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Lip biopsy results
Hi. I had a lip biopsy 3 weeks ago. Rheumatologist feels I've sjogrens but I'm serum neg. I have had dry eyes +mouth, mouth ulcers, sore swollen glands under my jaw, sore ears,sore joints in hands and feet and ankles and wrists,weakness in lower legs and arms , awful fatigue and restless legs. I have
Hi. I had a lip biopsy 3 weeks ago. Rheumatologist feels I've sjogrens but I'm serum neg. I have had dry eyes +mouth, mouth ulcers, sore swollen glands under my jaw, sore ears,sore joints in hands and feet and ankles and wrists,weakness in lower legs and arms , awful fatigue and restless legs. I have
Nellies47
in
The Australian Sjögren's Syndrome Association
3 years ago
Remedy for dry cough
I have dry cough over a month I have had X-rays check ups blood tests etc Need to find a cure for this irritating dry cough which comes at nite 😞 Any suggestions will help I have tired over the counter meds nothing helps Thanks in advance
I have dry cough over a month I have had X-rays check ups blood tests etc Need to find a cure for this irritating dry cough which comes at nite 😞 Any suggestions will help I have tired over the counter meds nothing helps Thanks in advance
Mystik
in
LUPUS UK
3 years ago
Shivering 4 days post ablation
Well it’s day 4, don’t know if this is normal, I can’t stop feeling cold and shivery, I feel cold anyway because of blood thinners but my body is sensitive and I feel so cold. Had a slight irregular HB this morning so trying hard not to be disappointed yet. Does colchicine make you cold by any chance
Well it’s day 4, don’t know if this is normal, I can’t stop feeling cold and shivery, I feel cold anyway because of blood thinners but my body is sensitive and I feel so cold. Had a slight irregular HB this morning so trying hard not to be disappointed yet. Does colchicine make you cold by any chance
Electricblue1
in
Atrial Fibrillation Support
3 years ago
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Off of sedation drugs for 1 week. Eyes r open and my friend is looking all around and up at the ceiling, that is all 😢
Does anyone know how long it takes before there starts to be a change where the brain begins to signal to the lungs to breathe on their own? My friend is still on the ventilator and Covid and pneumonia are gone but he’s not back with us yet. I’m assuming this is still from all the sedation drugs?
Does anyone know how long it takes before there starts to be a change where the brain begins to signal to the lungs to breathe on their own? My friend is still on the ventilator and Covid and pneumonia are gone but he’s not back with us yet. I’m assuming this is still from all the sedation drugs?
LCharles
in
ICUsteps
3 years ago
what is Ovarian hyperstimulation syndrome (OHSS)
Hi everyone! I had my First IVF app today! we start our fertility meds on 18th jan!! can't wait. Long story short.. I got told I have Ovarian hyper-stimulation syndrome (OHSS) has anyone ever suffered with this? the consultant said a normal percentage is 19.8 but mines 178. iv read up on google (I know
Hi everyone! I had my First IVF app today! we start our fertility meds on 18th jan!! can't wait. Long story short.. I got told I have Ovarian hyper-stimulation syndrome (OHSS) has anyone ever suffered with this? the consultant said a normal percentage is 19.8 but mines 178. iv read up on google (I know
TTC1994
in
Fertility Network UK
3 years ago
ADAA released a podcast! "What is Trauma?" with Paul Greene
Do you have any questions about trauma or PTSD? ADAA had the opportunity to sit down with ADAA Member Paul Greene, PhD, to discuss the many aspects of trauma: what it is, how it’s different from PTSD and stress, and how to get help if suffering from a traumatic experience. So give this podcast a listen
Do you have any questions about trauma or PTSD? ADAA had the opportunity to sit down with ADAA Member Paul Greene, PhD, to discuss the many aspects of trauma: what it is, how it’s different from PTSD and stress, and how to get help if suffering from a traumatic experience. So give this podcast a listen
ADAATeamRachel
Administrator
in
Anxiety and Depression Support
3 years ago
Omg Prednisolone
I was diagnosed with PMR approx 18 months and for the last 6 weeks have been on 0mg Pred after following a very slow tapering plan ( advice given on this forum). I had a couple of set backs and had to increase the dose and start tapering again . I was very keen to get off the Pred but soon realised
I was diagnosed with PMR approx 18 months and for the last 6 weeks have been on 0mg Pred after following a very slow tapering plan ( advice given on this forum). I had a couple of set backs and had to increase the dose and start tapering again . I was very keen to get off the Pred but soon realised
Liby57
in
PMRGCAuk
3 years ago
Pressure from doctors to for feeding tube or trachea
My friend is still on a ventilator. The doctor is saying no more Covid, no more pneumonia. His parents are being told he has Covid brain. His eyes r open but brain won’t signal lungs to breathe? Doc says get a permanent feeding tube? It’s only been 6 days since sedation drugs left.
My friend is still on a ventilator. The doctor is saying no more Covid, no more pneumonia. His parents are being told he has Covid brain. His eyes r open but brain won’t signal lungs to breathe? Doc says get a permanent feeding tube? It’s only been 6 days since sedation drugs left.
LCharles
in
ICUsteps
3 years ago
Covid and a wet cough
Hello, I tested positive for covid today I have asthma and I’ve developed a wet cough and white phlegm , I’m constantly needed to clear my throat too. Has anyone had a wet cough with covid at the start? Thank you in advance!
Hello, I tested positive for covid today I have asthma and I’ve developed a wet cough and white phlegm , I’m constantly needed to clear my throat too. Has anyone had a wet cough with covid at the start? Thank you in advance!
