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Pelvic floor pain
Hello again ladies! I am 10 weeks post rectocele repair and started seeing a pelvic floor physiotherapist ( https://www.physiomobility.com/pelvic-floor-physiotherapy-toronto-north-york/ ) this week to strengthen my pelvic floor and hopefully prevent further prolapses in the future. We'll, she assessed
Hello again ladies! I am 10 weeks post rectocele repair and started seeing a pelvic floor physiotherapist ( https://www.physiomobility.com/pelvic-floor-physiotherapy-toronto-north-york/ ) this week to strengthen my pelvic floor and hopefully prevent further prolapses in the future. We'll, she assessed
TravisSturgis
in
Pain Concern
5 years ago
Lung rehabilitation
Hi everyone, I joined in May this year,then I haven't been on in a while,just started my second time of lung rehab,it really helps, I knew I needed to go to get my lungs working a bit better,I'm doing more minutes and reps of all the excersises than I did last year as I had lung surgery, felt my self
Hi everyone, I joined in May this year,then I haven't been on in a while,just started my second time of lung rehab,it really helps, I knew I needed to go to get my lungs working a bit better,I'm doing more minutes and reps of all the excersises than I did last year as I had lung surgery, felt my self
Dollybow
in
Lung Conditions Community Forum
5 years ago
What I did on Holiday, as promised.
Dear All, I went to 'Sandpipers', which is Run by ReVitalise, formerly the Winged Fellowship Trust- founded by Joan Brander MBE. (If anyone want more details, on this, please contact me.) The Centre is, about a mile- or so- outside Southport and at the far end of the, absolutely beautiful, Marine Lake
Dear All, I went to 'Sandpipers', which is Run by ReVitalise, formerly the Winged Fellowship Trust- founded by Joan Brander MBE. (If anyone want more details, on this, please contact me.) The Centre is, about a mile- or so- outside Southport and at the far end of the, absolutely beautiful, Marine Lake
AndrewT
in
Vasculitis UK
5 years ago
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Living in hope
Hello everyone been diagnosed with PMR and started taking 12mg of Deflazacort for 4 days ..not noticed any change ..still lot of pain . Do you think I could take an extra tablet daily or do I wait it out a bit longer..many thanks Lulu
Hello everyone been diagnosed with PMR and started taking 12mg of Deflazacort for 4 days ..not noticed any change ..still lot of pain . Do you think I could take an extra tablet daily or do I wait it out a bit longer..many thanks Lulu
Seaglassgirl
in
PMRGCAuk
5 years ago
Neuromod. Feedback from my official review
Hello folks, I have been back to Dublin for my official first review. I have to report that there has been no lessening in the level of noise or intrusiveness of my T. Also, in my left ear, the Hyperacusis has got slightly worse. That is the down side. They enquired in relation to my use of the device
Hello folks, I have been back to Dublin for my official first review. I have to report that there has been no lessening in the level of noise or intrusiveness of my T. Also, in my left ear, the Hyperacusis has got slightly worse. That is the down side. They enquired in relation to my use of the device
ade-the-pade
in
British Tinnitus Association
5 years ago
Living with a Lung Condition
Hello, I am new to this community. I was diagnosed with Legionaires Disease two years ago and I have recently been told that I now have Bronchiectasis. I am finding it quite difficult to adjust to this news and understand what this means for me generally and long term. It's been really positive to read
Hello, I am new to this community. I was diagnosed with Legionaires Disease two years ago and I have recently been told that I now have Bronchiectasis. I am finding it quite difficult to adjust to this news and understand what this means for me generally and long term. It's been really positive to read
Bluestone36
in
Lung Conditions Community Forum
5 years ago
Vagus Nerve Stimulation in Rheumatoid Arthritis
I recently saw a news item on Sky News (from 2014) which showed a trial of Vagus Nerve Stimulation (VNS) that had proven very effective in the treatment of Rheumatoid Arthritis. I have looked on the web and contacted Dr Peter Tak who led the trial to see if there had been any developments - he said
I recently saw a news item on Sky News (from 2014) which showed a trial of Vagus Nerve Stimulation (VNS) that had proven very effective in the treatment of Rheumatoid Arthritis. I have looked on the web and contacted Dr Peter Tak who led the trial to see if there had been any developments - he said
Dennyh24
in
NRAS
5 years ago
Day 19 = some changes
Thank you to everyone for all your best wishes and kind words on these posts about the small person. I’ve got to be honest, I’ve hit the proverbial wall a bit today, so the nurses know not to mind me if they come in and I’m sat in the corner laughing like a loon 👀😂 I’m waiting for the doc to come and
Thank you to everyone for all your best wishes and kind words on these posts about the small person. I’ve got to be honest, I’ve hit the proverbial wall a bit today, so the nurses know not to mind me if they come in and I’m sat in the corner laughing like a loon 👀😂 I’m waiting for the doc to come and
Hidden
in
Lung Conditions Community Forum
5 years ago
Unable to reduce Pred. Any ideas?
