Hi everyone
I’m a newbie here who is looking for some advice.
I was recently diagnosed with RRMS which is having a negative impact on my day to day life. Both myself and my partner think it would be best to reduce my hours at work to focus on my health a bit more. I currently work full time 35 hours a week over 5 days. Ideally I would like to work 21 hours over 3 days, which my employer has agreed I can do if I need to.
The catch is that in order for me to reduce my hours I would need my critical illness cover to pay out to make the financial side of life easier. The cover was taken out through my employee benefits (I work for a high street bank) and no medical questionaire was required before the cover began.
I submitted a claim and have received a letter from them today rejecting my claim on the basis that a few years before I took out the cover I was referred to a Neurologist due to my migraine headaches/tingling in finger tips. A cervical spine MRI was carried out to check for a trapped nerve. Nothing was found on the scan and the Neuro didn’t take his investigations any further. I was referred back to my GP who prescribed migralieve tablets and I was sent on my merry way.
My ciritcal illness cover has therefore decided that this was probably my first sign of MS and the Neuro should have known this!!? They are therefore not willing to pay out as I probably had MS before the cover was taken out (the cover began last year).
How was I supposed to know I had MS if no-one told me and also why should I lose out because the Neuro I saw was either incompetent or didn’t think MS was a possibility?!!
In addition, I don’t see how they can reject a claim on previous medical history if they didn’t even bother to question it before the cover was taken out.
Has anyone on here had a similar experience or can anyone give me any advice/opinions in relation to this matter.
It has really knocked me for six today. I thought I had protected myself and my family by taking out critical illness and now I don’t know how we will carry on financially. It feels as though I will have to either compromise my families standard of living or my health.
It just doesn’t seem fair.