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Shingles and covid vaccine !
Don’t know if this is significant but I had my first dose of covid vaccine in January then 3 weeks later I got shingles on my upper torso I had my second dose of vaccine 3 weeks ago and now I have neuralgia which is also shingles I found out I have never experienced shingles in my life and have been
Don’t know if this is significant but I had my first dose of covid vaccine in January then 3 weeks later I got shingles on my upper torso I had my second dose of vaccine 3 weeks ago and now I have neuralgia which is also shingles I found out I have never experienced shingles in my life and have been
Strumpet
in
Thyroid UK
3 years ago
Rate control strategy
Does anyone just take a fast acting metoprolol or Diltiazam when they go into AFIB, vs. taking a slow release 24 hour dose every single day. It almost seems my AFIB comes on easier when my heart rate and blood pressure is in the low range. Thanks!
Does anyone just take a fast acting metoprolol or Diltiazam when they go into AFIB, vs. taking a slow release 24 hour dose every single day. It almost seems my AFIB comes on easier when my heart rate and blood pressure is in the low range. Thanks!
Kmm96
in
AF Association
4 years ago
Feeling Deflated
Started Couch to 5k again and I have been struggling this time, but I've kept going I've repeated Wk 1 a few times. Now I'm really enjoying it but I'm in so much pain after it with my knee. I'm taking pain killers using deep heat gel and also tried a tens machine but my knee still hurts. Are there any
Started Couch to 5k again and I have been struggling this time, but I've kept going I've repeated Wk 1 a few times. Now I'm really enjoying it but I'm in so much pain after it with my knee. I'm taking pain killers using deep heat gel and also tried a tens machine but my knee still hurts. Are there any
Kemali
in
Couch to 5K
3 years ago
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Have you ever used a patch to record the rhythm of your heart at home?
We think diagnostic technologies like this can be especially useful during the COVID-19 pandemic, allowing a patient to first have a telephone/video consultation before the patch is sent direct to their home. Zio is a promising new ECG patch which can be worn for up to 14 days. The National Institute
We think diagnostic technologies like this can be especially useful during the COVID-19 pandemic, allowing a patient to first have a telephone/video consultation before the patch is sent direct to their home. Zio is a promising new ECG patch which can be worn for up to 14 days. The National Institute
TracyAdmin
ArrhythmiaAlliance
in
Arrhythmia Alliance
4 years ago
Have you ever used a patch to record the rhythm of your heart at home?
We think diagnostic technologies like this can be especially useful during the COVID-19 pandemic, allowing a patient to first have a telephone/video consultation before the patch is sent direct to their home. Zio is a promising new ECG patch which can be worn for up to 14 days. The National Institute
We think diagnostic technologies like this can be especially useful during the COVID-19 pandemic, allowing a patient to first have a telephone/video consultation before the patch is sent direct to their home. Zio is a promising new ECG patch which can be worn for up to 14 days. The National Institute
TracyAdmin
Partner
in
AF Association
4 years ago
Recent diagnosis of Paroxysmal AF and underlining Lown-Ganong-Levine (LGL) syndrome
Hello all, I haven't written on here before but thought I would see if anyone knows some further information then what I could find on Google... ( which has not been helpful) At the end of January this year I ended up in hospital with AF. My resting heart rate was around 160 bpm and irregular, normally
Hello all, I haven't written on here before but thought I would see if anyone knows some further information then what I could find on Google... ( which has not been helpful) At the end of January this year I ended up in hospital with AF. My resting heart rate was around 160 bpm and irregular, normally
ladybird16
in
Atrial Fibrillation Support
4 years ago
Low blood pressure and AF ?
