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Insomnia- solutions?
Many of you will know that I have been battling insomnia for quite a while. I went to a sleep clinic in August and discovered I also had sleep apnoea. I have been treated by the clinic since then with “ infallible” treatments. The problem is, I don’t think my sleep is getting any better and part of
Many of you will know that I have been battling insomnia for quite a while. I went to a sleep clinic in August and discovered I also had sleep apnoea. I have been treated by the clinic since then with “ infallible” treatments. The problem is, I don’t think my sleep is getting any better and part of
suzy1959
in
PMRGCAuk
1 year ago
had b12 results and called in to discuss
hello… I’ve just had my b12 levels done and they are >2000 (range 200-900) I started my supplement with oral b12 and decided to trial SI after much reading as very symptomatic and matched myself to possible b12d. I have been hypothyroid for app 32 years and am on Levothyroxine t4 and more recently
hello… I’ve just had my b12 levels done and they are >2000 (range 200-900) I started my supplement with oral b12 and decided to trial SI after much reading as very symptomatic and matched myself to possible b12d. I have been hypothyroid for app 32 years and am on Levothyroxine t4 and more recently
Delilahmy
in
Pernicious Anaemia Society
1 year ago
mountain air stone house problems?
I grew up on the coast of Maine, USA, so elevation 0 and wooden houses and salty sea air. I attended college inland in a small city elevation ~100m. But was only there for 4 years and lived half the time in a concrete apartment and the rest in a wooden house. Then I moved to Munich, Germany, elevation
I grew up on the coast of Maine, USA, so elevation 0 and wooden houses and salty sea air. I attended college inland in a small city elevation ~100m. But was only there for 4 years and lived half the time in a concrete apartment and the rest in a wooden house. Then I moved to Munich, Germany, elevation
stevedavid
in
Lung Conditions Community Forum
1 year ago
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It’s so noisy!
As l am a new cpap user can anybody possibly help me ,l have been trying to use the Fisher and Parker Eason nasal mask. The one I originally received was medium and much to large .l now have a small one,it fits ok and no air leaks but ,should l be able to hear myself breathe? The idea of this device
As l am a new cpap user can anybody possibly help me ,l have been trying to use the Fisher and Parker Eason nasal mask. The one I originally received was medium and much to large .l now have a small one,it fits ok and no air leaks but ,should l be able to hear myself breathe? The idea of this device
Limping-along
in
Sleep Matters
1 year ago
Asthma/copd and tracheobronchomalacia
been diagnosed with tracheobronchomalacia, I’m only mild at the moment but my breathlessness is already awful, I’m struggling to get out and about, I have cpap for at home but does anyone know of anything I can have/use when out and about. Thank you x
been diagnosed with tracheobronchomalacia, I’m only mild at the moment but my breathlessness is already awful, I’m struggling to get out and about, I have cpap for at home but does anyone know of anything I can have/use when out and about. Thank you x
Cooperhart
in
Lung Conditions Community Forum
1 year ago
Need Help in Sleeping After Meningitis
It’s been just over four months since my on set of bacterial meningitis. I have made a significant recovery in both my physical and my mental abilities. I am still doing therapy on both areas. The biggest problem I have right now is being able to sleep. My primary care physician sent me to a sleep specialist
It’s been just over four months since my on set of bacterial meningitis. I have made a significant recovery in both my physical and my mental abilities. I am still doing therapy on both areas. The biggest problem I have right now is being able to sleep. My primary care physician sent me to a sleep specialist
Wparrishjr
in
Mental Health Support
1 year ago
Any support greatly appreciated!
