Royal United Hospital, Combe Park, Bath BA1 3NG, UK, ,
About Business
Bath Centre for Pain Services
Review
4.0
(5 Review)
5
4
4
0
3
0
2
0
1
1
Feb 12, 2016
May 20, 2018
Oct 30, 2017
Outstanding medical facility
Apr 20, 2015
This is where my life changed for the best. Met great Drs but for the month I stayed here I learnt how to live with my pain, More important though we're the other people on the course with me, going through the same things in life.
I met the most fantastic people that soon became very close friends. Jane, Aileen, Irene, Joy, Tracey, Barry and Kevin. Love and miss them all xxxx
Jan 03, 2023
I went here when I was 13 for "Chronic Pain Syndrome". Got told by a leading EDS specialist I didn't have Ehlers-Danlos. However, I have a positive family history, and enough clinical signs for diagnosis. I have a diagnosis at 17.
The idea of paediatric physiotherapy was to make a suicidal 13 year old (I was being beaten up every day at shcool) crawl around and make animal noises. My pain actually got WORSE after going here and due to stress eating I gained 5kg.
I was denied medicines and services after discharge as they were apparently still part of my medical team when i asked for them to be removed as aresult of the terrible care.
If I had had the EDS diagnosis when I went, I would have been saved a lot of bad incidents when I was 13-17.
Food was good though. Otherwise I'd try and work out how to give 0 stars.
Monday: 8:30 AM – 4:30 AM Tuesday: 8:30 AM – 4:30 AM Wednesday: 8:30 AM – 4:30 AM Thursday: 8:30 AM – 4:30 AM Friday: 8:30 AM – 4:30 AM Saturday: Closed Sunday: Closed
Outstanding medical facility
This is where my life changed for the best. Met great Drs but for the month I stayed here I learnt how to live with my pain, More important though we're the other people on the course with me, going through the same things in life. I met the most fantastic people that soon became very close friends. Jane, Aileen, Irene, Joy, Tracey, Barry and Kevin. Love and miss them all xxxx
I went here when I was 13 for "Chronic Pain Syndrome". Got told by a leading EDS specialist I didn't have Ehlers-Danlos. However, I have a positive family history, and enough clinical signs for diagnosis. I have a diagnosis at 17. The idea of paediatric physiotherapy was to make a suicidal 13 year old (I was being beaten up every day at shcool) crawl around and make animal noises. My pain actually got WORSE after going here and due to stress eating I gained 5kg. I was denied medicines and services after discharge as they were apparently still part of my medical team when i asked for them to be removed as aresult of the terrible care. If I had had the EDS diagnosis when I went, I would have been saved a lot of bad incidents when I was 13-17. Food was good though. Otherwise I'd try and work out how to give 0 stars.