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COVID restrictions are lifting but Pelvic Radiation Disease will keep many in ongoing lockdown | Guest Blog


COVID restrictions are lifting but Pelvic Radiation Disease will keep many in ongoing lockdown | Guest Blog


Each year, many of the 22,000 people treated with pelvic radiotherapy have debilitating side effects which can reduce their quality of life as a result of pelvic radiation disease (PRD). With correct treatment the quality of life of patients can be improved, bringing relief to thousands of patients and support is out there. The Pelvic Radiation Disease Association (PRDA) work to help those living with PRD and improve their day to day lives. Here they tell us about some of their initiatives and how they are able to help, especially given the restrictions of lockdown due to COVID-19.

"Following radiotherapy primarily for prostate, bowel, cervical and endometrial cancers, people can develop Pelvic Radiation Disease (PRD) which is a debilitating and complex group of long-lasting symptoms, including serious problems with bladder and bowel control, sexual health, fertility, mobility and related mental health problems.

People with PRD frequently experience problems such as needing frequent, urgent access to a toilet, chronic fatigue, pain, sleep disturbance and overall being unable to live a normal life. The knock-on effect on personal relationships and finances is often life-changing.

One of our trustees, who has also been a volunteer at the Pelvic Radiation Disease Association (PRDA) for over 10 years, has personal experience of the loneliness that both patients and partners can feel. “Many people have daily problems with bowel and bladder control, which makes leaving the house extremely problematic,” she explains. “People with PRD often plan and organise trips out based on precise knowledge of where accessible toilets are. But coronavirus has caused so many shops, cafes and public toilets to close or have long queues, and many people are left almost completely housebound which has just made their sense of isolation even worse.”

PRDA offers a free ‘Just Can’t Wait’ card which may help you to jump toilet queues, or gain access to toilets which are not normally open to the public.

Since April 2020, our volunteer has been phoning many people with PRD to find out how they are getting on.  As one of these people said “When I first found you, I felt waves of relief that there was hope, that I was not alone, you are the first person I have talked to in lockdown who understands”. PRDA is there to help people, and anyone with concerns our questions is very welcome to phone our helpline 01372 744338.

Having just launched its Online Community in June 2020, PRDA aims to provide support to many more people. Discussions on the Community so far include coping with lockdown, bowel incontinence treatment, and radiation-induced neuropathy.

Sarah is the Community administrator and is delighted to see the response so far. “People find it so hard to talk to family, friends or even their doctor about the embarrassing problems of PRD. Our Community forum is a great place for people to chat anonymously with others who are in a very similar situation. I have PRD myself and know what it’s like to feel isolated, confused and anxious. It really helps people feel less lonely if they can chat online, or phone our Helpline, and share experiences with someone who can probably help them to deal with an issue that they might think was unique to them.”