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Pudendal Nerve Symptoms? Please read.
Not diagnosed yet, but after three years and my gyno thinking I’m crazy, I saw a new one today and he thinks it’s definitely my pudendal nerve. I am finally getting referred for an MRI and starting pelvic floor therapy. My symptoms come and go and are brought on by stress, exercise (lifting weights maybe
Not diagnosed yet, but after three years and my gyno thinking I’m crazy, I saw a new one today and he thinks it’s definitely my pudendal nerve. I am finally getting referred for an MRI and starting pelvic floor therapy. My symptoms come and go and are brought on by stress, exercise (lifting weights maybe
Hidden
in
Pelvic Pain Support Network
4 years ago
l-Lysine
I have been diagnosed with shingles and recommended to take L-Lysine 500 mgs on an empty stomach. Will I still have to leave it an hour after I take my Levothyroxine before I take the L-Lysine? It was ask recommend to me to during apple cider vinegar on an empty stomach so I thought I’d take the L-Lysine
I have been diagnosed with shingles and recommended to take L-Lysine 500 mgs on an empty stomach. Will I still have to leave it an hour after I take my Levothyroxine before I take the L-Lysine? It was ask recommend to me to during apple cider vinegar on an empty stomach so I thought I’d take the L-Lysine
Citta
in
Thyroid UK
4 years ago
Symptoms, triggers, flare ups, pain relief...what are yours?
Hello ladies- hope you are all well and coping ok during this horrid period in time. I was wondering if you could describe your pain (where, what it feels like), when you have a flare up and what triggers it and any other symptoms you experience as a result of adenomyosis. Thought it might help to know
Hello ladies- hope you are all well and coping ok during this horrid period in time. I was wondering if you could describe your pain (where, what it feels like), when you have a flare up and what triggers it and any other symptoms you experience as a result of adenomyosis. Thought it might help to know
Gill1977
in
Adenomyosis Advice Association
4 years ago
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Got thinking....
I am out with a friend but currently st doctors office waiting for nerve block. This friend knows me pretty good and we were catching up about well my withdrawal, state of relationship etc... I have always valued this persons opinion and trusted that they would give it to me straight. It seems with
I am out with a friend but currently st doctors office waiting for nerve block. This friend knows me pretty good and we were catching up about well my withdrawal, state of relationship etc... I have always valued this persons opinion and trusted that they would give it to me straight. It seems with
CanuckAnon
in
Anxiety and Depression Support
4 years ago
Show Your Face /Stay At home Campaign -PLEASE READ AND PROMOTE-THANKYOU
SHARE, SHARE,SHARE PLEASE JUST STAY HOME FOR US ELDERS /IMMUNE COMPROMISED LETS TELL OUR STORIES AND SHOW OUR FACES. SO EVERYONE KNOWS WHO WE ARE. I am 53, a daughter, sister, wife, mother of 2 and friend. I was a primary school teacher for 13 years and have been a child protection social worker for
SHARE, SHARE,SHARE PLEASE JUST STAY HOME FOR US ELDERS /IMMUNE COMPROMISED LETS TELL OUR STORIES AND SHOW OUR FACES. SO EVERYONE KNOWS WHO WE ARE. I am 53, a daughter, sister, wife, mother of 2 and friend. I was a primary school teacher for 13 years and have been a child protection social worker for
SASSY196
in
My Ovacome
4 years ago
Advice for pushing to get a lap
Hi everyone, I've been dealing with a variety of symptoms over a period of years and for a long time I didn't link the likes of my sciatica (scheduled MRI was cancelled on the day because consultant told me he could "feel" a slipped disk) and IBS (had colonoscopy - clear of course) because I was on
Hi everyone, I've been dealing with a variety of symptoms over a period of years and for a long time I didn't link the likes of my sciatica (scheduled MRI was cancelled on the day because consultant told me he could "feel" a slipped disk) and IBS (had colonoscopy - clear of course) because I was on
Haylz95
in
Endometriosis UK
4 years ago
Continued rant
Some of you may have seen my post yesterday about those people who have been stripping the supermarkets bare without any thought for others, particularly those who are more vulnerable or at high risk, in fact a surprising number of people replied and most seem to have had similar experiences which prompted
Some of you may have seen my post yesterday about those people who have been stripping the supermarkets bare without any thought for others, particularly those who are more vulnerable or at high risk, in fact a surprising number of people replied and most seem to have had similar experiences which prompted
mickam
in
NRAS
4 years ago
Nerve pain after ICD repositioning nerve block.
