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Swollen penis between cut area and below the head.
I had the circumcision done last weekend exactly a week ago after being diagnosed with phimosis . So far I have been on rest for the first week. The first change of dressing was done right after two days of the operation and two days later( 4th day) the dressings removed by the doctor. Ever since that
I had the circumcision done last weekend exactly a week ago after being diagnosed with phimosis . So far I have been on rest for the first week. The first change of dressing was done right after two days of the operation and two days later( 4th day) the dressings removed by the doctor. Ever since that
Aray2018
in
Men's Health Forum
7 years ago
Which type of Arthritis?
Hi everyone, I have joint hypermobility and have just been told by Rheumatologist I have Arthritis in my feet which is likely caused by the hypermobility, he didnt say which type. Any ideas?
Hi everyone, I have joint hypermobility and have just been told by Rheumatologist I have Arthritis in my feet which is likely caused by the hypermobility, he didnt say which type. Any ideas?
Queencara78
in
Ehlers-Danlos Support UK
7 years ago
I got my first stocking yesterday but it's made my big toe nail red...
Hi, I got my first stocking yesterday. I asked for toeless but there was an error. I thought it would be ok but it's not. It's all red around the nail on my big toe and it's throbbing. Unfortunately I don't think I can wear it. Do you know if I can cut it at the toe until I get some toeless stockings
Hi, I got my first stocking yesterday. I asked for toeless but there was an error. I thought it would be ok but it's not. It's all red around the nail on my big toe and it's throbbing. Unfortunately I don't think I can wear it. Do you know if I can cut it at the toe until I get some toeless stockings
eleanorshutie
in
LSN
7 years ago
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Should I go to the doctors with these symptoms
Hi guys!!! I'm new here but I am wondering whether I should go to see a Doctor with this? I am 21 and I'm fairly sure this stuff is not normal. All my life my joints have been really loose. As in they would click and crack all the time, my jaw sometimes got stuck out of place if I yawned too widely
Hi guys!!! I'm new here but I am wondering whether I should go to see a Doctor with this? I am 21 and I'm fairly sure this stuff is not normal. All my life my joints have been really loose. As in they would click and crack all the time, my jaw sometimes got stuck out of place if I yawned too widely
Emilyeagleowl
in
Ehlers-Danlos Support UK
7 years ago
EDS and Bladder Failure
Hi Everyone, I had urodynamic tests today that showed that the nerves and muscles are doing nothing at all which explains why I haven't been able to pee without a catheter for the year. However, the consultant has said he doesn't know what to do about it because I have EDS. I was wondering if anyone
Hi Everyone, I had urodynamic tests today that showed that the nerves and muscles are doing nothing at all which explains why I haven't been able to pee without a catheter for the year. However, the consultant has said he doesn't know what to do about it because I have EDS. I was wondering if anyone
EBashford
in
Ehlers-Danlos Support UK
7 years ago
Diagnosis.. can anyone help me with the understanding of it all please
Hi, I was refered and recently now been diagnosed with hypermobility spectrum disorder bordering EDS (2017 EDS criteria) and chronic widespread pain-musculoskeletal predominant. That was on the 14th of July.. does this mean I have EDS? I am in so much pain..even more so, in my shoulders..one is so much
Hi, I was refered and recently now been diagnosed with hypermobility spectrum disorder bordering EDS (2017 EDS criteria) and chronic widespread pain-musculoskeletal predominant. That was on the 14th of July.. does this mean I have EDS? I am in so much pain..even more so, in my shoulders..one is so much
Leahmead1
in
Ehlers-Danlos Support UK
7 years ago
Skin irritation
I am new to this website and would like to find some answer's to this condition. My right thigh gets very itchy most at nights when in bed, some times the is a severe momentary pain in the thigh something like being stabbed with a red hot needle, I am driven to scratch the area severely, some times
I am new to this website and would like to find some answer's to this condition. My right thigh gets very itchy most at nights when in bed, some times the is a severe momentary pain in the thigh something like being stabbed with a red hot needle, I am driven to scratch the area severely, some times
joferking
in
MY SKIN
7 years ago
Need some advice, Please.
