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Pelvic nerve damage
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House like a Pharmacy
After having another crappy night and day in pain I had a mild panic today when I thought I'd ran out of Rennie's, non left in the 'bedside pharmacy' so ran to the large shelf I now have in the kitchen. On opening the cupboard I was greeted with a large box of pain killers falling on my head, whilst
After having another crappy night and day in pain I had a mild panic today when I thought I'd ran out of Rennie's, non left in the 'bedside pharmacy' so ran to the large shelf I now have in the kitchen. On opening the cupboard I was greeted with a large box of pain killers falling on my head, whilst
RedTeddy
in
IBS Network
3 years ago
Hypothyroidism-Lyme disease connection?
Has anyone here with Hashimoto's/hypothyroidism discovered they also have Lyme disease? Or that they've had it for years? A couple of knowledgeable friends have insisted I get checked for it, but the last time I knowingly got a few ticks was back in 1995! And, yes, some of my problems might have started
Has anyone here with Hashimoto's/hypothyroidism discovered they also have Lyme disease? Or that they've had it for years? A couple of knowledgeable friends have insisted I get checked for it, but the last time I knowingly got a few ticks was back in 1995! And, yes, some of my problems might have started
DandyThyro
in
Thyroid UK
3 years ago
Lucy Dawson: the model who got a mystery headache, a misdiagnosis – and a new mission in life
We see repeated failure to take seriously, failure to diagnose properly and long term consequences. Although not thyroid, this is an interesting article which raises the profile of autoimmune encephalitis. [i]
Lucy Dawson: the model who got a mystery headache, a misdiagnosis – and a new mission in
We see repeated failure to take seriously, failure to diagnose properly and long term consequences. Although not thyroid, this is an interesting article which raises the profile of autoimmune encephalitis. [i]
Lucy Dawson: the model who got a mystery headache, a misdiagnosis – and a new mission in
helvella
Thyroid UK
in
Thyroid UK
3 years ago
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Waiting for biologicals to kick in!
Hi guys, hope your all keeping well. Well as you know I started Humeria a month ago and it has been an agony time! I have been in so much pain all over, especially my hands and wrists! I phoned rumey nurse up on Thursday and then phoned back on Friday. I asked for some steroids or a steroid shot to help
Hi guys, hope your all keeping well. Well as you know I started Humeria a month ago and it has been an agony time! I have been in so much pain all over, especially my hands and wrists! I phoned rumey nurse up on Thursday and then phoned back on Friday. I asked for some steroids or a steroid shot to help
Carolsos
in
NRAS
3 years ago
Cholesterol-lowering drug to be offered to thousands on the NHS
The treatment will be rolled out to those who have already suffered a heart attack or stroke. A cholesterol-lowering drug that could save tens of thousands of lives over the next decade will be offered to people on the NHS. Inclisiran, described as a “game-changer”, is hoped to prevent thousands of
The treatment will be rolled out to those who have already suffered a heart attack or stroke. A cholesterol-lowering drug that could save tens of thousands of lives over the next decade will be offered to people on the NHS. Inclisiran, described as a “game-changer”, is hoped to prevent thousands of
2greys
in
Lung Conditions Community Forum
3 years ago
Deeply grateful to all the replies about agonising shoulder pain
Many thanks to all of you Kind people for your advice regarding my agonising shoulder pain. I am currently trying my Tens machine which I had forgotten about and which someone had suggested. I found paracetamol was useless, as was Ibuprofen. I previously suffered from duodenitis when taking nsaids,
Many thanks to all of you Kind people for your advice regarding my agonising shoulder pain. I am currently trying my Tens machine which I had forgotten about and which someone had suggested. I found paracetamol was useless, as was Ibuprofen. I previously suffered from duodenitis when taking nsaids,
butterflyfarm
in
PMRGCAuk
3 years ago
Great piece in the New York Times
NOTHING COULD PREPARE ME FROM WATCHING MY WIFE, JUDY, SLIP AWAY By Tom Coughlin Mr. Coughlin, a two-time Super Bowl-winning head coach, led the New York Giants, Jacksonville Jaguars and Boston College Eagles. Someone recently asked me why my wife, Judy, isn’t in any of the photos from our Jay Fund Foundation
NOTHING COULD PREPARE ME FROM WATCHING MY WIFE, JUDY, SLIP AWAY By Tom Coughlin Mr. Coughlin, a two-time Super Bowl-winning head coach, led the New York Giants, Jacksonville Jaguars and Boston College Eagles. Someone recently asked me why my wife, Judy, isn’t in any of the photos from our Jay Fund Foundation
Regann
in
PSP Association
3 years ago
On going pain.
