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Been on the IC since April 24h….bit fed up now!
Hi, I completed C25K a few years ago, and run regularly. I started having pain in both feet earlier this year, which felt like Plantar Fasciitis, which I had had very successful surgery for over 20 years ago! ( I must have been REALLY lucky with the results, as it’s hardly done now, as it’s not thought
Hi, I completed C25K a few years ago, and run regularly. I started having pain in both feet earlier this year, which felt like Plantar Fasciitis, which I had had very successful surgery for over 20 years ago! ( I must have been REALLY lucky with the results, as it’s hardly done now, as it’s not thought
Dansac29
Graduate
in
Couch to 5K
11 months ago
Positive clonus and lupus
Hello :) I've recently been diagnosed with rheumatoid arthritis and a lupus overlap. I have now been told I have a positive clonus reflex. I don't know if I should be concerned that it is linked or the physio is just being thorough referring me to my GP for further investigation. If anyone has had
Hello :) I've recently been diagnosed with rheumatoid arthritis and a lupus overlap. I have now been told I have a positive clonus reflex. I don't know if I should be concerned that it is linked or the physio is just being thorough referring me to my GP for further investigation. If anyone has had
Sunshine634
in
LUPUS UK
11 months ago
Levodopa end-of-dose dystonia successfully treated by neuromuscular taping: A case report
Most of us experience this havoc and its very cumbersome and disturbing. While searching on the topic I came across this article and found it worth sharing. Neuromuscular taping (NMT) is a physical therapy technique where an elastic drug free tape is applied without tension in order to lift the skin
Most of us experience this havoc and its very cumbersome and disturbing. While searching on the topic I came across this article and found it worth sharing. Neuromuscular taping (NMT) is a physical therapy technique where an elastic drug free tape is applied without tension in order to lift the skin
Farooqji
in
Cure Parkinson's
11 months ago
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Chronic shoulder pain
Was initially diagnosed with PMR in April 2022 only to be told a month later by Rheumatologist that it wasn’t PMR but a nasty viral infection. Also had long standing shoulder pain now for over 2 years and neck also very stiff.Had shoulder scanned recently shoeing no tests but SASD bursa distended consistent
Was initially diagnosed with PMR in April 2022 only to be told a month later by Rheumatologist that it wasn’t PMR but a nasty viral infection. Also had long standing shoulder pain now for over 2 years and neck also very stiff.Had shoulder scanned recently shoeing no tests but SASD bursa distended consistent
Countybowler
in
PMRGCAuk
11 months ago
Adult Degenerative Scoliosis
I have suffered from increasing pain in my back and legs since a fall in November 2021 when I fractured my left humerus in 3 places. I have had Polymyalgia Rheumatica since January 2021 and at first it was thought my pain was due to this. Eventually in July 2022 my GP agreed to send me for an XRay of
I have suffered from increasing pain in my back and legs since a fall in November 2021 when I fractured my left humerus in 3 places. I have had Polymyalgia Rheumatica since January 2021 and at first it was thought my pain was due to this. Eventually in July 2022 my GP agreed to send me for an XRay of
Jomaur
in
Pain Concern
11 months ago
Sternoclavicular Joint Popping / Snapping?
