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Exercise and PMR
I am posting an update and a question. Since discovering I have PMR in Sept 2023 and starting on Pred at 15 mg, I have had a slightly bumpy start to my PMR journey. Was getting used to being on Pred when I had a visit from the Covid fairy which took a couple of weeks to clear, but I still feel I have
I am posting an update and a question. Since discovering I have PMR in Sept 2023 and starting on Pred at 15 mg, I have had a slightly bumpy start to my PMR journey. Was getting used to being on Pred when I had a visit from the Covid fairy which took a couple of weeks to clear, but I still feel I have
Indigo2417
in
PMRGCAuk
7 months ago
Cough After Eating
This is the most recent episode of my mum’s PSP, she barely chokes, now we are dealing with after a meal cough, she coughs few mins after having her meals(different meals). I got her a cough syrup that helps after a while. Has this happened to anyone or experienced this, any solution? Her next appointment
This is the most recent episode of my mum’s PSP, she barely chokes, now we are dealing with after a meal cough, she coughs few mins after having her meals(different meals). I got her a cough syrup that helps after a while. Has this happened to anyone or experienced this, any solution? Her next appointment
Candor8
in
PSP Association
18 days ago
High Peak Flow but Wheezing and Phlegm x 4+ Months and Intense Fatigue
High Peak Flow but Wheezing and Phlegm x 4+ Months and Intense Fatigue I usually only get asthma as a secondary condition - with hayfever or a chest cold, etc. Since the first week of January, I've had constant fluid on the lungs - now a yellowy brown, which I cough up - but wouldn't say I have a
High Peak Flow but Wheezing and Phlegm x 4+ Months and Intense Fatigue I usually only get asthma as a secondary condition - with hayfever or a chest cold, etc. Since the first week of January, I've had constant fluid on the lungs - now a yellowy brown, which I cough up - but wouldn't say I have a
mmprospers
in
Asthma Community Forum
21 days ago
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Colds and flu…🧐🥹?
”Why don’t lupus patients catch cold? Many, many patients comment on this observation – that during cold and flu epidemics they seem to be the only family member not affected…?”
Professor Graham Hughes, [the London Lupus Centre] 2008
Just wondering about this observation but I personally have
”Why don’t lupus patients catch cold? Many, many patients comment on this observation – that during cold and flu epidemics they seem to be the only family member not affected…?”
Professor Graham Hughes, [the London Lupus Centre] 2008
Just wondering about this observation but I personally have
Suvi8901
in
LUPUS UK
6 months ago
Prescribed Naproxine 250 twice a day for hip bursitis is that dangerous with Pred
I was prescribed Naproxine 250 twice a day yesterday for bursitis ? on right hip. Pain is so bad dr. gave a steroid injection. Suggested I take up to 4g of Paracetamol if necessary. Just read of NHS site that Naproxine and Pred are not compatible. Is this true for short time use? If so what
I was prescribed Naproxine 250 twice a day yesterday for bursitis ? on right hip. Pain is so bad dr. gave a steroid injection. Suggested I take up to 4g of Paracetamol if necessary. Just read of NHS site that Naproxine and Pred are not compatible. Is this true for short time use? If so what
Motida
in
PMRGCAuk
7 months ago
obrilant bronchiolitis
hello all...my son was diagnosed he have obrilant bronchiolitis...he is in early position....only hard breathing when he runs around but without any oxygen...what can i expect from this?how long he can live with his own lungs?how fast this dissease progresive?
hello all...my son was diagnosed he have obrilant bronchiolitis...he is in early position....only hard breathing when he runs around but without any oxygen...what can i expect from this?how long he can live with his own lungs?how fast this dissease progresive?
care20
in
Lung Conditions Community Forum
24 days ago
QoL-Lick the spoon
This is an IF, WHEN and NOW thought process. I know many of you have already been through this stage because of your cancer but a few people ( new members and a few regulars) haven’t embraced these ideas. How many of you have probably said to yourself IF this treatment works we’re going to go on a
This is an IF, WHEN and NOW thought process. I know many of you have already been through this stage because of your cancer but a few people ( new members and a few regulars) haven’t embraced these ideas. How many of you have probably said to yourself IF this treatment works we’re going to go on a
MouseAddams
in
Advanced Prostate Cancer
7 months ago
Fatigue..again...Moderna jab?
