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Help needed
Hi Has anyone here ever had
nerve
block
for head pain I am due to have it but am unsure about it I know it’s injections but that’s all I know any help and advice would be appreciated thanku x
Hi Has anyone here ever had
nerve
block
for head pain I am due to have it but am unsure about it I know it’s injections but that’s all I know any help and advice would be appreciated thanku x
Braininjurysurvivor
in
Headway
5 years ago
Diagnosis of nerve injury following pelvic surgery
In another case, a lady probably has pudendal neuropathy following a gynaecological procedure and really is in terrible pain with constant mobility issues but has experienced some, but not complete, pain relief from
nerve
block
injections to date.
In another case, a lady probably has pudendal neuropathy following a gynaecological procedure and really is in terrible pain with constant mobility issues but has experienced some, but not complete, pain relief from
nerve
block
injections to date.
CMSol
in
Pelvic Pain Support Network
4 years ago
Apixaban
I have changed from Xarelto to Apixaban . I now have really upset gut and tight chest . Is it just me being neurotic or have others experienced this ? I don stand much chance of getting it changed now. I cMe iff Xarelto because of increasing joint pain. Hope you are all well.
I have changed from Xarelto to Apixaban . I now have really upset gut and tight chest . Is it just me being neurotic or have others experienced this ? I don stand much chance of getting it changed now. I cMe iff Xarelto because of increasing joint pain. Hope you are all well.
Luludean
in
AF Association
4 years ago
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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
Shingles vax
I am nearly at 4 years with pmr and have been on various doses of prednisone and still cant go below 5mg without gout like symptoms. I became ill with 2 months of having the shingles vaccine. I have always been healthy til then. I am coming up 65. Was never advised of the side effects. Has ruined my
I am nearly at 4 years with pmr and have been on various doses of prednisone and still cant go below 5mg without gout like symptoms. I became ill with 2 months of having the shingles vaccine. I have always been healthy til then. I am coming up 65. Was never advised of the side effects. Has ruined my
Babbaganoush
in
PMRGCAuk
4 years ago
Tens machine recommendations
Hi everyone! I'd like to get a TENS machine - does anyone have one they'd recommend? I'm UK based, so something that will ship here preferably. Thank you!
Hi everyone! I'd like to get a TENS machine - does anyone have one they'd recommend? I'm UK based, so something that will ship here preferably. Thank you!
SarahMia227
in
Endometriosis UK
4 years ago
Chronic Back Pain
Hi, I'm looking for some advice, I am 21 and have chronic lower back pain. I have had pain for over a year and it's getting worse. I have restricted movement now and cannot flex my back or arch my back. Sitting can be painful when I try to stand. I'm being woken up at night by the pain but the doctors
Hi, I'm looking for some advice, I am 21 and have chronic lower back pain. I have had pain for over a year and it's getting worse. I have restricted movement now and cannot flex my back or arch my back. Sitting can be painful when I try to stand. I'm being woken up at night by the pain but the doctors
BertieB_280616
in
Pain Concern
4 years ago
Should I ask my PG for a referral to a cardiologist?
I have recently been informed that I have Left Bundle Branch Block 3, but not given any more info or follow-up! Apparently, a partial block was detected 10 years ago, which they didn't tell me about! It is now a category 3, and causes pain, palpitations, missing beats, and makes me feel dizzy as if I'm
I have recently been informed that I have Left Bundle Branch Block 3, but not given any more info or follow-up! Apparently, a partial block was detected 10 years ago, which they didn't tell me about! It is now a category 3, and causes pain, palpitations, missing beats, and makes me feel dizzy as if I'm
Lesleyr14
in
Arrhythmia Alliance
4 years ago
Crippling Hip Pain
I was wondering if others have had experience of crippling pain in and around their hip joint, especially so at night? I had surgery for removal of endometriosis from the uterosacral ligament (1 year ago) but these symptoms all had come following surgery. I do not know if this pain is related or an
I was wondering if others have had experience of crippling pain in and around their hip joint, especially so at night? I had surgery for removal of endometriosis from the uterosacral ligament (1 year ago) but these symptoms all had come following surgery. I do not know if this pain is related or an
Ema4390
in
Endometriosis UK
4 years ago
Fears over fluttering in chest
I’ve had bouts of tachycardia and PVCs for 7 years, usually controlled by Flecainide and Verapamil. The tachycardia’s started again lately - 6 bouts over the past 6 weeks, heart rate about 100bpm, lasting 2 hours usually. Also now I have a fluttering/quivering sensation in my chest, and a different feeling
I’ve had bouts of tachycardia and PVCs for 7 years, usually controlled by Flecainide and Verapamil. The tachycardia’s started again lately - 6 bouts over the past 6 weeks, heart rate about 100bpm, lasting 2 hours usually. Also now I have a fluttering/quivering sensation in my chest, and a different feeling
Bedlington14
in
Arrhythmia Alliance
4 years ago
Restless Legs in Pregnancy
Hi everyone, I am not even sure why I am writing this message - partly because I want to vent; partly because I would like some advice. I have had about 2-3 episodes of mild and short lasting (3ish days) of restless legs outside of pregnancy. I remember the restless legs to be quite bad in my first pregnancy
Hi everyone, I am not even sure why I am writing this message - partly because I want to vent; partly because I would like some advice. I have had about 2-3 episodes of mild and short lasting (3ish days) of restless legs outside of pregnancy. I remember the restless legs to be quite bad in my first pregnancy
TanjaRLS
in
Restless Legs Syndrome
4 years ago
Pacemaker battery change due now
Hi all. Hope you are well and not stir crazy. I have sick sinus syndrome tachy/brady variety. 20 years. 3 ablations. Last one partially effective. Prof Schilling reluctant to do more. Anyway I am on the list at Barts for an update as my current (2nd) pacemaker has a few months battery left. Had
Hi all. Hope you are well and not stir crazy. I have sick sinus syndrome tachy/brady variety. 20 years. 3 ablations. Last one partially effective. Prof Schilling reluctant to do more. Anyway I am on the list at Barts for an update as my current (2nd) pacemaker has a few months battery left. Had
Icenae
in
Atrial Fibrillation Support
4 years ago
Apixaban.