Hi everyone, i had my icd repositioned under the muscle, via sedation and a nerve block Friday. Has anyone else had this done, as im 4 days in and still have alot of pain in my arm and shoulder feels like nerve pain which im assuming is from the injections as didnt have this ist time around, pain killers
Hi everyone, i had my icd repositioned under the muscle, via sedation and a nerve block Friday. Has anyone else had this done, as im 4 days in and still have alot of pain in my arm and shoulder feels like nerve pain which im assuming is from the injections as didnt have this ist time around, pain killers
Eastwood25
in
British Heart Foundation
4 years ago
Can Ozone Therapy Really Cure Virsuses such as COVID-19?
A Plausible “Penny” Costing Effective Treatment for Corona Virus – Ozone Therapy by ROWENSU CLINIC Pre-publication Study Comments by Dr. Rowen I have just uploaded a paper with high relevance to coronavirus to my office website. Due to formatting, the scientific references were omitted. However,
A Plausible “Penny” Costing Effective Treatment for Corona Virus – Ozone Therapy by ROWENSU CLINIC Pre-publication Study Comments by Dr. Rowen I have just uploaded a paper with high relevance to coronavirus to my office website. Due to formatting, the scientific references were omitted. However,
bepo
in
Cure Parkinson's
4 years ago
More TENS stuff
I added more TENS and EMS vids for you all to marvel at. https://www.vlcfa.org/viewtopic.php?f=37&t=249 https://youtu.be/KO9VbAw6KCc?list=PL8tJ0qedhHX7aG_jlbev8EjP8ybEEu9Zg And, I have started adding links to some of the science behind TENS and spasticity. https://www.vlcfa.org/viewtopic.php?f=37&t=
I added more TENS and EMS vids for you all to marvel at. https://www.vlcfa.org/viewtopic.php?f=37&t=249 https://youtu.be/KO9VbAw6KCc?list=PL8tJ0qedhHX7aG_jlbev8EjP8ybEEu9Zg And, I have started adding links to some of the science behind TENS and spasticity. https://www.vlcfa.org/viewtopic.php?f=37&t=
monkeybus
in
AMN EASIER
4 years ago
Checking in
Hello everyone ,I've been on this site for a year since I started having my neuromuscular pelvic floor dysfunction.I would love to know people's journeys that you've been on and what has worked and what hasn't worked... if it's ongoing or if it has resolved... As for me I did the usual round the doctors
Hello everyone ,I've been on this site for a year since I started having my neuromuscular pelvic floor dysfunction.I would love to know people's journeys that you've been on and what has worked and what hasn't worked... if it's ongoing or if it has resolved... As for me I did the usual round the doctors
kalecolbe12
in
Pelvic Pain Support Network
4 years ago
Advice on taking Nefopam please
Hi, I have fibromyalgia- diagnosed last year. I also have depression and anxiety. The fibro pain has been getting worse daily for at least a year now. I’ve been taking 30mg/500mg cocodomol which didn’t help so have weaned off of that on dr’s advice, tried naproxen..helped for around a week and then
Hi, I have fibromyalgia- diagnosed last year. I also have depression and anxiety. The fibro pain has been getting worse daily for at least a year now. I’ve been taking 30mg/500mg cocodomol which didn’t help so have weaned off of that on dr’s advice, tried naproxen..helped for around a week and then
Hidden
in
Pain Concern
4 years ago
TENS/FES
I did a little write up on TENS/FES, see the pic, that's my leg, that is. I did a vid as well. I'll post some more over the weekend. I love TENS. https://www.vlcfa.org/viewtopic.php?f=37&t=222&p=244#p244
I did a little write up on TENS/FES, see the pic, that's my leg, that is. I did a vid as well. I'll post some more over the weekend. I love TENS. https://www.vlcfa.org/viewtopic.php?f=37&t=222&p=244#p244
monkeybus
in
AMN EASIER
4 years ago
Need Home Care Suggestions. ANYTHING That will help. Alone With Just a Heating Pad! Going Crazy
I have been to so many doctors and specialists to see what was wrong with me. It took becoming incontinent and going to a urologist, she sent me to a PT that worked with pelvic floor rehabilitation. I was going there once a week for manual inner vaginal muscle pressure. Then my state insurance stopped
I have been to so many doctors and specialists to see what was wrong with me. It took becoming incontinent and going to a urologist, she sent me to a PT that worked with pelvic floor rehabilitation. I was going there once a week for manual inner vaginal muscle pressure. Then my state insurance stopped
Hidden
in
Pelvic Pain Support Network
4 years ago
Never guess were solutions may be found!
