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Lost in a maze
Ive tryed so hard to keep my head up but its starting to go down hill again i hate this feeling and fuzzy head and pain its a roundabout im stuck on ive asked doctor to send me for nerve block injection he wont , ive ask for nerve conduction test he wont , he said i can go private ive already spent thousands
Ive tryed so hard to keep my head up but its starting to go down hill again i hate this feeling and fuzzy head and pain its a roundabout im stuck on ive asked doctor to send me for nerve block injection he wont , ive ask for nerve conduction test he wont , he said i can go private ive already spent thousands
paul078
in
Mental Health Support
4 years ago
Tips on managing pain please:)
Really struggling with severe pain. Waiting for my GP to get funding for a nerve block injection so there's a very long wait. Any ideas on how to cope with severe pain when meds aren't strong enough? Will have to try an alternative and someone has suggested Pregablin instead of Gabapentin but any tips
Really struggling with severe pain. Waiting for my GP to get funding for a nerve block injection so there's a very long wait. Any ideas on how to cope with severe pain when meds aren't strong enough? Will have to try an alternative and someone has suggested Pregablin instead of Gabapentin but any tips
Chocaholic41
in
Fibromyalgia Action UK
4 years ago
Meningitis/encephalitis/brain illness
To all you wonderful people who have suffered with all types of this debilitating illness, did you know that you come under The Mental Health umbrella????? Mainly because your brain doesn't function properly? Poor memories ,mixed ones, lost ones, you need to ask the people close to you to be honest and
To all you wonderful people who have suffered with all types of this debilitating illness, did you know that you come under The Mental Health umbrella????? Mainly because your brain doesn't function properly? Poor memories ,mixed ones, lost ones, you need to ask the people close to you to be honest and
Hexy
in
Meningitis Now
4 years ago
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tens
Did anyone try tens patches on their legs?
Did anyone try tens patches on their legs?
silvia10
in
Restless Legs Syndrome
4 years ago
Update..1 year post Cyberknife, 2 years post HIFU
Just a quick update: (brief reminder of my Hx: diagnosis at 50...PSA around 8 (2018). Opted for HIFU to try and preserve erectile function. After HIFU had erectile function but PSA dropped then rose..indicating failure. In 2019 had Cyberknife...PSA was 2.5 pre and 2.4 post...but now in July 2020, PSA
Just a quick update: (brief reminder of my Hx: diagnosis at 50...PSA around 8 (2018). Opted for HIFU to try and preserve erectile function. After HIFU had erectile function but PSA dropped then rose..indicating failure. In 2019 had Cyberknife...PSA was 2.5 pre and 2.4 post...but now in July 2020, PSA
rf3rf3
in
Prostate Cancer Network
4 years ago
So much knee pain!
Evening Everyone! Just a liitle moan if I may, as everyone else is fed up hearing the words "it hurts s much!". I have been on mtx for the last 6 years (tablets) which were changed last week to the Metoject Pen, I was also prescribed Prednisolone starting at 15mg a day for a week, then reducing weekly
Evening Everyone! Just a liitle moan if I may, as everyone else is fed up hearing the words "it hurts s much!". I have been on mtx for the last 6 years (tablets) which were changed last week to the Metoject Pen, I was also prescribed Prednisolone starting at 15mg a day for a week, then reducing weekly
Diamondpainting
in
NRAS
4 years ago
Pain relief patches?
Hello again Has anyone tried pain relief patches or tens machines. If soo do they help are the tens machines worth investing in. Need to try and manage this pain. Been allergic to most pain relief is not helping my situation at all.
Hello again Has anyone tried pain relief patches or tens machines. If soo do they help are the tens machines worth investing in. Need to try and manage this pain. Been allergic to most pain relief is not helping my situation at all.
Graduate2020
in
Endometriosis UK
4 years ago
Say no to hormones?
Does anyone actually say no to hormones and try to handle it in a more natural way? I’m on a double dose of cerazette at the moment. My hair is falling out massively, I haven’t had a libido in YEARS and I can’t stop putting weight on. Plus I’m still having a cycle (but no bleeding) under a double dose
Does anyone actually say no to hormones and try to handle it in a more natural way? I’m on a double dose of cerazette at the moment. My hair is falling out massively, I haven’t had a libido in YEARS and I can’t stop putting weight on. Plus I’m still having a cycle (but no bleeding) under a double dose
Hidden
in
Endometriosis UK
4 years ago
Living with Chronic Neuropathic Pain
There is much money in the pain and drug industry. Ethics and the recipients of these drugs do not factor into the bottom line. Profit and Loss Statements mean percentage increases at any cost. It is sad that chronic pain patients are made to feel like drug addicts and treated in a most callous way.
There is much money in the pain and drug industry. Ethics and the recipients of these drugs do not factor into the bottom line. Profit and Loss Statements mean percentage increases at any cost. It is sad that chronic pain patients are made to feel like drug addicts and treated in a most callous way.
Hidden
in
Pain Concern
4 years ago
Living with Myeloproliferative Neoplasm - ET Jak2+ and Chronic Neuropathic Pain
There is much money in the pain and drug industry. Ethics and the recipients of these drugs do not factor into the bottom line. Profit and Loss Statements mean percentage increases at any cost. It is sad that chronic pain patients are made to feel like drug addicts and treated in a most callous way.
There is much money in the pain and drug industry. Ethics and the recipients of these drugs do not factor into the bottom line. Profit and Loss Statements mean percentage increases at any cost. It is sad that chronic pain patients are made to feel like drug addicts and treated in a most callous way.
Hidden
in
MPN Voice
4 years ago
Save the children !
