20 things I love about multiple sclerosis
Vertigo – I get to pretend that I am on a Trans-Atlantic sea cruise every day… plus I like wearing Hawaiian shirts.
Disabling Fatigue – I get to take naps and snuggle with my pillow.
Insomnia –
Positive Living with MS was started by Penelope Conway after she was diagnosed with MS. She found few resources for positive encouragement; to laugh, cry, share, and just feel normal in the midst of a life of chaos; so she decided to start something herself. Positive Living with MS was birthed out of Penelope’s desire to show others that regardless of the challenges, we can all enjoy life to the fullest and find a smile in the storm.
Vertigo – I get to pretend that I am on a Trans-Atlantic sea cruise every day… plus I like wearing Hawaiian shirts.
Disabling Fatigue – I get to take naps and snuggle with my pillow.
Insomnia –
How can something you can’t see hurt so badly? That’s the problem with multiple sclerosis. It’s not visible and it makes you feel alone.
MS challenges? Pfft, they’ve got nothing on me! I’m like a bulldozer, smashing through obstacles with sheer willpower.
After much thought, research and prayer, this year I made the decision to no longer use any MS therapy drugs to treat my MS.
Ladies and gentlemen, this is the non-stop flight to a life with multiple sclerosis. On behalf of the Captain and the entire crew, welcome aboard.
Multiple sclerosis is going to give you troubles at some point in your life. All of us go through them but everyone faces it differently. Many times it feels like it’s a constant struggle. Other times you may get a reprieve and have a moment of sanity and calm.
Even if you can’t do something as you once could, you have to keep trying. Be calm, be brave, don’t quit on life and never quit on yourself. The world needs you. I need you.
You may feel like you’re on a roller coaster of emotions. Accepting what’s going on one day and angry about it the next.
Since MS has taken up residence in my body, I have discovered many things that affect me that never did before. It seems like symptoms show up out of nowhere and have a tendency to hang around for a long, long time… sometimes forever.
I try my best to stay active because I know there will come a day when my body will be limited in the things it can do.