The nurse was the one who spilled the beans. Can you believe it? She just assumed that my sister’s steroid treatment was for MS and she addressed my sister with some nonchalant statement that began with “lots of my MS patients…” She had no idea that I would be the one who Jackie called, asking, “Does this mean that I have MS?” I didn’t even know what MS was, and I sure as hell didn’t trust the blabbermouth nurse, but something in my gut told me that there was no way she could have gotten that wrong.

I remember listening as my sister confirmed the nurse’s words after an appointment with a neurologist. I sat in front of my classroom computer late at night (I am a recovering workaholic) and I did what any other normal person would do: I shoved the phone between my shoulder and ear, double clicked on Internet Explorer, and googled it. Then I cried. Silently. And told my sister it would be fine. She is my baby sister, for pete’s sake. Even if a Tsunami was headed directly at our heads, I would tell her it would be fine.

In that moment I realized how lucky we were. We had suffered some unlikely tragedies in our family, but we were all still alive and happy. Even my father, who had been diagnosed with a weak heart after a series of small heart attacks, had outlived the original 5 year timeline we were given.

And as I processed the diagnosis, I wallowed in a ton of guilt. At that point in my life, I had a successful and rewarding teaching job, a stellar long term boyfriend who had recently proposed, and a house in the suburbs with a gym membership that kept me remotely healthy and active. Jackie was living at home, struggling to find a job, struggling even more to keep her relationship together and couldn’t afford a pair of running shoes. Why her? And how the hell was I supposed to help her, when just being me was probably nauseating?

I remember feeling like I couldn't possibly understand what she was going through. She needed other people who has been diagnosed with MS, young and old. She needed to find community, and I was so proud of her when she decided to try and unite the young MSers by using her talents in writing and design. MS.Understood was a feat of strength, as far as I’m concerned, and I hope that TheMSBlog creates an even bigger community of people who “get it.”

 


Comments




Leave a Reply

    RSS Feed

    Calling All Family & Friends

    From what I hear, the friends and family of those with MS can often feel just as isolated as those with the disease. Here we'll post entries from the friends and family of people with MS. Perhaps they can find some useful information here as well.

    So send us your stories, advice, and personal accounts on how you've dealt with being a "care giver".*

    So email us your stories

    *I absolutely HATE this term.

    Categories

    All
    Daughters
    Mothers
    Sisters