Search
Search
About
Log in
Join
Experiences with
Pelvic nerve damage
Posts
Communities
2,317 public posts
Filter results
What to try next
Anyone out there with suggestions of what I can bring up with my pain clinic doctor is much appreciated. I've had chronic pain from 2 lower back prolapsed discs for 14 years. I maintained quite well for several years with swimming and exercise up until a flare up just over 5 years ago that just won't
Anyone out there with suggestions of what I can bring up with my pain clinic doctor is much appreciated. I've had chronic pain from 2 lower back prolapsed discs for 14 years. I maintained quite well for several years with swimming and exercise up until a flare up just over 5 years ago that just won't
Sazntef
in
Pain Concern
9 years ago
Hands!
Hi, i was wondering whether anyone else suffers with pain, pins and needles and numbness in hands. It's driving me crazy and is much worse at night and keeps me awake and wakes me up. I find it hard to do anything involving my hands, even lifting a cuppa is painful. If anyone suffers from this do you
Hi, i was wondering whether anyone else suffers with pain, pins and needles and numbness in hands. It's driving me crazy and is much worse at night and keeps me awake and wakes me up. I find it hard to do anything involving my hands, even lifting a cuppa is painful. If anyone suffers from this do you
Cacenffrwytha
in
Fibromyalgia Action UK
9 years ago
Mollaret's Meningitis.
Hi, I thought I would raise awareness about this awful condition. I have had three episodes of viral meningitis and hospitalised due to this condition, each bout has been confirmed with a Lumbar puncture as encephalitis viral meningitis. I have been confirmed as having Mollarets meningitis/encephalitis
Hi, I thought I would raise awareness about this awful condition. I have had three episodes of viral meningitis and hospitalised due to this condition, each bout has been confirmed with a Lumbar puncture as encephalitis viral meningitis. I have been confirmed as having Mollarets meningitis/encephalitis
Hidden
in
Meningitis Now
9 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Thanks for tip!
I can't remember who mentioned this on here but thanks for the tip about getting the large electrode pads for my tens unit. Makes a very great difference.
I can't remember who mentioned this on here but thanks for the tip about getting the large electrode pads for my tens unit. Makes a very great difference.
Calceolaria
in
Pain Concern
9 years ago
Cervical DDD multiple slipped disks,moderate stenosis, nerve compression, bone spurs, just need a chat!!
Hi there I'm a newbie to this site I think it would help having people to talk to who are familiar with my situation or similar issues. I have five disk's in my neck that have lost there water & two of which are impinging a c4 left lateral nerve root and a c8 these disks all have tears prolapses or protrusions
Hi there I'm a newbie to this site I think it would help having people to talk to who are familiar with my situation or similar issues. I have five disk's in my neck that have lost there water & two of which are impinging a c4 left lateral nerve root and a c8 these disks all have tears prolapses or protrusions
Ktchard
in
Pain Concern
9 years ago
Shingles!!!!
Hi everybody Here I am into the second week of shingles, so painful, I am taking 3 lots of tablets and cream, I have booked to see my doctor to ask for tablets instead of capsules, I worry I should be taking some form of URSO, does anybody not take anything, if so are they ok ?
Hi everybody Here I am into the second week of shingles, so painful, I am taking 3 lots of tablets and cream, I have booked to see my doctor to ask for tablets instead of capsules, I worry I should be taking some form of URSO, does anybody not take anything, if so are they ok ?
