Thanks to Caregivers Who Share Our MS Load

Thanks to Caregivers Who Share Our MS Load

But, sometimes all of the blogs and guides in the world might not be of much help to a caregiver who feels depressed. It may take a patient to provide the best medicine. Here’s the start of “An Open Letter to My Caregivers” that I discovered on the Life with an Illness blog, written by Mackenzie:

“Having a chronic illness, a lot of people have vanished in my life, but you have never left my side. You have seen me through the good times and you haven’t left my side through the dark times.”

Whether you’re a caregiver or a patient, it’s worth your while to go to Mackenzie’s blog and read the whole letter. Then, ask yourself when the last time was that you thanked the person, or people, who help you make it through your day.

You’re invited to follow my personal blog at


Note: Multiple Sclerosis News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of Multiple Sclerosis News Today, or its parent company, BioNews Services, and are intended to spark discussion about issues pertaining to multiple sclerosis.

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