Hypermobility of joints
Does anybody else with RA have hypermobility of their joints? I feel like a freak because I can bend my fingers in ways that apparently other...
EDS or HMS
Hi, In June 2015 I was diagnosed with mild joint hypermobility and bilateral pes planus ( flat feet ). after being diagnosed with hypermobili...
Hypermobility syndrome, fybromyalgia
hi, I'm just new here and was hoping for some advice, I have been suffering for years with joint and muscle pain ( amongst other things ) onl...
Hypermobile EDS & Endometrosis
Has anyone with hEDS been diagnosed with Endometriosis and if so, what treatment did you have and how did it affect you?...
Understanding Needed Please
I scored 4/9 on the Beighton score and now being sent for heart scan and neck scan. Also if I'm found to have a cardio/ blood vessel problem ...
Hi all, I have just discovered I also have Hypermobility on top of Fibromyalgia, Raynaud's phenomenon, Photosensitivity, Trigeminal neuralgia...
Hypermobility Syndrome or EDS
I am new here and after seeing my rheumatologist for my RA, he diagnosed me with hypermobility syndrome too. I am just wondering what the dif...
Hypermobile joint syndrome and h-EDS
I have recently also been given a probable diagnosis of chronic fatigue syndrome to explain my other symptoms ( but this was by a neurologist...
Stomping Your TOE & Hypermobility Syndrome
Like really HOW do hou know if done damage to toes if stomp your toe and suffering from Hypermobility Syndrome or as its also known Ehlers Da...
Running with hypermobility and unstable ankles
They hurt a lot while running today and I'm worried that they will be my downfall....
fibromyalgia and joint hypermobility
I also have bipolar and S.p.t.s.d and I feel mental health in very much so a friend of fibro.....
Where To Go In London?
Hi all - I have Sjogren's and connective tissue disease, but over the past year I have been in excruciating pain and been to the GP and physi...
Need to lose 3 stone, under active thyroid and joint hypermobility syndrome
Hi, I'm new to this app but I'm determined to get myself sorted. I've been going to the gym for the last year, but on a very casual ' 10 mins...
Since receiving my daughter diagnosis of Hypermobility have researched the condition and it resembles my symptoms the doctor has now classed ...
May have been misdiagnosed
My sister has just been diagnosed with EDS type 3, she told my mum and my mum looked it up on google, she immediately thought of me. What do ...
My physiotherapist and also a doctor at the Pain Clinic told me in passing that I have JHS. I have often thought I had but my joints aren't m...
Vascular EDS...not even sure where to start
Hello people! I'm doing so-so of late....
Diagnosis? Is this Ehlers-Danlos?
I coped for years but over the past two years my health has declined to include muscle pain, IBS/ urine problems , faintness, vertigo and lig...
EDS and claiming disability.
She is working but it's becoming increasingly difficult and I was wondering if it was possible to claim disability benefits with a diagnosis ...
Hello everyone, I have finally had an assessment for a Pulmonary Rehabilitation in my local area, after a year on the waiting list.
I certainly don't want to turn this treatment down as I have read many times on this site that it is really helpful ( I have bronchiectasis a...
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