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Pelvic nerve damage
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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
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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
CRPS- Feet and toes.
What do people find helpful for CRPS in both legs? At the moment my toes turn red and feel like they are on fire? Any medication that help? Or nerve blocks, patches?
What do people find helpful for CRPS in both legs? At the moment my toes turn red and feel like they are on fire? Any medication that help? Or nerve blocks, patches?
Bunce
in
Pain Concern
9 years ago
Lyme disease - new research
I thought this might be interesting to those of you who have been told your Lyme disease is cured despite continuing symptoms.
The Search for Persisters
[i]Lyme disease–causing bacteria can outmaneuver antibiotics in vitro and manipulate the mouse immune system.[/i] http://www.the-scientist.com
I thought this might be interesting to those of you who have been told your Lyme disease is cured despite continuing symptoms.
The Search for Persisters
[i]Lyme disease–causing bacteria can outmaneuver antibiotics in vitro and manipulate the mouse immune system.[/i] http://www.the-scientist.com
PinkNinja
in
Thyroid UK
9 years ago
Pain every day no diagnosis!!
Hi all, wondered if anyone is still in the same position as me. I've been in pain every day for the past year. Still have no diagnosis! I've had a laparoscopy where I was diagnosed with endometriosis to find in fact t wasn't that at all! Biopsy were all clear. Still in pain after hormone treatment that
Hi all, wondered if anyone is still in the same position as me. I've been in pain every day for the past year. Still have no diagnosis! I've had a laparoscopy where I was diagnosed with endometriosis to find in fact t wasn't that at all! Biopsy were all clear. Still in pain after hormone treatment that
Georgialouise91
in
Pelvic Pain Support Network
9 years ago
Anyone had intercostal nerve block?
Hi everyone, I'm due to have an intercostal nerve block procedure next week. Anyone had one of those? Just want to hear about their experience.
Hi everyone, I'm due to have an intercostal nerve block procedure next week. Anyone had one of those? Just want to hear about their experience.
prodromos
in
Pain Concern
9 years ago
pudendal neuralgia diagnosis
Hello - this week I have finally be diagnosed.... relief (at the journey to find the expertise I needed and a diagonosis) is mixed with an intense awareness that this is it..... short of the miraculous there seems to be little hope for a significant degree of recovery.. I was very optimistic about specialist
Hello - this week I have finally be diagnosed.... relief (at the journey to find the expertise I needed and a diagonosis) is mixed with an intense awareness that this is it..... short of the miraculous there seems to be little hope for a significant degree of recovery.. I was very optimistic about specialist
_hope
in
Pelvic Pain Support Network
9 years ago
Searching for private treatment with Lidocaine
Hello again, I'm re-posting with a new title to be more specific. I'm looking for a private physician who has experience in intercostal nerve block Lidocaine injections on the thorax. Anyone who could help me on that?
Hello again, I'm re-posting with a new title to be more specific. I'm looking for a private physician who has experience in intercostal nerve block Lidocaine injections on the thorax. Anyone who could help me on that?
prodromos
in
Pain Concern
9 years ago
Need a doctor in UK for Lidocaine injections
Hi, six months after my left-side thoracotomy I was yesterday told by my surgeon (USA) that I need to get Lidocaine intercostal nerve-block injections for a persistent pain issue I'm having. So, I need to find someone in UK who has experience on this type nerve-block (intercostal Lidocaine injections
Hi, six months after my left-side thoracotomy I was yesterday told by my surgeon (USA) that I need to get Lidocaine intercostal nerve-block injections for a persistent pain issue I'm having. So, I need to find someone in UK who has experience on this type nerve-block (intercostal Lidocaine injections
prodromos
in
Pain Concern
9 years ago
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