Hi, Hope everyone is doing well, Its been a long time since I last posted. Its coming up on 9 years now since I was diagnosed with RA, feels like a lifetime ago! Just recently I have been experiencing what I can only describe as a feeling of popping / snapping in my sternoclavicular joint (only on
Hi, Hope everyone is doing well, Its been a long time since I last posted. Its coming up on 9 years now since I was diagnosed with RA, feels like a lifetime ago! Just recently I have been experiencing what I can only describe as a feeling of popping / snapping in my sternoclavicular joint (only on
JamesCH
in
NRAS
11 months ago
Minor Calf Strains (Pulled Calf)
As many know by now, I've been firmly placed onto the injury couch again, so my next posts will not be about running, or walking, rowing, dancing, stretching, weightlifting 😩 but …. yes … recovery and rehabilitation. I’ll share my journey to hold myself to account, but also in case it helps anyone
As many know by now, I've been firmly placed onto the injury couch again, so my next posts will not be about running, or walking, rowing, dancing, stretching, weightlifting 😩 but …. yes … recovery and rehabilitation. I’ll share my journey to hold myself to account, but also in case it helps anyone
CBDB
Administrator
in
Strength & Flex
11 months ago
Diet plan consultation
Has anyone got any information about diet or supplements? There was a post about berberine and 5HTP along with other medicines. My sister who is 43 years old has GBM grade 4. It was diagnosed in April 2023. She also had her tumour removed and radiotherapy in May/ June. She has hardly no feeling on her
Has anyone got any information about diet or supplements? There was a post about berberine and 5HTP along with other medicines. My sister who is 43 years old has GBM grade 4. It was diagnosed in April 2023. She also had her tumour removed and radiotherapy in May/ June. She has hardly no feeling on her
Speed_of_light
in
Glioblastoma Support
11 months ago
looking for answers
81 yr old husband got covid at physical therapy, ended up at er where they said he also had pneumonia, they also found (and removed) a quart of fluid from around his right lung. Said he had atrial fibrillation and he also needs an angioplasty. Took too long but finally got everything treated and surgery
81 yr old husband got covid at physical therapy, ended up at er where they said he also had pneumonia, they also found (and removed) a quart of fluid from around his right lung. Said he had atrial fibrillation and he also needs an angioplasty. Took too long but finally got everything treated and surgery
Spring15-3
in
AF Association
11 months ago
DAY 7 OF SICK DAYS, ET AL
Last Wednesday evening increased Pred from 16 to 20 mg. It has been 7 days. Still on antibiotics to avert any infection from that cut on my shin. Almost done with the AB. VON says it looks ok. Took my first shower this morning. Salined the cut. Also ran some saline solution.down my back, just in case
Last Wednesday evening increased Pred from 16 to 20 mg. It has been 7 days. Still on antibiotics to avert any infection from that cut on my shin. Almost done with the AB. VON says it looks ok. Took my first shower this morning. Salined the cut. Also ran some saline solution.down my back, just in case
Missus835
in
PMRGCAuk
11 months ago
5k 2 Couch and Reality Bites
Hi All, Over the summer I graduated on the Couch to 5k plan. Things were going great and I had completed around six consolidation runs, then on that last run, I felt pain in my Achilles Tendon and couldn't run. I posted about the injury saying it was all part of the challenge, part of the journey, but
Hi All, Over the summer I graduated on the Couch to 5k plan. Things were going great and I had completed around six consolidation runs, then on that last run, I felt pain in my Achilles Tendon and couldn't run. I posted about the injury saying it was all part of the challenge, part of the journey, but
Frankenfoot23
Graduate
in
Couch to 5K
11 months ago
Physio
Well Les had physio round today and she seems to think he should be able to get his strength back with exercise, She didn’t seem to know much about MSA so I’m concerned that as she doesn’t know about the disease she is just assuming that les just needs rehabilitation, has anyone else come across this
Well Les had physio round today and she seems to think he should be able to get his strength back with exercise, She didn’t seem to know much about MSA so I’m concerned that as she doesn’t know about the disease she is just assuming that les just needs rehabilitation, has anyone else come across this
DeeMilo25
in
Multiple System Atrophy Trust
11 months ago
The ParkinsonNet dream
Because we believe that the best possible care for this complex disease is only possible when patients are completely involved and through expertise and patients and healthcare professionals working together as one team.ParkinsonNet is endorsed by professional healthcare organizations (e.g. for
physiotherapy
Because we believe that the best possible care for this complex disease is only possible when patients are completely involved and through expertise and patients and healthcare professionals working together as one team.ParkinsonNet is endorsed by professional healthcare organizations (e.g. for
physiotherapy
Esperanto
in
Cure Parkinson's
1 year ago
Plantar fascia tear, due to long-term prednisone use?
