EDMESH | HealthUnlocked

upcoming #UniteToFight2024 conference on May 15th and 16th, dedicated to advancing understanding and research on LongCovid and ME/CFS.

Hi. I’m new to this forum but have had asthma and hyperthyroidism so have been on others. I only recently saw that I have a lot of similar symptoms to CFS so...

Hi everyone, I’ve suffered with fatigue for as long as I can remember. It’s a kind of fatigue that makes my whole body feel exhausted, I feel weak all the...

Hi! So i recently went to a neurologist. She said I couldn't have CFS because I've had problems with fatigue since I was little and it comes after a virus or...

Hi everyone, I have just recently be told I have Chronic Fatigue syndrome. When my doctor told me that I thought - I feel like I’ve had it for 30 years!...

Thank you for your welcome I read some posts from yrs ago so my info may not be useful to others now. But: 1. Breathing- I found it was the intercostal...

I’v read some of the posts. Re vaccine and long Covid. They are doing a study in USA Re long Covid and similarities to CFS. Many see the similarity. My CFS...

Hi. I’ve had CFS since 1972 following glandular fever in 68, followed by E.coli in 71. It was very bad for several yrs but gradual improvement once they...

Starting with neck pain, I went to visit a chiropractor. The day the pain went away, I started having something similar to absence seizures accept I was able...

Hello all I have been having a particularly rough time recently dealing with my CFS as I’ve had it for 8 years and am worst then I have been in a very long...

Just been referred to a pain clinic in grmbsy at Hugh's. Anybody else go there is it anygood

One of the Most Underestimated Health Care ProblemProtection For Chronic Pain Patients.Support this Petition 🙏healthcarepetition.com

I still work and have been advised to take lots of rest breaks to recharge through the day. Sounds simple enough but i dont know what rest is. I am always in...

Hi everyone there is a free week's conference which is everyday for 1 week with guest speakers and free gifts and peoples personal recovery stories and tips....

After years of a toxic environment at work I finally took voluntary redundancy. I felt I was not properly supported and terms of our contract were likely to...

I have set up a petition on Change.org.uk. link below! http://chng.it/v76rwLSH To abolish the current Atos/Pip assessments that use the Lima tick boxing...

Hello I’m new here. M.E sufferer for almost 4 years. Looking to connect with people from Edinburgh in the same position

Hi I am new here and have had chronic fatigue for 2 years now. I got it as a result of having autoimmune disease followed by chronic stress chronic migraines...

I have ME/cfs and multiple auto immune conditions. I am looking for help to support my immune system

Got to see Gp finally today ! I have had every test done on me now I think I have had mild asthma fir over 15 years had a bad chest infection last August and...

Hi all! I'm new to this forum and just wanted to share my story and see if it is a familiar story to others with a diagnosis. Essentially I'm in search of a...

Hi I have had CFS for nearly ten years. A question I want to ask is I was under a lot of stress last year,more then usual from around April till middle of...

Hi I am really struggling again with tiredness and constant viral infections. Does anyone know of any supplements or anything I could suggest to my gp that I...

Has anyone else had problems with severe dizziness that is unbearable when I’m standing or sitting I also have a feeling of pressure inside my head and it...

How do people deal with negativity I have a lot of it myself as I get down why I have a bad flare up and feel it’s very unfair but how do you deal with it when...

I have my first appointment next month with the cfs clinic in St Albans. Can anyone advise what to expect on my first visit so I can be prepared?

I've been suffering Tenesmus since April. It disappeared pretty much in October and now it's back with a vengeance. I've had aa colonoscopy which has not shown...

I am in the process of getting tested for pots as well as my me/cfs does anyone else suffer with sever bloating no mater how big or how little you eat through...

Reading a mountaineering book I was struck by how similar cfs is to altitude sickness. ME,CFS lists insomnia, dizziness, fatigue, headache, feeling sick, fast...

Should help us