Hi everyone, my daughter had Ehlers - Danlos, Husband and I where told that we where carries of the gene. I have always ached and been in pain but recently I have lost weight thinking that it would help but I feel that I am constantly in pain, bones clicking and crunching, muscles aching. Had blood tests
Hi everyone, my daughter had Ehlers - Danlos, Husband and I where told that we where carries of the gene. I have always ached and been in pain but recently I have lost weight thinking that it would help but I feel that I am constantly in pain, bones clicking and crunching, muscles aching. Had blood tests
bighel
in
Ehlers-Danlos Support UK
7 years ago
Advice please
Hi I'm new here. I'm after some advice on diagnosis of ehlers-danlos. My brother and sister were diagnosed with it as kids (5 years old), I don't think I presented any symptoms then so I don't think I was taken to the clinic. From teens onwards I've had hypermobile joints, I've had 2 operations on one
Hi I'm new here. I'm after some advice on diagnosis of ehlers-danlos. My brother and sister were diagnosed with it as kids (5 years old), I don't think I presented any symptoms then so I don't think I was taken to the clinic. From teens onwards I've had hypermobile joints, I've had 2 operations on one
Hidden
in
Ehlers-Danlos Support UK
7 years ago
EDS type h and Cerebrospinal fluid leaks
Hi all, just a quick question is there anyone on here who has spontaneous CSF Leaks due to EDS type H? I have had recurrent leaks since 2007 and this March EDS type H was diagnosed as the cause.
Hi all, just a quick question is there anyone on here who has spontaneous CSF Leaks due to EDS type H? I have had recurrent leaks since 2007 and this March EDS type H was diagnosed as the cause.
DJML
in
Ehlers-Danlos Support UK
7 years ago
Benign hyper mobility is the same as EDS?
Wondering if benign hyper-mobility is still EDS? My primary doc said the U of M doc didn't say I have EDS. But center pain syndrome & Benign hyper mobility. Anyone know?
Wondering if benign hyper-mobility is still EDS? My primary doc said the U of M doc didn't say I have EDS. But center pain syndrome & Benign hyper mobility. Anyone know?
Thelittlebrowngirl
in
Ehlers-Danlos Support UK
7 years ago
Pregnancy and Ehlers Danlos Type 3
Hi all, I was diagnosed with Ehlers Danlos Type 3 Hyper-mobility around 3 years ago (at age 20) after numerous doctor and consultant visits, as many of you may relate. I score 9/9 on the Beighton scale and dislocate daily, but being so bendy means that 99% of the time my joints relocate on their own
Hi all, I was diagnosed with Ehlers Danlos Type 3 Hyper-mobility around 3 years ago (at age 20) after numerous doctor and consultant visits, as many of you may relate. I score 9/9 on the Beighton scale and dislocate daily, but being so bendy means that 99% of the time my joints relocate on their own
sophieviolet94
in
Ehlers-Danlos Support UK
7 years ago
EDS Hypermobility and CSF leaks
Hi all, just a quick question is there anyone on here who has spontaneous CSF Leaks due to EDS type H? I have had recurrent leaks since 2007 and this March EDS type H was diagnosed as the cause.
Hi all, just a quick question is there anyone on here who has spontaneous CSF Leaks due to EDS type H? I have had recurrent leaks since 2007 and this March EDS type H was diagnosed as the cause.
