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Pelvic nerve damage
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SO MUCH PAIN - and I get married in 2 weeks :(
Hi everyone I have posted a few times before, so I don't want to repeat myself! To give you a bit of background information - diagnosed with Endo 2014 after suffering for many years, have undergone 3 operations specifically for Endo, but had a few others that are kind of related to Endo, been on every
Hi everyone I have posted a few times before, so I don't want to repeat myself! To give you a bit of background information - diagnosed with Endo 2014 after suffering for many years, have undergone 3 operations specifically for Endo, but had a few others that are kind of related to Endo, been on every
Hidden
in
Endometriosis UK
6 years ago
anyone had a nerve block procedure done?
my son had an accident 18 months ago boxing. His recovery has been slow , recent mri scans are good and now his neuro has told him he has "nerve damage" . He is on amitripyline and gabapetin . On monday he is having a "nerve block" procedure which will be injected into the base of his skull , has anyone
my son had an accident 18 months ago boxing. His recovery has been slow , recent mri scans are good and now his neuro has told him he has "nerve damage" . He is on amitripyline and gabapetin . On monday he is having a "nerve block" procedure which will be injected into the base of his skull , has anyone
joben45
in
Headway
6 years ago
Hi Everyone, I'm Brandon
New to the forum and believe I have either CPPS (as a result of Prostatitis) or Pudendal Neuralgia. ' My symptoms include a vibration deep within my pelvis, a burning pain in my perineum (on and off - it also travels through different paths), left testicular pain (oh yeh, I'm a man!) and pain in the
New to the forum and believe I have either CPPS (as a result of Prostatitis) or Pudendal Neuralgia. ' My symptoms include a vibration deep within my pelvis, a burning pain in my perineum (on and off - it also travels through different paths), left testicular pain (oh yeh, I'm a man!) and pain in the
ga138650
in
Pelvic Pain Support Network
6 years ago
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My tens machine
What settings would you ladies advice x
What settings would you ladies advice x
Amieeellismay
in
Endometriosis UK
6 years ago
Shingles
Oh wise ones - please give me some advice. I am due to spend my usual Wednesday with my almost 98 year old mother tomorrow but I’ve just phoned her to confirm arrangements only to be told she has developed shingles, poor thing. Now, I’ve just been reading up about it and it seems to me that you can’t
Oh wise ones - please give me some advice. I am due to spend my usual Wednesday with my almost 98 year old mother tomorrow but I’ve just phoned her to confirm arrangements only to be told she has developed shingles, poor thing. Now, I’ve just been reading up about it and it seems to me that you can’t
LizzieGuinn
in
PMRGCAuk
6 years ago
Tens machine
Trying out my tens machine for the first time.. very nervous what setting do you guys use
Trying out my tens machine for the first time.. very nervous what setting do you guys use
Amieeellismay
in
Endometriosis UK
6 years ago
Going Crazy!!!!!!!!!!!
I feel like I am going crazy..... nothing helps my RLS.........nothing. I have tried everything, cold/hot packs, tens machine, heat creams and sprays, GABA, magnesium, pramipexole, tramadol, muscle relaxer......and the list goes on. It shifts from one arm to the other, one leg to the other.... then
I feel like I am going crazy..... nothing helps my RLS.........nothing. I have tried everything, cold/hot packs, tens machine, heat creams and sprays, GABA, magnesium, pramipexole, tramadol, muscle relaxer......and the list goes on. It shifts from one arm to the other, one leg to the other.... then
lalake
in
Restless Legs Syndrome
6 years ago
Hiya ladies has anyone tried tens machine..
Would really like some feed back before I buy
Would really like some feed back before I buy
Amieeellismay
in
Endometriosis UK
6 years ago
REPOSTED - replies wanted - help please! Adenomyosis and answers
nerve
damage
(from where the deep endometriosis from previous surgeries has been removed, the nerve endings it grew remain and still cause symptoms etc) 3) adenomysosis Now, they have told me that my above symptoms, and the fact that the medical menopause was so beneficial to me (it seriously got
nerve
damage
(from where the deep endometriosis from previous surgeries has been removed, the nerve endings it grew remain and still cause symptoms etc) 3) adenomysosis Now, they have told me that my above symptoms, and the fact that the medical menopause was so beneficial to me (it seriously got
Hidden
in
Endometriosis UK
6 years ago
REPOSTED - replies wanted - help please! Adenomyosis and questions
nerve
damage
(from where the deep endometriosis from previous surgeries has been removed, the nerve endings it grew remain and still cause symptoms etc) 3) adenomysosis Now, they have told me that my above symptoms, and the fact that the medical menopause was so beneficial to me (it seriously got
nerve
damage
(from where the deep endometriosis from previous surgeries has been removed, the nerve endings it grew remain and still cause symptoms etc) 3) adenomysosis Now, they have told me that my above symptoms, and the fact that the medical menopause was so beneficial to me (it seriously got
Hidden
in
Pelvic Pain Support Network
6 years ago
Thyroid,coeliacs,b12????