I'm having real difficulty reducing my Pred dosage below 8mg. Any ideas? I started with PMR in December 2017 after a cycling accident, though it wasn't diagnosed for 3 months. I started on 25mg of pred and got down to 12.5mg without problem. But from that point on it's been extremely difficult to
I'm having real difficulty reducing my Pred dosage below 8mg. Any ideas? I started with PMR in December 2017 after a cycling accident, though it wasn't diagnosed for 3 months. I started on 25mg of pred and got down to 12.5mg without problem. But from that point on it's been extremely difficult to
Cycling_bloke
in
PMRGCAuk
5 years ago
Hospice-ask your doctor and look into it.
Our neurologist recommended hospice for my husband in dec 2018. My father was dying and put off until now. We met, he was approved and I can’t tell you how helpful after one visit -all within an hour and a half. His lift recliner had broken, we got a new one this afternoon. He will get a hospital bed
Our neurologist recommended hospice for my husband in dec 2018. My father was dying and put off until now. We met, he was approved and I can’t tell you how helpful after one visit -all within an hour and a half. His lift recliner had broken, we got a new one this afternoon. He will get a hospital bed
susantigner
in
PSP Association
5 years ago
New strange symptom
Hi Everyone, Hope you are all well, I’ve been experiencing some strange sensation when I’ve been drinking cold drinks and it’s really hard to explain but here goes. When I drink a cold drink I have one part of the roof and back of my mouth that go numb - it’s as if I’m about to get brain freeze but
Hi Everyone, Hope you are all well, I’ve been experiencing some strange sensation when I’ve been drinking cold drinks and it’s really hard to explain but here goes. When I drink a cold drink I have one part of the roof and back of my mouth that go numb - it’s as if I’m about to get brain freeze but
Leenie0811
in
LUPUS UK
5 years ago
Thursday
Got to sleep until 4:30 today. Got up exhausted. Walking into Larry’s bedroom. He was half on the floor holding a plastic urinal in his hands. He was trying to put it down after using it. Fell halfway out of bed. Was sort of kneeling leaning against the bed. Had to pry the urinal out of his hands. He
Got to sleep until 4:30 today. Got up exhausted. Walking into Larry’s bedroom. He was half on the floor holding a plastic urinal in his hands. He was trying to put it down after using it. Fell halfway out of bed. Was sort of kneeling leaning against the bed. Had to pry the urinal out of his hands. He
Hidden
in
PSP Association
5 years ago
Raising awareness and support for PMRGCAuk ... climbing an Ultimate Mountain
I'm still in remission with Polymyalgia Rheumatica, and as the PMRGCA North East coordinator I'm raising awareness and support for PMRGCAuk by climbing one of the world's highest, coldest, remotest and most dangerous mountains in the high Nepal Himalayas in October/November. I'm on a 32-day expedition
I'm still in remission with Polymyalgia Rheumatica, and as the PMRGCA North East coordinator I'm raising awareness and support for PMRGCAuk by climbing one of the world's highest, coldest, remotest and most dangerous mountains in the high Nepal Himalayas in October/November. I'm on a 32-day expedition
Skinnyjonny
in
PMRGCAuk
5 years ago
Liver pain
Anyone? I suspect it’s liver pain, it comes and goes and is more often a dull pain above my right hip and below my ribs. I can’t find any pattern to it and I’ve had it on and off for a couple of years. I have no other symptoms other than thyroid ones! And yes, I will see my gp 😉
Anyone? I suspect it’s liver pain, it comes and goes and is more often a dull pain above my right hip and below my ribs. I can’t find any pattern to it and I’ve had it on and off for a couple of years. I have no other symptoms other than thyroid ones! And yes, I will see my gp 😉
Murphysmum
in
Thyroid UK
5 years ago
In remission with PMR and climbing one of the World's most dangerous mountains
Today the Durham Times (UK) has reported my forthcoming attempt in Oct/Nov to climb Annapurna IV (7525m / 24,700ft) to raise awareness of my condition Polymyalgia Rheumatica. Six years ago I was advised I wouldn't climb again and now I'm attempting the ultimate challenge ... to put my body against one
Today the Durham Times (UK) has reported my forthcoming attempt in Oct/Nov to climb Annapurna IV (7525m / 24,700ft) to raise awareness of my condition Polymyalgia Rheumatica. Six years ago I was advised I wouldn't climb again and now I'm attempting the ultimate challenge ... to put my body against one
Skinnyjonny
in
PMRGCAuk
5 years ago
Mountains are definitely a metaphor of life ...
