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Shingles jab and PMR
A lady I know believes her PMR was caused by the shingles jab she was recently offered at the age of 70. I’d never heard this before and I wondered if it’s a widely shared view and if so is there any evidence to back it up?
A lady I know believes her PMR was caused by the shingles jab she was recently offered at the age of 70. I’d never heard this before and I wondered if it’s a widely shared view and if so is there any evidence to back it up?
Casia
in
PMRGCAuk
4 years ago
Tension myositis syndrome
Hello my names scott and I have had a constant pain in the back of my head, the temples and jaw since may 5th 2011. I have been diagnosed with chronic refractory migraine, chronic interactable migraine, new daily persistent headache and chronic trapezius myalgia. I have tried every medicine including
Hello my names scott and I have had a constant pain in the back of my head, the temples and jaw since may 5th 2011. I have been diagnosed with chronic refractory migraine, chronic interactable migraine, new daily persistent headache and chronic trapezius myalgia. I have tried every medicine including
scottlondon
in
National Migraine Centre
4 years ago
Pudendal nerve injections - should they be performed after 10 weeks of having pudendal neuralgia?
Advice, please on how long you should try manual therapy and neuromodulation drug before resorting to the nerve blocks. Thank you
Advice, please on how long you should try manual therapy and neuromodulation drug before resorting to the nerve blocks. Thank you
2977reader
in
Pelvic Pain Support Network
5 years ago
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Apixaban and indigestion
After an ecg about 3 months I was diagnosed with AF and put on anti coagulants, first rivaroxaban and for past month apixaban. This is pretty free from side effects apart from indigestion a couple of hours after a meal. today I had some cranberry cheese and two hours later I had very severe burping
After an ecg about 3 months I was diagnosed with AF and put on anti coagulants, first rivaroxaban and for past month apixaban. This is pretty free from side effects apart from indigestion a couple of hours after a meal. today I had some cranberry cheese and two hours later I had very severe burping
Zinzendorf0
in
AF Association
4 years ago
Pudendal Nerve
Had ups & downs with Pudendal nerve issues - Anyone tried a tens machine? Where have you had success placing the pads?
Had ups & downs with Pudendal nerve issues - Anyone tried a tens machine? Where have you had success placing the pads?
RobertVerde
in
Pelvic Pain Support Network
4 years ago
Recommended doctor for pudendal nerve blocks?
Please could anyone recommend a doctor for pudendal nerve blocks in the U.K? Thank you very much
Please could anyone recommend a doctor for pudendal nerve blocks in the U.K? Thank you very much
2977reader
in
Pelvic Pain Support Network
5 years ago
Unbearable Full Body Pain. Please Help :(
Anyway, because my trapped
nerve
thing wasn't properly helped, I only got the
nerve
block
last month after FIVE years of constant pain, replying on cocodamol and lidocaine patches which done nothing really. I have IBS too and allergies.
Anyway, because my trapped
nerve
thing wasn't properly helped, I only got the
nerve
block
last month after FIVE years of constant pain, replying on cocodamol and lidocaine patches which done nothing really. I have IBS too and allergies.
angelwin
in
Pain Concern
5 years ago
Chronic pain I was on this forum some time ago under the name of Gemini 71, I am trying to change it back. Sorry for the confusion
I’ve been offered a
nerve
block
by my pain specialist,but I’ve refused it,as I know they don’t work. Now I’m not asking for a miracle,but the pain after tea has started to get harder to deal with. So I’m just asking for ANY suggestions.
I’ve been offered a
nerve
block
by my pain specialist,but I’ve refused it,as I know they don’t work. Now I’m not asking for a miracle,but the pain after tea has started to get harder to deal with. So I’m just asking for ANY suggestions.
Breathless1943
in
Pelvic Pain Support Network
5 years ago
Tens machine
Good Morning, Could i ask if using a tens is considered safe if you have Afib.I know that it is not recommended if you have any implants like pacemaker etc, but if not, is it O.K. for relieving muscle pain?
Good Morning, Could i ask if using a tens is considered safe if you have Afib.I know that it is not recommended if you have any implants like pacemaker etc, but if not, is it O.K. for relieving muscle pain?
Renault4
in
AF Association
4 years ago
Misty Rushing is a CRNA (nurse anesthesiologist) and a Functional Medicine 25th Dec 2019
Misty Rushing is a CRNA (nurse anesthesiologist) and a Functional Medicine Advocate. She has been dealing with chronic illness since contracting lyme disease from a known tick bite in 2009. In 2010, she was diagnosed with lupus but later learned she had lyme disease after being tested. Doxycycline antibiotic
Misty Rushing is a CRNA (nurse anesthesiologist) and a Functional Medicine Advocate. She has been dealing with chronic illness since contracting lyme disease from a known tick bite in 2009. In 2010, she was diagnosed with lupus but later learned she had lyme disease after being tested. Doxycycline antibiotic
liveurlife
Volunteer
in
LDN Research Trust
4 years ago
Chronic lower back pain, nerve pain flare up. Advice needed please!
Hello all. This is my first post even though I joined this great community over a year ago. Just got home after an 8 hour stint at A&E. My GP sent me for an emergency MRI to rule out Cauda Equine Syndrome due to yet another episode of climbing the walls with back pain and a nerve pain flare up with
Hello all. This is my first post even though I joined this great community over a year ago. Just got home after an 8 hour stint at A&E. My GP sent me for an emergency MRI to rule out Cauda Equine Syndrome due to yet another episode of climbing the walls with back pain and a nerve pain flare up with
Rosie777
in
Pain Concern
4 years ago
Significant RLS improvement!
