Friday, 7 September 2018

PROVE your deaf child needs to sign.



Wales has NO deaf schools, we manage OK...

A seven-year-old deaf boy who has been out of education for eight months, can’t get the specialist schooling he needs because Cheshire East hasn’t completed vital paperwork, his parents claim. 


Jenson Lindop Lamens, of Sandbach, suffered brain damage and hearing loss when he contracted meningitis at the age of 16 months. His parents, Richard and Jenny, took him out of school last December because he wasn’t receiving the specialist signing and bilingual help he needs and he was becoming increasingly upset at not being able to communicate. 

The couple say Cheshire East doesn’t have a school which provides for children who need sign language and when they found Jenson a school in Stockport – just four miles from his old school – the new school was unable to take him until there is evidence in his plan that he needs British Sign Language support. Cheshire East, as the local education authority, is legally required to keep an up-to-date ‘manual’ of the education and health care requirements for every special needs child. 

Jenson’s parents say this hasn’t been updated since December 2015 so it doesn’t include a later review which stated he needs a signing resource – and this is why another school can’t take him. Jenny said: “The paperwork from the meeting last September, where it was agreed that Jenson would be entitled to full-time one-to-one signing support, seems to have mysteriously gone missing so that information is not going to be put into his plan because, according to Cheshire East, it doesn’t exist. 

“But it does exist... we’ve got emails from his old school to say that they were trying to put it in place because of the meeting, but Cheshire East are just refusing to put it in his EHCP because apparently, they don’t have any evidence he needs to sign.” 

She added: “The school in Stockport can’t accept him until his paperwork says this child needs this. If I consult with another school they’re going to say exactly the same to me and it’s not because that school is not appropriate for Jenson, it’s because his paperwork doesn’t reflect the child that he is.” Jenny said she was also amazed that, when she took Jenson out of school in December, no-one at the council checked on his welfare. “We took him out of school without one single email or phone call from Cheshire East to say ‘why’s your son out of education?’ 

I reported myself to child welfare in March to say, ‘can you please come and prosecute me or do something because my child’s out of education and Cheshire East won’t do anything’,” she said. “I emailed to say ‘I’ve taken him out of school, you don’t know where he is, you don’t know what he’s doing, this is a complete welfare issue’ and nobody’s contacting me. 

Living with an invisible disability


My social circle shrunk after I became Deaf. People did not know how to deal with it or unfortunately can't be bothered ...
My social circle shrunk after I became Deaf. People did not know how to deal with it or unfortunately can't be bothered ... My social circle shrunk after I became Deaf. People did not know how to deal with it or unfortunately can't be bothered dealing with you. Making friends as an adult is hard. 

Making friends when you have a disability is even harder. There is a sense of fear and anxiety when striking up a conversation that the other person will get uncomfortable if they see you look different or they struggle to communicate with you and so they get frustrated and give up. 

I was born with hearing and due to a neurological medical condition and subsequent surgery, I became deaf in my left ear. The battle with being lonely in a new town I was told that as I got into my late 20s, early 30s, it was almost a given that I would become profoundly deaf. However, I was 16, naive and figured that was a long time away so continued life as normal. human touch.

I was an extrovert, had a large group of friends and enjoyed socialising. My friends used to joke that I'd walk into a room and by the end of the event I'd know everyone's life story and be best friends with the dog. They were joking of course. I would have been friends with the dog first. 

Roll forward nine years to the end of 2009, I had recently gotten married and my husband and I were in the big city and enjoying the big city life. Unfortunately, my surgeon's warning came true, over a space of three weeks I lost my remaining hearing and was now Profoundly Deaf. The following 18 months were a blur of specialist appointments, test, scans, surgery and heartbreak to get my hearing back. But alas, it wasn't too be. 

I had to learn how to live being Deaf in a hearing world, whereas as little as 12 months before, I was a part of that hearing world with no problems. It's a huge mind shift to get to grips with and one my social circle struggled with. I still struggle with loneliness and depression after losing my hearing, but I have a group of friends I can call on. I still struggle with loneliness and depression after losing my hearing, but I have a group of friends I can call on. I looked the same, sounded the same, worked in the same job, yet my communication needs were different now. This lead to the unintentional shrinking of my social group. 

People naturally gravitate away due to not knowing how to deal with it or unfortunately, can't be bothered dealing with you. The saying that; 'When things get hard, you find out who your true friends are' certainly came true. I fought so hard against being Deaf, I didn't want to be. It was a whole new world for me and unfortunately, there was very little support I received. 

Not medically, of course, I had an abundance of that, but mentally. I had no idea where I could go to access help and support for myself and husband (nearly 10 years on now, I know what's available to me but at the time there was no information given to me). This led to me shying away from social events. 

It was too hard to communicate in a large group within a noisy setting. This led to depression and loneliness as I didn't want to be a bother to anyone. About five months after I became Deaf, it became apparent that my husband and I needed a proper way to communicate.

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