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Nerve block
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Trigger (Not only fools and horses)
I have been trying for months to establish a trigger that sets off attacks of AF. I’m lucky at present that I’m only on blood pressure and anti coagulative medication as the attacks are short lived and are around every two to three weeks. I realise that they will increase over time which is similar
I have been trying for months to establish a trigger that sets off attacks of AF. I’m lucky at present that I’m only on blood pressure and anti coagulative medication as the attacks are short lived and are around every two to three weeks. I realise that they will increase over time which is similar
Firstbusman
in
AF Association
3 years ago
Deeply grateful to all the replies about agonising shoulder pain
Many thanks to all of you Kind people for your advice regarding my agonising shoulder pain. I am currently trying my Tens machine which I had forgotten about and which someone had suggested. I found paracetamol was useless, as was Ibuprofen. I previously suffered from duodenitis when taking nsaids,
Many thanks to all of you Kind people for your advice regarding my agonising shoulder pain. I am currently trying my Tens machine which I had forgotten about and which someone had suggested. I found paracetamol was useless, as was Ibuprofen. I previously suffered from duodenitis when taking nsaids,
butterflyfarm
in
PMRGCAuk
3 years ago
Abnormal ecg
Hi everyone, I have been having a few symptoms, which I’ve posted about previously - tight chested, lightheaded, dizzy and feeling like I’m not getting enough air. Today the dr wanted an ecg to be done, it was done by a nurse who then took the results to be looked at by the dr. When she came back
Hi everyone, I have been having a few symptoms, which I’ve posted about previously - tight chested, lightheaded, dizzy and feeling like I’m not getting enough air. Today the dr wanted an ecg to be done, it was done by a nurse who then took the results to be looked at by the dr. When she came back
Knic
in
Anxiety Support
3 years ago
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Any advice
After 2 years of telling my doctor that I was experiencing "palpations", I had a 24 hours ecg just before Christmas. This led to my gp rining me to tell me I had PAF. I was prescribed Apixaban 5mg and bisoprolol 1.25 my. Had a very short telephone conversation with a consultant who said the results of
After 2 years of telling my doctor that I was experiencing "palpations", I had a 24 hours ecg just before Christmas. This led to my gp rining me to tell me I had PAF. I was prescribed Apixaban 5mg and bisoprolol 1.25 my. Had a very short telephone conversation with a consultant who said the results of
Trimley
in
AF Association
3 years ago
Sciatica flare up?
I’m currently waiting for a
nerve
root
block
injection. In the last 2 weeks. I have been experiencing considerable pain in my legs. My feet feel cold but I can still feel them. My legs just don’t want to work. I’m shuffling around like I’m drunk. Very unsteady.
I’m currently waiting for a
nerve
root
block
injection. In the last 2 weeks. I have been experiencing considerable pain in my legs. My feet feel cold but I can still feel them. My legs just don’t want to work. I’m shuffling around like I’m drunk. Very unsteady.
Danlos166
in
Pain Concern
3 years ago
Great piece in the New York Times
NOTHING COULD PREPARE ME FROM WATCHING MY WIFE, JUDY, SLIP AWAY By Tom Coughlin Mr. Coughlin, a two-time Super Bowl-winning head coach, led the New York Giants, Jacksonville Jaguars and Boston College Eagles. Someone recently asked me why my wife, Judy, isn’t in any of the photos from our Jay Fund Foundation
NOTHING COULD PREPARE ME FROM WATCHING MY WIFE, JUDY, SLIP AWAY By Tom Coughlin Mr. Coughlin, a two-time Super Bowl-winning head coach, led the New York Giants, Jacksonville Jaguars and Boston College Eagles. Someone recently asked me why my wife, Judy, isn’t in any of the photos from our Jay Fund Foundation
Regann
in
PSP Association
3 years ago
On going pain.
