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Remembering Nathan Ridd aka The Riddla
Ann Ridd
Remembering Nathan Ridd aka The Riddla
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Nathan Ridd also know to his mates as Riddy or the Riddla, who passed Tuesday 1 September 2020 was diagnosed with MND in late 2011. He was given 1-2 years to live and nearly made 10. But he never got bitter or complained, he just got on with his life living it to the fullest and making adjustments to not allow MND to stop him enjoying time with his daughter and his large group of great friends. Nathan was also passionate about supporting the MND Association of NSW as they helped him and other suffers with MND. A yearly Riddla mnd Golf Fundraiser was held in honour of Nathan since 2012, where our first year we had 62 players and by 2019 we were achieving over 135 players. We appreciate that you may like to send flowers or gifts to convey your sympathy for the family, but we feel that donating that money to the MND Association of NSW would be the way Nathan would have wanted it. Again we are honouring his memory in donating in his name.. Thank you
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Motor Neurone Disease New South Wales Limited
Motor Neurone Disease NSW is the only organisation in NSW/ACT working to support people living with all types of motor neurone disease, their families and carers. MND NSW provides: • Information and support for people living with MND. This includes regular telephone contact and home visits. • Literature to assist in coping with MND on an everyday basis • An information line to assist newly diagnosed and anyone looking for additional information. • Information evenings for people who are newly diagnosed, their carers & families. • Information and education sessions for health professionals to promote the best possible care for people living with MND. • Loan equipment, including, electric wheel chairs, communication devices, electric beds, walking frames and more. • Meetings, workshops and seminars to share ideas, support one another, demonstrate equipment and share the knowledge of experts in the management for members with MND and those involved in their care. • Advocacy on behalf of people with MND to increase awareness of needs and ensure equity of access to available services and resources. • Funding for Research.
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