DJML
in
Ehlers-Danlos Support UK
7 years ago
Rheumatologist consultant
Hi I'm new here , and trying to get a final diagnosis for my daughter, possible EDS . She has now received an appointment to see a consultant Rheumatologist. My question is has anybody else seen Dr Y M A Elmiedany , as I here a lot of consultants do not recognise Hypermobility EDS . If so is he the right
Hi I'm new here , and trying to get a final diagnosis for my daughter, possible EDS . She has now received an appointment to see a consultant Rheumatologist. My question is has anybody else seen Dr Y M A Elmiedany , as I here a lot of consultants do not recognise Hypermobility EDS . If so is he the right
Sjac
in
Ehlers-Danlos Support UK
7 years ago
Hypermobility and EDS
For those suffering with Ehlers Danlos Syndrome (EDS), there's a new and revised international classification criteria for it here http://ehlers-danlos.com/2017-eds-international-classification/. Each heading has an article link. For those suffering with MCAS as well, there is an article written by
For those suffering with Ehlers Danlos Syndrome (EDS), there's a new and revised international classification criteria for it here http://ehlers-danlos.com/2017-eds-international-classification/. Each heading has an article link. For those suffering with MCAS as well, there is an article written by
Purpletop
in
LUPUS UK
8 years ago
Rheumatology appointment
Hi everyone I have had my first rheumatology appointment this morning and I'm left feeling quite confused. I've been told that I'm definetly hyper mobile (already knew that) but that he can't diagnose EDS as I don't have family history of it. There is apparently no point in sending me to a geneticist
Hi everyone I have had my first rheumatology appointment this morning and I'm left feeling quite confused. I've been told that I'm definetly hyper mobile (already knew that) but that he can't diagnose EDS as I don't have family history of it. There is apparently no point in sending me to a geneticist
OTskywalker
in
Ehlers-Danlos Support UK
8 years ago
the continuing 10 month saga yet again after being free for 4 years back with a vengance
knee clinic sent me down to walk in centre due to could not exersise on foot big problems trying to motivate big toe They say never seen anything like this before EHH well u have now mate ankle still giving way pain in knee, but i can Get upstars on it cos i push but that ankle im sure took the knee
knee clinic sent me down to walk in centre due to could not exersise on foot big problems trying to motivate big toe They say never seen anything like this before EHH well u have now mate ankle still giving way pain in knee, but i can Get upstars on it cos i push but that ankle im sure took the knee
minka
in
NRAS
8 years ago
The continuing 10 month saga of it will be alright on the night doc
knee clinic sent me down to walk in centre due to could not exersise on foot big problems trying to motivate big toe They say never seen anything like this before EHH well u have now mate ankle still giving way pain in knee, but i can Get upstars on it cos i push but that ankle im sure took the knee
knee clinic sent me down to walk in centre due to could not exersise on foot big problems trying to motivate big toe They say never seen anything like this before EHH well u have now mate ankle still giving way pain in knee, but i can Get upstars on it cos i push but that ankle im sure took the knee
minka
in
LUPUS UK
8 years ago
Scotland based EDS and bladder specialist
Hi, i think I might be asking too much, but is anyone aware of a specialist in gynae probs and an interest in EDS?? I've previously had a TVTO , and I don't want anymore surgery really, so want to find the best person this time that will take into account my EDS. Many thanks
Hi, i think I might be asking too much, but is anyone aware of a specialist in gynae probs and an interest in EDS?? I've previously had a TVTO , and I don't want anymore surgery really, so want to find the best person this time that will take into account my EDS. Many thanks
tdoll
in
Ehlers-Danlos Support UK
8 years ago
Finally got some answers
Went to the hospital Wednesday and I got the diagnosis I was expecting I have EDS type 3 but Bristol is trying to move away from calling it that as people seem to panic when they are told they have EDS , because as soon as they are told it could be EDS they look it up on the internet and see some of
Went to the hospital Wednesday and I got the diagnosis I was expecting I have EDS type 3 but Bristol is trying to move away from calling it that as people seem to panic when they are told they have EDS , because as soon as they are told it could be EDS they look it up on the internet and see some of
Annemac
in
Ehlers-Danlos Support UK
8 years ago
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