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Physiotherapy
Hi All - reading many of you posts I do feel fortunate that my PRD is fairly mild. I finished treatment in September 2020. I have mild nausea, tender abdomen, a lot of wind, gel discharge and occasional uncontrollable bm. I told my Oncologist I am most anxious about bm so he has referred me to a
Hi All - reading many of you posts I do feel fortunate that my PRD is fairly mild. I finished treatment in September 2020. I have mild nausea, tender abdomen, a lot of wind, gel discharge and occasional uncontrollable bm. I told my Oncologist I am most anxious about bm so he has referred me to a
Triumph-Girl
in
Pelvic Radiation Disease Association
Have you ever had Physiotherapy for endometriosis?
I am researching
Physiotherapy
post laparoscopy or just helping symptoms. Please comment if you have ever had any
Physiotherapy
or post op or to help with conditions. I writing a paper on it and would love to change the rehabilitation and condition management!
I am researching
Physiotherapy
post laparoscopy or just helping symptoms. Please comment if you have ever had any
Physiotherapy
or post op or to help with conditions. I writing a paper on it and would love to change the rehabilitation and condition management!
Runner92
in
Endometriosis UK
Physiotherapy and hydrotherapy questions
hi I have been diagnosed with fibromyalgia since March time it has taken 15 months to get this diagnosed with a rheumatologist. Anyway, I wanted to put this question out there and ask if anyone has had physio for this and do you have to get referred by a doctor and does anyone know if you can get hydrotherapy
hi I have been diagnosed with fibromyalgia since March time it has taken 15 months to get this diagnosed with a rheumatologist. Anyway, I wanted to put this question out there and ask if anyone has had physio for this and do you have to get referred by a doctor and does anyone know if you can get hydrotherapy
fibrogirl41
in
Fibromyalgia Action UK
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Looking to connect with male adult particular 40 plus guys for emotional support
Physiotherapy
saved my life
Physiotherapy
saved my life
Mohammad-341
in
Anxiety and Depression Support
Spinal Stenosis
I was diagnosed with this condition almost 3 years ago and initially advised to consider surgery (not urgent) which looking at the details, was for me quite scary, so with some
physiotherapy
and occasional paracetamol help, I am coping.
I was diagnosed with this condition almost 3 years ago and initially advised to consider surgery (not urgent) which looking at the details, was for me quite scary, so with some
physiotherapy
and occasional paracetamol help, I am coping.
Davidpeaty
in
AF Association
Occupational therapist
My hip slightly better doing
physiotherapy
but gp said it's going to take some time to heal I'm struggling getting over bath into shower any feed back be appreciated
My hip slightly better doing
physiotherapy
but gp said it's going to take some time to heal I'm struggling getting over bath into shower any feed back be appreciated
Betsy50
in
Pain Concern
IT band syndrome!!
As I was just about to start a 50 mile challenge throughout May to raise money for Samaritans I end up with an IT band injury that requires
physiotherapy
! Such good timing! Anyone got any words of advice of how to keep up my fitness so I don't fall back with my running?
As I was just about to start a 50 mile challenge throughout May to raise money for Samaritans I end up with an IT band injury that requires
physiotherapy
! Such good timing! Anyone got any words of advice of how to keep up my fitness so I don't fall back with my running?
Skiddle1
Graduate10
in
Bridge to 10K
Recommended Rheumatologist in London to confirm diagnosis
I've been diagnosed with RA by one rheumotologist and prescribed hydroxychloroquine immediately but the second one said he didn't think I had it and should stop medication for at least one month and just do
physiotherapy
.
I've been diagnosed with RA by one rheumotologist and prescribed hydroxychloroquine immediately but the second one said he didn't think I had it and should stop medication for at least one month and just do
physiotherapy
.
AAMum
in
NRAS
NHS Physio appointment
Rheumatology gave me an urgent referral to
Physiotherapy
. They dealt with it fast. I had a phone consultation with a lovely chap this morning. He can see some muscular skeletal issues on my MRI that he may be able to help me with. I have my first face to face in 2 weeks.
Rheumatology gave me an urgent referral to
Physiotherapy
. They dealt with it fast. I had a phone consultation with a lovely chap this morning. He can see some muscular skeletal issues on my MRI that he may be able to help me with. I have my first face to face in 2 weeks.
Seacat30
in
PMRGCAuk
Stuffed but working on it.
Polymyalgia Rheumatica Treatments MOST EFFECTIVE #1 Panafcort (Brand names: Panafcort) Prednisone Drug | 1332 reports #2 Prednisolone (Category: drug) Drug | 524 reports #3 Methotrexate injection Methotrexate Drug | 236 reports #4
Physiotherapy
Physical therapy | 113 reports....... ...........
