replies1 Like
CFS = me losing my mind.
Sybariss23 days agoPOPULAR
I just found this website tonight, I'm a noob...so not sure where to start. I turned 43 this past week and the last 2+ years have been the h...
27 Replies4 Likes
Clare2206a month ago
Hi I'm Clare ,46 female frome the Highlands in Scotland . I suffer from under active thyroid , fibromalgia , depression , borderline persona...
Thoughts on Mickle Therapy
Plena month ago
Hello, This is my first post reaching out for advice. I hope I'm not asking questions which have already been discusssed.
I have been diagno...
scoobydoo87a month ago
Hi everyone, I got the dreaded letter this morning .
To explain more .
I claimed Pip less than 2 years ago , I had a gruelling assessment whi...
Get Well Soon
Nick817a month ago
Hello all. I’ve had fatigue for a few years now, and spent a long time trying desperately to get better while navigating all the controversy...
A Bit about me and the things that i currently suffer from.
marvelfan23a month ago
Hi my name is Lizzy. I am 26 and have joined this site to help me find support and to support people who have or understand what conditions ...
Wanting to be a helpful partner
Hannah221ba month ago
My boyfriend recently has been diagnosed with CFS/ME and it does explain a lot about how his health and energy throughout the day isn't what...
Cfs me -- antibiotics
Ohms140a month ago
Has anyone tried long term antibiotics for cfs me and/or Fibro? They worked for me and I was in bad shape for a year. They also worked for...
Cfs/ME and antibiotics
Hi everyone I'm new here and just wanted to introduce myself. My name is Karen. About 8 years ago I suffered from C...
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bakeacake33a month ago
Hi, I'm 21 and I'm in my final year of university in the UK. I have just been diagnosed with Chronic Fatigue Syndrome and I just want some a...
10 Replies1 Like
Has anyone tried D-Ribose?
kittenmittens2 months ago
After reading this information on Dr Myhill's page I'm going to give D-Ribose a go.
Has anyone foun...
4 Replies2 Likes
At breaking point.
scoobydoo872 months ago
I don’t write on here very often , but read the posts regularly. They’re my lifeline.
I was diagnosed with ME/ Fibro 2 yrs ago , I also have ...
Mountain Wheelchair Project
mountainwheelchair2 months ago
Hello all. My daughter, who previously won the "Junior Adventurer of the Year" competition, was diagnosed with Myalgic Encephalomyelitis las...
Support DR Myhill eat al re ME PACE Please read
fidders2 months ago
*** DR MYHILL HAS COMPLAINED TO THE GMC ABOUT THE PACE AUTHORS ***
*** SHE WANTS YOUR HELP ***
**PLEASE DO COPY YOUR LETTER OF SUPPORT TO cr64...
1 Reply1 Like
Effort3 months ago
An interview with Dr David Tuller conducted by a severely ill patient
Onlyme28123 months ago
Hi all! I know a lot of people resort to alternative therapy for CFS/ME and was wondering if any worked for you? I tried acupuncture but fel...
Optimum health Clinic for chronic fatigue syndrome
martha_taunt4 months ago
I was diaongones this summer with crunch fatigue after two years of Beeing really ill
Have been picked up by my local chronic fatigue team i...
Thyroid test results - Do these look normal ?
digga24 months ago
In brief: been suffering from CFS for over 15+ months.
Most symptoms have subsided except the muscle soreness in my thighs, general energy le...
a big thank you!!!!!
tobby14285 months ago
you might recall that I tried to write a blog about the terrible time I had with guillane barre syndrome over 20 years ago.i thought by writ...
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Jenni155 months ago
I am new to this site and looking for support I just discovered that my referral to Chronic Fatigue clinic has been lost and the original ho...
Samartime15 months ago
Hi everyone, hope your taking it easy. I suffer from a few conditions and one of them is ME. Nice to know that their are other people livi...
Transdermal B12, what's the best area
digga25 months ago
I have been using this transdermal spray - salesatdrmyhill.co.uk/trans...
Is there a particular area on the skin that absorbs better? I have ...
Onlyme28125 months ago
Hello everyone. I'm currently having a tough time with my employers. I recently got diagnosed with cfs (this year August) and been off work ...
Please leave me alone
Maxibonus5 months ago
Totally worn out.
Been in bed most of summer.
I hate mornings as I hate telephone calls and people at the door. Become a night bird.
2 Replies1 Like
heatherthornton5786 months ago
Hello Everyone Its been awhile since Ive been on here and I am now 16 and still suffering with CFS. I've been bruising very easily and in th...
Effort6 months ago
Please sign and share this as widely as possible
2 Replies2 Likes
Diagnosed with CFS, is there any where to go ?
digga27 months ago
End of 2016, son was born prematurely. Many days and nights in the hospital.
Beginning of 2016, energy levels are reduced, yearly ...
11 Replies2 Likes
If you have claimed ESA, or been migrated from another benefit to ESA, at what stage is your claim? Please comment if you want to explain further.
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