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Sarah's avatar

How interesting. I have an MSc in this stuff (sort of - my MSc is in Food Policy and I wrote my dissertation on UK household food insecurity) but I never really thought about how "deprivation" might affect me. I'm enormously privileged. I attended a fee paying school, and had the means to do three university degrees (the first two were Political Science and Law). I ended up working in local government like the bleeding heart liberal I actually am, not the cut throat lawyer my parents wanted me to be.

I was living in one of the most deprived LSOAs in the country at disease onset. A large, notorious council estate. It was close to work and uni and the rent was at a level that enabled me to save some money towards a deposit. Then I used that deposit to buy a flat in another slightly less deprived area, still as close as I could afford to my central London job. My parents ended up giving me the rest of my deposit.

I've since moved within the same area as I absolutely love it. I have close friends nearby. It is a "rapidly gentrifying" area and my friends are all mid-career professionals who also own their own homes.

Where I live now I'm the only owner-occupier. I'm in a two bed ground floor Victorian conversion. My upstairs neighbours are private tenants. The houses on either side have been converted into HMOs. I couldn't tell you how many people live there but they are seriously overcrowded.

The area is grimy. But I'm very involved in my local community. I have not been offered social prescribing but I imagine I do the very things they would recommend - I am a Run Director at my local parkrun and I volunteer with GoodGym. I keep trying to persuade my local GP surgery to become a "parkrun practice" but I don't think the doctors are that sold on running. It is a very good practice though.

Anyway I'm off to volunteer at parkrun now in my beautiful local park - another thing my area does very well.

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Jill Pack's avatar

So important to raise this now as disabled people's social security incomes are being attacked in the UK (and the notion of social 'security' is being undermined). This research should be required reading for the Labour government that is proposing savage cuts to those in receipt of Personal Independence Payments (PIP). I saw figures the other day that indicated that those with MS who have struggled to receive this benefit (it is very hard to claim) are among the most vulnerable to losing it with the proposed change of rules. This will plunge many thousands into poverty with dire consequences not just for individuals but for the health of our society. Write to your MP to oppose these cruel cuts.

I have MS but I am so lucky as I am comfortably off - I know I would be more disabled without access to, for example, good nutrition and a warm home. I don't have to live with the daily stress of living on a low income, we all know that stress impacts our symptoms.

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