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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 others cannot. I thought it was normal until my doc recently told me that not everybody can bend their fingers outwards the way I can. I have attached a pic from the
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 others cannot. I thought it was normal until my doc recently told me that not everybody can bend their fingers outwards the way I can. I have attached a pic from the
enthusiatjc
in
NRAS
7 years ago
Fat Shamed By Doctor
Ok. I'm new to this site. First time to post. Wanted a little love to come my way. Had a horrible doctors appoint today. Didn't even want to go, because I have gained weight, but knew I had to. She told me my weight is out of control and that I have to have an honest conversation with myself and to stop
Ok. I'm new to this site. First time to post. Wanted a little love to come my way. Had a horrible doctors appoint today. Didn't even want to go, because I have gained weight, but knew I had to. She told me my weight is out of control and that I have to have an honest conversation with myself and to stop
STTM67
in
Weight Loss Support
7 years ago
Introduction to shalomladydi
hi all, I'm introducing myself. I just recently turned 51 and was told last week that I need a total hip replacement for my left hip. I have had 2 previous surgeries on this hip to repair issues, but they have not worked. Surgery is scheduled for November 20th. I have Osteoarthritis in the whole lower
hi all, I'm introducing myself. I just recently turned 51 and was told last week that I need a total hip replacement for my left hip. I have had 2 previous surgeries on this hip to repair issues, but they have not worked. Surgery is scheduled for November 20th. I have Osteoarthritis in the whole lower
shalomladydi
in
Arthritis Action
7 years ago
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Knuckle joint replacement
Hi , I am a hairstylist and need my mcp knuckle replaced. Has anyone ever had this done? How long before you can go back to work? Or can you? Any advice is appreciated. Aloha, Bonnie
Hi , I am a hairstylist and need my mcp knuckle replaced. Has anyone ever had this done? How long before you can go back to work? Or can you? Any advice is appreciated. Aloha, Bonnie
Hasselleb
in
NRAS
7 years ago
Running with hypermobility and unstable ankles
Hi everyone, I'm a newbie to couch to 5k. I started last week and completed W2R1 today. I'm loving it! I started running to help me try and beat post natal depression. I'm so proud to have started. So far it's having a brilliant impact on my mental health and I can really feel a difference already
Hi everyone, I'm a newbie to couch to 5k. I started last week and completed W2R1 today. I'm loving it! I started running to help me try and beat post natal depression. I'm so proud to have started. So far it's having a brilliant impact on my mental health and I can really feel a difference already
laura_starts_running
in
Couch to 5K
7 years ago
SI joint dysfunction
Has anybody had an SI joint fusion done in the North of England and if so where please?
Has anybody had an SI joint fusion done in the North of England and if so where please?
Emma2017
in
Action on Pain
7 years ago
New here - RA sufferer - sad & lonely!
Hi everyone, my name is Julia and I was diagnosed with RA at the age of 29, I'm now 52. I have had numerous joint replacements, both hips, shoulder and triple foot fusion to name a few. I have been told i need my left hip replacing again and I am on the waiting list and have been for 16 weeks. Also
Hi everyone, my name is Julia and I was diagnosed with RA at the age of 29, I'm now 52. I have had numerous joint replacements, both hips, shoulder and triple foot fusion to name a few. I have been told i need my left hip replacing again and I am on the waiting list and have been for 16 weeks. Also
NannyJ
in
NRAS
7 years ago
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) only to have first been diagnosed with fibromyalgia, they have now confirmed that some of the pain could be caused by hypermobility in my younger years and over stretching
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) only to have first been diagnosed with fibromyalgia, they have now confirmed that some of the pain could be caused by hypermobility in my younger years and over stretching
audrey123
in
Ehlers-Danlos Support UK
7 years ago
Hypermobile joint syndrome and h-EDS
Hello, I've just been diagnosed with hypermobile joint sydrome. I've had significant health issues for about 11 years now but things got a lot worse over the past 6 months. I've had joint and muscle pains for more years than this but mostly self managed and saw an osteopath (which did help a bit)
Hello, I've just been diagnosed with hypermobile joint sydrome. I've had significant health issues for about 11 years now but things got a lot worse over the past 6 months. I've had joint and muscle pains for more years than this but mostly self managed and saw an osteopath (which did help a bit)
Kajarvie1985
in
Ehlers-Danlos Support UK
7 years ago
Pain in the leg
Just joined, first got restless leg in the Army where the cure was a run, then after 19 years things out of my control meant I left disabled with amongst other things a nervous system which was not what it was, I've had everything from restless legs to involuntary spasms that can throw me out of bed
Just joined, first got restless leg in the Army where the cure was a run, then after 19 years things out of my control meant I left disabled with amongst other things a nervous system which was not what it was, I've had everything from restless legs to involuntary spasms that can throw me out of bed
blue_is_the_colour
in
Restless Legs Syndrome
7 years ago
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?
