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Wanting to learn from you...
Hello! I am here to learn what kinds of things you experience after breast cancer surgery. I am a physical therapist and I see people who seem to have similar experiences of not being given good advice as to what to do, what therapies to seek, what exercises to do, or anything pre or post surgically
Hello! I am here to learn what kinds of things you experience after breast cancer surgery. I am a physical therapist and I see people who seem to have similar experiences of not being given good advice as to what to do, what therapies to seek, what exercises to do, or anything pre or post surgically
MFR4life
in
SHARE Breast Cancer Support
2 months ago
Physical therapy, anyone?
They're coming to my house to assess me so I'm going to throw myself on the floor to get my money's worth.š
They're coming to my house to assess me so I'm going to throw myself on the floor to get my money's worth.š
falalalala
in
My MSAA Community
2 months ago
Sciatica and numbness in leg.
Ok so now definitely diagnosed with sciatica. Have seen physio for first session and had treatment plus acupuncture. He says that numbness in the calf and lower leg is not uncommon. I am struggling to walk tho and VERY off balance. Using walking canes to help. Anyone else have tingling and pretty
Ok so now definitely diagnosed with sciatica. Have seen physio for first session and had treatment plus acupuncture. He says that numbness in the calf and lower leg is not uncommon. I am struggling to walk tho and VERY off balance. Using walking canes to help. Anyone else have tingling and pretty
gillsky8
in
PMRGCAuk
2 months ago
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A little moan about the NHS and positive outcome come on my private consultation with 2 consultants Hip and Back
Ok so I have been having serious issues with my Back and hip both separate issues and the NHS seem to take it as my back as a degenerative issue even after having an MRI done(seen by spinal team )š¤·š¤¦ . My hip was said to be a muscular issue which needed physio. Was seeing 2 different sets of physio
Ok so I have been having serious issues with my Back and hip both separate issues and the NHS seem to take it as my back as a degenerative issue even after having an MRI done(seen by spinal team )š¤·š¤¦ . My hip was said to be a muscular issue which needed physio. Was seeing 2 different sets of physio
KnitSewPurl
in
LUPUS UK
2 months ago
ED medications for assistance with incontinence recovery
2 months post Robotic daVinci prostatectomy. Non nerve sparing. Will Viagra or other ED meds help with incontinence issues along with Pelvic Floor Physical Therapy? Still mostly incontinent. Found and using a penile clamp 2-3 hours at a time for training the bladder to fill and empty. Appreciate
2 months post Robotic daVinci prostatectomy. Non nerve sparing. Will Viagra or other ED meds help with incontinence issues along with Pelvic Floor Physical Therapy? Still mostly incontinent. Found and using a penile clamp 2-3 hours at a time for training the bladder to fill and empty. Appreciate
HerbalGrower
in
Prostate Cancer Network
2 months ago
Cionic Neural Sleeve
Has anyone ever heard of this Cionic Neural Sleeve? I heard about it on a podcast and then did some digging. I received an email from my physical therapist about an upcoming webinar on May 22 about this device. Itās supposed to help normalize walking using electrodes to create muscle stimulation. Might
Has anyone ever heard of this Cionic Neural Sleeve? I heard about it on a podcast and then did some digging. I received an email from my physical therapist about an upcoming webinar on May 22 about this device. Itās supposed to help normalize walking using electrodes to create muscle stimulation. Might
Rezzy3
in
Ataxia UK
2 months ago
WEEKLY CHAT 20 to 26 MAY: After the Lord Mayorās Show?
