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Covid and fibromyalgia (lupus)
hi great forum people, I have been getting worse after Covid infection in December and have been going to GP with chest pains tightness pains in across top of my back told increase gaberpentin. this week went to see GP and said I need blood test to check vitamins as getting worse and like drained
hi great forum people, I have been getting worse after Covid infection in December and have been going to GP with chest pains tightness pains in across top of my back told increase gaberpentin. this week went to see GP and said I need blood test to check vitamins as getting worse and like drained
Geeforce99
in
Fibromyalgia Action UK
6 months ago
Millar 69
I am a57 year old man used to work in a fencing firm was as fit as a butcher’s dog before covid started new job before Covid took hold we all went out on ferlo but I txt my boss because I was always used to working i don’t drink or take drugs have had all Covid jabs but have went down hill badly went
I am a57 year old man used to work in a fencing firm was as fit as a butcher’s dog before covid started new job before Covid took hold we all went out on ferlo but I txt my boss because I was always used to working i don’t drink or take drugs have had all Covid jabs but have went down hill badly went
Pjpuk
in
Ataxia UK
6 months ago
Covid 2 years ago
I have asthma for many years but was controlled and well managed until I caught covid at work 2 years agoSince then my asthma is good for a few months then knocked for six steroids antibiotics etc I live an healthy active lifestyle has anyone experienced this please
I have asthma for many years but was controlled and well managed until I caught covid at work 2 years agoSince then my asthma is good for a few months then knocked for six steroids antibiotics etc I live an healthy active lifestyle has anyone experienced this please
Vegan8835
in
Asthma Community Forum
6 months ago
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cellulitis again….
Ugh! Woke up at 5am bank holiday weekend and realised I have cellulitis… No GP cover so 40 minutes holding for NHS 111 and now on 2 hour wait for GP call back to get some antibiotics. Why does it always turn up at the most inconvenient time? Tried to explain to the call handler that, although I can
Ugh! Woke up at 5am bank holiday weekend and realised I have cellulitis… No GP cover so 40 minutes holding for NHS 111 and now on 2 hour wait for GP call back to get some antibiotics. Why does it always turn up at the most inconvenient time? Tried to explain to the call handler that, although I can
Lyndy
in
LSN
1 year ago
Covid and the heart presentation
Here is a link to a Fb post that came my way to a presentation on the effects of Covid on the heart. My AF was drastically increased by Covid 19 infection. I live in BC, Canada, where a group of physicians here is working to get more science-based information out there in the public domain, and to secure
Here is a link to a Fb post that came my way to a presentation on the effects of Covid on the heart. My AF was drastically increased by Covid 19 infection. I live in BC, Canada, where a group of physicians here is working to get more science-based information out there in the public domain, and to secure
Letofeyd
in
AF Association
6 months ago
FET in 4 days and nasty cold
I am so worried now, our FET is this Thursday and some nasty cold got me this weekend. I am afraid to take any cold/flu meds so it won't mess up with my lining etc 🙈 Has anyone been not well before or during transfer and it affected the outcome?
I am so worried now, our FET is this Thursday and some nasty cold got me this weekend. I am afraid to take any cold/flu meds so it won't mess up with my lining etc 🙈 Has anyone been not well before or during transfer and it affected the outcome?
Glaedy
in
Fertility Network UK
5 months ago
High BP
Hi I am 63 years old male had 4 heart attacks last one was 8 years ago. All has been apart from covid and long covid and also never had raised BP in past .2 weeks was asked to do a weekly BP reading and all readings were high never this hi before. GP surgery called to make appointment for this it is
Hi I am 63 years old male had 4 heart attacks last one was 8 years ago. All has been apart from covid and long covid and also never had raised BP in past .2 weeks was asked to do a weekly BP reading and all readings were high never this hi before. GP surgery called to make appointment for this it is
Ouzo20_19
in
British Heart Foundation
6 months ago
Trimbow update
I have been on the Trimbow three weeks now and it does seem to be working , I noticed I was walking faster and the use of my ventolin is much reduced . I still have a chesty cough lingering on after a cold but no infection , I need to ask the question does Trimbow make you cough? Just wondered as I
I have been on the Trimbow three weeks now and it does seem to be working , I noticed I was walking faster and the use of my ventolin is much reduced . I still have a chesty cough lingering on after a cold but no infection , I need to ask the question does Trimbow make you cough? Just wondered as I
MrsP70
in
Lung Conditions Community Forum
5 months ago
covid afibs???/
I had covid in September of 2023 and soon thereafter developed a fibs, which I have never had in my life! I am 69. My question is this: Has this happened to anyone else and did they eventually go away, or is it a permanent thing?
I had covid in September of 2023 and soon thereafter developed a fibs, which I have never had in my life! I am 69. My question is this: Has this happened to anyone else and did they eventually go away, or is it a permanent thing?
peachtreepiggy
in
Atrial Fibrillation Support
6 months ago
slightly anxious and just looking for moral support
Hoping you all had a good Christmas. Mine has been a bit rough as the whole family has been unwell including me with this cold/throat bug that is going around. It didn’t go to my chest this year, thankfully and I was recovering okay when I noticed my throat and ears started hurting again and my mouth
Hoping you all had a good Christmas. Mine has been a bit rough as the whole family has been unwell including me with this cold/throat bug that is going around. It didn’t go to my chest this year, thankfully and I was recovering okay when I noticed my throat and ears started hurting again and my mouth
Abcd123455
in
PMRGCAuk
8 months ago
Starting Pegasys soon
Hi all and merry belated Christmas So… chemo…. I was diagnosed with ET about a year ago and finally found an MPN specialist in Montreal after a few months with a hemo who, unfortunately, knew very little about ET. I should be starting Pegasys sometime in January and I have a few questions :
Hi all and merry belated Christmas So… chemo…. I was diagnosed with ET about a year ago and finally found an MPN specialist in Montreal after a few months with a hemo who, unfortunately, knew very little about ET. I should be starting Pegasys sometime in January and I have a few questions :
IsabelleHo
in
MPN Voice
8 months ago
Covid vaccine
I am going to put it out there . Did anyone get ill with encephalitis after taking the Covid vaccine? This has been something that has been playing in my mind for a while My mom was in later 60s in good health and active before having the vaccine.