Has anyone with hEDS been diagnosed with Endometriosis and if so, what treatment did you have and how did it affect you?
piperpiper1
in
Ehlers-Danlos Support UK
7 years ago
EDS or HMS
Hi, In June 2015 I was diagnosed with mild joint hypermobility and bilateral pes planus ( flat feet ). Since then my condition has only got worse, at the time I was only in a large amount of pain and my joints wouldn't dislocate. my joints constantly dislocate, I suffer from chronic pain and fatiague
Hi, In June 2015 I was diagnosed with mild joint hypermobility and bilateral pes planus ( flat feet ). Since then my condition has only got worse, at the time I was only in a large amount of pain and my joints wouldn't dislocate. my joints constantly dislocate, I suffer from chronic pain and fatiague
life_as_me_2003
in
Ehlers-Danlos Support UK
7 years ago
I am new to this forum
. I am a 78 years old Female and am recovering from a hip joint replacement operation in January and developed an infection straight away and had Antibiotics. Shortly afterwards got chest infection and more Antibiotics. Shortly after this I was diagnosed by my GP with PMR two weeks ago and taking a 5mg
. I am a 78 years old Female and am recovering from a hip joint replacement operation in January and developed an infection straight away and had Antibiotics. Shortly afterwards got chest infection and more Antibiotics. Shortly after this I was diagnosed by my GP with PMR two weeks ago and taking a 5mg
Hidden
in
PMRGCAuk
7 years ago
Joint dislocations
Does anyone else have trouble with finger /hand or toe/foot bone dislocations or subluxations? I keep getting a dislocation of a couple of metatarsals. Just got back from a GP apt (not my own named GP), who agreed it looked as if it had dislocated again and just says wear supportive shoes for a few weeks
Does anyone else have trouble with finger /hand or toe/foot bone dislocations or subluxations? I keep getting a dislocation of a couple of metatarsals. Just got back from a GP apt (not my own named GP), who agreed it looked as if it had dislocated again and just says wear supportive shoes for a few weeks
Rubylu
in
LUPUS UK
7 years ago
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 on the treadmill then an hour in the spa' way, and having weighed myself today I'm horrified by how much the numbers have gone up! I need to lose 3 stone to be
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 on the treadmill then an hour in the spa' way, and having weighed myself today I'm horrified by how much the numbers have gone up! I need to lose 3 stone to be
Hidden
in
Weight Loss Support
7 years ago
New to the group - Fed up
Hi; My 1st post. Im in my early 40's and got a diagnosis of Fibromyalgia early this year after having chronic pain in various parts of my body for just over 10 years. I was always very sporty and slim, and after getting a few injuries reduced my activity levels due to the high levels of pain. It started
Hi; My 1st post. Im in my early 40's and got a diagnosis of Fibromyalgia early this year after having chronic pain in various parts of my body for just over 10 years. I was always very sporty and slim, and after getting a few injuries reduced my activity levels due to the high levels of pain. It started
TaylorCat
in
Fibromyalgia Action UK
7 years ago
Start Here: There Will Be a Quiz Later
Welcome to life without Glycols! If you’ve just discovered you have a sensitivity or allergy to polyethylene glycol or other glycol compounds, you’ll need to learn how to find it, how to avoid it, and what alternatives there are. This is a community where you can find resources and share your experience
Welcome to life without Glycols! If you’ve just discovered you have a sensitivity or allergy to polyethylene glycol or other glycol compounds, you’ll need to learn how to find it, how to avoid it, and what alternatives there are. This is a community where you can find resources and share your experience
linabella
Administrator
in
Allergic to Glycols
7 years ago
fibromyalgia and joint hypermobility
When I was 7 I was diagnosed with juvenile rheumatoid arthritis.. as I grew older it developed according to the specialist... when I turned 16 I was told it was fibromyalgia and joint hypermobility throughout my body. Unfortunately non of the medication helps my pain. I've tried swimming but found I
When I was 7 I was diagnosed with juvenile rheumatoid arthritis.. as I grew older it developed according to the specialist... when I turned 16 I was told it was fibromyalgia and joint hypermobility throughout my body. Unfortunately non of the medication helps my pain. I've tried swimming but found I
fluffyloz85
in
Fibromyalgia Action UK
7 years ago
Hypermobility
Hi all. Since receiving my daughter diagnosis of Hypermobility have researched the condition and it resembles my symptoms the doctor has now classed as "nerve problems in the lower back". Is one of the symptoms not being able to gain weight as this has been a problem for me since I was young and have
Hi all. Since receiving my daughter diagnosis of Hypermobility have researched the condition and it resembles my symptoms the doctor has now classed as "nerve problems in the lower back". Is one of the symptoms not being able to gain weight as this has been a problem for me since I was young and have
John-bacon
in
Ehlers-Danlos Support UK
7 years ago
So surgery...
It seems that after about 4 years I'll need to fuse my ankle. Unfortunately the subtler joint fusion I received in August didn't fuse all the way and the infection I got in November and second surgery in December to remove the screws didn't help. I recently just got a steroid shot (again) and of course
It seems that after about 4 years I'll need to fuse my ankle. Unfortunately the subtler joint fusion I received in August didn't fuse all the way and the infection I got in November and second surgery in December to remove the screws didn't help. I recently just got a steroid shot (again) and of course
allard4life
in
NRAS
7 years ago
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