How to Craft a Mission Statement When You Have a Chronic Illness

How to Craft a Life’s Mission Statement

Learning to live well with a disease like MS requires understanding ourselves at a deep level.

How to Craft a Life’s Mission Statement
Dominic Dähncke/Stocksy

Those of you who have been reading the Life With Multiple Sclerosis column for any time at all know that I’m one for analogies, metaphors, and allegories when describing what it’s like to have multiple sclerosis.

Analogies (or metaphors or allegories) seem to pop up at every turn in my days, although I don’t always notice or appreciate them at the time. Sometimes it’s weeks later as I sit down to write that an experience bubbles up and ends up in a post.

One of those experiences occurred recently.

Long Lists of Words Can Feel Meaningless

I’ve been helping to launch a network of food producers in my area of the world. Anyone who has ever started something from a large bunch of ideas that came from an even larger bunch of passionate individuals knows that it can be very rewarding work … but work nonetheless.

At one point, I felt like the My Fair Lady character Eliza Doolittle when we were trying to write the network’s mission, vision, and values statements.

For months, our assembled group spouted words about who we wanted to be. Words representing aspirations and direction. Words about place, goals, and history. Scores of words on virtual whiteboards (we often met on video chat because of the pandemic) became hundreds of words via email and text.

“Words, words, words. I’m so sick of words!” I understand you, Eliza.

As it came time to compile and compress this continually growing list of words into concepts, sentences, and a document of mission, vision, and values, I came to realize that that list is backward — in reverse order of how I have come to first define and then live my life with multiple sclerosis (MS).

Values Come First, Then Vision, Then Mission

It’s impossible to set out on a mission (to live my best life in the constant companionship of an incurable, degenerative disease) without a vision of where I want that life to lead me.

Equally, it’s a fool’s errand to try to lay out that vision without first understanding and acknowledging where my values in living that life lie.

We were doing it all backward. Once we flipped our first priority to establishing our values as an organization, it was like the fog lifted and our path forward cleared.

Understand the ‘Why’ Before the ‘What’ and ‘How’

I don’t know if they’re still a “thing,” as I’ve tried to avoid much of the online world since it’s become a series of echo chambers and bot-shared memes, but formulating a personal mission statement used to be a common suggestion for people making or going through major changes in their lives. Changes like being diagnosed with an incurable disease.

I may (or may not) have given a go at one of these in my days of rehabilitation psychotherapy, when it all seemed too much near the beginning. I don’t write that “may or may not” part flippantly. Much of those early days is “what’s too painful to remember, we simply choose to forget” stuff.

If, however, I were to endeavor to write such a mission statement today, I would start by assessing the values part first.

Understanding the “why” before we try and figure out the “what” and “how” seems clear in hindsight. In the throes of the battle, however, we might focus too intensely on the other two — particularly the what — without first doing the soul-searching work of determining the underlying principles upon which we’ll build that new life we’re trying to define and devise for ourselves and our families.

The Right Words Can Have a Lot of Power

Living with MS and trying to make it down this new path can be difficult. It’s nice to have a few lines jotted down on the fridge or the bathroom mirror to keep us from wandering too far off our intended path.

Rather than a mission or vision statement, however, I feel like a few words to fall back on about who I am (or at least aspire to be) might be more helpful as I hitch up my trousers, lace up my boots, and head down this new path.

Mission (and vision, but most importantly, values) accomplished.

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.