I am going to put it out there . Did anyone get ill with encephalitis after taking the Covid vaccine? This has been something that has been playing in my mind for a while My mom was in later 60s in good health and active before having the vaccine.
GIL910
in
Encephalitis International
6 months ago
Lymphedema & Knee bursitis
I have Inflammatory arthritis, Sjogren's and OA. I have been on Methotrexate and Imraldi since 2017, before that I was on Benepali. I have had a new hip in 2017 and I also suffered with my knees which despite many steroid injections they are no longer having any effect. I saw my rheumatologist
I have Inflammatory arthritis, Sjogren's and OA. I have been on Methotrexate and Imraldi since 2017, before that I was on Benepali. I have had a new hip in 2017 and I also suffered with my knees which despite many steroid injections they are no longer having any effect. I saw my rheumatologist
Bailybiscuit
in
NRAS
6 months ago
Hip Replacement while on treatment??
My husband, who is in a Clinical Trial at MDA for Richter's, needs a hip replacement badly - such that his severe arthritis is a bigger deal to his quality of life than the Richter's. He saw an orthopedic pain management specialist last week who had nothing to offer, stating that a steroid injection
My husband, who is in a Clinical Trial at MDA for Richter's, needs a hip replacement badly - such that his severe arthritis is a bigger deal to his quality of life than the Richter's. He saw an orthopedic pain management specialist last week who had nothing to offer, stating that a steroid injection
laurieq
in
CLL Support
6 months ago
Paxlovid for “mild” COVID?
hello all. Just wondering what your experiences have been regarding taking Paxlovid. I realize you can’t advise but I would love to hear from fellow immune suppressed types like me. I have taken it before but when I had it last year I felt pretty bad and taking the Paxlovid was a no brainer. This time
hello all. Just wondering what your experiences have been regarding taking Paxlovid. I realize you can’t advise but I would love to hear from fellow immune suppressed types like me. I have taken it before but when I had it last year I felt pretty bad and taking the Paxlovid was a no brainer. This time
Bon1
in
NRAS
6 months ago
Back to square one
Hi, I first started having coughing problems back in November 2022 when I caught what I thought was just a bad cold or covid, I was getting phlegm stuck in my airways which was tough to get out when coughing, and sometimes I struggled to breath. Sometimes to the point where I actually cried because
Hi, I first started having coughing problems back in November 2022 when I caught what I thought was just a bad cold or covid, I was getting phlegm stuck in my airways which was tough to get out when coughing, and sometimes I struggled to breath. Sometimes to the point where I actually cried because
amygx25
in
Asthma Community Forum
6 months ago
What to do after prednisolone rescue ended?
Has anyone any advice how to get back down to my normal dose of inhaled steroid after a short prednisolone course and chest infection please? Story: I’m maintained on 1 or 2 puffs once a day of Alvesco 80, PF max 380 and very occasional use of Ventolin. I caught a cold virus about 12 days ago and despite
Has anyone any advice how to get back down to my normal dose of inhaled steroid after a short prednisolone course and chest infection please? Story: I’m maintained on 1 or 2 puffs once a day of Alvesco 80, PF max 380 and very occasional use of Ventolin. I caught a cold virus about 12 days ago and despite
Merryroundabout
in
Asthma Community Forum
8 months ago
Lyme Disease
Hello, I hope everyone is feeling as well as possible. Can I ask about links between Lyme Disease and RA? What is actually known? My daughter was talking about ticks the other day (we are both walkers) when I said I had had (in my late teens) a bullseye mark from a tick on my leg, she said ‘well that
Hello, I hope everyone is feeling as well as possible. Can I ask about links between Lyme Disease and RA? What is actually known? My daughter was talking about ticks the other day (we are both walkers) when I said I had had (in my late teens) a bullseye mark from a tick on my leg, she said ‘well that
Lyndy
in
NRAS
1 year ago
ADT and crying
Does anyone else that has been on ADT drugs for years have trouble with tears or crying for no real reason? I tear up anymore at just the thought of something sad. It’s a major pain in the ass, not to mention embarrassing because I am still employed. Wondering if there is a solution other than stopping
Does anyone else that has been on ADT drugs for years have trouble with tears or crying for no real reason? I tear up anymore at just the thought of something sad. It’s a major pain in the ass, not to mention embarrassing because I am still employed. Wondering if there is a solution other than stopping
joeguy
in
Advanced Prostate Cancer
8 months ago
GPA flare, is it likely even if I only have 1 symptom
I was diagnosed with GPA in 2017, I have had 3 flares since initial diagnosis and although the symptoms have got milder each time, I always have the same symptoms - pain and loss of hearing in my ear, discomfort and blood in my nose, pain and stiffness in my finger joints and extreme fatigue. I regularly
I was diagnosed with GPA in 2017, I have had 3 flares since initial diagnosis and although the symptoms have got milder each time, I always have the same symptoms - pain and loss of hearing in my ear, discomfort and blood in my nose, pain and stiffness in my finger joints and extreme fatigue. I regularly
stuc
in
Vasculitis UK
8 months ago
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