I'm in remission with Polymyalgia Rheumatica and I'll be climbing one of the world's highest, remotest, coldest and deadliest mountains as the ultimate challenge. Annapurna IV (7525m / 24,700ft) is in the Nepal Himalayas and the expedition will take 30 days with technical climbing and four high camps
I'm in remission with Polymyalgia Rheumatica and I'll be climbing one of the world's highest, remotest, coldest and deadliest mountains as the ultimate challenge. Annapurna IV (7525m / 24,700ft) is in the Nepal Himalayas and the expedition will take 30 days with technical climbing and four high camps
Skinnyjonny
in
PMRGCAuk
5 years ago
Caught between consultants & GP
I was referred to royal Brompton cons' he suggested not all symptoms were asthma so had a challenge test - said I have hypersensitive airways (which I knew). Was then asked to have a Mannitol test - reacted to first dose, needing x3 nebilising to sort asthma attack out! Now stuck between cons' and local
I was referred to royal Brompton cons' he suggested not all symptoms were asthma so had a challenge test - said I have hypersensitive airways (which I knew). Was then asked to have a Mannitol test - reacted to first dose, needing x3 nebilising to sort asthma attack out! Now stuck between cons' and local
Jules22
in
Asthma Community Forum
5 years ago
Hydrotherapy and exercise
Just one of those late evening thoughts. Seldom do we have posts on hydrotherapy here. Liz used to have one to one hydrotherapy with a neuro-physiotherapist. Her lack of balance was not an issue in the water. She was able to do exercises and swim and the resistance of the water gave her a good work
Just one of those late evening thoughts. Seldom do we have posts on hydrotherapy here. Liz used to have one to one hydrotherapy with a neuro-physiotherapist. Her lack of balance was not an issue in the water. She was able to do exercises and swim and the resistance of the water gave her a good work
Kevin_1
in
PSP Association
5 years ago
Support please
Hi there. I am new to this site. My mom was sadly diagnosed with PSP and frontotemporal dementia 4 years ago, I just need some support and would like to hear from others in a similar situation or even meet up with people. I feel very alone in terms of others understanding this horrific disease. I
Hi there. I am new to this site. My mom was sadly diagnosed with PSP and frontotemporal dementia 4 years ago, I just need some support and would like to hear from others in a similar situation or even meet up with people. I feel very alone in terms of others understanding this horrific disease. I
Lydia_May
in
PSP Association
5 years ago
Fibromyalgia
I’ve been suffering for years with back & hip pain. Legs keep going numb also pins & needles in both legs & arms. Finally got told about 2mths ago that I had fibromyalgia this was after 2 doctors stating I didn’t show symptoms of it. Then I saw a 3rd doctor about 6mths after the 1st doctor and he finally
I’ve been suffering for years with back & hip pain. Legs keep going numb also pins & needles in both legs & arms. Finally got told about 2mths ago that I had fibromyalgia this was after 2 doctors stating I didn’t show symptoms of it. Then I saw a 3rd doctor about 6mths after the 1st doctor and he finally
Bev-1
in
Fibromyalgia Action UK
5 years ago
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