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- About MND
- Support and information
Louise's special day
Louise from Bedford has made the courageous decision to attend her own funeral to celebrate her life with family and friends, all whilst raising money for the…
- About MND
- Support and information
Mike's special day
When Mike was recording a video message during the pandemic and noticed a change in his voice, he was immediately filled with horror and concern. Mike’s voice…
- About MND
- Support and information
Linda's special day
Despite her diagnosis, Linda continues to fundraise and engage in activities like pottery which she finds therapeutic. Linda emphasises the importance the…
- About MND
- Support and information
Jay's special day
Jay, who is living with MND, is determined not to let the disease take away his sense of community or adventure. Since being diagnosed with MND in 2009, Jay…
- About MND
- Support and information
Andrew's special day
Former BBC news reporter Andrew Hartley gave the speech of his life at his brother’s wedding in April – four months after being diagnosed with MND. Having…
- About MND
- Support and information
Jim's special day
When MND took away the use of Jim’s arms and legs hobbies he once loved, Jim became fascinated with the night sky and a grant from the MND Association now…
- About MND
- Support and information
Anna's special day
Anna was just 39 when she started experiencing problems with her speech. After her devastating diagnosis, Anna, was invited to the MND Association’s EnCouRage…
- Research
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- Professionals
Dysarthria
Many people with MND experience weakness in the bulbar region, affecting muscles of the mouth, throat and tongue. This can lead to problems with speech and…