Hi, I'm new to this forum. My best friend has MSA-P. head drop syndrome and nocturnal stridor, Maggie just turned 70. She was diagnosed Aug 22 but we think had symptoms for 5 years. First diagnosed with Parkinson's then A-Typical Parkinism. At the moment she's in constant pain with her neck and head
Hi, I'm new to this forum. My best friend has MSA-P. head drop syndrome and nocturnal stridor, Maggie just turned 70. She was diagnosed Aug 22 but we think had symptoms for 5 years. First diagnosed with Parkinson's then A-Typical Parkinism. At the moment she's in constant pain with her neck and head
Whitefeather1
in
Multiple System Atrophy Trust
2 years ago
Why is my brother as he is
Had problems with breathing. Put on oxygen.Then CPAP mask. Was talking. Able to walk move everything as normal. Overnight placed on induced coma. Eventually brought out of it after a considerable time. Unable to talk or move. Can now speak albeit slurred and non understandable at times. Can move
Had problems with breathing. Put on oxygen.Then CPAP mask. Was talking. Able to walk move everything as normal. Overnight placed on induced coma. Eventually brought out of it after a considerable time. Unable to talk or move. Can now speak albeit slurred and non understandable at times. Can move
Twoblu
in
ICUsteps
2 years ago
what is people taking for asthma and mucus I have sleep apnoea but can not use CPAP machine when I have a cold
can anyone recommend something to clear mucus not montelukast as it interferes with my liver as.i don't have a gallbladder
can anyone recommend something to clear mucus not montelukast as it interferes with my liver as.i don't have a gallbladder
Myasthma1
in
Asthma Community Forum
2 years ago
Side Effects of Rivaroxaban?
In my early 40's I was prescribed Warfarin after DVT thrombosis in leg and two PE's circa 2004. Had what I would call accepted side effects, feeling cold, easily bruised had to change my diet slightly as grapefruit juice, cranberries, leafy greens were apparently not good whilst taking Warfarin. Around
In my early 40's I was prescribed Warfarin after DVT thrombosis in leg and two PE's circa 2004. Had what I would call accepted side effects, feeling cold, easily bruised had to change my diet slightly as grapefruit juice, cranberries, leafy greens were apparently not good whilst taking Warfarin. Around
Hidden
in
Anticoagulation Support
2 years ago
New here
hi just thought I would come in and say hi. I have had obstructive sleep apnea for years but diagnosed and managed for about six years, using cpap nightly to good effect. Unfortunately due to my diabetes and needing to wee more than usual my night is always broken. I am happy to help anyone on here
hi just thought I would come in and say hi. I have had obstructive sleep apnea for years but diagnosed and managed for about six years, using cpap nightly to good effect. Unfortunately due to my diabetes and needing to wee more than usual my night is always broken. I am happy to help anyone on here
Hidden
in
Sleep Matters
2 years ago
The issues!
I am new to this forum. I spend most of my time on the RLS forum, but I also have (treated) sleep apnea. I always tell people that I don't have insomnia. I could sleep just fine if I weren't walking around! Well-meaning people are always making suggestions to me regarding getting to sleep. If only
I am new to this forum. I spend most of my time on the RLS forum, but I also have (treated) sleep apnea. I always tell people that I don't have insomnia. I could sleep just fine if I weren't walking around! Well-meaning people are always making suggestions to me regarding getting to sleep. If only
ratfancy
in
Sleep Matters
2 years ago
Diet book for PMR - anyone know of it?
