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Saturday, 31 March 2018

Spread The Word

Nothing much to say about easter eggs and bunnies and happy families . But as someone who has seen so many families and lives destroyed by the Government in their disability cull . Read this ...its not fake news , its not written by a biased press, its just someone who has to live without a future .
Spread the word , this is the reality of life today in the UK

https://write.as/9xj6wngoh5yyi

13 comments:

  1. Sorry, link does not work for me.

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  2. I appreciate you won't publish this comment.

    I have an adult son with very severe disabilities.

    I have worked as a volunteer helping people with disabilities and their families fill out forms for 25 yesra pluc.

    I have worked with the severely disabled for 25 years plus.

    EVERYBODY gets their correct benefits that they apply for. ALL OF THEM. This is not a coincidence this is a fact.

    This country gives VERY generous benefits to its very disabled and in 25 years I have never come across anyone who has not received them when correctly applied for, There have been occasions when parents with learning difficulties have needed support filling out forms correctly but they all got their benefits. I am talking about a base group of several hundred people over the 25 years.

    You post about your personal reality and claim it as the whole picture . It is not.

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    Replies
    1. Is your real name Ian Duncan Smith? Theresa May? Alas, you are delusional. And very, very rude.....

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    2. 25 years worth of facts is delusional ? And up to date working/living with and volunteering for the last 25 years. Living the 24/7 reality.

      No, love I am not delusional

      Nope. If people want to post their personal reality then great but don't claim its the whole picture cos its not.

      I'm on the frontline/coalface actually living the reality and also working with cos I care and want the best for those less able and volunteering because ..........again....I want to help those less able who perhaps have been scared by incorrect social media .

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    3. Lol. I suggest you re-read this lady's posts 'love'. Then re-read your patronising, un caring, big headed, know-all, judgemental, biased reply. If you want to actually help people and not just blow your own trumpet, help them. Don't post anonymous comments telling them that their life and experiences aren't the truth and that of thousands of others too, wake up!

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    4. I love the idea that the facts are somehow "biased " . Call me what you like but its the reality, which seems to really bother you.

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    5. Lol. Alas, your "reality" doesn't bother me in the slightest -your poor attitude to other folks problems is where you come unstuck.

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  3. The article is so right, we know.
    Briony
    x

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  4. We had the same thing happen to us,after 12 years,with my Hubbys health getting worse.I cant get the link..but i do read your blogs and we was going through the same thing.We have given up now.The stress was making my Hubby really ill and couldnt carry on.They make me so angry.xx

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  5. I,m so glad we have the safety net of NHS. We will never need to sell our homes or be turned away for healthcare. We all pay in to the pot. Admit there will always be those who can,t or won,t work who abuse the systemn. The i,m entitled and others will pay scenario makes me angry!. The NHS is full of the worried well looking for the magical diagnosis for benefits!. Ye gods a generation searching for sickness so others will pay for them!. They don,t and will not ever get it!.

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    Replies
    1. The Holby City Generation , theres so many things that cant be cured in 10 minutes , people have watched to much TV and think a magic wand can be waved and theyll be leaving the hospital hop skip and jumping in half an hour. Long term chronic health conditions can only be managed not cured

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  6. Well this is getting interesting !! now as most of you know i dont censor comments , I let you get on with it . But i must point out that the anonymous person who doesnt agree with me is also right in some ways , severe disability that is very visable is treated far better by the system , so are disabled children mainly i suspect because it would illicit bad press everyone gets their payments in the end , but it is currently taking them months and even years to sort their act out under the new system. Those whose disabilities are new and have applied under the ESA PIP new system have had horrendous problems and we are part of that reality it does not mean we are thick or stupid , it means we are being used as Lab Rats by the State to test drive the new system . The New System will work eventually correctly but it isnt doing now and the horror stories you read in the press are for the most part true

    ReplyDelete