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Author Archives: PSPA Ireland
Neurology Patients Would Welcome More Information When They Are Diagnosed
A newly published report by the Neurological Alliance reveals that over half of patients surveyed reported they did not receive sufficient information at the time of diagnosis, including details of relevant patient support organisations. The findings come from the first … Continue reading
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Aware for All – Wednesday 5th December 2018
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Irish Hospice Foundation public information evening – LIVING WITH LOSS – 1st November 2018
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Niall Coughlan fundraising for PSPA Ireland in the Dublin Marathon Sunday 28th October 2018
Niall Coughlan is running in the SSE Airtricity Dublin Marathon to raise funds for PSPA Ireland and Diabetes Ireland. Niall’s mother -in- law battled with PSP for 5 years. Clodagh was not only a wonderful mother-in law, mother and wife … Continue reading
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AGM – Tues. October 2nd in Marco Centre
Notice of AGM of PSPA Ireland Continue reading
Video – We all need support
PSPA Ireland would like to acknowledge the work of Zoë Boss in the filming and production of this clip.
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A BIG SHOUT OUT to thank Mary & Mick who’s organised a Birthday Fundraiser for PSP
Making a difference Mary Whelan presenting a cheque to PSPA Ireland. Mary’s husband Michael has PSP and recently celebrated his birthday by doing a fundraiser and having a big party. What a great couple. A big thank you to Mary, … Continue reading
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5K for PSPA Ireland – Virtual Race – Sign up Now
You Deserve a Medal Sign up Now! 5K for PSPA Ireland Join our virtual race and raise funds to support people with PSP & CBD and fund research. Take advantage of this great weather from Sat 18th August- Sun … Continue reading
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MY BROKEN BRAIN: RTE1 Tuesday 17 July 2018 9.35pm
A documentary on tonight about various Neurological conditions including Parkinson’s disease, Motor Neuron Disease and Dementia. The programme looks at the work of Professor Tim Lynch and the Dublin Neurological Institute.
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Friday July 20th – PSPA Ireland Regional Support Group Meeting – ARDEE
The aim of this meeting is to offer people diagnosed with Progressive Supranuclear Palsy (PSP) and Corticobasal Degeneration (CBD), their carers, families and friends an opportunity to meet with us and ask questions, share experiences and concerns over a cup … Continue reading
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