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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
1 month 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
7 months ago
Dry coughs
Hi everyone, I have had a persistent dry cough for about the last eight months. It has being given different diagnosis and put on treatments that haven't helped yet. This cough comes like a tickling sensation at the sides of my throat then I cough for about 2-3 minutes, drinking water doesn't stop
Hi everyone, I have had a persistent dry cough for about the last eight months. It has being given different diagnosis and put on treatments that haven't helped yet. This cough comes like a tickling sensation at the sides of my throat then I cough for about 2-3 minutes, drinking water doesn't stop
IlvJesus
in
Lung Conditions Community Forum
2 months ago
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Pegasys is applying for formal approval in MPN treatment
Dear friends, I came across a EMA document recently and found that Pegasys is applying for indication extension to PV and ET. It provides, on page 53: “Grouped application consisting of: Extension of indication to include treatment of Polycythaemia Vera (PV) and Essential thrombocytopenia (ET) for
Dear friends, I came across a EMA document recently and found that Pegasys is applying for indication extension to PV and ET. It provides, on page 53: “Grouped application consisting of: Extension of indication to include treatment of Polycythaemia Vera (PV) and Essential thrombocytopenia (ET) for
TimothyHLuff
in
MPN Voice
9 months ago
Wife getting MMR vaccine booster - isolate or not?
I'm an SLL patient, 55 years old, now about 2.5 years into remission after 6 FCR treatments. I just recovered from a recent (and thankfully mild) bout of shingles. My shingles was so mild that my GP wasn't convinced it actually was shingles! She had me tested for herpes zoster antibodies, and for good
I'm an SLL patient, 55 years old, now about 2.5 years into remission after 6 FCR treatments. I just recovered from a recent (and thankfully mild) bout of shingles. My shingles was so mild that my GP wasn't convinced it actually was shingles! She had me tested for herpes zoster antibodies, and for good
xpro3
in
CLL Support
6 months ago
Inhaler post pneumonia, awaiting lung scarring diagnosis?
Hi first time posting - hoping someone can help! I’m basically after some advice in knowing when to ask for an inhaler. 40 y old female fit and healthy until last September when I got severe pneumonia. One lung was a white out with atelectasis (bits inside the lung dying; they’re still dead) and the
Hi first time posting - hoping someone can help! I’m basically after some advice in knowing when to ask for an inhaler. 40 y old female fit and healthy until last September when I got severe pneumonia. One lung was a white out with atelectasis (bits inside the lung dying; they’re still dead) and the
SirCoughalot
in
Lung Conditions Community Forum
6 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
7 months ago
Tuesday's Tips
[i]
Two of the common conditions associated with PBC are thyroid conditions and with those that cause anemia. This is because they both have shared genetic factors that affect our immune response.
[/i] [i]
An underactive thyroid is caused by an autoimmune response to the gland itself.
[
[i]
Two of the common conditions associated with PBC are thyroid conditions and with those that cause anemia. This is because they both have shared genetic factors that affect our immune response.
[/i] [i]
An underactive thyroid is caused by an autoimmune response to the gland itself.
[
DonnaBoll
Administrator
in
PBC Foundation
2 months ago
Mumps contact 😷
Hi Peeps 🙂 I hope this post finds you as well as can be 🫠 I am writing to ask about contact with mumps. I have RA and my main meds are Tocilizumab (injection), Methotrexate (injection) and Sulphasalazine. Do I have to be particularly careful that I do not come in contact with a child who possibly has
Hi Peeps 🙂 I hope this post finds you as well as can be 🫠 I am writing to ask about contact with mumps. I have RA and my main meds are Tocilizumab (injection), Methotrexate (injection) and Sulphasalazine. Do I have to be particularly careful that I do not come in contact with a child who possibly has
Moomin8
in
NRAS
9 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
7 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
7 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
7 months ago
pneumonia jab
hi , I’ve booked to have a jab privately as I wasn’t having any luck requesting it from the gp. Is this definitely safe for me to have with liver disease. Thanks
hi , I’ve booked to have a jab privately as I wasn’t having any luck requesting it from the gp. Is this definitely safe for me to have with liver disease. Thanks
Etymolog
in
British Liver Trust
9 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
7 months ago
Tuberculosis
I have been talking medication for lymph node tb for 4 months now, however i have been developing fever and night sweats for the past few day. Is it common to have fever and nights sweats 4 months into the treatment? My lymph node is secreting pus and is very itchy.
I have been talking medication for lymph node tb for 4 months now, however i have been developing fever and night sweats for the past few day. Is it common to have fever and nights sweats 4 months into the treatment? My lymph node is secreting pus and is very itchy.
Premika
in
TB Alert
9 months ago
touched a nerve
Hi you wonderful people. I’m overwhelmed by your responses and support resulting from my recent post concerning doctors refusal to prescribe Buprenorphine and it’s moved me m ok re than I can say but I think it’s time to close it down now, I didn’t realise I had poked a hornets 🐝 nest and but realise
Hi you wonderful people. I’m overwhelmed by your responses and support resulting from my recent post concerning doctors refusal to prescribe Buprenorphine and it’s moved me m ok re than I can say but I think it’s time to close it down now, I didn’t realise I had poked a hornets 🐝 nest and but realise
HipHop1972
in
Restless Legs Syndrome
6 months ago
COVID-19
Been battling Covid for 17 days. I am negative but have a lot of physical issues achy big time. Always exhausted. No motivation. Starting to take a toll on me mentally. Doctor says that sometimes it takes weeks or months to get rid of everything. I hate feeling like this
Been battling Covid for 17 days. I am negative but have a lot of physical issues achy big time. Always exhausted. No motivation. Starting to take a toll on me mentally. Doctor says that sometimes it takes weeks or months to get rid of everything. I hate feeling like this
Trainchaser
in
Anxiety and Depression Support
7 months ago
COVID & sulfasalazine?
After all these years hubby has passed COVID to me! Contacted GP, they have referred me to respiratory@home still waiting for them to call. Question is do I keep taking sulfasalazine.? I've called my Rheumy helpline but they've not got back to me and I've looked on here but can't find anything saying
After all these years hubby has passed COVID to me! Contacted GP, they have referred me to respiratory@home still waiting for them to call. Question is do I keep taking sulfasalazine.? I've called my Rheumy helpline but they've not got back to me and I've looked on here but can't find anything saying
Haz58
in
NRAS
7 months ago
COPD and Long Covid
Hi all, I've been ill for over three years with Long Covid and just last week diagnosed with COPD stage 2. Looking through my medical history COPD was mentioned back in 2005, but I was told it was Asthma! Just joined my local Breathe Easy group who are great and very supportive.
Hi all, I've been ill for over three years with Long Covid and just last week diagnosed with COPD stage 2. Looking through my medical history COPD was mentioned back in 2005, but I was told it was Asthma! Just joined my local Breathe Easy group who are great and very supportive.
SimonJJJ
in
Lung Conditions Community Forum
7 months ago
Covid - Reflux
Just out of interest has anyone's reflux problems come on after having Covid? I had it back in early December and got problems in middle of January. I have read somewhere that there could be a link .
Just out of interest has anyone's reflux problems come on after having Covid? I had it back in early December and got problems in middle of January. I have read somewhere that there could be a link .
Pinkcatfairy
in
Acid Reflux Support
7 months ago
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