For over nine years now, I have suffered pain, which over the years has worsened each and every year. At the begining I felt very much that my GPs didn’t believe me at all, one even saying to me that it’s time I let go of this, as there’s nothing wrong with me. I have tried pain management, bought practically
For over nine years now, I have suffered pain, which over the years has worsened each and every year. At the begining I felt very much that my GPs didn’t believe me at all, one even saying to me that it’s time I let go of this, as there’s nothing wrong with me. I have tried pain management, bought practically
Judo1010
in
Pain Concern
3 years ago
Tens
Glad my tens post started some laughs
Glad my tens post started some laughs
edwangy
in
IBS Network
3 years ago
Tens machine
Has anyone tried tens machine? I have terrible pain and trapped wind IBS C and thought I'd try a tens machine. I bought a reasonably priced one and it really helps with trapped gas. Just place the contacts on your belly where you are in pain it helps to relax the colon allow gas to pass. There is also
Has anyone tried tens machine? I have terrible pain and trapped wind IBS C and thought I'd try a tens machine. I bought a reasonably priced one and it really helps with trapped gas. Just place the contacts on your belly where you are in pain it helps to relax the colon allow gas to pass. There is also
edwangy
in
IBS Network
3 years ago
Past VM and the COVID Vaccine
Has anyone with a past history of VM taken the COVID-19 Vaccine? And If so how did you feel afterwards? And what brand did you take? My son had viral meningitis four years ago and is concerned that the vaccine will trigger a a viral meningitis attack. With this new Delta variant I am much more concerned
Has anyone with a past history of VM taken the COVID-19 Vaccine? And If so how did you feel afterwards? And what brand did you take? My son had viral meningitis four years ago and is concerned that the vaccine will trigger a a viral meningitis attack. With this new Delta variant I am much more concerned
Dutch22
in
Meningitis Now
3 years ago
Failed rectocele/cystocele surgery
I had both repaired in 2018 but feel that I am back to square one, the physio says that I have some
nerve
damage
to the
pelvic
floor and the exercises aren’t really working. I have a pessary but to it out to clean it and now can’t get it back in. Has anyone had successful repeat surgery for this?
I had both repaired in 2018 but feel that I am back to square one, the physio says that I have some
nerve
damage
to the
pelvic
floor and the exercises aren’t really working. I have a pessary but to it out to clean it and now can’t get it back in. Has anyone had successful repeat surgery for this?
weegiesmam
in
Pelvic Pain Support Network
3 years ago
What I have learned from 1 year with Early Onset PD - "Glass Half Full"
I decided to keep a journal of my journey - it has been quite a year but I have learned a lot. some of which maybe relevant for new and older PD people. I am not a doctor and this is not a medical opinion but there is lots available to make a stand against PD https://fightparkinsonsdisease.files.wordpress.com
I decided to keep a journal of my journey - it has been quite a year but I have learned a lot. some of which maybe relevant for new and older PD people. I am not a doctor and this is not a medical opinion but there is lots available to make a stand against PD https://fightparkinsonsdisease.files.wordpress.com
blazyb
in
Cure Parkinson's
3 years ago
Give me a break!
