Forrest * 0 Posted December 14, 2017 Share Posted December 14, 2017 Hi having read other topics with interest and seen the knowledge some of you have, I am asking for information. I have read the topic about IHR for fibromyalgia and the issue of permanence. My diagnosis is ME / CFS. I have been told that I am being sent down the ill health retirement route and so am keen to learn of any others with this illness, serving or retired. What happened to them? What additional evidence might I need to get from doctors for my IHR process? Frustrations are building and I could do without any additional stress to try and keep my illness stable. Thanks Link to comment Share on other sites More sharing options...
Stix * 0 Posted March 3, 2018 Share Posted March 3, 2018 Hi Forrest, I have been through the IHR process once already with a diagnosis of ME/CFS, it failed. It was a long and drawn out process that centred around the issue of permanence, the diability was agreed early on. To be brief, it failed as they felt that despite all of the CBT that i had, had i didn't have enough and that despite medical evidence stating that i wasn't suitable for GET, i had to do it as it would 'make me better in six months'! The process is incredibly corrupt and they will use any excuse to not grant it, you really do have to cover every angle in order to put them into a corner where they literally have nowhere to go but to say yes. I have now done more CBT and completed a course in GET, against my consultants advice and it has made me a lot more ill and a lot more disabled, angry is not the word right now! To cap it all, my Force have put me on Stage 2 UPP and are giving another action plan that i cannot achieve. I honestly am at the end of my tether and beign pushed into a very dark place, i honestly don't know what to do to get them to actually help me. If you or anyone else has any idea or know's anyone who can help with disability discrimination, i'd be really happy to hear from you. I wish you luck with you application, just pelase consider the above and get advice from the ME Association, they are really good with advising what can possibly help. Cheers....Stix. Link to comment Share on other sites More sharing options...
Recommended Posts
Create an account or sign in to comment
You need to be a member in order to leave a comment
Create an account
Sign up for a new account in our community. It's easy!
Register a new accountSign in
Already have an account? Sign in here.
Sign In Now