Keeping an MS Medical Journal

When I first developed multiple sclerosis, it was so vague and weird that I couldn’t quite describe the sensations to others, particularly to my family and friends. How do you explain fleeting neurological symptoms that sound like you’re having a stroke? Explaining to my then-primary doctor what was going on seemed even more challenging: he wanted to know WHAT kind of numbness I had. Did it feel like pins-and-needles or did the area lack ALL feeling? When did it come and when did it go? Was it restricting any of my activities and did it ever become painful? At this point I began a medical journal where I logged symptoms, durations, my feelings about these symptoms, dates, things that worsened these symptoms and so on. This journal has become my guide to my history with multiple sclerosis and a basic reference that I bring along with me to my doctors’ visits.

Keeping an MS medical journal is easy. Here’s what I find helpful:

Narrow a Medical Journal Down to One Topic

If you have more than one ailment— many of us do— then separate the problems into different journals within a notebook. Keep MS information in one area and (for example) low blood sugar, or hypoglycemia, in another section. Sometimes it’s difficult to tell where symptoms are coming from (particularly in the case of multiple autoimmune diseases) but if the illnesses are unrelated try to keep them unrelated in the journal to focus on what is precisely going on with each illness.

Be as Specific as Possible

I look back at my medical journal and my memory is jogged: I had this episode of vertigo at this point in time, I took this medication, my neurologist said such-and-such, the vertigo tapered off at such-and-such time. I would never remember this on my own and I’m glad that I took such descriptive details. Referencing entries with specific dates, durations, performed tests, my feelings about the symptoms, what medications I took, whether said medications helped or did nothing, and my doctors’ opinions has helped me to keep a mental idea of my MS journey thus far. It’s still of course mysterious, but I feel a little more in control of what’s going on.

Regularly Update Your Status, Including the Good Times

Being well is a point of reference within the journal. It’s important to document this as part of the journey. Just checking in every few months keeps the journal updated and current.

Record Feelings about the Attacks and the Symptoms

I was able to see a pattern of anxiety and depression which I shared with my therapist because of my noted feelings within my medical journal. The psychological elements are definitely a part of the greater whole.

Remember to Bring the Medical Journal Along with You to Doctors’ Visits

This journal aids not only you but your treatment team in better knowing your disease history and present status. You can also immediately record what your doctors say, requesting proper spellings and exact information. Sometimes it all sounds like mumbo jumbo if you wait until you get home.

Stick to the Basics

I don’t know about you but I prefer to keep this sort of journal in a standard wide-ruled notebook. I don’t get fancy and I keep to the basics of my case. This isn’t my autobiography; it’s a book of facts I need to keep. A basic notebook works for me.

9 comments

  • Thanks for the reminder! I stopped updating my MS/Health spreadsheet when I went on disability, so I need to update that darn thing. It is huge!

  • Jen

    Joan—

    You really are a ‘numbers’ kind of gal, huh? I’m embarrassed about my total buffoonery with Excel sheets. I can barely do Powerpoint either. Now there’s an idea: an MS medical journal as a slide presentation…!

    Any way we care to slice it, the information is still the same and is relevant to our overall medical records.

    Glad you’re up and about again, Joan.

    Jen (a smile)

  • I wish the Internet had been around when I was first DX. Great advice, Jen.

  • Jen

    I received this advice from my mom, who really doesn’t have much wrong with her (knock on wood.) She always tells me to write everything down— anything that can later cause a discrepancy or questions. I’m a huge list maker (it’s pretty embarassing actually) but it’s worked for me. I had a small notebook in the past specifically for an altercation with my insurance carrier and a provider who didn’t precertify me for a procedure (dragged on for a year and a half.) I learned then!

    Good morning, Diane..

  • I did this in the “beginning” 6 years ago and I stopped and now I need to do it again. It helps to be a reminder as well that “Hey – You, You have MS – take care of yourself.”

    I may do mine online this time, last time I wrote it down. I type much faster so online it will go! Good Post!

  • Jen

    Oooohhhh: like the online idea. Thanks for sharing it!

    PS: my notebook is a junky mess. Might try this idea myself.

  • Jill

    I have Lupus and keep a journal. Every day I write down what I ate, what meds I took & times, what I have to do (helps having everything on one page), and how I felt w/ specifics (good or bad), along with a little freewrite of things I want to remember (saw a bird, nice sunrise, good conversation, notes from docs, etc). I transfer the “how I felt” onto a monthly calendar when I have time (usually do it during work meetings when I should be paying attention), which is easier to look at rather than flipping through each page, for instance, if I had to count the number of days in a month with a headache, knee pain, etc. My journal will definitely help me keep track of trends, and memories I don’t want to forget.

  • Jen

    Hey Jill—

    Love ya lots! Great ideas that will help anyone who comes across this page. You’re doing an awesome job with this recent diagnosis. See ya Saturday.

    One of your oldest buddies–

    Jen (a big goofy smile)

  • I have mine on the computer so I can update it easily. I do the same for my list of meds and other things. It’s not easy keeping track of it all, but so important to write it down as it changes/happens or its gone from the memory!

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