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Scientist behind coronavirus shot says next target is cancer.
The scientist who won the race to deliver the first widely used coronavirus vaccine says people can rest assured the shots are safe, and the technology behind it will soon be used to fight another global scourge — cancer. Ozlem Tureci, who co-founded the German company BioNTech with her husband, was
The scientist who won the race to deliver the first widely used coronavirus vaccine says people can rest assured the shots are safe, and the technology behind it will soon be used to fight another global scourge — cancer. Ozlem Tureci, who co-founded the German company BioNTech with her husband, was
2greys
in
Lung Conditions Community Forum
3 years ago
Chronic pelvic pain
Hi,Could I use a tens machine for chronic pelvic pain
Hi,Could I use a tens machine for chronic pelvic pain
Breathless1943
in
IBS Network
3 years ago
Stress triggering meningitis
What are your thoughts on stress being a trigger for a viral infection and triggering viral meningitis and M.E? Do you think stress plays a contributing factor?
What are your thoughts on stress being a trigger for a viral infection and triggering viral meningitis and M.E? Do you think stress plays a contributing factor?
Sunny308
in
Meningitis Now
3 years ago
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Chronic Shingles & Hashi/Hypo
Anyone else get Shingles everytime their TSH rises due to Hashi’s & it’s time for an increase in Levo.mg’s? This has been my pattern for a year now. First round was face/neck second was armpits. Both times bilateral. Shingles vaccine has not been an option for me because I can’t go long enough in between
Anyone else get Shingles everytime their TSH rises due to Hashi’s & it’s time for an increase in Levo.mg’s? This has been my pattern for a year now. First round was face/neck second was armpits. Both times bilateral. Shingles vaccine has not been an option for me because I can’t go long enough in between
badgenes
in
Thyroid UK
3 years ago
Message from a hopeful Nana - don't give up
Dear everyone, I have been following this site for a few months now. I posted about how best to support my daughter and her wife, who have been on a very, very long journey, with ups and many downs. The proverbial rollercoaster. So - after over five years, one self-inseminated pregnancy that ended
Dear everyone, I have been following this site for a few months now. I posted about how best to support my daughter and her wife, who have been on a very, very long journey, with ups and many downs. The proverbial rollercoaster. So - after over five years, one self-inseminated pregnancy that ended
PollJ
in
Fertility Network UK
3 years ago
Advice on TENS machine
Hi everyone. I suffer from sciatic/nerve pain in my legs - there is nothing structurally wrong with my back or the disks in it. It's believed to be a central sensitisation problem, or a 'wind up' in pain over the years. It's very irritable. I tried a TENS machine for the first time last week after a
Hi everyone. I suffer from sciatic/nerve pain in my legs - there is nothing structurally wrong with my back or the disks in it. It's believed to be a central sensitisation problem, or a 'wind up' in pain over the years. It's very irritable. I tried a TENS machine for the first time last week after a
Margot89
in
Pain Concern
3 years ago
Pain relief
After a telephone consultation with my gynaecologist today, he has said they don't think there's anything else they can do 4 my endo pain as ive trued the pill running packs 4 3months, had the coil fitted while under for removal of endometriosis last Feb but since December I have had prolonged pain worse
After a telephone consultation with my gynaecologist today, he has said they don't think there's anything else they can do 4 my endo pain as ive trued the pill running packs 4 3months, had the coil fitted while under for removal of endometriosis last Feb but since December I have had prolonged pain worse
Mrsmcgrogan
in
Endometriosis UK
3 years ago
advice on home devices for pain treatment
so, covid has been going tough on my back... I'm looking for some advice on home devices such as Solio Alfa Plus or a tens unit, anyone with insights out there?
so, covid has been going tough on my back... I'm looking for some advice on home devices such as Solio Alfa Plus or a tens unit, anyone with insights out there?
painless2b
in
Cloudy with a Chance of Pain
3 years ago
Cryoblation didn’t work for me
I had pudenal cryoblation in France with dr Bautrant- it made my pain worse! I wouldn’t recommend. I get some relief with nerve blocks but the cryoblation it just felt like he missed. My skin felt burnt! / I had surgery with him right sided decompression surgery my nerve pain initially got better but
I had pudenal cryoblation in France with dr Bautrant- it made my pain worse! I wouldn’t recommend. I get some relief with nerve blocks but the cryoblation it just felt like he missed. My skin felt burnt! / I had surgery with him right sided decompression surgery my nerve pain initially got better but
1980natty
in
Pelvic Pain Support Network
3 years ago
Nerve block
So further to my post on nerve blocks I had it on 9th so far psin worse but not been a week.So we will see
So further to my post on nerve blocks I had it on 9th so far psin worse but not been a week.So we will see
Conolly20
in
Fibromyalgia Action UK
3 years ago
Struggling with pain
I was diagnosed with endometriosis and was diagnosed after the lap. Before I was diagnosed I spent years trying to manage pain and reduce bleeding using oral contraceptives. I’ve been on cerazette for about a year now and it’s definitely reduced bleeding but I’m still suffering from severe cramps throughout
I was diagnosed with endometriosis and was diagnosed after the lap. Before I was diagnosed I spent years trying to manage pain and reduce bleeding using oral contraceptives. I’ve been on cerazette for about a year now and it’s definitely reduced bleeding but I’m still suffering from severe cramps throughout
Rainb0w28
in
Endometriosis UK
3 years ago
Endo flare up
Hi Another day another flare up, I honestly cant take this much more. After 7 years I have tried every medicine they can you and still nothing is working. I have another endo surgery coming up but its put on hold with covid. I'm just ranting but also interested in what other people do for flare up days
Hi Another day another flare up, I honestly cant take this much more. After 7 years I have tried every medicine they can you and still nothing is working. I have another endo surgery coming up but its put on hold with covid. I'm just ranting but also interested in what other people do for flare up days
Megan170123
in
Endometriosis UK
3 years ago
Sclerosis
Hi today I had a nerve block injection in my l3/l4 disk.And the specialist said I have sclerosis?? Not overly sure what this is.plus we have a family history of padgets disease.Not helping with fibro the worry of this xx
Hi today I had a nerve block injection in my l3/l4 disk.And the specialist said I have sclerosis?? Not overly sure what this is.plus we have a family history of padgets disease.Not helping with fibro the worry of this xx
Conolly20
in
Fibromyalgia Action UK
3 years ago
updates from last post, warning: long, sorry!
