Recently I wrote to our local MP to highlight the current situation with PIP applications. i wanted him to look into this, possibly raise my concerns with other ministers, and approach ATOS with a query as to why I and so many others have been waiting months and months before our application is even looked at.
He was very kind and wrote to me straightaway promising to raise the issue and to make an enquiry for me. Within a week i had another letter with a letter from ATOS enclosed apologising for the delay in my application and promising to write to my Drs for information straight awa! WOW....good work local MP! TWO DAYS later I had a letter from the surgery saying they had received a request to access my records from ATOS!
So for all you people out there waiting patiently, try your own MPS to see if they will help. I cant say that the wait wont be long after the assessment, but i will just ask my MP again.
Just a couple of things more to add on this subject. I went to my GP last week for three things: to update and make accurate my medical records, to look at my medication and discuss my lymphodema and to ask for support in my application for PIP. When it came to the latter i was TOTALLY SHOCKED at my GPs response.
This is word for word what she said when I told her I had made an application, and written to my MP. "I don't approve of PIP. As a taxpayer, why should I pay for other people to have time off sick?"
What do you think of that then?!!!!
I was so shocked I couldn't speak. I tried to mumble that I wasn't off work sick, I had reduced my hours (in actual fact my manager is off for a couple of weeks so I am working every single day except Sunday for three weeks....needs must )....and she interrupted me to tell me in a very terse manner that a letter had been posted to me asking for my consent to release my records (you know....those ones which haven't been filled in properly, and scans, Xrays and requests for referrals are missing from). I have never claimed a penny in benefits and have worked for the NHS a good portion of my life.
I am really offended by her statement and what she is implying. (Just before this she had said regarding my swollen feet and legs, that the only solution was to put them higher than my head. Like i haven't tried to do that already. (She has been in trouble for her brusqueness and upsetting patients with her remarks before, and had to formally apologise on several occasions).
I despair of these GPS tbh. After finding out from my Neurosurgeon that I should have been on Lyrica as per his instruction to the GP three months ago, and my MRI wasn't missing at all, they just didn't request it, I am giving up dealing with them. I am changing surgeries, BEFORE I consent to my records being released. I am making an appointment with a new Dr from a new surgery and explaining my difficulties to them. A new broom sweeps clean.
Just thought i would let you all know.
In other news....I am back in BED! Fabulous. sort of. Finding it very uncomfortable first thing in the morning, but it is definitely better than the "throne" on the settee. Have been taking Lyrica for a week now, so too soon to tell about that, but side effects are few so that's good. Was given Naproxen too....it's rubbish and didn't work so i'm not bothering.
All thoughts on these issues most welcome, hope everyone is doing ok and finding some happiness in each day. Z x