Polymyalgia Rheumatica Treatments MOST EFFECTIVE #1 Panafcort (Brand names: Panafcort) Prednisone Drug | 1332 reports #2 Prednisolone (Category: drug) Drug | 524 reports #3 Methotrexate injection Methotrexate Drug | 236 reports #4
Physiotherapy
Physical therapy | 113 reports....... ...........
ignatz
in
PMRGCAuk
Pcd and parents
Since then, with inhalations and
physiotherapy
, she is much better. Still, I keep thinking she's sick. I can't accept that she really has PCD. How do other parents live with it ?.
Since then, with inhalations and
physiotherapy
, she is much better. Still, I keep thinking she's sick. I can't accept that she really has PCD. How do other parents live with it ?.
Olja
in
PCD Family Support Group (UK)
Vestibular pysio
Strange as seemingly back to 2018 as started vestibular
physiotherapy
again. 3 neurologists could not agree. I had a very bad fall hitting my head hard . Only thing that showed on z blood test was very low b12.
Strange as seemingly back to 2018 as started vestibular
physiotherapy
again. 3 neurologists could not agree. I had a very bad fall hitting my head hard . Only thing that showed on z blood test was very low b12.
Nackapan
in
Headway
Road block
Physiotherapy
to improve walking, might do that when the pension allows. Levodopa has stopped working after only 3 months, I was only allowed minimum dose, so the much hated jerking has returned, plus the weird walking. No suggestion how to improve slow speech or loss of fine motor skills.
Physiotherapy
to improve walking, might do that when the pension allows. Levodopa has stopped working after only 3 months, I was only allowed minimum dose, so the much hated jerking has returned, plus the weird walking. No suggestion how to improve slow speech or loss of fine motor skills.
MONIREN
in
Functional Neurological Disorder - FND Hope
Ankylosing spondylitis? What happens next?
I’ve had so much
physiotherapy
hasn’t really helped with pain.
I’ve had so much
physiotherapy
hasn’t really helped with pain.
Beau2016
in
NRAS
pain after sleeping
After months of
physiotherapy
and doctors visits I have been tentatively diagnosed with a trapped [pinched] nerve somewhere in my lower spine[ MRI scan 16 weeks wait to confirm] I am now taking Gabpentine300. but I don't know that it is doing any good, The big problem is Sleep, or the lack of it.
After months of
physiotherapy
and doctors visits I have been tentatively diagnosed with a trapped [pinched] nerve somewhere in my lower spine[ MRI scan 16 weeks wait to confirm] I am now taking Gabpentine300. but I don't know that it is doing any good, The big problem is Sleep, or the lack of it.
lubarr
in
Pain Concern
Right shoulder pain
Accessing
physiotherapy
treatment. I feel since I turn 40 my my pain has gotten worse. In addition I have Fibromyalgia. How are people dealing with shoulder pain x
Accessing
physiotherapy
treatment. I feel since I turn 40 my my pain has gotten worse. In addition I have Fibromyalgia. How are people dealing with shoulder pain x
Acocoa
in
Pain Concern
Feeling lost
I really feel like I’m being fobbed off and being referred for
physiotherapy
and an MRI scan may be needed if things don’t improve. Has anyone else been through this or is in a similar situation? My only symptoms are lower back pain and leg pain 😣
I really feel like I’m being fobbed off and being referred for
physiotherapy
and an MRI scan may be needed if things don’t improve. Has anyone else been through this or is in a similar situation? My only symptoms are lower back pain and leg pain 😣
Amy8970
in
Endometriosis UK
Pcd rsph4a compound heterozygosity
We do inhalations and
physiotherapy
. Tympanogram type As, but does not speak well. She had frequent respiratory infections, a wet cough, a diagnosis of non-allergic asthma. Sorry, my English is not good. Thank you in advance everyone.
We do inhalations and
physiotherapy
. Tympanogram type As, but does not speak well. She had frequent respiratory infections, a wet cough, a diagnosis of non-allergic asthma. Sorry, my English is not good. Thank you in advance everyone.
Olja
in
PCD Family Support Group (UK)
New here. I experienced two moments without tinnitus after 2 months
I'm trying to understand what happened...whether it was food, medicine,
physiotherapy
, acupuncture, peace, prayer, exercise. I'm looking for explanations. I had COVID in March 2021. I got vaccinated in May 2021. I took an area trip in June 2021 and I got tinnitus in July 2021.
I'm trying to understand what happened...whether it was food, medicine,
physiotherapy
, acupuncture, peace, prayer, exercise. I'm looking for explanations. I had COVID in March 2021. I got vaccinated in May 2021. I took an area trip in June 2021 and I got tinnitus in July 2021.
Overloq
in
British Tinnitus Association
aiming for diagnosis
I just had my appointment and they have said it could be fibro but because that diagnosis comes from the exclusion of others they cant be sure its not just intermittent yet, so im being referred back to msk for
physiotherapy
and ‘pain management’ as she found some hyper mobility in my joints, doesnt
I just had my appointment and they have said it could be fibro but because that diagnosis comes from the exclusion of others they cant be sure its not just intermittent yet, so im being referred back to msk for
physiotherapy
and ‘pain management’ as she found some hyper mobility in my joints, doesnt
aprilj15
in
Fibromyalgia Action UK
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