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post Viral symptoms
I returned from Australia with a heavy cold and painful cough. I have been confined to bed mostly for 2 weeks and really quite ill. A man coughed throughout our flight, this could be the source although my grandchildren were ill too. No sooner did I feel this virus improve it seemed to gain more impetus
I returned from Australia with a heavy cold and painful cough. I have been confined to bed mostly for 2 weeks and really quite ill. A man coughed throughout our flight, this could be the source although my grandchildren were ill too. No sooner did I feel this virus improve it seemed to gain more impetus
SheffieldJane
in
PMRGCAuk
7 months ago
covid vaccines
hi all. I’m sure many readers of this wonderful community will be tired of this subject. But I wanted to ask the question- I never had any AF episodes up to and including Covid. When I look at my vaccination dates I see a possible link. Is it possible that the jabs we all had did in fact interfere with
hi all. I’m sure many readers of this wonderful community will be tired of this subject. But I wanted to ask the question- I never had any AF episodes up to and including Covid. When I look at my vaccination dates I see a possible link. Is it possible that the jabs we all had did in fact interfere with
OscarN
in
AF Association
7 months ago
Has anyone heard of Parsonage Turner Syndrome? Out of interest.
Hello , I was diagnosed with PMR in September 2012 . I had returned from holiday , had my annual flu jab and noticed awful stiffness in my arms and hips whilst at Yoga . It increased to agonising electric shock pains , from shoulders downwards , my biceps would almost spasm and go hard , the pain
Hello , I was diagnosed with PMR in September 2012 . I had returned from holiday , had my annual flu jab and noticed awful stiffness in my arms and hips whilst at Yoga . It increased to agonising electric shock pains , from shoulders downwards , my biceps would almost spasm and go hard , the pain
Greensleeves
in
PMRGCAuk
7 months ago
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My PMR is basically gone, but now I got shingles on my right side of face.
All the drugs I took, take lowers my immune system. No prednisone anymore, but Methotrexate lowers immune response. About 4 days ago, got shingles on my face and forehead. It is super pain, bad pain. Before the shingles, I felt like my eyes were infected, eyes and skin all red and sore. Pain not quite
All the drugs I took, take lowers my immune system. No prednisone anymore, but Methotrexate lowers immune response. About 4 days ago, got shingles on my face and forehead. It is super pain, bad pain. Before the shingles, I felt like my eyes were infected, eyes and skin all red and sore. Pain not quite
sdowney717
in
PMRGCAuk
8 months ago
If you get sick...cold, flu, Covid...what did you do?
I'm just over 9 months kidney transplant from a living donor. I've felt great but I do worry, since it is cold and flu season, about getting sick. Probably my biggest worry at this point. I try to wear masks when I am out and take all precautions. I just wondered though if I should get sick what are
I'm just over 9 months kidney transplant from a living donor. I've felt great but I do worry, since it is cold and flu season, about getting sick. Probably my biggest worry at this point. I try to wear masks when I am out and take all precautions. I just wondered though if I should get sick what are
Tankjsl
in
Kidney Transplant
7 months ago
looking for a neurologist
Can anyone recommend a neurologist knowledgeable in RLS in the Bristol/ Bath (England) area ? I currently have a neurologist whom I rate quite highly but who cannot prescribe opioids as they are not on the formulary of the hospital where she practises. She has however asked my GP to prescribe Oxycodone
Can anyone recommend a neurologist knowledgeable in RLS in the Bristol/ Bath (England) area ? I currently have a neurologist whom I rate quite highly but who cannot prescribe opioids as they are not on the formulary of the hospital where she practises. She has however asked my GP to prescribe Oxycodone
etchea33
in
Restless Legs Syndrome
6 months ago
covid
hello iam suffering with covid had it since Sunday , symptoms don’t seem to be going away , has anybody had covid , with hashimotos , am I wrong in thinking having this condition makes illness worse and longer to recover , sorry but been told I have hashimotos, but not sure on how it works thanks for
hello iam suffering with covid had it since Sunday , symptoms don’t seem to be going away , has anybody had covid , with hashimotos , am I wrong in thinking having this condition makes illness worse and longer to recover , sorry but been told I have hashimotos, but not sure on how it works thanks for
Prosecco1997
in
Thyroid UK
7 months ago
Recurrent vaginal thrush- need urgent help
I had what looks like a vaginal thrush for the first time 3 weeks back. I'm 35 yrs old. My GP nurse saw me and suggested Canesten pessary. I took it but to no avail (also the pessary did not work properly) I went back to the doctor in 2 days and she suggested Flucanazole oral tabled (150 mg 1 dose) that
I had what looks like a vaginal thrush for the first time 3 weeks back. I'm 35 yrs old. My GP nurse saw me and suggested Canesten pessary. I took it but to no avail (also the pessary did not work properly) I went back to the doctor in 2 days and she suggested Flucanazole oral tabled (150 mg 1 dose) that
Rita89
in
Women's Health
6 months ago
11 months on.
