I'm from the UK and all my children have disabilities and the hoops that have to be jumped through to get DLA (Disability living allowance) are so strict, that for anyone to believe they are handed out willy nilly have no clue. The fight I had to get my son the highest rate for mobility took appealing two rejections and on the third had to go in front of board. After I prepared a War and Peace size document, they called me to say it didn't need to go before the board, I was correct that by their own definition my child met all the criteria and was finally awarded what they were entitled too. The stress as a parent fighting for your child who cannot speak for themselves is not one any parent or individual should have to take on board. So many just accept their initial decision and don't appeal. But this mother was like a dog with a bone, I was not letting go and in the end they knew they would not be successful at a tribunal and didn't want to pay the costs involved, hence why I got a very apologetic phone call and awarded the highest rate for my child in both categories. For this woman... and I use the term loosely to weaponise disabled people for her own political gain is beyond vile! My eldest child has ME aka CFS Chronic Fatigue Syndrome as well as a myriad of other diagnoses, to watch her as an adult trying to get PIP, as they now are swapping everyone over too, has been a ten year long battle. It makes me so angry that people like this speak in such negatively and in such an ill informed way about human being, who they and their families struggle with so many things in so many ways just makes my blood boil. She is literally a step away from saying "Burden on society, put them all in a chamber and unalive them!" like a German guy with a little moustache once tried. My goodness it is a world gone mad!!! Thank you Nell for bringing this, this... "Person" to our attention. I don't hope ill will go anyone but my goodness she needs to be cancelled! I hope this ends her political career asap!
Unfortunately, this isn't likely to end her political career - she's a racist, xenophobic, backwards thinking dinosaur who has said so many awful things I'm surprised she hasn't attacked in the street. And yet she is still able to stand in our parliament and make statement after statement that makes me sick to my stomach. But I can at least bring more outside eyes to her misinformation.
You certainly can Nell! Thank goodness for people like yourself who say No! Not on my watch! Keep on spreading the word 🙏🏻 Power to the people ✊🏻 ALL PEOPLE OF ALL ABILITIES, nothing less will do! I honestly do not know how people of such views sleep at night. My two youngest have no voice, literally and will never lead independent lives. If only this woman experienced what it's really like or if it effected her or a loved one of hers, I'm sure she would be singing a very different tune!
@@bellblue5527 Thank you for that encouragement! I won't stop lifting up my voice for those who have none, who just keep getting talked over by people who have absolutely no idea what they're talking about. What an absolute shame that people have the ability to speak, and absolutely waste it with bullshit.
I thousand times agree with you with everything and after Pauline Hanson one nation made me ashamed of biing on NDIS of that video and I hated that video. Same with taken that away too. Yes I do agree about the medications and see our doctor now we have pay over a hundred dollars to see the doctor because Mum seen the doctor and she told that we have to pay over a hundred dollars too. I think Pauline and one nation too die or live on nothing and we are lot of no bodies. I hope Pauline and one nation sees this video. I am that I got very nice and independent care to help me out. What would Pauline one nation do if they a disability person family. Will they help or get rid of them.
I think a lot of people who make videos like this or promote them might change their tune if disability affected them. It's easy for them to think this way when they don't go through it!
![Nell Tyler [Warning: Honesty Ahead]](http://yt3.ggpht.com/G_Wwm84VACPUWyxCE4K5INrJ2f3Fs-09xq8wDpYl968-FBUOkZQHOcFvS_xkUsMSo5gnUtOWFA=s48-c-k-c0x00ffffff-no-rj)
I'm from the UK and all my children have disabilities and the hoops that have to be jumped through to get DLA (Disability living allowance) are so strict, that for anyone to believe they are handed out willy nilly have no clue. The fight I had to get my son the highest rate for mobility took appealing two rejections and on the third had to go in front of board. After I prepared a War and Peace size document, they called me to say it didn't need to go before the board, I was correct that by their own definition my child met all the criteria and was finally awarded what they were entitled too. The stress as a parent fighting for your child who cannot speak for themselves is not one any parent or individual should have to take on board. So many just accept their initial decision and don't appeal. But this mother was like a dog with a bone, I was not letting go and in the end they knew they would not be successful at a tribunal and didn't want to pay the costs involved, hence why I got a very apologetic phone call and awarded the highest rate for my child in both categories.
For this woman... and I use the term loosely to weaponise disabled people for her own political gain is beyond vile!
My eldest child has ME aka CFS Chronic Fatigue Syndrome as well as a myriad of other diagnoses, to watch her as an adult trying to get PIP, as they now are swapping everyone over too, has been a ten year long battle. It makes me so angry that people like this speak in such negatively and in such an ill informed way about human being, who they and their families struggle with so many things in so many ways just makes my blood boil. She is literally a step away from saying "Burden on society, put them all in a chamber and unalive them!" like a German guy with a little moustache once tried. My goodness it is a world gone mad!!!
Thank you Nell for bringing this, this... "Person" to our attention. I don't hope ill will go anyone but my goodness she needs to be cancelled! I hope this ends her political career asap!
Unfortunately, this isn't likely to end her political career - she's a racist, xenophobic, backwards thinking dinosaur who has said so many awful things I'm surprised she hasn't attacked in the street. And yet she is still able to stand in our parliament and make statement after statement that makes me sick to my stomach. But I can at least bring more outside eyes to her misinformation.
You certainly can Nell! Thank goodness for people like yourself who say No! Not on my watch!
Keep on spreading the word 🙏🏻
Power to the people ✊🏻 ALL PEOPLE OF ALL ABILITIES, nothing less will do!
I honestly do not know how people of such views sleep at night. My two youngest have no voice, literally and will never lead independent lives. If only this woman experienced what it's really like or if it effected her or a loved one of hers, I'm sure she would be singing a very different tune!
@@bellblue5527 Thank you for that encouragement! I won't stop lifting up my voice for those who have none, who just keep getting talked over by people who have absolutely no idea what they're talking about. What an absolute shame that people have the ability to speak, and absolutely waste it with bullshit.
I thousand times agree with you with everything and after Pauline Hanson one nation made me ashamed of biing on NDIS of that video and I hated that video. Same with taken that away too. Yes I do agree about the medications and see our doctor now we have pay over a hundred dollars to see the doctor because Mum seen the doctor and she told that we have to pay over a hundred dollars too. I think Pauline and one nation too die or live on nothing and we are lot of no bodies. I hope Pauline and one nation sees this video. I am that I got very nice and independent care to help me out. What would Pauline one nation do if they a disability person family. Will they help or get rid of them.
I think a lot of people who make videos like this or promote them might change their tune if disability affected them. It's easy for them to think this way when they don't go through it!
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