Has anyone tried this book? It was recommended by my local pharmacist, a young guy that did a his university thesis on PMR. ( He also does a lot of research into CPAP machines having suffered a heart attack at age 28. It was discovered he had severe sleep apneoa). He's helped me a lot with both. Title
Has anyone tried this book? It was recommended by my local pharmacist, a young guy that did a his university thesis on PMR. ( He also does a lot of research into CPAP machines having suffered a heart attack at age 28. It was discovered he had severe sleep apneoa). He's helped me a lot with both. Title
Hidden
in
PMRGCAuk
2 years ago
Sputum bugs and OSA/COPD
HiI have COPD, asthma, severe OSA, hypothyroid and a few other things. I am 62 and have had these challenges for a good few years now. Last year I had 2 sputum samples 6 months apart. 1st was staph aureus, 2nd was coliform species. Treated with 1 and 2 weeks of ciprofloxacin As soon as Cipro finishes
HiI have COPD, asthma, severe OSA, hypothyroid and a few other things. I am 62 and have had these challenges for a good few years now. Last year I had 2 sputum samples 6 months apart. 1st was staph aureus, 2nd was coliform species. Treated with 1 and 2 weeks of ciprofloxacin As soon as Cipro finishes
MollyMoo53
in
Lung Conditions Community Forum
2 years ago
Sleep Help Needed
Hello Friends, Following my transplant in 2017, I have developed a rather big challenge in getting a full night's sleep. Very rarely can I pull off 7 hours. Mostly the average is less than 5 hours per night. I have read how this is a common challenge for transplant recipients. I also use a CPAP
Hello Friends, Following my transplant in 2017, I have developed a rather big challenge in getting a full night's sleep. Very rarely can I pull off 7 hours. Mostly the average is less than 5 hours per night. I have read how this is a common challenge for transplant recipients. I also use a CPAP
Vaderboy
in
Kidney Transplant
2 years ago
Snow Queen
Tonight was the first real snow of the year. It has me thinking will this be the last first snow that I will not be on dialysis. I am trying not to think that way. It's just hard. But you know I'm going to put a bright spin on it. It's okay if this is the last first snow, I truly enjoyed watch every
Tonight was the first real snow of the year. It has me thinking will this be the last first snow that I will not be on dialysis. I am trying not to think that way. It's just hard. But you know I'm going to put a bright spin on it. It's okay if this is the last first snow, I truly enjoyed watch every
HipHopQueen
in
Kidney Dialysis
2 years ago
Copd medication
I have just been given Uniphyllin Continus by my study doctor (Copd study for new drug) but forgot to ask if I should continue to use my ventolin during the day, does anyone know
I have just been given Uniphyllin Continus by my study doctor (Copd study for new drug) but forgot to ask if I should continue to use my ventolin during the day, does anyone know
Oldhippylynn
in
Lung Conditions Community Forum
2 years ago
Weight Loss, in a positive way
Unlike a lot with PD, I have had major issues losing weight. Pre-PD I was at 190lbs and maxed out at 230lbs before I started making some major changes in my lifestyle. I am not on any prescription drugs and have been very lucky to control most of my issues with supplementation. In the past, exercise
Unlike a lot with PD, I have had major issues losing weight. Pre-PD I was at 190lbs and maxed out at 230lbs before I started making some major changes in my lifestyle. I am not on any prescription drugs and have been very lucky to control most of my issues with supplementation. In the past, exercise
SAGoodman
in
Cure Parkinson's
2 years ago
Cpap users with servere copd
Does anyone have experience of using a cpap machine to remove CO2 in someone who has servere COPD? My husband has just been told he must wear one at least every night as his oxygen levels are low and he is retaining CO2. He us trying it but finding it impossible to sleep and is not too keen to continue
Does anyone have experience of using a cpap machine to remove CO2 in someone who has servere COPD? My husband has just been told he must wear one at least every night as his oxygen levels are low and he is retaining CO2. He us trying it but finding it impossible to sleep and is not too keen to continue
Camposdemurcia
in
Lung Conditions Community Forum
2 years ago
The mother of all flares!
I have been having my worst flare ever in the 10 plus years of PMR. I have increased pred to 22.5 from 11 mgs and it is still not yet fully under control. I wish I had increased my dose more quickly but I had no idea it was this bad. I don't usually have blood tests for CRP but this week it was 43 and
I have been having my worst flare ever in the 10 plus years of PMR. I have increased pred to 22.5 from 11 mgs and it is still not yet fully under control. I wish I had increased my dose more quickly but I had no idea it was this bad. I don't usually have blood tests for CRP but this week it was 43 and
suzy1959
in
PMRGCAuk
2 years ago
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