For over nine years now, I have suffered pain, which over the years has worsened each and every year. At the begining I felt very much that my GPs didn’t believe me at all, one even saying to me that it’s time I let go of this, as there’s nothing wrong with me. I have tried pain management, bought practically
For over nine years now, I have suffered pain, which over the years has worsened each and every year. At the begining I felt very much that my GPs didn’t believe me at all, one even saying to me that it’s time I let go of this, as there’s nothing wrong with me. I have tried pain management, bought practically
Judo1010
in
Pain Concern
3 years ago
After exercise
My normal resting heart rate is around 65. When I exercise (cycle) it will go to around 155. However once I finish my ride my heart rate will stay around 80 to 90 for hours with my heart feeling jumpy. I wouldn't say I'm pushing it very hard when riding but I feel I'm getting a workout. I'm 54 had
My normal resting heart rate is around 65. When I exercise (cycle) it will go to around 155. However once I finish my ride my heart rate will stay around 80 to 90 for hours with my heart feeling jumpy. I wouldn't say I'm pushing it very hard when riding but I feel I'm getting a workout. I'm 54 had
chris45558
in
AF Association
3 years ago
Tens
Glad my tens post started some laughs
Glad my tens post started some laughs
edwangy
in
IBS Network
3 years ago
Tens machine
Has anyone tried tens machine? I have terrible pain and trapped wind IBS C and thought I'd try a tens machine. I bought a reasonably priced one and it really helps with trapped gas. Just place the contacts on your belly where you are in pain it helps to relax the colon allow gas to pass. There is also
Has anyone tried tens machine? I have terrible pain and trapped wind IBS C and thought I'd try a tens machine. I bought a reasonably priced one and it really helps with trapped gas. Just place the contacts on your belly where you are in pain it helps to relax the colon allow gas to pass. There is also
edwangy
in
IBS Network
3 years ago
PAF, Propranolol and Apixaban
The EP has suggested Propranolol twice a day alongside my Apixaban and Carvedilol . I’ve been have an increase in PAF episodes . However, the GP has warned me of an increased bleed risk because of the interaction with Apixaban . Also, the propranolol can cause QT elongation which is dangerous and can
The EP has suggested Propranolol twice a day alongside my Apixaban and Carvedilol . I’ve been have an increase in PAF episodes . However, the GP has warned me of an increased bleed risk because of the interaction with Apixaban . Also, the propranolol can cause QT elongation which is dangerous and can
kalgs
in
AF Association
3 years ago
Past VM and the COVID Vaccine
Has anyone with a past history of VM taken the COVID-19 Vaccine? And If so how did you feel afterwards? And what brand did you take? My son had viral meningitis four years ago and is concerned that the vaccine will trigger a a viral meningitis attack. With this new Delta variant I am much more concerned
Has anyone with a past history of VM taken the COVID-19 Vaccine? And If so how did you feel afterwards? And what brand did you take? My son had viral meningitis four years ago and is concerned that the vaccine will trigger a a viral meningitis attack. With this new Delta variant I am much more concerned
Dutch22
in
Meningitis Now
3 years ago
Pregabalin and CBD Oil Query .
I have a year wait for a
nerve
block
and have been passed from a urologist to a pain clinic to a gynaecologist and also colorectal team . I have at least a 6 month wait to see any of these teams . Recently I’ve developed extremely loud tinnitus and I’m not sure if the pregabalin has caused this .
I have a year wait for a
nerve
block
and have been passed from a urologist to a pain clinic to a gynaecologist and also colorectal team . I have at least a 6 month wait to see any of these teams . Recently I’ve developed extremely loud tinnitus and I’m not sure if the pregabalin has caused this .
