Mental Health Resources for MS Patients

Multiple Sclerosis and Mental Health

When the brain is altered by a disease such as MS, it shouldn’t be a surprise that other aspects of brain health can be compromised.
Multiple Sclerosis and Mental Health
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The brain is an amazing organ. The longer I live with multiple sclerosis (MS), and the more I study the disease, its effects, and our brains’ responses to the disease, the more amazed I am by it.

The brain, however, is not the mind. And while the brain plays an important role in our emotions, it’s the mind that attempts to make sense of our experiences and the feelings they evoke.

Both play a role when it comes to mental health.

Mental Health Resources for People With MS

I’m not the only one thinking about mental health and MS. All of the major MS patient advocacy sites I use as resources have some level of coverage about MS and mental health.

The MS Society UK has extensive resources on the topic for people living with multiple sclerosis. Their coverage, ranging from depression and anxiety to grief and uncontrolled emotions, offers a lot for ourselves and our loved ones if we’re having trouble coping with the emotional effects of MS.

The National MS Society has information on emotional health for patients, as well as guidance for healthcare professionals who care for individuals with MS. It is so important to educate professionals about both general MS symptoms, as well as invisible symptoms, such as mental health issues, that patients themselves might have trouble acknowledging or describing.

I also found useful information on depression, anxiety, and pseudobulbar affect in an article entitled “Multiple Sclerosis and Mental Health: 3 Common Challenges,” published by Johns Hopkins Medicine.

My Own Contributions to the Discussion

As many of you know, I host a series of webcasts for MS Ireland called The Unspeakable Bits. While we’ve touched on issues related to mental health with topics like relationships, lost connections, and even getting through the stresses of Christmas with MS, we haven’t yet attacked some of the big ones like depression, anxiety, and grief. I’d say that we’ll be looking closely at that for our next series schedule.

I’ve signed off these Life With Multiple Sclerosis pieces for over 18 years with the same tagline, which wishes good health to all and their families. I suppose I’ve always been thinking of our physical health when doing so. But I suppose I also should be thinking of mental health when I write these words.

Wishing you and your family the best of health.

Cheers,

Trevis

Important: The views and opinions expressed in this article are those of the author and not Everyday Health.

Trevis Gleason

Author

Trevis L. Gleason is an award-winning chef, writer, consultant, and instructor who was diagnosed with secondary progressive multiple sclerosis in 2001. He is an active volunteer and ambassador for the National Multiple Sclerosis Society and speaks to groups, both large and small, about living life fully with or without a chronic illness. He writes for a number of MS organizations, like The Multiple Sclerosis Society of Ireland, and has been published in The Irish Times, Irish Examiner, Irish Independent, The Lancet, and The New England Journal of Medicine.

His memoir, Chef Interrupted, won the Prestige Award of the International Jury at the Gourmand International World Cookbook Awards, and his book, Dingle Dinners, represented Ireland in the 2018 World Cookbook Awards. Apart from being an ambassador MS Ireland and the Blas na hÉireann Irish Food Awards, Gleason is a former U.S. Coast Guard navigator. Gleason lives in Seattle, Washington and County Kerry, Ireland with his wife, Caryn, and their two wheaten terriers, Sadie and Maggie.