Sandie1
in
PBC Foundation
9 years ago
Shingles Vaccination
According to posters in my GPs' waiting room, I am now eligible for the shingles jab. However, I seem to remember advice on this forum saying that it's not advisable for patients receiving prednisolone. I have been looking at the Government's guidance for practitioners and unearthed the following: "
According to posters in my GPs' waiting room, I am now eligible for the shingles jab. However, I seem to remember advice on this forum saying that it's not advisable for patients receiving prednisolone. I have been looking at the Government's guidance for practitioners and unearthed the following: "
Annodomini
in
PMRGCAuk
9 years ago
Pelvic floor issues
Diagnosed with peudenal nerve entrapment, chronic pelvic pain (burning sensation in vaginal cavity), Have sever pain after walking over several 100 ft. Dr also diagnosed rectocele prolapse. Have tried PT, nerve blocks, pain meds. nothing works. Currently trying aquatic exercises to strengthen pelvic
Diagnosed with peudenal nerve entrapment, chronic pelvic pain (burning sensation in vaginal cavity), Have sever pain after walking over several 100 ft. Dr also diagnosed rectocele prolapse. Have tried PT, nerve blocks, pain meds. nothing works. Currently trying aquatic exercises to strengthen pelvic
Rossvillegal52
in
Pelvic Pain Support Network
9 years ago
Pregnancy and Fibro..........not me! I've been done lol.
Hi all, sorry it has been a while since I have been on, but I am alive Johnny five! Well just..... I have actually come on here to ask some advice as unfortunately my daughter has been diagnosed with Fibro and after months of fighting with her GP he finally decided last month to treat her for her symptoms
Hi all, sorry it has been a while since I have been on, but I am alive Johnny five! Well just..... I have actually come on here to ask some advice as unfortunately my daughter has been diagnosed with Fibro and after months of fighting with her GP he finally decided last month to treat her for her symptoms
vikki
in
Fibromyalgia Action UK
9 years ago
Newborn with aseptic meningitis
Hi. My newborn was diagnosed with meningitis on day 5. He was treated for 7 days and watched closely in the hospital. He had nothing abnormal in his blood or urine. His LP showed elevated levels of white blood in the 500's. Nothing ever grew from his cultures and they said he had aseptic meningitis.
Hi. My newborn was diagnosed with meningitis on day 5. He was treated for 7 days and watched closely in the hospital. He had nothing abnormal in his blood or urine. His LP showed elevated levels of white blood in the 500's. Nothing ever grew from his cultures and they said he had aseptic meningitis.
laurelm
in
Meningitis Now
9 years ago
Sacral nerve stimulator block
After numerous surgical procedures in and around the pelvic area, I am left in agony every time I pass urine, which continues for sometime after. Lots of tests and and trials after I am now to undergo a trial on the sacral nerve block. Has anyone had this procedure that could inform me please of any
After numerous surgical procedures in and around the pelvic area, I am left in agony every time I pass urine, which continues for sometime after. Lots of tests and and trials after I am now to undergo a trial on the sacral nerve block. Has anyone had this procedure that could inform me please of any
Relentless
in
Pelvic Pain Support Network
9 years ago
Still UCTD
Hi all, I am still in limbo as the rheumatologist (the one I went to for a 2nd opinion) is saying that my diagnosis will likely stay at UCTD for the time being until they catch other things going on in bloods / tests. Firstly, they definitely want to do a lip biopsy (should have been ordered 6 months
Hi all, I am still in limbo as the rheumatologist (the one I went to for a 2nd opinion) is saying that my diagnosis will likely stay at UCTD for the time being until they catch other things going on in bloods / tests. Firstly, they definitely want to do a lip biopsy (should have been ordered 6 months
bestbuddy
in
LUPUS UK
9 years ago
Post encephalitis
feeling isolated after recovering from encephalitis & not having much support from local consultants at my hospital or doctors as no one seems to think that any of my problems are down to having had encephalitis & if I'm honest they don't seem to have a clue about ongoing & lasting effects this has changed
feeling isolated after recovering from encephalitis & not having much support from local consultants at my hospital or doctors as no one seems to think that any of my problems are down to having had encephalitis & if I'm honest they don't seem to have a clue about ongoing & lasting effects this has changed
NickBossLewis
in
Headway
9 years ago
How Can I Speed Up Successful Pelvic Clitoral Myofascial Treatments w/ Trigger Point Release?
I have had success with myofascial phsio treatments all clitoral. One trigger point is released, pain there gone but the next sharp/burn point appears. It continues to heal and each new spot during treatment includes exposing the restricted myofascial band, releasing the trapped nerve and blood flow
I have had success with myofascial phsio treatments all clitoral. One trigger point is released, pain there gone but the next sharp/burn point appears. It continues to heal and each new spot during treatment includes exposing the restricted myofascial band, releasing the trapped nerve and blood flow
Pinky2233
in
Pelvic Pain Support Network
9 years ago
Success with nerve blocks for chronic pelvic pain?
