Hey all - please forgive the username, privacy and that.
I’m looking for some advice on structuring my MR letter, I was hoping someone could help.
I applied for PIP on the grounds of the following:
1) Generalised joint/muscular pain
2) Multiple MH issues - originally diagnosed as anxiety/depression, further investigation led to discussions on OCD and later still ADHD (diagnoses as of this last month!)
After a bit of a battle that involves Capita LOSING MY REPORT for my original video call assessment and rescheduling it for a telephone assessment a month later and not informing anyone (me or DWP) that it had been lost until I contracted them myself, I finally have received my report and decision and, in a turn of events that shouldn’t really have surprised me, I was awarded a grand total of 4 points.
The reasoning behind awarding me 0 points on each question were one or more of the following:
1) I own and can drive a manual car
2) I work 32 hours a week
3) I don’t have a prescription for pain medication/take regular high amounts of pain medication
4) I didn’t have official diagnoses other than the anxiety/depression
In each question, it appears than pulling this gotcha to award me 0 points if possible was the goal. If there were any issues with dexterity/mobility, they called on 1, any issues with motivation they called on 2, any issues with pain they called on 3, and any mention of OCD/ADHD they called on 4. However, I have entirely valid reasons as to why these issues do not constitute reasons to award 0 points.
1) I am physically able to drive, yes, but I made it clear in the assessment (and this is noted in the report) that at most I can drive on my own is a ten minute drive to my mothers house, following a specific, quieter, less direct route. This is due to severe anxiety around driving, meaning I cannot drive a route I do not know without someone else in the car. Panic attacks aren’t fun on the road. Also, whereas I can physically drive, it does cause me pain, so I can’t drive for extended periods. Plus, the activity involved in driving, although difficult, isn’t the type of activity that causes me my main issues (namely, repetitive motions especially in my wrists causing severe pain and swelling, and pain and fatigue from supporting my own body weight).
2) I work 32 hours a week, because if I didn’t I wouldn’t be able to pay my bills. This does not, however, mean that I find my work easy. In the two years since I’ve worked my home based contact centre role, I’ve had 2 occupational health reviews (the first of which resulted in a reasonable adjustment of adapted shift patterns, the second is ongoing and delayed due to my sick period), multiple instances of sick, one lasting six weeks and one that I’m currently on that is likely to last considerably longer, I’ve nearly had a disciplinary review due to poor performance and realistically I am only able to work the hours I do because the company is (mostly) incredibly supportive of my disabilities and because I have had to due to necessity.
3) I don’t have a prescription for pain medication because I had tried many, and nothing has helped with the pain. This has lead to me forgoing pain medication as I am quite frankly scared of what taking high doses of pain medication will do to my body long term especially if they don’t work. I am also incredibly reluctant to take an opiate painkiller, as I am predisposed to addiction and I do not need to add an opiate addiction to my life.
4) This is the fun one - although I was in discussions with GPs and MH nurses for years regarding my OCD symptoms, it looks like this was never recorded on my medical history, and was always listed as Anxiety/Depression. At one point, a MH nurse I was receiving help from (she was honestly) advised me that there would be limited use in going for a psychiatric assessment to log OCD as an issue because the treatment I would be offered she could offer me anyway, and I wouldn’t have to wait the huge waiting period for a psych evaluation. Probably not the best move looking back but it made sense at the time, as I downplayed my own issues and didn’t see myself as qualifying for support for it anyway.
I have recently however had an ADHD assessment, after which I was diagnosed with:
Adult ADHD
Mixed anxiety and depressive disorder
Traits of PTSD
After being on SSRIs for ~12 years and eventually realising they were doing more harm than good, I’ve now been put on ADHD medication, which I’m in my second week of. The fun bit is that due to waiting times, the ADHD assessment and the SECOND Capita assessment landed on the same day, with the PIP assessment first. This also happened to be my dads birthday, who died last year due to alcoholism (hence the opiate fear) so safe to say I wasn’t in the best of moods on the day. This would obviously mean that the PIP assessor didn’t have access to this medical information as I wasn’t able to mail a copy off until a week later when I was able to pick up the letter with the diagnoses. This would have arrived this last Tuesday, and I received the big old ‘Nah Fam’ from DWP today (Saturday) so the timeline would mean that they wouldn’t have received this before making the decision.
The pain issues are difficult to verify too, as for years I have kinda been palmed off about them, even though I was having X-rays and bloods done for them before my anxiety manifested originally (~13 years ago). I’m finally seeing a rheumatologist and so far we still don’t know what the issue is even after an MRI. The rheumatologist has provided a letter to the effect of ‘yes, there’s something wrong, no we don’t know what it is yet, give pip plz’. I initially gave the information in the letter over the phone and was advised I didn’t need to send a copy, until I called to provide the information about the ADHD diagnoses and was told actually, yes, plz send. So this letter also didn’t arrive until after the decision would have been made. Although both these letters would have been noted on my file (I was explicitly told they were) it doesn’t appear either were taken into account in any way judging by the wording of the response.
Anyway, sorry for the life story - my main questions really are:
1) Would providing the above information relating to my ‘disqualifications’ be beneficial in any way? The information I’ve seen about the MR letter I need to write seems to boil down to ‘look at the criteria, explain why the decision made is incorrect, explain why you believe you should have been given a different answer’ which seems pretty straightforward but I am concerned that this information will just be disregarded again like it was in the original assessment.
2) If I go for an MR now, and insist they look at the supporting evidence I sent after the assessment, would the fact that they now have this information realistically change anything?
3) I mixed up/forgot to include some of the above information in the assessment, as I was in a pit of grief, on four hours sleep, and angry and miserable that I had to go through the assessment process again (but I was ‘articulate’ apparently) - if I include this extra information will this be held against me due to the fact that it would differ to what is written in the assessment?
4) Should I request any further information from medical professionals to support the above? If so, what should I look for? My GP isn’t going to be able to confirm that I barely ever drive, for example, so I don’t know what extra information I can realistically give here.
Thanks for reading all this - sorry it’s so long. It’s just become very apparent that I probably did the assessment ‘wrong’ and I want to make sure I get the MR right as much as I can.