Dog2paws
in
Pelvic Pain Support Network
4 years ago
What I have learned from 1 year with Early Onset PD - "Glass Half Full"
I decided to keep a journal of my journey - it has been quite a year but I have learned a lot. some of which maybe relevant for new and older PD people. I am not a doctor and this is not a medical opinion but there is lots available to make a stand against PD https://fightparkinsonsdisease.files.wordpress.com
I decided to keep a journal of my journey - it has been quite a year but I have learned a lot. some of which maybe relevant for new and older PD people. I am not a doctor and this is not a medical opinion but there is lots available to make a stand against PD https://fightparkinsonsdisease.files.wordpress.com
blazyb
in
Cure Parkinson's
3 years ago
Thought it was under control after years of multiple serious surgeries and diet changes but now facing new battles - any advice welcome
Hello all, I was diagnosed with endometriosis aged 21 after 8 years of awful problems and symptoms. After my first laparoscopy I was initially told it was “just a few spots of endometriosis” and my options were chemically induced menopause (gnrh and add back HRT) or to get pregnant and they fitted
Hello all, I was diagnosed with endometriosis aged 21 after 8 years of awful problems and symptoms. After my first laparoscopy I was initially told it was “just a few spots of endometriosis” and my options were chemically induced menopause (gnrh and add back HRT) or to get pregnant and they fitted
Greys90
in
Endometriosis UK
3 years ago
Tachycardia episodes
Well thats me seen consultant re my tachycardia episodes (approx 1 per week) lasting from 10 minutes to 4 hours bpm around 120 to 130, frequent ectopics which can trigger an episode, all caught on my Kardia device. I made appt with my gp yesterday to see if she could explain what was causing them only
Well thats me seen consultant re my tachycardia episodes (approx 1 per week) lasting from 10 minutes to 4 hours bpm around 120 to 130, frequent ectopics which can trigger an episode, all caught on my Kardia device. I made appt with my gp yesterday to see if she could explain what was causing them only
Lbeat796
in
AF Association
3 years ago
SVT & Ectopics to NSR after ablation
Had Covid March 2020. Previously totally fit cardiac wise. Developed SVT and ectopics in August 2020 with SOBE, palpitations and fatigue Tried Bisoprolol and Flecainide. Worked initially, but bad side effects. Ablation in May 2021. Now been in Normal Sinus Rhythm for 5 weeks, thanks be to God. Off all
Had Covid March 2020. Previously totally fit cardiac wise. Developed SVT and ectopics in August 2020 with SOBE, palpitations and fatigue Tried Bisoprolol and Flecainide. Worked initially, but bad side effects. Ablation in May 2021. Now been in Normal Sinus Rhythm for 5 weeks, thanks be to God. Off all
Jim1954
in
Atrial Fibrillation Support
3 years ago
excessive blood loss
hi how's everyone doing? for those who don't know me, I've had issues with my periods since 13 and diagnosed with endometriosis since 05, I've been on every combination of hormonal treatments and pain relief medications u can imagine (to the point where I'd rattle when I walked) I've had so many operations
hi how's everyone doing? for those who don't know me, I've had issues with my periods since 13 and diagnosed with endometriosis since 05, I've been on every combination of hormonal treatments and pain relief medications u can imagine (to the point where I'd rattle when I walked) I've had so many operations
dodgeviperdiva
in
Endometriosis UK
3 years ago
Update to "Feeling Terrible Lately".
Hello all, Well the reason I felt so terrible was because I ended up having Lyme disease.. I ended up seeing my family Dr. as I was starting to feel bad again. I was on antibiotics for 15 days and am doing well now. It got me behind my knee, so I didn't notice it at first. They are areal problem in our
Hello all, Well the reason I felt so terrible was because I ended up having Lyme disease.. I ended up seeing my family Dr. as I was starting to feel bad again. I was on antibiotics for 15 days and am doing well now. It got me behind my knee, so I didn't notice it at first. They are areal problem in our
fxdx1
in
CLL Support
3 years ago
Shingrix OK For Immunocompromised Adults
This article was posted today on CLLSLL groups.io and is reposted here with permission from Dr. Furman https://groups.io/g/CLLSLL/message/31608?reply=1 [i] Re: Shingrix OK For Immunocompromised Adults [/i] [i]From: Rick Furman Date: Fri, 30 Jul 2021 08:43:32 EDT[/i] [i]-[/i] [i]Shingles is the result
This article was posted today on CLLSLL groups.io and is reposted here with permission from Dr. Furman https://groups.io/g/CLLSLL/message/31608?reply=1 [i] Re: Shingrix OK For Immunocompromised Adults [/i] [i]From: Rick Furman Date: Fri, 30 Jul 2021 08:43:32 EDT[/i] [i]-[/i] [i]Shingles is the result
lankisterguy
Volunteer
in
CLL Support
3 years ago
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