MS: Living in denial
Living Like You
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2y ago
Willeke reflects on her experience dealing with MS symptoms and coming to terms with her diagnosis ..read more
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The power of a caregiver
Living Like You
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2y ago
Our LLY blogger, Birgit, shares the hidden power of a caregiver ..read more
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The truth about my MS symptoms
Living Like You
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2y ago
LLY blogger, Declan, discusses some of his many MS symptoms, their impact on his daily life and solutions to working round them ..read more
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Gratitude and MS
Living Like You
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2y ago
Karen reflects on how she found gratitude during hard times, when she received her MS diagnosis and grieving loss of her mother ..read more
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The time MS stole my memory
Living Like You
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2y ago
LLY blogger, Willeke, talks about memory loss as a symptom of MS, and how she has dealt with it over the years ..read more
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MS and ageing
Living Like You
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2y ago
Our LLY blogger, Willeke, gives her thoughts on what it will be like growing old with MS ..read more
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Online Dating and MS
Living Like You
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2y ago
Ever tried online dating? Our LLY Blogger Karen reflects on her various online dating experiences and what she has learned from it ..read more
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COVID-19, MS and doctor’s appointments
Living Like You
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2y ago
COVID-19 has brought many challenges to people with MS in getting treatment, but the results are changing the future of MS care ..read more
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Telling your partner you have MS
Living Like You
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2y ago
Whether you’re in a new relationship or have been in one for a long time, explaining MS can be tricky ..read more
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What is NEDA?
Living Like You
by
2y ago
No evidence of disease activity (NEDA) is an emerging new goal for MS treatment. Here’s what it is and how it could help you ..read more
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