Andover Fibromyalgia & ME Community Group | HealthUnlocked

hi all.. hope everyone is looking after yourselves. Just a quick one that’s baffling me. When I have a fibromyalgia flare why do I crave salt and sugar so...

Hello there, I've recently been diagnosed with ME and FND after 7 months of fatigue and bizarre neurological symptoms. I had a lot of time off sick, and tried...

I won't write my whole saga, just to say my GP is thinking I have fibro and CFS, after first him and a specialist suggesting it was psychological of...

Is anyone else on Pregabalin and if so, how do you cope with 'zombiefying' side effects? I spend most of my working day on a computer and sometimes I feel like...

Hi. I am new to this group so wanted to introduce myself and see if anyone out there has some helpful suggestions that I haven't tried yet. I am 43 and a mum...

Hello I just got diagnosed with fibromyalgia just a few months ago I’m new here ...

is there any one that has hip pain,and if so what do you take and do for the pain.I’ve got osteoarthritis in both hips.all I take is gabapentin,and it don’t...

Hi all, I have had tender breasts for ever plus more recently (since menopause, I'm 73) very tender spots on my chest going round under my arms too....

Since I had Covid I've had burning nerve pain across my face, in my mouth and limbs. I feel that as I've no nerve damage that can be imaged that medicine has...

I really hope am not going out of the rules and guidelines to please for help, it’s killing me am just 25, I have exhausted everything I have yet I can’t do...

Can any long term suffers of fibro and cfs tell me if you ever find yourself ? By this meaning I don’t have a clue where my life’s going anymore I just feel...

I have been advised to do Tai Chi, but cannot find a class near me. I also looked into Pilates, but same thing. I live in Totton: anyone know of anything? Or...

Does anyone have me/cfs , fibromyalgia, but belive it could be lyme disease but cant get UK diagnoses

Hello I've got degenerative disc disease , occipital neuralgia, carpel tunnel ,and fibryomyalgia I believe, just bit worried about it all as I'm only 43,but...

Hi, I had diagnosedd with fibro 4 years ago. After long medication I got ulcers in stomach. Its been one year ulcers are not healing. I had IBS , cervical and...

Hi any else here on fire everyday😭

I'm p.nagakumar ,34 from India, New to this group, I have been diagnosed as fibromyalgia before that I went multiple hospitals for neck, shoulder blade, elbow...

I have been on Prednisolone for many years and with my rheumatologist's advice I am now trying to come off them. However after reducing from 10 mg to 5, I am...

Hi Members, Here's an excerpt with a quote from Des Quinn, Chair of Fibromyalgia Action UK (FMAUK) and from Pain Concern board of trustees chairman Dr Marin...

Excerpt from Action for ME's Newsletter 'At the start of September, Forward ME published an open letter addressing concerns and highlighting best practice with...

Please sign this PETITION: Change NICE guidelines for Chronic Pain. A recent article entitled Commonly used treatments for chronic pain can do more harm than...

Play the quiz in support of Andover Fibromyalgia & ME Community Group and make a difference. Grab your laptop or other device, cosy up and let’s have some...

Hi I just need to ask if people feel the same as me. When walking I feel like I’m walking in wet cement and feel like it’s pulling on my hip and my legs hurt...

Ahhhh woke up this morning with more pain than i had yesterday, my back, shoulders and both arms ahhh 😢💜

I get spasms everywhere. Legs fingers toes neck wrist. Its not painful just an idd feeling and i want to know if its to do with the fibro or something else.

Does anyone have issues sleeping due to fibro am finding it really hard to sleep, and when i do i get a few hrs and back awake again.

Going at a slower pace for me means I actually achieve more in the end. Have a good day everyone :)

Hi everyone any tips on energy much appreciated I’m so tired all the time x

Hi! I have fibromyalgia and M.E. and was wondering if anyone has any suggestions on living with m.e.

Peace love and joy to all xx