Following sudden and agonising heel pain on Monday morning, I've seen my physio. He says it's an unusual injury, but likely due to long-term steroids. I have a tear to my plantar fascia, where it inserts under the heel. He strapped it and suggested heel cups to lift my heel (Amazon) and only supportive
Following sudden and agonising heel pain on Monday morning, I've seen my physio. He says it's an unusual injury, but likely due to long-term steroids. I have a tear to my plantar fascia, where it inserts under the heel. He strapped it and suggested heel cups to lift my heel (Amazon) and only supportive
HelenDaisy
in
PMRGCAuk
11 months ago
How can they really know?
I'm a bit perplexed as to how they can really tell the difference between OA and RA.I have heard of so many people that are told they have RA, to later be told it's OA. My arthritis symptoms have changed somewhat and are affecting other areas of my body and I don't know whether to bother mentioning
I'm a bit perplexed as to how they can really tell the difference between OA and RA.I have heard of so many people that are told they have RA, to later be told it's OA. My arthritis symptoms have changed somewhat and are affecting other areas of my body and I don't know whether to bother mentioning
Soreallover
in
Arthritis Action
11 months ago
My Fibro specialist appointment - gut health
I posted last week about having an appointment with a pharmacist. My appointment was this morning and it was actually with a chronic pain specialist in fibromyalgia. He was really kind and listened to my history going back to migraines in primary school. He talked about genetic predisposition for my
I posted last week about having an appointment with a pharmacist. My appointment was this morning and it was actually with a chronic pain specialist in fibromyalgia. He was really kind and listened to my history going back to migraines in primary school. He talked about genetic predisposition for my
Brigga
in
Fibromyalgia Action UK
11 months ago
A-fib and low BP in a bent position
Hi - I am in persistent a-fib and in reasonable health. When I exert myself in a bent over position I get unusually short of breath (it escalates much quicker than seems in proportion to what I am doing) and often when I stand up I feel vertigo / loss of balance / loss of orientation. The loss of
Hi - I am in persistent a-fib and in reasonable health. When I exert myself in a bent over position I get unusually short of breath (it escalates much quicker than seems in proportion to what I am doing) and often when I stand up I feel vertigo / loss of balance / loss of orientation. The loss of
Jonathan_C
in
Atrial Fibrillation Support
11 months ago
Plantar fasciitis
I might have yet another inflammatory condition: sudden agonising heel and sole of foot pain. I think I've been ignoring it, but boy is it in the fore front of my mind now! I'm seeing a physio tomorrow. My question: I'm not supposed to take NSAIDs, although I have taken a couple. Also Co Codamol.
I might have yet another inflammatory condition: sudden agonising heel and sole of foot pain. I think I've been ignoring it, but boy is it in the fore front of my mind now! I'm seeing a physio tomorrow. My question: I'm not supposed to take NSAIDs, although I have taken a couple. Also Co Codamol.
HelenDaisy
in
PMRGCAuk
11 months ago
psp remission ?
My mom is now 81, she was diagnosed in 2018 with psp. Most notably her symptoms were a 90 degree slant of her body to the right, tremors (she has a battery and a system in her skull to stop them), inability to write or speak legibly, she permanently uses a wheelchair, eyesight issues, and choking with
My mom is now 81, she was diagnosed in 2018 with psp. Most notably her symptoms were a 90 degree slant of her body to the right, tremors (she has a battery and a system in her skull to stop them), inability to write or speak legibly, she permanently uses a wheelchair, eyesight issues, and choking with
Aljosh2013
in
PSP Association
11 months ago
Pain control
I’m just over a year down the line after my 2nd ablation and my quality of life is much improved with only 2 short episodes of AF . About 8 weeks ago I felt a sharp pain in my back which didn’t improve with rest so after having 3 physio appointments with no improvement and feeling a burning pain in
I’m just over a year down the line after my 2nd ablation and my quality of life is much improved with only 2 short episodes of AF . About 8 weeks ago I felt a sharp pain in my back which didn’t improve with rest so after having 3 physio appointments with no improvement and feeling a burning pain in
Hammerboy
in
AF Association
11 months ago
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