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Cortizone-5
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AV Nodal Re-Entrant Tachycardia
After seeing my EP today and giving him an EKG print-out of my tachycardia episode in the ER on October 2nd, I got some bad news. It seems my SVT wasn't caused by too much cortisone in my system prescribed by my GP, but that I have AV Nodal Re-Entrant Tachycardia. He said of the 1,000 or more ablations
After seeing my EP today and giving him an EKG print-out of my tachycardia episode in the ER on October 2nd, I got some bad news. It seems my SVT wasn't caused by too much cortisone in my system prescribed by my GP, but that I have AV Nodal Re-Entrant Tachycardia. He said of the 1,000 or more ablations
Snowgirl65
in
AF Association
2 years ago
Strength in good memories
My husband passed away on Oct 3rd, aged 65 after 19 months since diagnosis. He had the standard operation and chemotherapy and recovered really well but in last 7 months deteriorated losing movement in his right arm,and last 4 months his right leg was almost gone , and then last 2 weeks a wheelchair
My husband passed away on Oct 3rd, aged 65 after 19 months since diagnosis. He had the standard operation and chemotherapy and recovered really well but in last 7 months deteriorated losing movement in his right arm,and last 4 months his right leg was almost gone , and then last 2 weeks a wheelchair
Daybreak2
in
Glioblastoma Support
2 years ago
Pain Management
Hi All, My husband's pain seems to be out of control. He says he hurts everywhere all the time, but mostly his whole right side, from his shoulder, arm, wrist all the way to his toes. He uses magnesium and heat, a tens machine as well as massage, CBD and acupuncture. But nothing really helps or lasts
Hi All, My husband's pain seems to be out of control. He says he hurts everywhere all the time, but mostly his whole right side, from his shoulder, arm, wrist all the way to his toes. He uses magnesium and heat, a tens machine as well as massage, CBD and acupuncture. But nothing really helps or lasts
PDsux_10
in
Cure Parkinson's
2 years ago
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Very Scary SVT.
I ended up in the ER last night via ambulance because of a sudden heart rate of 198 -- it literally felt like it was beating out of my chest. I was breathless and panicky. I was told it was SVT, which I never had, and was given a drip of various drugs. It went down to 150, then finally six hours later
I ended up in the ER last night via ambulance because of a sudden heart rate of 198 -- it literally felt like it was beating out of my chest. I was breathless and panicky. I was told it was SVT, which I never had, and was given a drip of various drugs. It went down to 150, then finally six hours later
Snowgirl65
in
AF Association
2 years ago
My mother died
My mother died yesterday after a horrible period. My stress level is rocket high and my body needs cortisone. Puls over 100, so fatigue I have not felt since beginning of PMR, brain is a mess so I just lay here waiting for the extra 5 mg to kick in so I can sleep. I find this lack of cortisone production
My mother died yesterday after a horrible period. My stress level is rocket high and my body needs cortisone. Puls over 100, so fatigue I have not felt since beginning of PMR, brain is a mess so I just lay here waiting for the extra 5 mg to kick in so I can sleep. I find this lack of cortisone production
krillemy
in
PMRGCAuk
2 years ago
Epidural Injections for Back Pain for MPN Patient
I am scheduled for an epidural Friday and have some concerns since I have PV and ET. I have stopped taking aspirin as well as Eliquis; however, I am concerned about the possible risk involved with the epidural. I have been having some back and leg pain for about a month and went to an orthopedic dr
I am scheduled for an epidural Friday and have some concerns since I have PV and ET. I have stopped taking aspirin as well as Eliquis; however, I am concerned about the possible risk involved with the epidural. I have been having some back and leg pain for about a month and went to an orthopedic dr