Hiya,I was in a coma in jan-march for mixed overdose, CLABSI, cellulitis, gangrene to left thigh, sepsis, multi organ failure, end stage renal failure/on diyalsis, ventilation associated pneumonia and the list goes on. I came out of the hospital on 5th may with a walking frame and still 0 ability to
Hiya,I was in a coma in jan-march for mixed overdose, CLABSI, cellulitis, gangrene to left thigh, sepsis, multi organ failure, end stage renal failure/on diyalsis, ventilation associated pneumonia and the list goes on. I came out of the hospital on 5th may with a walking frame and still 0 ability to
Jjones210519
in
ICUsteps
8 months ago
Pegasys Update 1.0
Finally getting around to sharing my experiences of starting Pegasys. First a little background. Diagnosed with ET JAK2+ in 2019 after a decade of scintillating scotomas with increasing frequency at almost weekly. Aspirin cut this to approx. 90 days! Over the next three years increasingly struggled with
Finally getting around to sharing my experiences of starting Pegasys. First a little background. Diagnosed with ET JAK2+ in 2019 after a decade of scintillating scotomas with increasing frequency at almost weekly. Aspirin cut this to approx. 90 days! Over the next three years increasingly struggled with
Crossefield
in
MPN Voice
7 months ago
D Mannose
Hello everyone Just wondered if anyone here has used D Mannose tablets to manage recurrent urinary tract infections and if so with what success? I’ve had this problem for a few years now and the Urologist suggested daily low dose antibiotics which I want to avoid. Despite trying all of the self
Hello everyone Just wondered if anyone here has used D Mannose tablets to manage recurrent urinary tract infections and if so with what success? I’ve had this problem for a few years now and the Urologist suggested daily low dose antibiotics which I want to avoid. Despite trying all of the self
RosaD
in
LUPUS UK
7 months ago
Covid and Myelofibrosis
hi I’ve just tested positive for Covid, I have post pv Myelofibrosis. I’m waiting on 111 to see whether I need to have some treatment. What are your thoughts and is this necessary now? I think it’s going to be a long wait, so it might be tomorrow. Thank you Mal
hi I’ve just tested positive for Covid, I have post pv Myelofibrosis. I’m waiting on 111 to see whether I need to have some treatment. What are your thoughts and is this necessary now? I think it’s going to be a long wait, so it might be tomorrow. Thank you Mal
Mal42
in
MPN Voice
7 months ago
Aciclovir as prevention for shingles
I wish to express my deepest thanks to all fellow members who have responded to my recent enquiry. There has been consensus in all replies confirming that prescribing Aciclovir is standard practice.
I wish to express my deepest thanks to all fellow members who have responded to my recent enquiry. There has been consensus in all replies confirming that prescribing Aciclovir is standard practice.