I was tuned today on the laptop to "France 24" TV in English. French hospitals are inverstigating what might help patients with coronavirus infection. A number of substances were mentioned, and I just got the last of a word ending as "........clovir". Valacyclovir is a remedy after the onset of shingles
I was tuned today on the laptop to "France 24" TV in English. French hospitals are inverstigating what might help patients with coronavirus infection. A number of substances were mentioned, and I just got the last of a word ending as "........clovir". Valacyclovir is a remedy after the onset of shingles
vog292
in
CLL Support
4 years ago
Right L5S1 foraminotomy / Chronic back pain
I underwent surgery in May 2015 for Right L5S1 foraminotomy. I was discharged with dexamethasone for a few days to try and reduce the numbness I had in my right foot and toes, The numbness did not disappear, it got worse and spread. I returned to hospital 2 months later due to new onset reduced sensation
I underwent surgery in May 2015 for Right L5S1 foraminotomy. I was discharged with dexamethasone for a few days to try and reduce the numbness I had in my right foot and toes, The numbness did not disappear, it got worse and spread. I returned to hospital 2 months later due to new onset reduced sensation
misstopaz
in
Pain Concern
4 years ago
Nerve block
Hi everyone I had nerve block on Friday it was horrific absolutely terrible agony I had 5 injections in my face and I feel absolutely awful still after 3 days has anyone else had this? I don’t know how I’m supposed to be feeling I feel like someone has sucked the life out of me and I’m still in pain
Hi everyone I had nerve block on Friday it was horrific absolutely terrible agony I had 5 injections in my face and I feel absolutely awful still after 3 days has anyone else had this? I don’t know how I’m supposed to be feeling I feel like someone has sucked the life out of me and I’m still in pain
Braininjurysurvivor
in
Headway
4 years ago
Finally admitted the bad, ugly, sad path to realizing I messed up and needed help....
So new here. My story is complicated, messy and emotional... I was hurt at work in early 2015, I ended up working thru pain after physio was discontinued by workers compensation as I supposedly should have healed🤨. I had migraines, couldn’t bear lights, was dizzy, ears were ringing and so on. Aug of
So new here. My story is complicated, messy and emotional... I was hurt at work in early 2015, I ended up working thru pain after physio was discontinued by workers compensation as I supposedly should have healed🤨. I had migraines, couldn’t bear lights, was dizzy, ears were ringing and so on. Aug of
CanuckAnon
in
Anxiety and Depression Support
4 years ago
Levator muscle syndrome; Levator ani syndrome
Twelve years ago I was diagnosed with levator ani syndrome with excruciating pain. After seeing 19 doctors over 2 years, and trying botox injections, caudal epidural, acupuncture treatments, cold laser treatment, electric galvanic stimulation, cortisone shots, many kinds of pain medication and nerve
Twelve years ago I was diagnosed with levator ani syndrome with excruciating pain. After seeing 19 doctors over 2 years, and trying botox injections, caudal epidural, acupuncture treatments, cold laser treatment, electric galvanic stimulation, cortisone shots, many kinds of pain medication and nerve
nosagraft
in
Pelvic Pain Support Network
4 years ago
Diagnosis of nerve injury following pelvic surgery
Diagnosis of nerve injury following pelvic surgery Hi all, I am acting for various unfortunate ladies who have terrible chronic pelvic pain, affecting their groin/ legs etc and mobility after different types of pelvic surgery. In one case this is owing to the positioning of a staple in the pudendal nerve
Diagnosis of nerve injury following pelvic surgery Hi all, I am acting for various unfortunate ladies who have terrible chronic pelvic pain, affecting their groin/ legs etc and mobility after different types of pelvic surgery. In one case this is owing to the positioning of a staple in the pudendal nerve
CMSol
in
Pelvic Pain Support Network
4 years ago
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