Buggerbear
in
MPN Voice
2 years ago
Use of Corticoide to treat tight foreskin
Hey guys, Last July I had a Frenuloplasty to help me to retract more my foreskin. I didn’t had a bad phimosis, just couldn’t fully retract my foreskin when horny… I wanted to have it completely uncovered. I had a perfect and fast healing. Now I can retract without any discomfort when flaccid, but
Hey guys, Last July I had a Frenuloplasty to help me to retract more my foreskin. I didn’t had a bad phimosis, just couldn’t fully retract my foreskin when horny… I wanted to have it completely uncovered. I had a perfect and fast healing. Now I can retract without any discomfort when flaccid, but
AndyAvila
in
Men's Health Forum (Penis Health)
2 years ago
possible use of prednisone
I have inflamed sinuses and have taken short term prednisone before. If I were to do this again would it complicate or damage things? I was just diagnosed with the pre-cursor to CLL and do not have CLL yet. I want to do all I can to prevent it from developing further. I also have been getting cortisone
I have inflamed sinuses and have taken short term prednisone before. If I were to do this again would it complicate or damage things? I was just diagnosed with the pre-cursor to CLL and do not have CLL yet. I want to do all I can to prevent it from developing further. I also have been getting cortisone
DianeSH
in
CLL Support
2 years ago
Dealing with stressful situations and events while in prednisolon
I am on 17.5 mg. I have a clear feeling that my adrenals are not working very well anymore. I have to deal with a dying mother in and out of hospital and not mentally well. At the same time my oldest son 24 lost his girlfriend, and that has put him in to a crisis where he needs help daily. He had Tourettes
I am on 17.5 mg. I have a clear feeling that my adrenals are not working very well anymore. I have to deal with a dying mother in and out of hospital and not mentally well. At the same time my oldest son 24 lost his girlfriend, and that has put him in to a crisis where he needs help daily. He had Tourettes
krillemy
in
PMRGCAuk
2 years ago
does inflammation return after cortisone?
I had a cortisone injection into my shoulder joint last week and I’m concerned that the inflammation that’s been reduced to make me feel a little better will return after the injection wears off. Is this a thing?
I had a cortisone injection into my shoulder joint last week and I’m concerned that the inflammation that’s been reduced to make me feel a little better will return after the injection wears off. Is this a thing?
Lfh73
in
NRAS
2 years ago
Metacarpal boss
Hi, I have a left hand fracture that has developed into metacarpal boss. I've been given a cortisone injection that hasn't fully worked and I'm still getting pain.tWhat I can't understand is the pain is mainly from about 5pm until about 6am the following day so you can imagine sleeping ain't that
Hi, I have a left hand fracture that has developed into metacarpal boss. I've been given a cortisone injection that hasn't fully worked and I'm still getting pain.tWhat I can't understand is the pain is mainly from about 5pm until about 6am the following day so you can imagine sleeping ain't that
Amanfromtheuk
in
Sports Injury
2 years ago
Chronic pain
Hi I have suffered wide spread pain going on 4 yrs , had MRI scan ultra sounds cortisone injections for years to get diagnosed with fibromyalgia august 2022 I had a bad fall at work last year heightened pain and anxiety hit the roof I’m still off work cannot see light at end of tunnel , in so much
Hi I have suffered wide spread pain going on 4 yrs , had MRI scan ultra sounds cortisone injections for years to get diagnosed with fibromyalgia august 2022 I had a bad fall at work last year heightened pain and anxiety hit the roof I’m still off work cannot see light at end of tunnel , in so much
Cherish1961
in
Fibromyalgia Action UK
2 years ago
Anaphylaxis from Augmentin (amoxicillin) after pneumonia, no previous penicillin allergy.