I had a cardioversion 6 years ago which corrected my persistence AF. Sadly I am in now back in persistent AF and experiencing problems with low blood pressure. When my BP is normal I feel great and have no other symptoms but when my BP drops I feel absolutely awful and have to rest. Have been taking
I had a cardioversion 6 years ago which corrected my persistence AF. Sadly I am in now back in persistent AF and experiencing problems with low blood pressure. When my BP is normal I feel great and have no other symptoms but when my BP drops I feel absolutely awful and have to rest. Have been taking
Cricket24
in
Atrial Fibrillation Support
4 years ago
Amlodipine and Peripheral Neuropathy
I have been on 10mg amlodipine for about 10 years. Bp is great/controlled. I have the usual side effect of swollen feet/ankles, and am used to it. In the last several years I developed peripheral bilateral neuropathy on the bottoms of my feet - no pain, just loss of feeling. Questions: could this be
I have been on 10mg amlodipine for about 10 years. Bp is great/controlled. I have the usual side effect of swollen feet/ankles, and am used to it. In the last several years I developed peripheral bilateral neuropathy on the bottoms of my feet - no pain, just loss of feeling. Questions: could this be
Hidden
in
High Blood Pressure Support
3 years ago
Broad complex tachycardia
Has anyone experienced broad complex tachycardia on a 24 holter ? Should I be worried? GP has requested an echo! I had two episodes that lasted less than 3 seconds and no symptoms other than felt them. GP said my HR went to 146bpm. The rest was normal sinus rhythm. Feeling a bit stressed with it all
Has anyone experienced broad complex tachycardia on a 24 holter ? Should I be worried? GP has requested an echo! I had two episodes that lasted less than 3 seconds and no symptoms other than felt them. GP said my HR went to 146bpm. The rest was normal sinus rhythm. Feeling a bit stressed with it all
Robski501
in
Thyroid UK
4 years ago
Advice
I am currently suffering with extremely painful period pains which I'm quite positive could be endo as it runs through the family. like quite a few of you I am still waiting for an appointment from my referral for gyne. But I recently brought a tens machine as I saw that can be quite helpful does it
I am currently suffering with extremely painful period pains which I'm quite positive could be endo as it runs through the family. like quite a few of you I am still waiting for an appointment from my referral for gyne. But I recently brought a tens machine as I saw that can be quite helpful does it
Monkeydancer1202
in
Endometriosis UK
3 years ago
Flecainide and Metoprolol Combo Have Stopped Working
I've been a member for a while, but have never posted before. I am a 62-year-old male with what had been long-standing but well-controlled atrial fibrillation/flutter (Flecainide 200mg and Metoprolol 50mg). Quite suddenly these drugs stopped working and I am now in constant Atrial Flutter. I am on a
I've been a member for a while, but have never posted before. I am a 62-year-old male with what had been long-standing but well-controlled atrial fibrillation/flutter (Flecainide 200mg and Metoprolol 50mg). Quite suddenly these drugs stopped working and I am now in constant Atrial Flutter. I am on a
Quinney
in
AF Association
4 years ago
My Apple watch
I have been extremely surprised today when I saw my EP at the hospital. My watch was recording that I had AF and I felt dizzy and breathless. However my ECG tracing in the hospital recorded that I was in sinus rhythm. I have always trusted my watch but now in shock as it doesn’t seem very accurate.
I have been extremely surprised today when I saw my EP at the hospital. My watch was recording that I had AF and I felt dizzy and breathless. However my ECG tracing in the hospital recorded that I was in sinus rhythm. I have always trusted my watch but now in shock as it doesn’t seem very accurate.
maria68
in
AF Association
4 years ago
Snoo
I have had PMR for many years and am in fact now labelled inflammatory arthritis. The signs and symptoms are the same as is the treatment on and off Pred. I had shingles badly about three years ago and this year will qualify for the shingles vaccine. Has anybody had the vaccine while on Pred and were
I have had PMR for many years and am in fact now labelled inflammatory arthritis. The signs and symptoms are the same as is the treatment on and off Pred. I had shingles badly about three years ago and this year will qualify for the shingles vaccine. Has anybody had the vaccine while on Pred and were
Snoopy7
in
PMRGCAuk
4 years ago
'Could All the Experts Be Wrong About Parkinson's?'
