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Hypermobility
Thank you for accepting me on to your forum. My daughter has just been diagnosed with Hypermobility at 20. She has been offered physio and is coping well with her condition considering but is finding sleeping very hard and tosses and turns all night to get pain relief and ease her joints and spine
Thank you for accepting me on to your forum. My daughter has just been diagnosed with Hypermobility at 20. She has been offered physio and is coping well with her condition considering but is finding sleeping very hard and tosses and turns all night to get pain relief and ease her joints and spine
tamccart
in
Fibromyalgia Action UK
3 months ago
Never ending flare
I seem to be getting worse and having no good daysš¢.Any advice anyone ? I'm doing physio every morning. I'm eating less, but the burning skin spread today - Sunday- My mood has plummeted lately. Well you all known the symptomsšØš¤š Now I'm going to bed . I'll try to be cheery tomorrow hugs and love
I seem to be getting worse and having no good daysš¢.Any advice anyone ? I'm doing physio every morning. I'm eating less, but the burning skin spread today - Sunday- My mood has plummeted lately. Well you all known the symptomsšØš¤š Now I'm going to bed . I'll try to be cheery tomorrow hugs and love
Smilesalot
in
Fibromyalgia Action UK
3 months ago
Osteoarthritis in knee
Hello I am new on this site and would like to thank admin for letting me on here. Going back about January 2024 time my left knee started to feel a little odd at the back (ham) think this is what it's name is, anyhow about 6/8 weeks ago plucked up enough courage to see a G.P at my local doctors, a
Hello I am new on this site and would like to thank admin for letting me on here. Going back about January 2024 time my left knee started to feel a little odd at the back (ham) think this is what it's name is, anyhow about 6/8 weeks ago plucked up enough courage to see a G.P at my local doctors, a
completely-zero654
in
Couch to 5K
3 months ago
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Specialist womanās health Physio needed!
Hi, Iām a 49 year old woman and have been suffering with PN. Iāve read some of the stories on the Network, can anyone give me the name of specialist womenās health physio who was knowledgeable about PN? Iām in Cheltenham so Bristol or Birmingham or Wales even?
Hi, Iām a 49 year old woman and have been suffering with PN. Iāve read some of the stories on the Network, can anyone give me the name of specialist womenās health physio who was knowledgeable about PN? Iām in Cheltenham so Bristol or Birmingham or Wales even?
StepAerobics99
in
Pelvic Pain Support Network
3 months ago
Our Dad's journey
Our hearts are broken as our dad passed away on April 15th. We wanted to summarise his journey and symptoms to hopefully help others and to also raise awareness of gastric outlet obstruction. Our dad had a neurological degenerative disease called Progressive Supranuclear Palsy (PSP). We had not heard
Our hearts are broken as our dad passed away on April 15th. We wanted to summarise his journey and symptoms to hopefully help others and to also raise awareness of gastric outlet obstruction. Our dad had a neurological degenerative disease called Progressive Supranuclear Palsy (PSP). We had not heard
DALLY123
in
PSP Association
3 months ago
tear in my meniscus cartilage
What a difference two weeks can make. Two weeks ago I you asked if I should attempt a taper to try to force my adrenals to wake up. The circumstances were not very good and you advised me to leave it for a while so I took your advice. A few days later I somehow got a tear in the cartilage of my knee
What a difference two weeks can make. Two weeks ago I you asked if I should attempt a taper to try to force my adrenals to wake up. The circumstances were not very good and you advised me to leave it for a while so I took your advice. A few days later I somehow got a tear in the cartilage of my knee
jinoadby
in
PMRGCAuk
3 months ago
Back/pelvis/hip pain?