I have severe endometriosis and adenomyosis. They cause relentless pelvic pain so severe that I'm on morphine. I'm keen to try nerve blocks to try and make things more comfortable and I've been referred to a pain clinic. What sort of nerve blocks have people tried (particularly for uterine, bladder and
I have severe endometriosis and adenomyosis. They cause relentless pelvic pain so severe that I'm on morphine. I'm keen to try nerve blocks to try and make things more comfortable and I've been referred to a pain clinic. What sort of nerve blocks have people tried (particularly for uterine, bladder and
EE29
in
Pelvic Pain Support Network
9 years ago
Shingles & Flare
I haven't posted for about 10 months. Last I was moving back to our home after working away for three years. The move went well, we had almost 5 months at home, and being winter we got a lot of work done on inside of our house. It was fun and aside from the odd day on the couch it all went well.
I haven't posted for about 10 months. Last I was moving back to our home after working away for three years. The move went well, we had almost 5 months at home, and being winter we got a lot of work done on inside of our house. It was fun and aside from the odd day on the couch it all went well.
Chapter
in
LUPUS UK
9 years ago
Revitive
Simple question...anyone tried one with any good effect? Before you all start googling it - tray like device where you put your feet on and it wobbles sending electric currents up your lower legs. Seems rather like a TENS. Not cheap to buy although VAT free and some good offers around. But would like
Simple question...anyone tried one with any good effect? Before you all start googling it - tray like device where you put your feet on and it wobbles sending electric currents up your lower legs. Seems rather like a TENS. Not cheap to buy although VAT free and some good offers around. But would like
Bananas5
in
Pain Concern
9 years ago
Shoulder update.
Following up from my post "when its not Lupus or associated" Just got back from orthopedic appt. and told can't do surgery for rotator cuff and. Bicep slap tear (thanks physiotherapist for that!) as Crps has now set in good and proper and as barnclown said surgery and crps are a definite no no. So referred
Following up from my post "when its not Lupus or associated" Just got back from orthopedic appt. and told can't do surgery for rotator cuff and. Bicep slap tear (thanks physiotherapist for that!) as Crps has now set in good and proper and as barnclown said surgery and crps are a definite no no. So referred
littleeffie
in
LUPUS UK
9 years ago
Clinical Nerve Entrapment treatment in Nantes, France
Hi, I have a cluneal nerve entrapment of the Iliac crest diagnosed after 5 years of misery, by Mr Fitzgerald at The Spire, in Manchester. He told me that it is a common yet poorly understood condition. I told my pain clinic at Hope Hospital, who said they had never heard of the diagnosis. I have had
Hi, I have a cluneal nerve entrapment of the Iliac crest diagnosed after 5 years of misery, by Mr Fitzgerald at The Spire, in Manchester. He told me that it is a common yet poorly understood condition. I told my pain clinic at Hope Hospital, who said they had never heard of the diagnosis. I have had
HollyElsieN
in
Pelvic Pain Support Network
9 years ago
Pelvic Pain blog - hopeful, useful, especially about flare ups
Hello, I am 1 year into having chronic pelvic pain and wanted to share a resource which I have found particularly useful. It's a physio practice in San Francisco. They have a post which is about flare ups which I have come back to many times, it's so easy to forget the tools in it, but very useful and
Hello, I am 1 year into having chronic pelvic pain and wanted to share a resource which I have found particularly useful. It's a physio practice in San Francisco. They have a post which is about flare ups which I have come back to many times, it's so easy to forget the tools in it, but very useful and
Raybellene
in
Pelvic Pain Support Network
9 years ago
1
...
89
90
91
...
100
Next page
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Pain Concern
265 results
Meningitis Now
236 results
Endometriosis UK
229 results
View top 10 communities
Sort by
Most Relevant
Newest