Following a weekend of excitement around the HU10, and lots of brilliant posts, I have a feeling of āfollow that?ā, especially as I have yet to complete my run. But, my first task is obvious. I have to thank Ā Ā Ā linda9389 and Ā Ā Ā Irishprincess for all the hours of hard work they have put in to make the event
Following a weekend of excitement around the HU10, and lots of brilliant posts, I have a feeling of āfollow that?ā, especially as I have yet to complete my run. But, my first task is obvious. I have to thank Ā Ā Ā linda9389 and Ā Ā Ā Irishprincess for all the hours of hard work they have put in to make the event
Beachcomber66
Half Marathon
in
Fun Beyond 10K & Race Support
2 months ago
Ramblings from a calf strain sufferer
Apologies for the longer post, but I am trying to gather my thoughts and the physio advice received, to devise some sort of recovery and prevention plan addressing my reoccurring calf strains. In the off chance that someone might be in the same position, I thought Iād wrote it all down, as my ramblings
Apologies for the longer post, but I am trying to gather my thoughts and the physio advice received, to devise some sort of recovery and prevention plan addressing my reoccurring calf strains. In the off chance that someone might be in the same position, I thought Iād wrote it all down, as my ramblings
CBDB
Administrator
in
Strength & Flex
2 months ago
Pins & needles in obscure places...
Hi all, Just a random question... I get pins and needles in the top of my thighs if I stand still for more than a few minutes or if I walk for more than a few paces. I get pins & needles in my hands all the time they never go away even when I use compression gloves provided by physio, and I get pins
Hi all, Just a random question... I get pins and needles in the top of my thighs if I stand still for more than a few minutes or if I walk for more than a few paces. I get pins & needles in my hands all the time they never go away even when I use compression gloves provided by physio, and I get pins
Bacaloca
in
Fibromyalgia Action UK
2 months ago
Castleview back under another name
Ralph is doing okay, walking with a stick now, and managing 8 stairs. Showering himself, front anyway, can't do back or bottom as having physio on his shoulders due to them being tight through lack of use. He can also dress himself. He's still not allowed to get out of bed or walk without supervision
Ralph is doing okay, walking with a stick now, and managing 8 stairs. Showering himself, front anyway, can't do back or bottom as having physio on his shoulders due to them being tight through lack of use. He can also dress himself. He's still not allowed to get out of bed or walk without supervision
Gardenview10
in
British Heart Foundation
2 months ago
constipation leading to Pelvic Floor dysfunction
I have IBS - C and over the years the medical fraternity have prescribed laxatives for me. Iām following a low fermentation & FODMAP diet which works well for me. However my constipation due to a lot of straining has turned into PFD which basically means my anal muscles are out of sync. Does anyone suffer
I have IBS - C and over the years the medical fraternity have prescribed laxatives for me. Iām following a low fermentation & FODMAP diet which works well for me. However my constipation due to a lot of straining has turned into PFD which basically means my anal muscles are out of sync. Does anyone suffer
Profound15
in
IBS Network
2 months ago
Enemas for constipation
I am taking flecainide and bisoprolol for my afib. The medication is doing fine but Iāve got what I believe to be Pelvic Floor dysfunction. Basically one of my rectum muscles (at exit) is contracting when it should be relaxing. Iāve got biofeedback physio on Monday but wanted to know if anyone has experience
I am taking flecainide and bisoprolol for my afib. The medication is doing fine but Iāve got what I believe to be Pelvic Floor dysfunction. Basically one of my rectum muscles (at exit) is contracting when it should be relaxing. Iāve got biofeedback physio on Monday but wanted to know if anyone has experience
Profound15
in
Atrial Fibrillation Support
2 months ago
feeling a little hopeless!
hi all, First time posting on here! I have been reading all the threads and finding lots of comfort, so thought Iād reach out. I was diagnosed with psoriatic arthritis in mid-March. It took almost three years to get my diagnosis due to my symptoms not āfitting in a boxā (words of the Rheumy nurse
hi all, First time posting on here! I have been reading all the threads and finding lots of comfort, so thought Iād reach out. I was diagnosed with psoriatic arthritis in mid-March. It took almost three years to get my diagnosis due to my symptoms not āfitting in a boxā (words of the Rheumy nurse
Becrosep
in
NRAS
2 months ago
Treatment has hit a wall. I can not sit without pain.