A month or 2 ago, I got a new dog, he's bigger than my previous dog and he pulls on the lead. And I got stressed adapting to the change. Somewhere soon after that I picked up a bug, and the PMR "buzzing" in my shoulders, arms and calves popped back. Not really painful but aware of "the bucket" I stopped
A month or 2 ago, I got a new dog, he's bigger than my previous dog and he pulls on the lead. And I got stressed adapting to the change. Somewhere soon after that I picked up a bug, and the PMR "buzzing" in my shoulders, arms and calves popped back. Not really painful but aware of "the bucket" I stopped
Curious101
in
PMRGCAuk
3 months ago
vestibular dysfunction
Hello, I was diagnosed 7 years ago with SCA unknown cause, following blood tests. Does anyone else suffer with vestibular dysfunction? Iām seeing a vestibular physio this week. Thank you
Hello, I was diagnosed 7 years ago with SCA unknown cause, following blood tests. Does anyone else suffer with vestibular dysfunction? Iām seeing a vestibular physio this week. Thank you
mimosaholland
in
Ataxia UK
3 months ago
Exercise intolerance
Hi all. Does anyone have any idea how to tackle this please? Just over four months into PCS. At first I had to build exercise back up but managed to get to walking about five miles a few months ago. Not without symptoms and obviously pretty shattered the next day, but I could do it. Over the last
Hi all. Does anyone have any idea how to tackle this please? Just over four months into PCS. At first I had to build exercise back up but managed to get to walking about five miles a few months ago. Not without symptoms and obviously pretty shattered the next day, but I could do it. Over the last
Ideogram
in
Headway
3 months ago
Please can someone help me?
Hi All! Iām hoping someone on here can help me as I am having no luck with my doctors. I have been having pain and stiffness, strange rashes, blotchy red skin, swelling, my hips, knees and ankles are particularly affected. I have had very raised inflammatory markers in blood tests since 2009 but this
Hi All! Iām hoping someone on here can help me as I am having no luck with my doctors. I have been having pain and stiffness, strange rashes, blotchy red skin, swelling, my hips, knees and ankles are particularly affected. I have had very raised inflammatory markers in blood tests since 2009 but this
Capybara123
in
NRAS
3 months ago
To raise pred or not?
Following a medication review earlier this year when I was on 7mgs my GP told me I had to reduce by 1 mg a month and that any aches and pains I had now were not PMR. I have done as she said even though I had my doubts about this course of action and Iām now down to 4mg. I told her I still had pain in
Following a medication review earlier this year when I was on 7mgs my GP told me I had to reduce by 1 mg a month and that any aches and pains I had now were not PMR. I have done as she said even though I had my doubts about this course of action and Iām now down to 4mg. I told her I still had pain in
Decsgran
in
PMRGCAuk
3 months ago
PVā¦.is cupping contraindicated?
Hi All I hope everyone is well and enjoying whatever sunshine some of us are getting now. I have not been on here in a while. Life & work is manic but plan to pop an update on whats been happening with me. But for now, I have a quick question on use of cupping from massage / alternative practitioners
Hi All I hope everyone is well and enjoying whatever sunshine some of us are getting now. I have not been on here in a while. Life & work is manic but plan to pop an update on whats been happening with me. But for now, I have a quick question on use of cupping from massage / alternative practitioners
LittleLuna
in
MPN Voice
3 months ago
NASH progressed
Hi I've had fatty liver disease for many years nowIt progressed to NASH eventually Now on my latest fibroscan it shows 80 percent of fat in my liver (highest ever) And more scarring bringing me out of F4 fibrosis into suspected Cirrhosis All I can do is wait. I'm in the UK and drs don't prescribe the
Hi I've had fatty liver disease for many years nowIt progressed to NASH eventually Now on my latest fibroscan it shows 80 percent of fat in my liver (highest ever) And more scarring bringing me out of F4 fibrosis into suspected Cirrhosis All I can do is wait. I'm in the UK and drs don't prescribe the
LaurieRose
in
Living with Fatty Liver and NASH
3 months ago
Up then down
Mixed today. He's brilliant, walked the entire length of the ward and backšThey want the bed, so to start with were looking to go back to Sheffield Hallamshire ENT ward, then hoping to get him on Devonshire ward Calow Mon Fri and Sheffield weekends. Holding off on that possibly as he couldn't have the