Hi all, Would really appreciate some advice. A couple of days ago I developed anaphylaxis after taking an augmentin antibiotic tablet. I'm 42 and have no history of allergy to penicillin, have always been able to take it. I recently had bad pneumonia and was on a 3 week course of augmentin and had
Hi all, Would really appreciate some advice. A couple of days ago I developed anaphylaxis after taking an augmentin antibiotic tablet. I'm 42 and have no history of allergy to penicillin, have always been able to take it. I recently had bad pneumonia and was on a 3 week course of augmentin and had
Aquablue80
in
USAnaphylaxis
2 years ago
Still testing positive after 10 weeks
Hello everyone. I need some help. My mum has CLL and had been on venetoclax + rituximab since November 2021 (rituximab suspended early due to lowered neutrophils). We had several mishaps (e.g. frequent diarrhoea) however she was quite well until she got on 16 May and she tested covid positive. She
Hello everyone. I need some help. My mum has CLL and had been on venetoclax + rituximab since November 2021 (rituximab suspended early due to lowered neutrophils). We had several mishaps (e.g. frequent diarrhoea) however she was quite well until she got on 16 May and she tested covid positive. She
Marymary19
in
CLL Support
2 years ago
Long time no chat 😄
Well it’s been a while since I posted and what a journey I’ve been on. I try to keep it brief. I year ago I was told I’m steroid dependent. I carry and emergency injection kit of cortisone. I hope I never have to use it. I had a follow up cardiology appointment on January 4th this year. I was told I
Well it’s been a while since I posted and what a journey I’ve been on. I try to keep it brief. I year ago I was told I’m steroid dependent. I carry and emergency injection kit of cortisone. I hope I never have to use it. I had a follow up cardiology appointment on January 4th this year. I was told I
SuziCutie
in
PMRGCAuk
2 years ago
Asymptomatic AF - more comments
Well, I have now the time to sit leisurely and review all your kind and useful comments. Many thanks. I list what I understand to be symptoms of Covid Omicron Varient ( source NHS) and alongside what I can identify with. Lower back pain No Runny nose/congestion
Well, I have now the time to sit leisurely and review all your kind and useful comments. Many thanks. I list what I understand to be symptoms of Covid Omicron Varient ( source NHS) and alongside what I can identify with. Lower back pain No Runny nose/congestion
Hidden
in
AF Association
2 years ago
Shooting here in Copenhagen :(
Well I really needed my cortisone today. Devastated by the shooting episode here in Copenhagen near to my daughters home, and my grown children knowing the ill young man who had the riffel as a friends little brother.... I have been crying my eye out. I thought this was in USA only, but I guess that
Well I really needed my cortisone today. Devastated by the shooting episode here in Copenhagen near to my daughters home, and my grown children knowing the ill young man who had the riffel as a friends little brother.... I have been crying my eye out. I thought this was in USA only, but I guess that
krillemy
in
PMRGCAuk
2 years ago
Pain management alternatives
“Things I learned along the way” … in the event this may help others, I thought I’d share … If you or your loved one is struggling a great deal with pain, you may want to consider 1) having a pain pump placed 2) acupuncture. As my Jeff’s pain became harder to manage with his drug regimen, we were referred
“Things I learned along the way” … in the event this may help others, I thought I’d share … If you or your loved one is struggling a great deal with pain, you may want to consider 1) having a pain pump placed 2) acupuncture. As my Jeff’s pain became harder to manage with his drug regimen, we were referred
Pancake_Lefse
in
Advanced Prostate Cancer
2 years ago
Tronchanteric bursitis and joint space in hip
Hi everyone I had a cortisone injection las5 week hip was much better for three days then last night I started having pain again.
Hi everyone I had a cortisone injection las5 week hip was much better for three days then last night I started having pain again.
Gillybean123
in
AF Association
2 years ago
Reducing Prednisolone and normal test results.
I saw a consultant for the first time in April this year and he suggested slowly reducing prednisolone until I reached 2mg. I was diagnosed with PMR two years ago and according to the doctor in the hospital I should have been off steroids by June 2021. I have had flares over this time and been
I saw a consultant for the first time in April this year and he suggested slowly reducing prednisolone until I reached 2mg. I was diagnosed with PMR two years ago and according to the doctor in the hospital I should have been off steroids by June 2021. I have had flares over this time and been
Buzybe
in
PMRGCAuk
2 years ago
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