I have been taking Warfarin for about 2 years now since I was diagnosed with AF. I wanted to take Apixaban , as I have Coeliac the doctor said it was not suitable for me. Anyone on here taking Apixaban and have Coeliac ? I don't want to be going out if I can help it. My age is 76 so I should
I have been taking Warfarin for about 2 years now since I was diagnosed with AF. I wanted to take Apixaban , as I have Coeliac the doctor said it was not suitable for me. Anyone on here taking Apixaban and have Coeliac ? I don't want to be going out if I can help it. My age is 76 so I should
benmaise
in
AF Association
4 years ago
Crazy Neck Pain and Headaches Post Viral Meningitis
Hi all, 42 yr, female. I was diagnosed with viral meningitis in August 2019. After almost 7 months I am still dealing with the headaches, major neck pain and light sensitivity. There are days I feel like I could run a marathon (ok... not really a marathon but I feel pretty good!) and other times
Hi all, 42 yr, female. I was diagnosed with viral meningitis in August 2019. After almost 7 months I am still dealing with the headaches, major neck pain and light sensitivity. There are days I feel like I could run a marathon (ok... not really a marathon but I feel pretty good!) and other times
Practicingpatience
in
Meningitis Now
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
SVT back after ablation?
I had my ablation for STV on the 10th Feb. I was told at the time that they may not of got it due to being so close to my AV node abd I was going into heart block during the procedure. I've had a few little bumps etc since but no SVT. However today after eating my heart started to race which lasted
I had my ablation for STV on the 10th Feb. I was told at the time that they may not of got it due to being so close to my AV node abd I was going into heart block during the procedure. I've had a few little bumps etc since but no SVT. However today after eating my heart started to race which lasted
chris45558
in
AF Association
4 years ago
What could this be?
When I breathe in deep, my heart beats realllllly fast. Like, I know when you breathe in...your heart rate increases. But once I get to the point of maxing out my lungs with air, my heart goes THUMPTHUMPTHUMPTHUMP back to back, FAST, and returns to normal when I exhale. I dont get it. I know doctors
When I breathe in deep, my heart beats realllllly fast. Like, I know when you breathe in...your heart rate increases. But once I get to the point of maxing out my lungs with air, my heart goes THUMPTHUMPTHUMPTHUMP back to back, FAST, and returns to normal when I exhale. I dont get it. I know doctors
Notorious_Nick
in
Arrhythmia Alliance
4 years ago
Meningitis Now is still here to support you during this time
Hello Everyone, Hope you are keeping safe in these strange times. Although we are working with a reduce team at the moment, we are still here to support and provide information to anyone living in the UK who has been impacted by meningitis. Our nurse-led helpline is open from 9am until 4pm, Monday
Hello Everyone, Hope you are keeping safe in these strange times. Although we are working with a reduce team at the moment, we are still here to support and provide information to anyone living in the UK who has been impacted by meningitis. Our nurse-led helpline is open from 9am until 4pm, Monday
MNClaireD
Meningitis Now
in
Meningitis Now
4 years ago
TENS MACHINE
Has anyone tried a TENS machine for RLS? I take .75mg sifrol which is very effective. However, the TENS gives relief as well. I use one - it's worth a try.
Has anyone tried a TENS machine for RLS? I take .75mg sifrol which is very effective. However, the TENS gives relief as well. I use one - it's worth a try.
Hidden
in
Restless Legs Syndrome
4 years ago
Flecainide Journey Continued...
Hello again. Thank you to everyone for your support up to now. It has been massively appreciated. I’m 10 days in taking 2 x 50mg of Flecainide daily and had a horrible AF episode yesterday again. Really struggled to get it to slow down. Have spoken with GP who doesn’t want to change things without
Hello again. Thank you to everyone for your support up to now. It has been massively appreciated. I’m 10 days in taking 2 x 50mg of Flecainide daily and had a horrible AF episode yesterday again. Really struggled to get it to slow down. Have spoken with GP who doesn’t want to change things without
Apple88
in
AF Association
4 years ago
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