Mixed today. He's brilliant, walked the entire length of the ward and backšThey want the bed, so to start with were looking to go back to Sheffield Hallamshire ENT ward, then hoping to get him on Devonshire ward Calow Mon Fri and Sheffield weekends. Holding off on that possibly as he couldn't have the
Hidden
in
British Heart Foundation
3 months ago
Plans to help me and support,
Hi hope you are all okay, im wondering if people have had good support from their doctors re fibro, plans to help, therapies, hydro therapys, more physio or something. I dont feel i got much, i know its a complex thing but i asked to be referred for hydrotherapy where i live but apparantly it was denied
Hi hope you are all okay, im wondering if people have had good support from their doctors re fibro, plans to help, therapies, hydro therapys, more physio or something. I dont feel i got much, i know its a complex thing but i asked to be referred for hydrotherapy where i live but apparantly it was denied
fibrogirl41
in
Fibromyalgia Action UK
3 months ago
Urinary incontinence post surgery
One month post daVince robotic prostatectomy. 70 years old. Active (could exercise more) Catheter removed day 8. Persistent incontinence. Doing Kegel exercises. Awaiting contacts with local Physical Therapists for Pelvic floor, core and post surgical rehab program. Open to ideas from others post surgery
One month post daVince robotic prostatectomy. 70 years old. Active (could exercise more) Catheter removed day 8. Persistent incontinence. Doing Kegel exercises. Awaiting contacts with local Physical Therapists for Pelvic floor, core and post surgical rehab program. Open to ideas from others post surgery
HerbalGrower
in
Prostate Cancer Network
3 months ago
PMR/Sciatica
I have had PMR since autumn 2016 and have been on 5mg for some time..I do try regularly to reduce ,so far unsuccessfuly..hopefully I will get there eventually.I also am Hypo thyroid. In mid January this year I had Sciatica,and have been applying weekly Morphine pain patches. Recently both my physio
I have had PMR since autumn 2016 and have been on 5mg for some time..I do try regularly to reduce ,so far unsuccessfuly..hopefully I will get there eventually.I also am Hypo thyroid. In mid January this year I had Sciatica,and have been applying weekly Morphine pain patches. Recently both my physio
Mellow-Yellow
in
PMRGCAuk
3 months ago
Exercise
I wondered how people approach exercise to try to maintain their fitness. I am going to a respiratory physio as too much exercise tends to leave me rather fatigued and asthmatic. So I decided that my normal approach of pushing it, needed modification, so I sought advice. The physio has helped me improve
I wondered how people approach exercise to try to maintain their fitness. I am going to a respiratory physio as too much exercise tends to leave me rather fatigued and asthmatic. So I decided that my normal approach of pushing it, needed modification, so I sought advice. The physio has helped me improve
Homely2
Administrator
in
Asthma Community Forum
3 months ago
Mom's Journey
Hi all. I haven't been on in a while. Last month, my mom with psp fell and broke her pelvis. After hospitalization, she was moved to a rehab facility. It seems as if the injury and trauma of it have sped up the disease tremendously. We are deciding between two long term care homes for her to live
Hi all. I haven't been on in a while. Last month, my mom with psp fell and broke her pelvis. After hospitalization, she was moved to a rehab facility. It seems as if the injury and trauma of it have sped up the disease tremendously. We are deciding between two long term care homes for her to live
christie329
in
PSP Association
3 months ago
anismus
I have chronic constipation. I think it is casued by various muscles not relaxing as the symptoms fit what I have read online. There are vaious names for this, anismus, dysssergenic defaecation and obstruced defaecation. I looked on this site and this is one of the groups that seems appropriate to post
I have chronic constipation. I think it is casued by various muscles not relaxing as the symptoms fit what I have read online. There are vaious names for this, anismus, dysssergenic defaecation and obstruced defaecation. I looked on this site and this is one of the groups that seems appropriate to post
Grassmower
in
IBS Network
3 months ago
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