- #myDLA My fight to change the law for students goes on. Please visit mad4mel.co.uk Protect those who need it! #Freudwerenotallfrauds
“#myDLA My fight to change the law for students goes on. Please visit mad4mel.co.uk Protect those who need it! #Freudwerenotallfrauds- “My son went through a 15 month assessment process which was highly stressful for him before being diagnosed with #autism for #myDLA
- “After one assessment, the assessor wrote down the wrong distance I could walk & #myDLA was stopped. It took a year of appeals to reinstate..
- “#myDLA My condition is progressive and won't get better. I Paid NI & tax when I worked so DLA is NOT FREE! Took me 18 months to get it after
- “#myDLA for Nate is not 'just because I filled out a form' but because he is at risk of sudden death and requires overnight home ventilation
- “Ignore tabloid lies like today's Daily Mail and read the #myDLA hashtag for real picture: DLA is about independence not benefit scrounging
- “I have a genetic inherited progressive incurable neuromuscular disease #myDLA the clue is in the diagnosis waste of money retesting
- “independence can be reading your own post,cooking a meal unaided etc,though this govt want to penalise independent disabled,shameful #myDLA
- “my dla helps with transport,communication &technology costs. i'm blind, dla keeps me independent.we don't all have helpers on tap #myDLA tbc
- “#myDLA was awarded 23 yrs ago without a medical because I have a progressive genetic condition that will in all likelihood be the end of me.
- “#MyDLA was awarded 2 me after 9 months of applying-appealing & going 2 tribunal even though i've had some conditions since birth.
- “I was turned down first app for #myDLA awarded on appeal I have progressive MS wouldn't be mobile without it - lets me have a life + a job
- “#myDLA My Aspie daughter's DLA was supported by a paediatrician, psychiatrist & her GP. Who else is she supposed to see?
- “#myDLA Application form v intrusive and stressful. In tears over it. Mental stress knocked me out for days. MS won't go away. Fear DLA will.
- “#myDLA Awarded 12yrs ago. Help with form from SocServ Link Worker. Wld be w/out transport w/out DLA. V rural, no public transport. Have MS.
- “#myDLA isn't mine, it's my sisters - means she can live an amazingly independent life as part of a Garvald community rather than be in care
- “I had to fight for years to get #myDLA even though I've had a progressive autoimmune condition since aged 3.
- “#myDLA I had to fight for DLA lasting more than 2 yrs at a time despite having Progressive MS. I still only re… (cont)deck.ly/~pyYwm
- “Like many people, transport costs, care costs, extra other costs. It doesn't cover it all but is necessary help. #DLA #myDLA
- “#mydla I won't say why my wife has DLA but without it we would be living in a cardboard box. It has been a godsend though its still not engh
- “#myDLA My Son grew from an autistic child into an autistic adult. That how these incurable things work you see. DLA allows him independence.
- “#myDLA was *refused* without an atos medical - and then reinstated at appeal, still without an atos medical.
- “#myDLA awarded because of evidence on my forms from my NHS and social services professionals. Why should they need atos medical as well?
Monday, 16 January 2012
#spartacusstories and #myDLA - how DLA helps 10 - #spartacusreport
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