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Nerve block
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Atrial Flutter and Shingles
Two years ago, after ankle reconstruction surgery, I was diagnosed with SVT. After two unsuccessful ablations (and Verapamil and Flecainide) my specialist said that I have Multifocal Atrial Tachycardia (MAT) and put me on Sotalol (40mg twice a day). That mostly kept things under control and if I had
Two years ago, after ankle reconstruction surgery, I was diagnosed with SVT. After two unsuccessful ablations (and Verapamil and Flecainide) my specialist said that I have Multifocal Atrial Tachycardia (MAT) and put me on Sotalol (40mg twice a day). That mostly kept things under control and if I had
Kaz747
in
AF Association
6 years ago
Svt
Hi. This is my first post on this page. I had an svt attack on Thursday and was rushed to hospital with a heart rate of 250 for two hours. I stayed in hospital for 10hrs and they let me go saying they would do me an urgent referral to the heart specialist. They would have a 7 day monitor fitted and arrange
Hi. This is my first post on this page. I had an svt attack on Thursday and was rushed to hospital with a heart rate of 250 for two hours. I stayed in hospital for 10hrs and they let me go saying they would do me an urgent referral to the heart specialist. They would have a 7 day monitor fitted and arrange
LMor
in
AF Association
6 years ago
OA and Degenerative disc disease
Prior to surgery my doc (who has been brilliant) suggested trying
nerve
branch root
block
injections.
Prior to surgery my doc (who has been brilliant) suggested trying
nerve
branch root
block
injections.
Jojohope
in
Osteoarthritis Action
6 years ago
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OA and Degenerative disc disease
Prior to surgery my doc (who has been brilliant) suggested trying
nerve
branch root
block
injections.
Prior to surgery my doc (who has been brilliant) suggested trying
nerve
branch root
block
injections.
Jojohope
in
Arthritis Action
6 years ago
The not so merry Merry Go Round
I've started
block
nerve
injections. I've had years worth of physiotherapy. I've been attending a psychiatrist for 5 years. I practice distraction therapy, but over the last month I feel like I've taken 10 steps back. Has anyone else experienced a slump like this? If yes, did it pass?
I've started
block
nerve
injections. I've had years worth of physiotherapy. I've been attending a psychiatrist for 5 years. I practice distraction therapy, but over the last month I feel like I've taken 10 steps back. Has anyone else experienced a slump like this? If yes, did it pass?
Catmag
in
National Migraine Centre
6 years ago
I am really at the end of my tether,please can anyone help.
Last July I had a
nerve
block
,so I believe my pain specialist thinks it's due to the Prudendal nerve,and to use his words I'm very complicating,because I have quite a few other health issues,so lots of medication,I don't believe it done anything for me,but he want to do another one the middle of this
Last July I had a
nerve
block
,so I believe my pain specialist thinks it's due to the Prudendal nerve,and to use his words I'm very complicating,because I have quite a few other health issues,so lots of medication,I don't believe it done anything for me,but he want to do another one the middle of this
Hidden
in
Pelvic Pain Support Network
6 years ago
Viral Meningitis- After effects
Hi, I am Dave and live in Sydney Australia. I had VM last April 2017 and it took me 6 months to recover. VM was diagnosed via lumbar puncture in hospital. At age 59 I was fit and healthy and VM slammed me. I lost a lot of time off work. I have substantially improved since and keep active but if I get
Hi, I am Dave and live in Sydney Australia. I had VM last April 2017 and it took me 6 months to recover. VM was diagnosed via lumbar puncture in hospital. At age 59 I was fit and healthy and VM slammed me. I lost a lot of time off work. I have substantially improved since and keep active but if I get
Daver19021958
in
Meningitis Now
6 years ago
Tens
Just wondering if anyone has had any experience with using tens treatment for their child in overactive bladder diagnosis? My bladder and bowel nurse has mentioned about trialling some treatment for my little girl instead of meds. I’m open to it but can’t find a lot of information on it. Any experiences
Just wondering if anyone has had any experience with using tens treatment for their child in overactive bladder diagnosis? My bladder and bowel nurse has mentioned about trialling some treatment for my little girl instead of meds. I’m open to it but can’t find a lot of information on it. Any experiences
Iamskiff
in
ERIC
6 years ago
Vulvodynia or pudundel neuropathy?!?!?!?
Also, my other dr wants me to get pudundel
nerve
block
.
Also, my other dr wants me to get pudundel
nerve
block
.
Leahc23
in
Pelvic Pain Support Network
6 years ago
Article in 'The Times' on Antidepressants etc. causing Dementia
"Common antidepressants, bladder drugs and anti-Parkinson’s medication account for tens of thousands of cases of dementia and doctors need to use them more sparingly, the most comprehensive study of its kind has found. Millions of older people are on cocktails of pills and GPs must take more seriously
"Common antidepressants, bladder drugs and anti-Parkinson’s medication account for tens of thousands of cases of dementia and doctors need to use them more sparingly, the most comprehensive study of its kind has found. Millions of older people are on cocktails of pills and GPs must take more seriously
Polaris
in
Pernicious Anaemia Society
6 years ago
W6 R1 alarm set early!
Great run which was a relief as calf muscle trouble so stepped back a week. Swimming , strength & flex & tens machine seem to have done the trick. I think I needed to build up muscles elsewhere & flexibility to maintain a good technique....strength & flex tomorrow.
Great run which was a relief as calf muscle trouble so stepped back a week. Swimming , strength & flex & tens machine seem to have done the trick. I think I needed to build up muscles elsewhere & flexibility to maintain a good technique....strength & flex tomorrow.
