Can`t make my mind up if it is funny or too close to the truth to laugh at. sue
As the subject at the moment is attit... - Fibromyalgia Acti...
As the subject at the moment is attitudes to the disabled I thought I would post this.
![](https://images.hu-production.be/post/post_40e06240910743d98aaf45cac32b3b7c_635281552459732000.jpg)
Sunday satire sue Heehehehhehheh xx
Hi other I think a bit of both ,,I really do not understand why so many people with genuine illnesses or disableitys have such a hard time get the right benefits that states in black and white that they are inteitaled to them..why do people who have longterm illnesses or disabiltys get such a hard time getting them or they have to fight for everyfin or have to prove them selfs to people who havint the first I dear A about the illness B if u can cook a meal or put or own clothes on ..I find they hole thing from DLA to pip and they way people get treated for applying for it having to goto medicals or sit in front of people and b treated like a lier is shocking ...I no ther is people on these benefits and ther is not a thing wrong with them ...they should b gave. A Oscar xx
Thats exactly how My hubby and I felt when having to to tribunals.That we were on trial for some thing we had not done Hubby has 4 major illnesses 3 of which are life threatening. but was still found fit for work...sue
![amanda2277 profile image](https://images.hu-production.be/avatars/c1ae9f587eb8d6413a8b37fbedc4a261_small@2x_100x100.jpg)
Hi Maryrose I find that disgusting ..I hope yous both fright this all they way .have u been to your MP I wood take this to a lawyer its shocking ..I get really angry wen I hear story's like yours wen I c people and no of people who get thes benefits for a skin condistion or having accolostomy.. av worked with people who have thes condition and u wouldn't no they had them ...but others people out other and the bottom line is they should not be no DLA or PIP cause other nothing wrong with them when they can drink everyday go other own shopping ther not in any pain they take the systom for every penny they can get ITS wrong ..I really hope you both get this sorted out soon don't give up ..xx
I should have said that both times the tribunal found in his favour. The second time they gave Atos a reccomendation that he not be reasessed within 2 yrs and Atos still put him in the work support group. He went to job centre and they told him to go home and forget it That there was no way they were going to make him look for work. sue
.
Now that's a result xx
You're so right that's how we were made to feel too every time. It's ridiculous.
With respect to the toon it's meant to be satire and most definitely to me is ribbing ATOS more than us............. we already feel like that anyway so it would be a pointless joke if aimed in our direction!!
I used to know a few peeps back in the early 90's that would turn up at their assessments act terrified and cry a lot and deemed unfit for work whilst people who were sick had to go to tribunal which is why it's so hard today................ it's partially thanks to them!! The system has not changed same processes differing names!!
Rant over and apologies for said rant
xxx flufies on route to make up for it
It's both. Satire can be really hurtful to the prejudiced and they really deserve it. I wonder if I have the courage to send it to my MP
I've just failed Emma's PIP and ESA self tests.
There are people on these benefits where there is notHing wrong however I have been in both situation I have been diagnosed with fibro for 18 months but been suffering for. 3 years however 10 years ago I had a serious flare of my eczema my arms were covered from top to bottom covered in bandages everytime I moved they bled and the pain was unbearable so there are situations where skin conditions can stop you working I even ended up in hospital 70miles from home for weeks on end
Hi mayrose54
I sincerely hope that you and your husband are feeling as well as you can be today?
I think this picture is a statement of modern life, from the media to politics. If I were to contact my MP and show them this picture I would be simply wasting my time as I cannot change the mind of the politically afflicted, this is now making me wonder if they are the real disabled?
Al my hopes and dreams for you.
Ken x
Ouch! But where would we be without sense of humour?
I also think it's both....really funny though. I think we find it funny cos we can all see the irony in it!! XX
a modern day witch hunt and we're the witch's
Hi Sue I saw this a while back and honestly chuckled but at that time if it had been posted uproar would have occurred!!
And I agree it is very ambiguous
How are you doing, and how is Grandad coming along?
May fluffies on route to you filled with sunshine smiles
xxxsianxxx
Hi Zeb .I was very careful with the timeing I had had it on my pinterest site for months until the timeing seemed right and then was very careful with the wording. The last thing I wanted was a riot.
At the moment I don`t have the energy or the motivation to do much of anything but I am still working it out in my mind, actually I have a picture of a conservative MP on pinterest who has a very `interesting ` face that I may use as a model
Good luck with your group,wish I lived nearer. Hugs sue xxx
Aw thanks Sue I think we should have a rally day somewhere so that we could meet each other and also help FibroAction at the time
Sorry you're not so good at the mo a bit of R&R maybe
I'm with you on the energy and motivation issues too and I have hydro this aft then a train journey and a car journey I'll be wiped out and I need to be up and sorted for tomorrow
I'll be running on lucozade and adrenaline LOL
This illness has marvelous timing for being inconvenient!
Theres a basket of mixed fluffies filled with sunshine smiles for you
xxxsianxxx