Experiences with

Physiotherapy

Hello everyone, So I've been having pelvic floor physiotherapy for an overly tight pelvic floor/vaginismus for about a month now and I have seen some improvement and less pain. But I was wondering how long it takes to see a bigger change?

Hello everyone, My Dr has suggested physiotherapy for me for my various pelvic floor issues (vulvodynia, vaginismus and potential levator ani syndrome) and I'd like to hear of any success stories anyone may have?

Hannah Beecham BSc Hons, MSc, MCSP, the Clinical Lead of the Pelvic Health team and an Advanced Physiotherapy Practitioner at the Royal Free London NHS Trust, will be speaking on how endometriosis can affect sex, services available for support, and top physiotherapy tips during lockdown.

I searched online for some solutions and came to know about in-home physiotherapy treatments( https://www.physiomobility.com/home-health-care/). I'm thinking about trying it as I hope it can reduce my pain. Has anyone tried in-home physiotherapy? Was it effective? Kindly share your opinions.

I m doing physiotherapy how can l get back to my full strength

Hi All, I just wondered, anyone who is diagnosed with liver issues - fatty liver, Fibrosis etc who has flank/back pain has benefited from Physiotherapy to help with pain relief?

I am awaiting physiotherapy but would like advice. Many thanks

I’ve tried acupuncture, pelvic floor physiotherapy, deep breathing exercises, yoga and pain killers but I still suffer with what has now become chronic pain in the muscles in and around the urethra, a constant urge to pee and my mental health has suffered greatly because of this.

Does anyone have any advice for my aunt (65) who has been learning disable since birth, she has broke her hip and had a hip replacement and will now look to rehabilitate with physiotherapy etc. My aunt has the mental capacity of a 7 yo, cannot absorb information, or follow instructions.

Once you or your loved one has returned home, many NHS trusts offer physiotherapy session for a period of time, these are designed to get you mobile again.

I was undergoing women's physiotherapy and have had psychosexual counselling, but due to Covid19 my treatment has been stopped- Huge shame. I'm so afraid of having a baby due to the pre natal invasive exams, insemination/conception, child birth itself and everything in between and beyond.

Even though we took her for physiotherapy treatment, there was no improvement. When we did an online search to find an alternate solution, we found this chiropractic centre that does chiropractic treatment https://www.oakvillechiropractic.com/chiropractic-centre-burlington .

Hello everyone, So over the last few months I've been having botox injections, pelvic floor physiotherapy and psychosexual counselling for a variety of pelvic pain issues (endometriosis, vaginismus, vulvodynia, hypertonic pelvic floor...)

MRI and checked with radiology doctor he said i have issue in pudendal nerve , he injected me by anesthesia but pain come again after one day only from procedure, I ask doctor he said we can turn it off the nerve and iron it , I'm afraid from this decision and I’m applying for one month back for physiotherapy

There is some evidence that training with immersive virtual reality and physiotherapy is a promising approach for ataxic gait and balance etc. Just to let you all know that because i m as thick as a brick and have the same IQ as a dead fish I’ve made some changes to my life.

In these difficult times we have been in Malta unable to return home to the UK, but are very happy with the health service we have received - what I would like to know is that I have been given by the physiotherapy a Philips respironics threshold IMT which I have been told to use for 5 mins twice a day

I have mainly asked for sensible physiotherapy because I know I won't get it through NHS. In fact, in the weeks before my diagnosis I was having physiotherapy and then as soon as I was diagnosed it stopped! WTF?

I am undergoing medical treatment with nerve conduction tests, physiotherapy and scans. I’ve also been given medication to take, Co-Codamaol, Pregabalin, Tramadol, Naproxen and more. As i have been on these medications since the injury occurred i believe i have become reliant on them.

My recovery has taken 3 months, not 3 weeks I was led to believe, and was quite painful (and I am quite tough) Ten excellent physiotherapy sessions later, my quads have built almost back to normal and I have completed two very nervous, very steady week 1 sessions.

I am currently doing physiotherapy which has been struggle. I am not sure what else I can do. So maybe seeking help from The London Lupus & Rheumatology Centre. The prices are insane. A new patient consultation is £240 and follow-up consultation is £215. Other tests could be £700 and upwards.