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Trelegy and pneumonia?
In April this year, I was prescribed Trelegy after an exacerbation that resulted in respiratory failure. I have read that people who are on Trelegy are a lot more likely to get pneumonia but I had the vaccination a couple of years ago so I am a little confused. Does anyone know anything about this?
In April this year, I was prescribed Trelegy after an exacerbation that resulted in respiratory failure. I have read that people who are on Trelegy are a lot more likely to get pneumonia but I had the vaccination a couple of years ago so I am a little confused. Does anyone know anything about this?
Coughingalltheway
in
Lung Conditions Community Forum
3 months ago
Alcohol
My husband has AF but after two ablations things seem thankfully quite stable. The only problem is that since he is taking Dabigatran he is no longer able to enjoy alcohol - red wine tastes like vinegar and also causes gastric issues., as well as whiskey and beer. He is sorry he can no longer enjoy
My husband has AF but after two ablations things seem thankfully quite stable. The only problem is that since he is taking Dabigatran he is no longer able to enjoy alcohol - red wine tastes like vinegar and also causes gastric issues., as well as whiskey and beer. He is sorry he can no longer enjoy
tannin
in
Atrial Fibrillation Support
3 months ago
jaw pain
A few weeks ago I noticed that I couldn’t open my mouth as wide as I normally could without pain on the left side. Also, if I yawn and forget not to open it too wide I get a horrible pain and twisted feeling in my neck and throat. I went to the doctor’s surgery this week and saw a senior health practitioner
A few weeks ago I noticed that I couldn’t open my mouth as wide as I normally could without pain on the left side. Also, if I yawn and forget not to open it too wide I get a horrible pain and twisted feeling in my neck and throat. I went to the doctor’s surgery this week and saw a senior health practitioner
Gaycreasey
in
PMRGCAuk
3 months ago
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TB diagnosis
I have recently been diagnosed with TB after being very ill in hospital with Covid. My immune system was so low that latent TB led to active TB, I would be interested to know of anyone also suffering from TB and in particular related to Covid.
I have recently been diagnosed with TB after being very ill in hospital with Covid. My immune system was so low that latent TB led to active TB, I would be interested to know of anyone also suffering from TB and in particular related to Covid.
cheeseaddict
in
TB Alert
8 days ago
Dienogest
Hi all, My 17 year old daughter has just had her follow up post op appointment following a laparoscopy which she had last October. She has confirmed Endometriosis and all the surface (that they could see) Endo was removed. Unfortunately her pain has not improved and she says it's the same as before the
Hi all, My 17 year old daughter has just had her follow up post op appointment following a laparoscopy which she had last October. She has confirmed Endometriosis and all the surface (that they could see) Endo was removed. Unfortunately her pain has not improved and she says it's the same as before the
Welshpearl
in
Endometriosis UK
3 months ago
NHS London statement on Synnovis ransomware cyber attack
I am posting this using the NHS' own website version - it is covered across news sites as well. It seems it is having a major impact on blood tests - which might immediately affect some members. As well as the rest of the impact. [i]
NHS London statement on Synnovis ransomware cyber attack
[
I am posting this using the NHS' own website version - it is covered across news sites as well. It seems it is having a major impact on blood tests - which might immediately affect some members. As well as the rest of the impact. [i]
NHS London statement on Synnovis ransomware cyber attack
[
helvella
Thyroid UK
in
Thyroid UK
3 months ago
b 1 Therapy
Hello fellow readers. My name is Sakina. I am soo confused about the b1 therapy. I have been taking b1 sublingual 100 mg three times in a week under the tongue for quite a while l, but have noticed no difference. So now I am taking 100mgs of Thiamine Mononitrate. Which is better Thiamine Hydrochloride