I have tried soo many things to improve my RLS...taking magnesium, iron, tens machines, ice baths and acupuncture! I’m on Parapexole, but I was sure this was contributing to the worsening of my symptoms, so managed to cut down after a week or two of painful, agonising nights. I was always sure it must
I have tried soo many things to improve my RLS...taking magnesium, iron, tens machines, ice baths and acupuncture! I’m on Parapexole, but I was sure this was contributing to the worsening of my symptoms, so managed to cut down after a week or two of painful, agonising nights. I was always sure it must
RachelMary77
in
Restless Legs Syndrome
4 years ago
Normal MRI, EEG -don’t feel normal Vm from shingles
Hi Things keep coming back ‘normal’ but I still get tired and have jerks and a little bit of “ataxia” when tired. I don’t think this is a “functional” or conversion disorder, since this only happened after meningitis but I keep wondering what’s wrong with me? Is it just meningitis recovery?
Hi Things keep coming back ‘normal’ but I still get tired and have jerks and a little bit of “ataxia” when tired. I don’t think this is a “functional” or conversion disorder, since this only happened after meningitis but I keep wondering what’s wrong with me? Is it just meningitis recovery?
greenocean
in
Meningitis Now
4 years ago
Sharing my experience
I've just replied to someone's post but thought I'd start my own aswell.. Been to A&E for my last 4 episodes, last one was Friday morning after a night shift, I don't know what the usual heart rate is but mine was 158bpm the 104bmp when they discharged me. I used to be in 2.5mg biosprol and 180mg Adizem
I've just replied to someone's post but thought I'd start my own aswell.. Been to A&E for my last 4 episodes, last one was Friday morning after a night shift, I don't know what the usual heart rate is but mine was 158bpm the 104bmp when they discharged me. I used to be in 2.5mg biosprol and 180mg Adizem
MrSkins
in
AF Association
4 years ago
Constant bleeding - should I ask for deeper tests?
I had my first laparoscopy in September. Endo is now confirmed. I started I really strong contraceptive which has halved my pain, but I'm bleeding constantly - and I don't mean spotting. It's been a few months now and I'm still bleeding, with cramps every now and then. I'm starting to wonder if I should
I had my first laparoscopy in September. Endo is now confirmed. I started I really strong contraceptive which has halved my pain, but I'm bleeding constantly - and I don't mean spotting. It's been a few months now and I'm still bleeding, with cramps every now and then. I'm starting to wonder if I should
Petit-ange
in
Endometriosis UK
4 years ago
Optimising TENS Machine?
Hi, I was wondering if anyone has any tips on getting the most possible pain relief out of a TENS? So far TENS is one of the few things that have helped me deal with pain. Today I have had 2 doses of 30mg of dihydrocodeine and my TENS on 150hz/120 pulse at a dial setting of 5 (out of 8), but am still
Hi, I was wondering if anyone has any tips on getting the most possible pain relief out of a TENS? So far TENS is one of the few things that have helped me deal with pain. Today I have had 2 doses of 30mg of dihydrocodeine and my TENS on 150hz/120 pulse at a dial setting of 5 (out of 8), but am still
deafhound
in
Endometriosis UK
4 years ago
"Sticky Blood" - Antiphospholipid Syndrome, POTS, Chronic Fatigue Syndrome and Fibromyalgia - The Dysautonomia Conference
by Cort Johnson | Aug 15, 2018 | This blog is part IV in a series of blogs covering the issues presented at the 2018 Dysautonomia International Conference in Nashville, Tennessee. APS and POTS and ME/CFS This is the fourth blog on issues presented in the 2018 Dysautonomia International Conference.
by Cort Johnson | Aug 15, 2018 | This blog is part IV in a series of blogs covering the issues presented at the 2018 Dysautonomia International Conference in Nashville, Tennessee. APS and POTS and ME/CFS This is the fourth blog on issues presented in the 2018 Dysautonomia International Conference.
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
4 years ago
It never rains it pours ☔️ update
Anaesthetist came while I was there and they are going to put a nasal tube in for anaesthetic cos he couldn’t face another
nerve
block
- can’t say I blame him - and they don’t want to undo any of the Max Fac work.
Anaesthetist came while I was there and they are going to put a nasal tube in for anaesthetic cos he couldn’t face another
nerve
block
- can’t say I blame him - and they don’t want to undo any of the Max Fac work.
Nerak12
in
PMRGCAuk
5 years ago
Recent atfib diagnosis
Hi everyone! I'm Clive and I was finally diagnosed with Atrial fibrillation a couple of months ago after wondering what the hell was going on and then ending up in A+E after 6 crazy hours of missed beats, 160 bpm heartrate, so on, absolutely shat myself. Anyway, was put on apixaban and bisoprolol, still
Hi everyone! I'm Clive and I was finally diagnosed with Atrial fibrillation a couple of months ago after wondering what the hell was going on and then ending up in A+E after 6 crazy hours of missed beats, 160 bpm heartrate, so on, absolutely shat myself. Anyway, was put on apixaban and bisoprolol, still
Bigbilldup
in
AF Association
4 years ago
Feeling like “the old me”
Well I was .... I had been feeling great. Last week I flew across the country for a work dinner (fabulous gala event with delicious food and dancing) and an overnight stay. Then quite a busy weekend with a concert Friday, dinner out on Saturday and Sunday lunch with friends. I had a bit of a headache
Well I was .... I had been feeling great. Last week I flew across the country for a work dinner (fabulous gala event with delicious food and dancing) and an overnight stay. Then quite a busy weekend with a concert Friday, dinner out on Saturday and Sunday lunch with friends. I had a bit of a headache
Kaz747
in
AF Association
4 years ago
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