- #myDLA NEVER pays for my bungee-jumping holidays because I have never slept anywhere other than MY bed for the past 12 years.
“#myDLA pays for new mattresses, pillows, bedding, night clothes that get soiled when I am sick or accidentally incontinent.
“This year I bought £300 of Ice Melt, I live in an ungritted cul-de-sac then told ALL #myDLA and motability car will cease 6th Dec '11/- “#myDLA without it I couldn't get out, couldn't afford the equipment I need and would be completely bed ridden. #wearen'tallscroungers
- “Remember that you can't know that you might not be disabled in the future. I'm sure you would want respect & dignity. DLA is vital. #myDLA
- “#myDLA is what helps me to live more independently. Without it I would be more reliant on others for help
- “#myDLA pays for mobile phones so I am in constant contact with my carer, if I fall or run out of water I can call for help
- “#myDLA means I can put the heating on BEFORE it's so cold I have headache, two winters ago that's how it was. Cold makes my condition worse!
- “#myDLA never had a Dr assesment but have had 3 tribunals, can't walk without another person, can't transfer, had to appeal to get MRC
- “#myDLA - the only thing preventing complete financial dependency on partner or family. What price dignity?
- “When contribution based ESA is time limited DLA will be the only personal income some disabled people have. #myDLA
- “I've got to fill in another ltd cap 4 work form. Its making me feel like hitting the bottle or suicide #MyDLA.
- “I suffer with/from depression & its getting harder to cope from day to day. Its getting more difficult to think of waking up anymore #MyDLA
- “I live in a residential home and #myDLA is only paid when I'm at home with my mum at weekends, my needs don't go away during the week though
- “@Bubblejet #myDLA goes towards my heating and lighting bills amongst other things. It helps me,you and others survive.
- “@Quinonostante I was lucky, my 3rd form & I got indefinite. With changes I think we'll all have to 'prove' ourselves frequently #myDLA
- “#myDLA - how humiliating and distressing it is to detail just how pathetic you health problem makes you and how crap it makes your life.
- “A 50 page form to explain how you poo, wee, sleep, walk, eat, sleep & then possible medical, yes, that's an easy way out isn't it? #myDLA
- “I could use the extra money from #myDLA to go out now and again and eat properly. But claiming makes me too suicidal to be worthwhile.
- “I have serious, long term psychiatric problems. I don't claim #myDLA because the application process is too damaging to my health.
- “And while I'm at it, #myDLA pays for a Motability vehicle that allows me to stay in work. We are not scroungers or cheats.
- “#myDLA was awarded without an assessment because MS is progressive and currently incurable. #rapidlyevolvingsevereRRMS
- “@Tanni_GT #myDLA means I can eat real food, despite problems preparing it, and get cabs or similar on journeys most would walk
“@Rachela53 I'm trying not to think about what's going to happen if I lose #myDLA it's too worrying :(
Spartacus Stories
Here is a collection of Stories written by many different disabled people about the impact that DLA has on their lives. It also includes stories of fear about the proposed changes to personal independence payment.
Admin: benefitscroungingscum, Lucia and Lucy
to add your story email us at spartacusstories @ g mail . com (without the spaces) (your posts are there, just being scheduled throughout the day) (can you add how you want your 'name' to appear ta)
Admin: benefitscroungingscum, Lucia and Lucy
to add your story email us at spartacusstories @ g mail . com (without the spaces) (your posts are there, just being scheduled throughout the day) (can you add how you want your 'name' to appear ta)
Monday, 16 January 2012
#spartacusstories and #myDLA - how DLA helps 2 - #spartacusreport
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