*"This approach can be tested now by using the drug metyrosine to partially
block
the synthesis of dopamine within the
nerve
cells." "We've lived in the dopaminergic era since the 1970s and that has allowed for millions of people with Parkinson's to feel some improvement in their symptoms.
*"This approach can be tested now by using the drug metyrosine to partially
block
the synthesis of dopamine within the
nerve
cells." "We've lived in the dopaminergic era since the 1970s and that has allowed for millions of people with Parkinson's to feel some improvement in their symptoms.
PDConscience
in
Cure Parkinson's
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
4 years ago
Serious Endo, some things have helped my Stage 4
Hi there, Well yes for many, some it stays the same, some it goes away. Mine started when I was 10. Diagnosis at 24. Between 24 and 36 it had become stage 4. Several operations. Had it in my lungs, down to Pouch of Douglas, repro organs twisted, cysts, on bladder, bowel bedded down with adhesions,
Hi there, Well yes for many, some it stays the same, some it goes away. Mine started when I was 10. Diagnosis at 24. Between 24 and 36 it had become stage 4. Several operations. Had it in my lungs, down to Pouch of Douglas, repro organs twisted, cysts, on bladder, bowel bedded down with adhesions,
JOSANDY40
in
Endometriosis UK
3 years ago
Viral meningitis
I have had VM, unfortunately the virus was not a usual strain so I did not respond to any IV treatments they usually give to VM patients. I had to fight it myself with a temp of 40.2. How long will the headaches last? Been in hospital 3 weeks only recently discharged and scared for the future .Any advice
I have had VM, unfortunately the virus was not a usual strain so I did not respond to any IV treatments they usually give to VM patients. I had to fight it myself with a temp of 40.2. How long will the headaches last? Been in hospital 3 weeks only recently discharged and scared for the future .Any advice
UptoonGirl1
in
Meningitis Now
4 years ago
AF Cure
Good News from Seventy Nine member It would appear NHS had got me in Good Place . After a long time suffering with AFP They have finally cracked it I will be 81 in March hope to go back to Tennis certainly Golf . Along with 2 complete replacement Knees and Right Hip joint I’ve had 2 cardio Versions
Good News from Seventy Nine member It would appear NHS had got me in Good Place . After a long time suffering with AFP They have finally cracked it I will be 81 in March hope to go back to Tennis certainly Golf . Along with 2 complete replacement Knees and Right Hip joint I’ve had 2 cardio Versions
Seventy9
in
AF Association
4 years ago
Does shingles cause Hashimoto’s to flare up?
I have had Hashimoto’s now for about 3 years and I’m still finding it hard navigating my way through the symptoms and flare ups. I have suffered from very bad crippling anxiety over the last year and half which hasn’t helped with the lockdown and dealing a 4 year old and 1.5 year old while attempting
I have had Hashimoto’s now for about 3 years and I’m still finding it hard navigating my way through the symptoms and flare ups. I have suffered from very bad crippling anxiety over the last year and half which hasn’t helped with the lockdown and dealing a 4 year old and 1.5 year old while attempting
Purple_dog
in
Thyroid UK
4 years ago
Lyme's Disease long term arthritis
Is there anyone out there who has long term joint issues due to Lyme's Disease. I had it in 2019 but now struggle to walk 1 mile due to my knees apparently having crumbled and I have cysts on the cartlidge too. Is anyone having similar problems please ? Any advice too thanks.
Is there anyone out there who has long term joint issues due to Lyme's Disease. I had it in 2019 but now struggle to walk 1 mile due to my knees apparently having crumbled and I have cysts on the cartlidge too. Is anyone having similar problems please ? Any advice too thanks.
Bessie22
in
Pain Concern
4 years ago
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