I asked the wife Am I the only one in your life ? She replied Yes all the others were nine and tens !
I asked the wife Am I the only one in your life ? She replied Yes all the others were nine and tens !
Bazzak
Reading Rabbits
in
Positive Wellbeing During Self-Isolation
4 years ago
Chronic pelvic floor pain and bleeding after bowel movements
Got examined again today, not hemorrhoids from what they could see.. About 2.5 years ago I had a hip arthroscopic surgery on my left hip. For about 1.5 years I was feeling awesome and pain free. But then this last year I have had chronic pelvic floor floor pain that gets worse after sex and sitting for
Got examined again today, not hemorrhoids from what they could see.. About 2.5 years ago I had a hip arthroscopic surgery on my left hip. For about 1.5 years I was feeling awesome and pain free. But then this last year I have had chronic pelvic floor floor pain that gets worse after sex and sitting for
Pelvicfloorpainhurts
in
Pelvic Pain Support Network
4 years ago
CBD Oil for Back Pain?
I have suffered with back problems for the past 20years which over the last 7/8 years have gradually got worse. It started of with pain in my lower back which was helped by regular trips to a Chiropractor. This allowed me to continue walking with my local walking group. But slowly over the past
I have suffered with back problems for the past 20years which over the last 7/8 years have gradually got worse. It started of with pain in my lower back which was helped by regular trips to a Chiropractor. This allowed me to continue walking with my local walking group. But slowly over the past
Spursboy
in
Pain Concern
4 years ago
Pain in side?
I have had severe pain in my right side for 8 months or so. Had CT scan during admission but as always my lungs to precedence. Seen pain management in February after scan showed tiny impact fracture. But it's not that. I do have lots of bone pain and may have another nerve block. This pain is at waist
I have had severe pain in my right side for 8 months or so. Had CT scan during admission but as always my lungs to precedence. Seen pain management in February after scan showed tiny impact fracture. But it's not that. I do have lots of bone pain and may have another nerve block. This pain is at waist
Dianemc01234
in
Pain Concern
4 years ago
Postherpetic neuralgia from Shingles
I am 75 and I have Postherpetic neuralgia from Shingles, which I had on my perineum. It has now been over one year and I am feeling really low. There is nothing the doctors seem to be able to do as they say there is no other treatment and it has to take its course. I am on 200mg per day Pregabalin
I am 75 and I have Postherpetic neuralgia from Shingles, which I had on my perineum. It has now been over one year and I am feeling really low. There is nothing the doctors seem to be able to do as they say there is no other treatment and it has to take its course. I am on 200mg per day Pregabalin
geniveve27
in
Pain Concern
4 years ago
Shingles and cll
I have been on ibrutinib since aug 2019 and now that things have opened up a bit my sister was going to come for a visit. Only problem is she now has shingles. If we eat outside and she uses the downstairs washroom are we ok? I have had the shingles vacine...but then again so has she and got it anyway
I have been on ibrutinib since aug 2019 and now that things have opened up a bit my sister was going to come for a visit. Only problem is she now has shingles. If we eat outside and she uses the downstairs washroom are we ok? I have had the shingles vacine...but then again so has she and got it anyway
Imbub
in
CLL Support
4 years ago
Coronavirus: Warning thousands could be left with lung damage.
Tens of thousands of people will need to be recalled to hospital after a serious Covid-19 infection to check if they have been left with permanent lung damage, doctors have told the BBC. Experts are concerned a significant proportion could be left with lung scarring, known as pulmonary fibrosis. The
Tens of thousands of people will need to be recalled to hospital after a serious Covid-19 infection to check if they have been left with permanent lung damage, doctors have told the BBC. Experts are concerned a significant proportion could be left with lung scarring, known as pulmonary fibrosis. The
2greys
in
Lung Conditions Community Forum
4 years ago
What’s left
16 year ago. D left op later back in th muscle not stitched more pain back in wrong joint fitted p kept upping tablets till 20 mg oxy norm a 160 mg quick release I book private found nerve damage had spinal nerve block fitted needed 2 knees did let after a week back in because of infection two weeks
16 year ago. D left op later back in th muscle not stitched more pain back in wrong joint fitted p kept upping tablets till 20 mg oxy norm a 160 mg quick release I book private found nerve damage had spinal nerve block fitted needed 2 knees did let after a week back in because of infection two weeks
Hidden
in
Pain Concern
4 years ago
Soooo freaking panicky
I’m going to go get nerve block shots in the back of both sides of my head. I’m freakin scared of that, and I’m taking a transportation service. I’ll be alone in a car with a driver. Now that makes me nervous. I don’t trust people easily. I’m shaking and sweating and just can’t calm down. I’m trying
I’m going to go get nerve block shots in the back of both sides of my head. I’m freakin scared of that, and I’m taking a transportation service. I’ll be alone in a car with a driver. Now that makes me nervous. I don’t trust people easily. I’m shaking and sweating and just can’t calm down. I’m trying
Ubud2021
in
Anxiety and Depression Support
4 years ago
Ticks/Lyme disease and hypothyroidism
I have just removed two ticks, two others broke off and the mouth part remains stuck in me. I have seen things on here before about ticks in relation to thyroid, but have never read them because I’ve never had one attached before. I presume I need to see a nurse to get the remains removed? Will it be
I have just removed two ticks, two others broke off and the mouth part remains stuck in me. I have seen things on here before about ticks in relation to thyroid, but have never read them because I’ve never had one attached before. I presume I need to see a nurse to get the remains removed? Will it be
CornishChick
in
Thyroid UK
4 years ago
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