Hello everyone. Reduced to 2.75, working slowly towards 2.5. Back from lovely break in Ireland tracing my roots. Had Moderna jab, aching arm and headache, then, coincidentally, full flu, nose like a tap, cough etc. Altho some neighbours had flu and not the jab. Cold symptoms finally going after 2 weeks
Hello everyone. Reduced to 2.75, working slowly towards 2.5. Back from lovely break in Ireland tracing my roots. Had Moderna jab, aching arm and headache, then, coincidentally, full flu, nose like a tap, cough etc. Altho some neighbours had flu and not the jab. Cold symptoms finally going after 2 weeks
Temoral
in
PMRGCAuk
24 days ago
Small Airways Disease
I had an infection the end of Jan (still not sure what it was - maybe RSV). Didn’t really start like a cold but airways closed up & excessive mucus. Mucus tested & nothing so no antibiotics. Things slowly got worse, although I was continuing to exercise to clear my chest of mucus (my primary issues is
I had an infection the end of Jan (still not sure what it was - maybe RSV). Didn’t really start like a cold but airways closed up & excessive mucus. Mucus tested & nothing so no antibiotics. Things slowly got worse, although I was continuing to exercise to clear my chest of mucus (my primary issues is
PW_R
in
Lung Conditions Community Forum
24 days ago
Covid & dosing
Hi, I tested +ve for covid this morning. It's the first time I've had it. I've had 5 vacs. My temperature is high & I'm taking paracetamol for that.My question is, should I alter my T4/NDT dose? I haven't been ill at all since I started on thyroid meds in 2015. I wondered if I should increase, decrease
Hi, I tested +ve for covid this morning. It's the first time I've had it. I've had 5 vacs. My temperature is high & I'm taking paracetamol for that.My question is, should I alter my T4/NDT dose? I haven't been ill at all since I started on thyroid meds in 2015. I wondered if I should increase, decrease
amala57
in
Thyroid UK
7 months ago
Have COVID - should I get Paxlovid/
I have CLL and in W&W and also have ET. I am 67 yrs old, fully vaccinated and otherwise in good health Tested positive yesterday for COVID. Day three of my symptoms are uncomfortable but bearable. Should I get Paxlovid?
I have CLL and in W&W and also have ET. I am 67 yrs old, fully vaccinated and otherwise in good health Tested positive yesterday for COVID. Day three of my symptoms are uncomfortable but bearable. Should I get Paxlovid?
Lambo1
in
CLL Support
7 months ago
Always cold.
Hi suffer from OB since 14 have stayed stable for couple years but just wondered if its normal to be so cold all the time and my skin is so transparent and pale always has a blueish tint to it .
Hi suffer from OB since 14 have stayed stable for couple years but just wondered if its normal to be so cold all the time and my skin is so transparent and pale always has a blueish tint to it .
Cornflake123
in
Lung Conditions Community Forum
26 days ago
Cough
So, since having a virus causing a sinus cold at the start of Easter holidays, I have had a flare up which has gradually gotten worse since. I think, symptoms-wise I might have stabilized. Anyhow, I have realized that since about halfway through April I started with a light cough and it has increased
So, since having a virus causing a sinus cold at the start of Easter holidays, I have had a flare up which has gradually gotten worse since. I think, symptoms-wise I might have stabilized. Anyhow, I have realized that since about halfway through April I started with a light cough and it has increased
Obsdian
in
Thyroid UK
28 days ago
Mirena Coil Side Effects
hi everyone, I am desperate for some advice/help. I had the mirena coil fitted 6 months ago. 10 days after the coil was fitted I contacted my GP complaining of severe shoulder pain. I am still in agony most days, and nights are the worst. I am getting by on anywhere between 0-3 hours sleep due to being
hi everyone, I am desperate for some advice/help. I had the mirena coil fitted 6 months ago. 10 days after the coil was fitted I contacted my GP complaining of severe shoulder pain. I am still in agony most days, and nights are the worst. I am getting by on anywhere between 0-3 hours sleep due to being
Emily1107
in
Women's Health
7 months ago
Is this Scabies?
