Living With MS ~ Looking on the Bright Side #LivingWithMS

Living With MS isn’t the end of life it is just life reimagined.

When I was first diagnosed with MS after my coma(read the story HERE). The journey and work required to get back on my feet was hard not gonna lie. It seemed life had become a series of misfortunate events. I knew life as I had known it was gone. In its place a new life one I would have to learn to live with and live fully.

In the years since my diagnosis, I have learned three valuable lessons.  One is humor. I have learned

One is humor. I have learned to laugh at myself and my symptoms. I will tell more about this lesson later.

Two never give in or give up. this is a life lesson for everyone. even when life is tough we can never give in or give up on what we want to accomplish.

Three MS is a disability felt not seen. there have been so many rumors around my small town about me due to my MS symptoms. You may wonder why that is well because MS isn’t always visible to the people around you. Let me tell you why by sharing some of my daily symptoms.


Living With MS Symptoms

Living With MS

Yes, both heat and cold affect me. The heat seems to hit me hard and my symptoms flare up more when I am hot. Things like my foot-dragging or just being extra cranky. Think of a two-year not getting a nap and that’s me.

Living With MS

Dizziness and vertigo is a real problem sometimes. If I move my head just right or standing up too quick it hits hard.

Living With MS

Vision issues yes. This is the main reason I don’t drive. I don’t just see two of everything I see like 3 sometimes 4. Like the picture says that’s ok if it’s chocolate or a handsome pirate(AKA Johnny Depp) but for everything else not so much. I can no longer drive which is a pain. I also have an issue with seeing things in a distance like when people are on stage or wave across the room. No, I am not being rude I just don’t see you waving so try hollering I will answer.

Living With MS

Numbness is a big thing I find getting up and moving helps, but most of the time I feel my toes and sometimes even my fingers.

Living With MS

No, I am not drunk is correct. I don’t know how many times I have heard the rumor I was drunk at 7AM dropping off my son at school.  I can’t tell you how many walls, doors and/or tables I have bumped into in my life. I have lost count.  and yes. that is only water in my cup.

Living With MS

Fatigue doesn’t even begin to describe the feeling. Think how you feel after 2 days of no sleep and hard labor that bone tired can’t move my body tired and then multiple that by 10 and that is how I feel. On a good day I can handle anything on a bad I can’t move out of bed.

There are many other signs and symptoms of MS these are just a few I deal with daily.  To see more illustrations and to learn more check out website  Positive Living With Ms.

Let’s Talk:

Do you know someone with Ms?  What did you learn that surprised you?

Living With MS


Disclaimer:  Photos are from the website Positive Living With MS.

About Rebecca 2510 Articles
Rebecca is a boy mom, traveler, Disney addict, chocolate lover, and tea drinker. She lives in Florida and enjoys good food, good music, and a great book. Her goal in life is to live in the moment and to always be open to new things.


  1. Invisible ilnesses are so difficult to deal with. Those without them really have no idea what it is like and sometimes are too quick to judge or get annoyed. I’m familiar with MS and one of my family member’s has it and I can appreciate all of the symptoms you have posted here. Keep doing what you are doing and living your life!

    • Always there is too much to see and do to let a little Ms throw me off.

  2. loisaltermark says:

    I have a couple of other friends who have MS, too, so I’m always eager to learn more so I can help. I’m sorry you have to live with this but you have such a great attitude and are so inspiring.

    • Thank you and as the saying goes when life gives you lemons make grape juice and what they wonder.

  3. My bosses mom had MS and it was the first time I have ever heard of the disease before.
    She described it as opening up the electrical panel and randomly cutting wires and waiting to see what happens. Hopefully they find a cure soon!

    • That is exactly how it is. All the wiring gets crossed and mangled so you never know.

  4. My neighbor suffers from MS and I always feel so awful for her on very warm days and frigid cold days because I know she is suffering bad!

  5. There is a lot I didn’t know about MS. I didn’t know that the weather affects people with MS so bad.

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