Experiences with

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

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!

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

Physiotherapy saved my life

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.

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

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?

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.

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.

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....... ...........

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 ?.

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.

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.

I’ve had so much physiotherapy hasn’t really helped with pain.

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.

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

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 😣

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.

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 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