Please tell me if this looks like scabies? This is right under the armpit. I have tried to crop and focus on the problem area but can share another version of this photo if it is not clear. I am morbidly obese so a lot of skin stretching is happening.
Please tell me if this looks like scabies? This is right under the armpit. I have tried to crop and focus on the problem area but can share another version of this photo if it is not clear. I am morbidly obese so a lot of skin stretching is happening.
TryingItOn
in
MY SKIN
29 days ago
Cough, chest pressure, GCA
I am being treated for GCA, but had a negative biopsy. I am now taking 40 mg of prednisone and will drop to 35 mg tomorrow. My first rheumatology appointment is May 16. I am in no pain but I am very fatigued and I continue to cough, especially when I speak, and have chest heaviness. My primary care
I am being treated for GCA, but had a negative biopsy. I am now taking 40 mg of prednisone and will drop to 35 mg tomorrow. My first rheumatology appointment is May 16. I am in no pain but I am very fatigued and I continue to cough, especially when I speak, and have chest heaviness. My primary care
Moaningxcat
in
PMRGCAuk
1 month ago
Second Treatment -Feeling scared
My husband has CLL and finished FCR in April 2019. Due to low platelets, enlarged spleen and ALC doubling he needs to start his next treatment even though he feels wellV&R is the treatment starting on 15th May. I have researched extensively including within this group, and am aware of the treatment
My husband has CLL and finished FCR in April 2019. Due to low platelets, enlarged spleen and ALC doubling he needs to start his next treatment even though he feels wellV&R is the treatment starting on 15th May. I have researched extensively including within this group, and am aware of the treatment
Sanders9
in
CLL Support
1 month ago
Methotrexate and a head cold
Hi, I have been on methotrexate for 9 weeks and am starting with a head cold.Do I need to inform anyone? It's the first "illness" since starting methotrexate.
Hi, I have been on methotrexate for 9 weeks and am starting with a head cold.Do I need to inform anyone? It's the first "illness" since starting methotrexate.
pattypatchwork
in
LUPUS UK
1 month ago
Natural cycle FET likely to be cancelled due to ovulation on small follicle. What does this mean about my eggs/ ovaries? Having a wobble
Oh it's been a trial. Last month my cycle was cancelled due to COVID and this month, my bloods show I'm due to ovulate but follicle is only 12mm. I have been quite ill with Covid and pretty stressed getting ready to start a new job but was so hopeful to get this transfer done before Christmas but my
Oh it's been a trial. Last month my cycle was cancelled due to COVID and this month, my bloods show I'm due to ovulate but follicle is only 12mm. I have been quite ill with Covid and pretty stressed getting ready to start a new job but was so hopeful to get this transfer done before Christmas but my
Minniemouse88
in
Fertility Network UK
7 months ago
Taking Prolia with Rusolitinib (Jakafi)
I have been taking Jakafi (15 mg) twice a day for the last 3 years for my polycythemia vera. I also take blood thinners for my thrombocytosis since I have had blood clots in my lungs twice in the last 2 years. I have had osteoporosis for a while, but my T scores from bone density test are really
I have been taking Jakafi (15 mg) twice a day for the last 3 years for my polycythemia vera. I also take blood thinners for my thrombocytosis since I have had blood clots in my lungs twice in the last 2 years. I have had osteoporosis for a while, but my T scores from bone density test are really
Buggerbear
in
MPN Voice
1 month ago
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