Hi all , I hope everyone is doing ok.
Just a question regarding what my GP said.
I have Fybro, arthritis in my spine , had a hip replacement at 46, need a crutch or walking stick on good days , have plantar fascitis, PTSD and other forms of physical restrictions. Recent diagnosis of severe restrictive sleep apnoea, which is causing daytime hypoxia with severe exhaustion. (Waiting treatment)On top of Fybro fog and widespread pain.
My Gp filled out a form asked for by the lovely supportive and positive people (tongue in cheek) of the DWP.
The question asks.
Is the patient able to attend and assessment by using public transport, ie bus or taxi.
He ticked YES.
I was referred by the same Gp recently to a specialist service for PTSD counciling. There is a waiting list and I've been told 9 months at the least. The GP is not aware of why I have PTSD not do I intend to tell them because he's not trained to deal with it hence the referral for specialist care.
Given all the above I want to know people's thoughts regarding it because I get really triggered and overwhelming psychological distress thinking it might me my mental health thinking is there something wrong with my thought process.
How can a GP given all of the above information even consider that I am able to leave the house never mind embark on a journey on Public transport. I don't even go to see the Gp alone and it's only 3 miles away.
Thoughts please and advice regarding addressing this issue that's now on my medical records.
Many thanks for reading sorry it's a bit long.