RamsesII
in
CLL Support
6 months ago
dont give up the fight against Afib
I have been a member of this forum for some years and learned a few things from its members but up until now i have never posted anything but i thought my story may give some of you people a bit of hope. I first went into afib in 2018 sudenly without any warning my heart rate was 222 and the top line
I have been a member of this forum for some years and learned a few things from its members but up until now i have never posted anything but i thought my story may give some of you people a bit of hope. I first went into afib in 2018 sudenly without any warning my heart rate was 222 and the top line
Dikytiker
in
AF Association
7 months ago
Covid and Party
👋 Party is this coming Sat . I feel OK with going now after people's advice , so thank you all. Got my N95 mask. Will have sanitiser on me all the time . However I am now facing difficulties, flare up in both knees and one hip in agony and lower back , getting in and out of bed , turning in bed
👋 Party is this coming Sat . I feel OK with going now after people's advice , so thank you all. Got my N95 mask. Will have sanitiser on me all the time . However I am now facing difficulties, flare up in both knees and one hip in agony and lower back , getting in and out of bed , turning in bed
Stavrou1
in
CLL Support
7 months ago
Types of asthma
I was diagnosed with non specific asthma 2 years ago at 69. My type starts with a tickle in the throat, coughing and sadly incontinence. My dad a smoker had cold. How many types of asthma are there. My friend says I probably only have chronic cough
I was diagnosed with non specific asthma 2 years ago at 69. My type starts with a tickle in the throat, coughing and sadly incontinence. My dad a smoker had cold. How many types of asthma are there. My friend says I probably only have chronic cough
Msccruises
in
Asthma Community Forum
21 hours ago
Persistent cough and possible asthma diagnosis
Hello. I’m new here and keen to find out if other people with asthma have experienced the symptoms I have. I have had a persistent cough for about 4 months. Generally I feel a pressure in my chest and lower throat where it feels like a can’t breath. I then cough as this feels like it relieves the pressure
Hello. I’m new here and keen to find out if other people with asthma have experienced the symptoms I have. I have had a persistent cough for about 4 months. Generally I feel a pressure in my chest and lower throat where it feels like a can’t breath. I then cough as this feels like it relieves the pressure
SunnyDaySunshine
in
Asthma Community Forum
5 days ago
symbicort 200 user
Over 2 months ago I was dx with asthma, bronchitis and lower right pneumonia. My lungs were shit. I have been taking symbicort 2puffs 2x daily. Also taking Monttelukast 10 mg 1x a day. So if an expert or MD is in here I want to say I quit taking the symbicort completely and feel better not taking it.
Over 2 months ago I was dx with asthma, bronchitis and lower right pneumonia. My lungs were shit. I have been taking symbicort 2puffs 2x daily. Also taking Monttelukast 10 mg 1x a day. So if an expert or MD is in here I want to say I quit taking the symbicort completely and feel better not taking it.
Cougher1001
in
Asthma Community Forum
8 days ago
Rituximab
Hi all, well after 6 months on hyrimoz and no improvement they want to start me on Rituximab. Does anyone know how long you have to wait before you can start, ie this wash out period were you have nothing?? The steroid injections have worn off again, inflammation crp up again tiredness back and the
Hi all, well after 6 months on hyrimoz and no improvement they want to start me on Rituximab. Does anyone know how long you have to wait before you can start, ie this wash out period were you have nothing?? The steroid injections have worn off again, inflammation crp up again tiredness back and the
Akaka
in
NRAS
7 months ago
latest results, confused, please advise!
My last results a month ago before treatment with 50 mcg were : Serum free t4 level. 10.2 pmo/L TSH level 7.28 IU/mL After a month of Levothyroxine my results are now:- serum free t4 level. 15.6 TSH 2.87 I asked for, and was told my T3 would be checked but I can’t see it on printout unless
My last results a month ago before treatment with 50 mcg were : Serum free t4 level. 10.2 pmo/L TSH level 7.28 IU/mL After a month of Levothyroxine my results are now:- serum free t4 level. 15.6 TSH 2.87 I asked for, and was told my T3 would be checked but I can’t see it on printout unless
Benjipuss
in
Thyroid UK
7 months ago
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