Hello fellow readers. My name is Sakina. I am soo confused about the b1 therapy. I have been taking b1 sublingual 100 mg three times in a week under the tongue for quite a while l, but have noticed no difference. So now I am taking 100mgs of Thiamine Mononitrate. Which is better Thiamine Hydrochloride
Springbreak
in
Cure Parkinson's
4 months ago
Eye Supplement Concern
Eye doctor highly recommended taking supplement Preservision. I cleared with hematology re peginterferon but after buying it, researching ingredients and checking interactions am concerned. Twice a day ingredients: C = 250 mg, E = 90 mg, zinc= 40 mg, copper = 1 mg, Lutein = 5 mg. Except Lutein,
Eye doctor highly recommended taking supplement Preservision. I cleared with hematology re peginterferon but after buying it, researching ingredients and checking interactions am concerned. Twice a day ingredients: C = 250 mg, E = 90 mg, zinc= 40 mg, copper = 1 mg, Lutein = 5 mg. Except Lutein,
Mishie14
in
MPN Voice
4 months ago
exposure to chickenpox during ivf
Hi, I have been exposed to chicken pox a lot whilst taking my buserelin for my down regulation. I have a scan on Friday to check how my down regulation is going. I will inform them of the chicken pox but just wondered if people thought it would impact this cycle. Would I be considered having a weakened
Hi, I have been exposed to chicken pox a lot whilst taking my buserelin for my down regulation. I have a scan on Friday to check how my down regulation is going. I will inform them of the chicken pox but just wondered if people thought it would impact this cycle. Would I be considered having a weakened
IVFnewbie1
in
Fertility Network UK
4 months ago
Equivocal Dsdna
hi, I was diagnosed with SLE in 2022 and have had positive and negative antibody results since this time but my most recent test came back as equivocal which is a first for me. I’m on Benlysta monthly infusions which has massively dampened down my symptoms. Has anyone had this equivocal result and could
hi, I was diagnosed with SLE in 2022 and have had positive and negative antibody results since this time but my most recent test came back as equivocal which is a first for me. I’m on Benlysta monthly infusions which has massively dampened down my symptoms. Has anyone had this equivocal result and could
Mooncat111
in
LUPUS UK
4 months ago
Hand, Foot & Mouth
Be aware of the childhood desease HF&M. My 2 year old grand twins caught HF&M last year.Unfortunately I caught it from them & it was a nightmare. Because of the thickness of my skin due to SS, the spots & sores could not break out on the surface of my skin. They errupted below the skin on my hands
Be aware of the childhood desease HF&M. My 2 year old grand twins caught HF&M last year.Unfortunately I caught it from them & it was a nightmare. Because of the thickness of my skin due to SS, the spots & sores could not break out on the surface of my skin. They errupted below the skin on my hands
Ildivolover
in
Scleroderma & Raynaud's UK (SRUK)
4 months ago
Sjorgren syndrome
Following months of repeated eye infections, I have now been diagnosed with dry eyes, and drops certainly seem to be helping. However I came across an article on Sjorgren syndrome,. The list of symptoms include dry mouth, IBS, dry eyes, dry skin, joint problems, all of which I suffer from. I also get
Following months of repeated eye infections, I have now been diagnosed with dry eyes, and drops certainly seem to be helping. However I came across an article on Sjorgren syndrome,. The list of symptoms include dry mouth, IBS, dry eyes, dry skin, joint problems, all of which I suffer from. I also get
Pippapot
in
MPN Voice
4 months ago
RA got worse after pneumonia
After pneumonia my ra took a turn for the worse. Could a medicine change help
After pneumonia my ra took a turn for the worse. Could a medicine change help
Vonnie69
in
NRAS
4 months ago
Help with steroid induced hyperglycaemia
My story is in my bio as it’s rather long! Is there anyone out there managing Steroid Induced Hyperglycaemia? As I started on 70mg and had to stay on it for 6 weeks after diagnosis, I quickly developed SIH and have found it a daily battle to control it despite being on a very low Carb diet indeed! Diabetic