Milo1996
in
Asthma Community Forum
3 years ago
No support from GP - need to change meds
Hi everyone and Merry Christmas! This is my first post to the forum and I'm sorry it's quite a long one. I'm hoping that someone can advise me about a change of medication. I've had RLS since a teenager (now in my 50s). I augmented on Pramipexole about 5 years ago and went through hell to stop. I tried
Hi everyone and Merry Christmas! This is my first post to the forum and I'm sorry it's quite a long one. I'm hoping that someone can advise me about a change of medication. I've had RLS since a teenager (now in my 50s). I augmented on Pramipexole about 5 years ago and went through hell to stop. I tried
Night_raven
in
Restless Legs Syndrome
3 years ago
What is Covid brain? My friend has suffered from Covid pneumonia and been off sedation drugs for 4 full days, he’s not awake yet?
They want him to start trying to use his lungs and have his brain connect to that! But they say he has Covid brain?
They want him to start trying to use his lungs and have his brain connect to that! But they say he has Covid brain?
LCharles
in
ICUsteps
3 years ago
Just too much sometimes
Hi, I'm just wondering if anyone else gets totally overwhelmed with Fibro? The last couple of years have sent my fibromyalgia off the scale with symptoms and its becoming very overwhelming. I have worked right through this pandemic in a job thats stressful at the best if times but the last couple of
Hi, I'm just wondering if anyone else gets totally overwhelmed with Fibro? The last couple of years have sent my fibromyalgia off the scale with symptoms and its becoming very overwhelming. I have worked right through this pandemic in a job thats stressful at the best if times but the last couple of
Elle247
in
Fibromyalgia Action UK
3 years ago
Friend just came off sedation drugs after having Covid pneumonia.
They’re doing EEG tomorrow to see if his brain will tell his lungs to breathe? So far everything else has been okay. Just concerning about his EGG
They’re doing EEG tomorrow to see if his brain will tell his lungs to breathe? So far everything else has been okay. Just concerning about his EGG
LCharles
in
ICUsteps
3 years ago
Increasing Prednisone when you have the flu or Covid
I read 6 months ago somewhere that if we have pmr and are taking prednisone and then get the flu that we should increase the dosage substantially for a few days till our flu symptoms improve. What happens to us and what should we do if we get Covid as well. I have had pmr since may and started on 40
I read 6 months ago somewhere that if we have pmr and are taking prednisone and then get the flu that we should increase the dosage substantially for a few days till our flu symptoms improve. What happens to us and what should we do if we get Covid as well. I have had pmr since may and started on 40
Skier321
in
PMRGCAuk
3 years ago
I think I know what a Pin Cushion feels like🤨
Dear All, not only have I now had Three Covid Jabs with, in all probability, a Booster to come but also 'Flu' and Pneumonia too. Not that I'm really complaining- especially if it keeps me 'Well'😊 However today I had another TEN Blood Samples taken, for Both of my Consultants plus my GP, this only involved
Dear All, not only have I now had Three Covid Jabs with, in all probability, a Booster to come but also 'Flu' and Pneumonia too. Not that I'm really complaining- especially if it keeps me 'Well'😊 However today I had another TEN Blood Samples taken, for Both of my Consultants plus my GP, this only involved
AndrewT
in
Vasculitis UK
3 years ago
Year long cough
Year-long cough I had PMR symptoms a year ago December. At that time I started a cough. I would cough once a day and then may be a week later a couple times a day and it progressed from there until now I am now coughing a lot of times during the day. I am not coughing up anything I have no tickle in
Year-long cough I had PMR symptoms a year ago December. At that time I started a cough. I would cough once a day and then may be a week later a couple times a day and it progressed from there until now I am now coughing a lot of times during the day. I am not coughing up anything I have no tickle in
Bajg
in
PMRGCAuk
3 years ago
Erosion of a historically good marriage due to my FND
After a year’s onset of various symptoms, I was diagnosed with FND July 2021. Thanks be to God that I live near a world renown hospital and have a cutting-edge neurologist who is a movement specialist My husband is not responding well to this. He refuses to read any of the literature and doctor notes
After a year’s onset of various symptoms, I was diagnosed with FND July 2021. Thanks be to God that I live near a world renown hospital and have a cutting-edge neurologist who is a movement specialist My husband is not responding well to this. He refuses to read any of the literature and doctor notes
HenriettaPoultryfoot
in
Functional Neurological Disorder - FND Hope
3 years ago
Woo Hoo
Just finished my first non stop 20 minute run since mid December. It's been a slow build up after a cold and chesty cough. Hard work but worth the effort!!
Just finished my first non stop 20 minute run since mid December. It's been a slow build up after a cold and chesty cough. Hard work but worth the effort!!
69upandrunning
Graduate
in
Couch to 5K
3 years ago
Went to ER for asthma exacerbation, tested positive for Omicron and some pneumonia on X-ray
Not the way I thought my Thursday was going to go. I’d already had a negative COVID test 2 days before. Now I have COVID, asthma exacerbation and pneumonia. They sent me home after IV steroids, IV magnesium and a RX for antibiotics. Not a lot of details about what to do or expect. I am vaccinated and
Not the way I thought my Thursday was going to go. I’d already had a negative COVID test 2 days before. Now I have COVID, asthma exacerbation and pneumonia. They sent me home after IV steroids, IV magnesium and a RX for antibiotics. Not a lot of details about what to do or expect. I am vaccinated and
Shadowcat04
in
Asthma Community Forum
3 years ago
Support group in the US?
Hello Everyone! Is there a support group for the US? I’ve been diagnosed with hyper mobility spectrum disorder and in July I see a geneticist for EDS testing. Thank you!
Hello Everyone! Is there a support group for the US? I’ve been diagnosed with hyper mobility spectrum disorder and in July I see a geneticist for EDS testing. Thank you!
TurquoiseTime
in
Ehlers-Danlos Support UK
3 years ago
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