I have not been able to sit without horrid pain since August. I did too much ā and I have not recovered. On top of that, the nerve blocks I have been getting to try to help this pain for years, like pudendal nerve block, trigger point injections into my pelvic floor, si joint injections, and caudal injections
I have not been able to sit without horrid pain since August. I did too much ā and I have not recovered. On top of that, the nerve blocks I have been getting to try to help this pain for years, like pudendal nerve block, trigger point injections into my pelvic floor, si joint injections, and caudal injections
kellerfly
in
Pelvic Pain Support Network
2 months ago
Pain Clinics
1. I attended my 1st PC in 2012 (Cambridge) following spinal decompression which was successful but I also had fibromyalgia. 2. Transferred to 2nd Peterborough PC due to travel problems. Sat through excruciatingly painful group sessions relating to the Biopsychosocial Model and Mindfulness. Course
1. I attended my 1st PC in 2012 (Cambridge) following spinal decompression which was successful but I also had fibromyalgia. 2. Transferred to 2nd Peterborough PC due to travel problems. Sat through excruciatingly painful group sessions relating to the Biopsychosocial Model and Mindfulness. Course
Blackwitch
in
Pain Concern
2 months ago
PMR flare or sciatica getting worse!?
All the original discomfort and pain of the first bout of PMR seems to have returned. In my hips and thighs, so very painful and I feel thoroughly exhausted. I am still on 10mg of prednisone and now considering whether I should ask for increase again. I have enough to up dose at home and tempted
All the original discomfort and pain of the first bout of PMR seems to have returned. In my hips and thighs, so very painful and I feel thoroughly exhausted. I am still on 10mg of prednisone and now considering whether I should ask for increase again. I have enough to up dose at home and tempted
gillsky8
in
PMRGCAuk
2 months ago
whiplash pain and interferon
hi everyone I started interferon about 6 weeks ago and apart from a bit of nausea and the odd ache the day after seem ( fingers crossed) to be tolerating it ok. However, weāre on Anglesey with friends ( all 70 ish) and thinking we all feel like spring chickens, we decided to book a rib ride under the
hi everyone I started interferon about 6 weeks ago and apart from a bit of nausea and the odd ache the day after seem ( fingers crossed) to be tolerating it ok. However, weāre on Anglesey with friends ( all 70 ish) and thinking we all feel like spring chickens, we decided to book a rib ride under the
Loubprv
Volunteer
in
MPN Voice
2 months ago
Is it time to give up?
I started the programme during lockdown at the age of 66. Iād never run before and I loved it. I was reasonably fit having been a keen hiker for most of my life but it took me almost 2 years to complete the programme because of a series of injuries along the way, including shin splints, plantar fasciitis
I started the programme during lockdown at the age of 66. Iād never run before and I loved it. I was reasonably fit having been a keen hiker for most of my life but it took me almost 2 years to complete the programme because of a series of injuries along the way, including shin splints, plantar fasciitis
Upsidaisy
Graduate
in
Couch to 5K
2 months ago
Please... Help is it possible i have fibromyalgia as well as hypermobility?
I'm diagnosed bipolar and EUPD have bad anxiety I just can't cope with this much longer, I need help to know what's wrong with me... no medical professional I've seen helps, Dr's,
physiotherapy
, specialist
physiotherapy
, surgeons for ligament rupture (without a injury) ... all blame hypermobility with
I'm diagnosed bipolar and EUPD have bad anxiety I just can't cope with this much longer, I need help to know what's wrong with me... no medical professional I've seen helps, Dr's,
physiotherapy
, specialist
physiotherapy
, surgeons for ligament rupture (without a injury) ... all blame hypermobility with
Tnt88
in
Fibromyalgia Action UK
1 year ago
Capsular pain?
Hi diagnosed in January with liver cirrhosis . Never drunk alcohol, kpa 14 .. since the fibrosis in January i have had constant pain in and around my rib cage on the right side.. had x rays and physio with no improvement... my question is... Could this be capsular pain ive heard of on this forum ?
Hi diagnosed in January with liver cirrhosis . Never drunk alcohol, kpa 14 .. since the fibrosis in January i have had constant pain in and around my rib cage on the right side.. had x rays and physio with no improvement... my question is... Could this be capsular pain ive heard of on this forum ?
Jender58
in
British Liver Trust
2 months ago
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