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Clare woman speaks about living with Multiple Sclerosis ahead of World MS Day

A CLARE woman living with Multiple Sclerosis has spoken about her “life changing” diagnosis and the challenges she has faced this year ahead of World MS Day 2021. Margaret Lohan Gunning, said, “I have Multiple Sclerosis, MS, for many years. It is a life-changing diagnosis where one must rethink life’s goals and expectations. “The past year has brought added challenges. While I was concerned about contracting Covid, I knew I had to stay physically active. Margaret told the Champion that physical activity is important for people with MS, for their mental, physical and social wellbeing. “My physical activity consisted of short walks outdoors, face to face group physiotherapy classes and yoga. All that changed in March 2020. I was however able to participate in exercise classes online. “Group exercise classes, organised by the MS community worker and led by a physiotherapist, were delivered via zoom.” World MS Day takes place on Sunday, May 30, with the aim of raising awareness …

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MS sufferer loses free drugs

THE HSE has been accused of “pulling the carpet from under the feet” of a Doonbeg Multiple Sclerosis (MS) sufferer, following the withdrawal of a free drug. Angela Fitzpatrick has also questioned why the HSE didn’t make the necessary arrangements to pay for an alternative drug before it decided to withdraw the reimbursement of Fampridine from her husband, Nick, under the GMS and other schemes from July 1 next. Nick, who was  diagnosed with MS 12 years ago, at the age of 48, has been taking Fampridine, otherwise known as Famprya, for the last 18 months. “It was a huge shock to us when our pharmacist informed us the drug would be withdrawn and, if we wanted it, we would have to pay between €300 and €500 a month, which isn’t viable for us and other MS sufferers who are on a limited income. “It is scary because his body has got used to this drug now. It would have …

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