Social worker’s experience of motor neurone disease inspires ‘silent challenge’ fundraising effort

Challenge aims to raise awareness of the the impact on individuals of losing your voice through the condition.

From left to right: Sally, Maureen and Lynn

Maureen Carson has received a lifetime achievement award for her contribution to social work. Two years ago she was diagnosed with motor neurone disease and the illness led to her losing her speech.

Unable to communicate through speech, Maureen resigned from her job as an independent reviewing officer for looked after children with disabilities. She felt she could no longer chair the meetings without a voice. She now communicates via an iPad with a specialist predictive speech application.

This week, Lynn Baxter, Maureen’s best friend and a former social work colleague, and Sally Roberts, Maureen’s niece, are taking on a ‘silent challenge’. The week-long sponsored silence aims to raise awareness of the impact on individuals of losing your voice through motor neurone disease.

The duo will both only communicate through the same iPad technology that Maureen now relies on. They will also blog each day about their experience. The pair are raising funds for the Motor Neurone Disease association in south London.

MND EDIT from Sarah Mills on Vimeo.

Writing about the challenge, Lyn said: “I thought it was particularly cruel of the disease to steal her voice first, as Maureen has always been a very sociable person, an entertainer and full of laughter and stories to tell. In her career as a social worker she was a skilled communicator and she had helped many vulnerable children to speak out about their abuse and pain. She had also developed training and tools to help other professionals listen better to children and to ensure that children had a voice in plans for their futures.

“…Even with her iPad by her side, we are aware that Maureen’s loss of ‘normal’ speech daily causes her frustration, discrimination and insensitive treatment from the general public and professionals. This is usually from people who lack awareness of motor neurone disease, those who jump to assumptions about her lack of speech, or who are just plain stupid and don’t think. For example, the GP who phones her to discuss new medication, the shop assistant who shouts at her as if she’s deaf or speaks slowly as if she’s stupid, or the district nurse who talks about her as if she’s not there.”

You can read more about Lynn and Sally’s fundraising effort here.

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