Can anybody help me The doctors say I have interactive thyroid and have been giving me 200 mcg of thyroxine and I still don't feel right . I have given up with the doctors as i feel much better not taking thyroxine , but about 3 weeks into not raking them I feel really tired so I start taking them for
Can anybody help me The doctors say I have interactive thyroid and have been giving me 200 mcg of thyroxine and I still don't feel right . I have given up with the doctors as i feel much better not taking thyroxine , but about 3 weeks into not raking them I feel really tired so I start taking them for
scarlet35
in
Thyroid UK
6 years ago
HELP PLEASE - adenomyosis and questions
nerve
damage
(from where the deep endometriosis from previous surgeries has been removed, the nerve endings it grew remain and still cause symptoms etc) 3) adenomysosis Now, they have told me that my above symptoms, and the fact that the medical menopause was so beneficial to me (it seriously
nerve
damage
(from where the deep endometriosis from previous surgeries has been removed, the nerve endings it grew remain and still cause symptoms etc) 3) adenomysosis Now, they have told me that my above symptoms, and the fact that the medical menopause was so beneficial to me (it seriously
Hidden
in
Pelvic Pain Support Network
6 years ago
HELP PLEASE - Adenomyosis questions
nerve
damage
(from where the deep endometriosis from previous surgeries has been removed, the nerve endings it grew remain and still cause symptoms etc) 3) adenomysosis Now, they have told me that my above symptoms, and the fact that the medical menopause was so beneficial to me (it seriously got rid
nerve
damage
(from where the deep endometriosis from previous surgeries has been removed, the nerve endings it grew remain and still cause symptoms etc) 3) adenomysosis Now, they have told me that my above symptoms, and the fact that the medical menopause was so beneficial to me (it seriously got rid
Hidden
in
Endometriosis UK
6 years ago
If it's not Chickenpox or Shingles...
I was diagnosed with phoritic RA ( as well as all the other arthritis ) put on a high dose of mexitrate by injection . Anyhow, broke out in a horrible rash on my hands and arms. Went to the chemist, they said heat rash and flogged me antihistamines. Rash continued to be really painful and incredibly
I was diagnosed with phoritic RA ( as well as all the other arthritis ) put on a high dose of mexitrate by injection . Anyhow, broke out in a horrible rash on my hands and arms. Went to the chemist, they said heat rash and flogged me antihistamines. Rash continued to be really painful and incredibly
Mcdebz
in
NRAS
6 years ago
Newbie: diagnosis of osteoarthritis not PA
Hi, wanted to pick some brains! I have had psoriasis for the last 24 years (am 44) which is on my elbows and few bits on my knees but haven't had any treatment for it for years. 18 months ago I went to my GP for some blood tests as I was feeling so tired I was falling asleep the minute I got home from
Hi, wanted to pick some brains! I have had psoriasis for the last 24 years (am 44) which is on my elbows and few bits on my knees but haven't had any treatment for it for years. 18 months ago I went to my GP for some blood tests as I was feeling so tired I was falling asleep the minute I got home from
Lulusymes
in
Beyond Psoriasis
6 years ago
Fed up
I'm new on here tonight came upon the site by accident, I have severe rls and don't really know which way to turn now, I'm on pregabalin already aswell as tramadol and oromorph, I've had a liver transplant last year and I'm also type 2 diabetic, I really need help, my GP has never acknowledged I've got
I'm new on here tonight came upon the site by accident, I have severe rls and don't really know which way to turn now, I'm on pregabalin already aswell as tramadol and oromorph, I've had a liver transplant last year and I'm also type 2 diabetic, I really need help, my GP has never acknowledged I've got
Hidden
in
Restless Legs Syndrome
6 years ago
Undiagnosed nerve pain
Hello. I am 44 years old, male from Sweden. Since October 2015 I've had really distressing nerve pain, most severe in my feet, but also in my face and lower back. I've had 4 neurological investigations (with EMG, nerve conduction studies and thermal thresholds), seen 7 neurologists and 30+ other doctors
Hello. I am 44 years old, male from Sweden. Since October 2015 I've had really distressing nerve pain, most severe in my feet, but also in my face and lower back. I've had 4 neurological investigations (with EMG, nerve conduction studies and thermal thresholds), seen 7 neurologists and 30+ other doctors
JakeBlake
in
Neuropathy Support
6 years ago
Effects of meningitis
Does people with the TB meningitis get (chronic granulomatous lymphadenitis) swelling in the neck forming pus. Does it will cure on it's own? Or it needs a surgery
Does people with the TB meningitis get (chronic granulomatous lymphadenitis) swelling in the neck forming pus. Does it will cure on it's own? Or it needs a surgery
Vissusaila
in
Meningitis Now
6 years ago
Viral Meningitis
I had viral meningitis with Influenza B in March 2018. I have had a horrible headache everyday since then. I also have major cognitive problems and I have trouble walking. I also was diagnosed with Chiari malformation but the doctor said I had it since childhood and that wasn’t the problem. I am off
I had viral meningitis with Influenza B in March 2018. I have had a horrible headache everyday since then. I also have major cognitive problems and I have trouble walking. I also was diagnosed with Chiari malformation but the doctor said I had it since childhood and that wasn’t the problem. I am off
buttons2ct
in
Meningitis Now
6 years ago
Pudendal nerve damage following insertion of Atoms Sling
Hi. My husband had an Atoms Sling installed for incontinence in November. He had a Prostatectomy done around 14 years ago, followed by a round of radiation therapy. The incontinence grew worse until he felt that he needed this device to improve the quality of his life. He felt intense pain after
Hi. My husband had an Atoms Sling installed for incontinence in November. He had a Prostatectomy done around 14 years ago, followed by a round of radiation therapy. The incontinence grew worse until he felt that he needed this device to improve the quality of his life. He felt intense pain after
Pudendal72
in
Pelvic Pain Support Network
6 years ago
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