Rebecca12
in
Couch to 5K
6 years ago
Newbie... suffering since 09,undiagnosed inner leg pain,thigh to ankle,burning buzzing,knees can't touch,worst at night,no zzz.help?ideas?x
Hypothyroid,B12 injector,Lyme Disease.Longterm Abx treatment.But wits end with leg pain.Anyone else out there like me with this type of pain? Ideas so welcome before I go mental x
Hypothyroid,B12 injector,Lyme Disease.Longterm Abx treatment.But wits end with leg pain.Anyone else out there like me with this type of pain? Ideas so welcome before I go mental x
Flutterfly1
in
NRAS
6 years ago
Endo and neuropathic pain
Hi Have had extensive surgery and have tried Prostap, both to little effect. My consultant thinks my pain is neuropathic. I have been referred to the pain clinic and she has asked my GP to prescribe gabapentin. I have a Tens machine, sometimes this helps. I have tried acupuncture to no avail. I have
Hi Have had extensive surgery and have tried Prostap, both to little effect. My consultant thinks my pain is neuropathic. I have been referred to the pain clinic and she has asked my GP to prescribe gabapentin. I have a Tens machine, sometimes this helps. I have tried acupuncture to no avail. I have
Catmum
in
Endometriosis UK
6 years ago
Why am i having abdominal pain following lateral nerve block injection?
Had my first
nerve
block
treatment on Thursday and knew would feel worse to begin with but now its day 4 and still having queasiness and pain in groin/abdomen area on right..had x ray guided injection just above right buttock and knew this would be sore for a few days but don't understand the related
Had my first
nerve
block
treatment on Thursday and knew would feel worse to begin with but now its day 4 and still having queasiness and pain in groin/abdomen area on right..had x ray guided injection just above right buttock and knew this would be sore for a few days but don't understand the related
Bea61
in
Pain Concern
6 years ago
Did I have Encephalitis?
I was in hospital for 3 months last year with a brain infection they described as "an encephalitic illness". I'm still getting letters from the hospital saying "it wasn't this, that or the other thing we've tested for". I'm so confused. I guess I didn't have Encephalitis, just brain swelling, but it
I was in hospital for 3 months last year with a brain infection they described as "an encephalitic illness". I'm still getting letters from the hospital saying "it wasn't this, that or the other thing we've tested for". I'm so confused. I guess I didn't have Encephalitis, just brain swelling, but it
cheddah
in
Headway
6 years ago
TENS machine
Just a thought! Anyone have experience using a TENS machine for their loved ones pains and stiffness. I did a search but nothing came up. My hubby is not in pain yet but I see many are in pain and I am looking ahead, building up a notebook of tips etc. As the TENS machine works on impulses to the nerves
Just a thought! Anyone have experience using a TENS machine for their loved ones pains and stiffness. I did a search but nothing came up. My hubby is not in pain yet but I see many are in pain and I am looking ahead, building up a notebook of tips etc. As the TENS machine works on impulses to the nerves
daffodil48
in
PSP Association
6 years ago
How slow can we go?
This is probably a doctor question, but it is Good Friday, so decised it can sit til monday. Just curious, Im just on PIP for my PAF. ( after much disagreement between cardiologist and EP, EP won the PIP debate). As my blood pressure is creeping up a little, they both agreed to put me on low dose metoprolol
This is probably a doctor question, but it is Good Friday, so decised it can sit til monday. Just curious, Im just on PIP for my PAF. ( after much disagreement between cardiologist and EP, EP won the PIP debate). As my blood pressure is creeping up a little, they both agreed to put me on low dose metoprolol
Hidden
in
AF Association
6 years ago
New Symptoms for an SVT sufferer
Hello All ! I am 29 years old , was diagnosed with SVT 2 years ago , in which I directly decided to do an ablation for (since doctors told me i had a 98% chance of success) well sucks for me i turned out to be from the 2% LOL. However after 6 months on med and clean living I have been doing great for
Hello All ! I am 29 years old , was diagnosed with SVT 2 years ago , in which I directly decided to do an ablation for (since doctors told me i had a 98% chance of success) well sucks for me i turned out to be from the 2% LOL. However after 6 months on med and clean living I have been doing great for
Fmak
in
AF Association
6 years ago
Post Op Symptoms
Hi. My name is Victoria. My husband had an AN removed 10 months ago. It was 3.5 cm, calcified, and pushing against his brain stem. They had to sacrifice some nerves(7th and 8th). He doesn't have any facial function on the left side, but has had the 5th to 7th nerve transfer and nerve reconstruction
Hi. My name is Victoria. My husband had an AN removed 10 months ago. It was 3.5 cm, calcified, and pushing against his brain stem. They had to sacrifice some nerves(7th and 8th). He doesn't have any facial function on the left side, but has had the 5th to 7th nerve transfer and nerve reconstruction
vmcnorton12
in
Acoustic Neuroma Support
6 years ago
Circulation boosters
Has anyone had experience with circulation boosters for rls? I have seen some reviews that seem to indicate so. I seem to have lost feeling in some of my toes which seem to indicate that my circulation is poor I take a daily beta blocker for SVT which may be responsible and I use a tens machine which
Has anyone had experience with circulation boosters for rls? I have seen some reviews that seem to indicate so. I seem to have lost feeling in some of my toes which seem to indicate that my circulation is poor I take a daily beta blocker for SVT which may be responsible and I use a tens machine which
Hooc
in
Restless Legs Syndrome
6 years ago
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