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'Words for the newly diagnosed from people living with MS’ – new book by Joan Jordan
For her very first MS and Me blog, Teresa McShane delivers a tale of her fast-paced and effervescent years as an advertising executive in London but soon discovered that life had other ideas.
Read the first blog for MS and Me from Katie St. Lawrence (24). She shares her experience of what it means to have fatigue, how she deals with it and how, thanks to being strategic about rest, energy and listening to her body, life is as enjoyable as ever.
From August 2011 up to February 2018, MS Ireland have been in a partnership agreement with Dolly Recycling. Through this partnership clothes would be donated into designated banks to be recycled and MS Ireland would receive a fee on this basis from Dolly Recycling.
Sensory Café Captures Customers ‘Experiencing’ Multiple Sclerosis (MS) Symptoms
With a combined 175 years of living with the diagnosis of multiple sclerosis, the MS & Me blog team shares some golden nuggets of lessons learned.
Patients Deserve Better
Kiss Goodbye to MS for research into Multiple Sclerosis and vital services
This week Christina McDonald goes deep into the experience of being diagnosed with MS. From being scared and grieving, she’s learned to doing things differently. More than ever before, she’s chasing her dreams.
The Board and Chief Executive of the Multiple Sclerosis Society of Ireland are committed to maintaining the highest standards of honesty, openness and accountability. Members and employees are often the first people who realise that there may be something seriously wrong within an organisation such as MS Ireland.