My story is in my bio as it’s rather long! Is there anyone out there managing Steroid Induced Hyperglycaemia? As I started on 70mg and had to stay on it for 6 weeks after diagnosis, I quickly developed SIH and have found it a daily battle to control it despite being on a very low Carb diet indeed! Diabetic
AmberGamble
in
PMRGCAuk
4 months ago
Azithromycin
Discharged recently from hospital after a long period of exacerbations and then pneumonia. After weeks of oral antibiotics and steroids had to have IV antibiotics. Next time I will probably have to begin IV immediately on flare up. I take 250 mg Azithromycin 3 times a week and was wondering does any
Discharged recently from hospital after a long period of exacerbations and then pneumonia. After weeks of oral antibiotics and steroids had to have IV antibiotics. Next time I will probably have to begin IV immediately on flare up. I take 250 mg Azithromycin 3 times a week and was wondering does any
kenta
in
Lung Conditions Community Forum
4 months ago
ToeNail fungus treatment and Methotrexate
I’ve recently been recommended Curanail by my footcare practitioner for a toe nail fungus condition. I wondered if any one has used this while taking weekly methotrexate, and sometimes Naproxen.My blood test results are all fine and RA is well controlled atm. Looking at the instructions it can take
I’ve recently been recommended Curanail by my footcare practitioner for a toe nail fungus condition. I wondered if any one has used this while taking weekly methotrexate, and sometimes Naproxen.My blood test results are all fine and RA is well controlled atm. Looking at the instructions it can take
L-ttie
in
NRAS
4 months ago
Night Terrors
Good morning everyone, I last posted about my night terrors , so I visited my doctor who changed the 30mg lansoprazole I was taking to 20 Esomeprazole but unfortunately still getting the disturbing night terrors feel so upset this morning the nightmare was so bad last night I was too scared to go
Good morning everyone, I last posted about my night terrors , so I visited my doctor who changed the 30mg lansoprazole I was taking to 20 Esomeprazole but unfortunately still getting the disturbing night terrors feel so upset this morning the nightmare was so bad last night I was too scared to go
lmpieroni
in
Scleroderma & Raynaud's UK (SRUK)
4 months ago
Sepsis - a timely reminder
[i]“The paramedics were reluctant to take me in,” he said. “They thought I should go and see my GP. I could have gone back to sleep. And I would have died I suppose. After a bit of remonstration they agreed [to take me]. No doubt at all Kati saved my life. If we had got there two hours later I would
[i]“The paramedics were reluctant to take me in,” he said. “They thought I should go and see my GP. I could have gone back to sleep. And I would have died I suppose. After a bit of remonstration they agreed [to take me]. No doubt at all Kati saved my life. If we had got there two hours later I would
bennevisplace
in
CLL Support
4 months ago
Thyroid Dysfunction and PD
So I thought I'd cross-search some of my health challenges and whadyaknow: https://academic.oup.com/cei/article/208/3/372/6578682. Shut your mush and take your Ldopa, though I'm non-responsive. Doc, I'm photophobic, can't open my eyes in the morning ALO, blepharospasm...Read it's predictive years before
So I thought I'd cross-search some of my health challenges and whadyaknow: https://academic.oup.com/cei/article/208/3/372/6578682. Shut your mush and take your Ldopa, though I'm non-responsive. Doc, I'm photophobic, can't open my eyes in the morning ALO, blepharospasm...Read it's predictive years before
Dabaa
in
Cure Parkinson's
4 months ago
Keeping Pegasys injections cool and monitoring temp
Hi, I have recently been diagnosed with Erdheim-Chester Disease after being treated for many years for an MPN, (ET) I have started on Pegasys Interferon and will be travelling by plane soon (yay) and am looking for advice to keep the injections cool. Does anyone use a fridge (or similar) thermometer
Hi, I have recently been diagnosed with Erdheim-Chester Disease after being treated for many years for an MPN, (ET) I have started on Pegasys Interferon and will be travelling by plane soon (yay) and am looking for advice to keep the injections cool. Does anyone use a fridge (or similar) thermometer
LeoTravels
in
MPN Voice
4 months ago
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