How is everyone doing today? It's quite a sunny day over here in CA and I'm waiting for one of the kids to finish their class for the day. They both got caught up in playing and that resulted in her being late to class. Kind of funny when you hear little miss being forced out of their room for goofing
How is everyone doing today? It's quite a sunny day over here in CA and I'm waiting for one of the kids to finish their class for the day. They both got caught up in playing and that resulted in her being late to class. Kind of funny when you hear little miss being forced out of their room for goofing
JennaShi
in
LUPUS UK
3 years ago
Itching and burning skin all over
Hi there . I've been suffering from burning and itching skin all over for nearly 2 years. Been tested for everything. They gave now decided its fibromyalgia. Have had ketamine infusions and nerve blocks. Stopped taking any medication I was on when it started about 4 months ago to see was it due to
Hi there . I've been suffering from burning and itching skin all over for nearly 2 years. Been tested for everything. They gave now decided its fibromyalgia. Have had ketamine infusions and nerve blocks. Stopped taking any medication I was on when it started about 4 months ago to see was it due to
Rebelpear1991
in
Pernicious Anaemia Society
3 years ago
I’m quite new to this site
I was interested to hear other peoples advice on meds. I’ve been taking tramadol for years and bupernorphine patches. I have now gone on pregabalin 150 3 times a day but don’t find them much good. I read from others that I should take them every day which I’ve not been doing, so I’ll try your advice
I was interested to hear other peoples advice on meds. I’ve been taking tramadol for years and bupernorphine patches. I have now gone on pregabalin 150 3 times a day but don’t find them much good. I read from others that I should take them every day which I’ve not been doing, so I’ll try your advice
Hidden
in
Fibromyalgia Action UK
3 years ago
Latent shingles and high BP
Has anyone had shingles lately and increase in BP...contracted shingles couple of weeks ago, felt very hot but not high temp and only few spots on left arm/bra line and left shoulder/back....phoned GP and mentioned headache and light headedness and sent photos..went to pick up script at pharmacy and
Has anyone had shingles lately and increase in BP...contracted shingles couple of weeks ago, felt very hot but not high temp and only few spots on left arm/bra line and left shoulder/back....phoned GP and mentioned headache and light headedness and sent photos..went to pick up script at pharmacy and
Bea61
in
Pain Concern
3 years ago
Has anyone had ACDF/Discectomy & Spinal Fusion Surgery?
Has anyone had this surgery? I’m a potential candidate for this is have large herniated discs in C5-6 & C7-8. My Neurosurgeon said that first option would be a nerve block of pain wasn’t improving (it isn’t) but I feel this would only help pain and wouldn’t sort out the problem itself. I’m a 30 year
Has anyone had this surgery? I’m a potential candidate for this is have large herniated discs in C5-6 & C7-8. My Neurosurgeon said that first option would be a nerve block of pain wasn’t improving (it isn’t) but I feel this would only help pain and wouldn’t sort out the problem itself. I’m a 30 year
nurseblue
in
Fibromyalgia Action UK
3 years ago
Has anyone had ACDF/Discectomy & Spinal Fusion Surgery?
Has anyone had this surgery? I’m a potential candidate for this is have large herniated discs in C5-6 & C7-8. My Neurosurgeon said that first option would be a nerve block of pain wasn’t improving (it isn’t) but I feel this would only help pain and wouldn’t sort out the problem itself. I’m a 30 year
Has anyone had this surgery? I’m a potential candidate for this is have large herniated discs in C5-6 & C7-8. My Neurosurgeon said that first option would be a nerve block of pain wasn’t improving (it isn’t) but I feel this would only help pain and wouldn’t sort out the problem itself. I’m a 30 year
nurseblue
in
Action on Pain
3 years ago
Has anyone had ACDF/Discectomy & Spinal Fusion surgery?
Has anyone had this surgery? I’m a potential candidate for this is have large herniated discs in C5-6 & C7-8. My Neurosurgeon said that first option would be a nerve block of pain wasn’t improving (it isn’t) but I feel this would only help pain and wouldn’t sort out the problem itself. I’m a 30 year
Has anyone had this surgery? I’m a potential candidate for this is have large herniated discs in C5-6 & C7-8. My Neurosurgeon said that first option would be a nerve block of pain wasn’t improving (it isn’t) but I feel this would only help pain and wouldn’t sort out the problem itself. I’m a 30 year
nurseblue
in
Pain Concern
3 years ago
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