So after contracting shingles in the eye over 4 & 1/2 months ago I’m still suffering with post herpetic neuralgia. Tried all sorts of drugs and a nerve block injection and nothing has helped. Initially the hospital upped my steroids from 12mg I was on to 25mg as they weren’t sure if it was GCA. After
So after contracting shingles in the eye over 4 & 1/2 months ago I’m still suffering with post herpetic neuralgia. Tried all sorts of drugs and a nerve block injection and nothing has helped. Initially the hospital upped my steroids from 12mg I was on to 25mg as they weren’t sure if it was GCA. After
Griggser
in
PMRGCAuk
3 years ago
Treatments for Erythromelalgia
Hello, Community. I have Lupus, severe Raynaud's and a long history of secondary erythromelalgia of my feet. It has got steadily worse over the last few years and the persistent effects are now deemed to be ischaemia reperfusion injury. It is much worse when the weather is hot or I have been walking
Hello, Community. I have Lupus, severe Raynaud's and a long history of secondary erythromelalgia of my feet. It has got steadily worse over the last few years and the persistent effects are now deemed to be ischaemia reperfusion injury. It is much worse when the weather is hot or I have been walking
skylark15
in
Scleroderma & Raynaud's UK (SRUK)
3 years ago
Lignocaine infusions for erythromelalgia
Hello, Community. I have Lupus, severe Raynaud's and a long history of secondary erythromelalgia of my feet. It has got steadily worse over the last few years and the persistent effects are now deemed to be ischaemia reperfusion injury. It is much worse when the weather is hot or I have been walking
Hello, Community. I have Lupus, severe Raynaud's and a long history of secondary erythromelalgia of my feet. It has got steadily worse over the last few years and the persistent effects are now deemed to be ischaemia reperfusion injury. It is much worse when the weather is hot or I have been walking
skylark15
in
LUPUS UK
3 years ago
Thought it was under control after years of multiple serious surgeries and diet changes but now facing new battles - any advice welcome
Hello all, I was diagnosed with endometriosis aged 21 after 8 years of awful problems and symptoms. After my first laparoscopy I was initially told it was “just a few spots of endometriosis” and my options were chemically induced menopause (gnrh and add back HRT) or to get pregnant and they fitted
Hello all, I was diagnosed with endometriosis aged 21 after 8 years of awful problems and symptoms. After my first laparoscopy I was initially told it was “just a few spots of endometriosis” and my options were chemically induced menopause (gnrh and add back HRT) or to get pregnant and they fitted
Greys90
in
Endometriosis UK
3 years ago
Update to "Feeling Terrible Lately".
Hello all, Well the reason I felt so terrible was because I ended up having Lyme disease.. I ended up seeing my family Dr. as I was starting to feel bad again. I was on antibiotics for 15 days and am doing well now. It got me behind my knee, so I didn't notice it at first. They are areal problem in our
Hello all, Well the reason I felt so terrible was because I ended up having Lyme disease.. I ended up seeing my family Dr. as I was starting to feel bad again. I was on antibiotics for 15 days and am doing well now. It got me behind my knee, so I didn't notice it at first. They are areal problem in our
fxdx1
in
CLL Support
3 years ago
Shingrix OK For Immunocompromised Adults
This article was posted today on CLLSLL groups.io and is reposted here with permission from Dr. Furman https://groups.io/g/CLLSLL/message/31608?reply=1 [i] Re: Shingrix OK For Immunocompromised Adults [/i] [i]From: Rick Furman Date: Fri, 30 Jul 2021 08:43:32 EDT[/i] [i]-[/i] [i]Shingles is the result
This article was posted today on CLLSLL groups.io and is reposted here with permission from Dr. Furman https://groups.io/g/CLLSLL/message/31608?reply=1 [i] Re: Shingrix OK For Immunocompromised Adults [/i] [i]From: Rick Furman Date: Fri, 30 Jul 2021 08:43:32 EDT[/i] [i]-[/i] [i]Shingles is the result
lankisterguy
Volunteer
in
CLL Support
3 years ago
excessive blood loss
hi how's everyone doing? for those who don't know me, I've had issues with my periods since 13 and diagnosed with endometriosis since 05, I've been on every combination of hormonal treatments and pain relief medications u can imagine (to the point where I'd rattle when I walked) I've had so many operations
hi how's everyone doing? for those who don't know me, I've had issues with my periods since 13 and diagnosed with endometriosis since 05, I've been on every combination of hormonal treatments and pain relief medications u can imagine (to the point where I'd rattle when I walked) I've had so many operations
dodgeviperdiva
in
Endometriosis UK
3 years ago
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