I had my first multiple sclerosis (MS) episode in 2005. I recollect it well. We had simply come off the most active storm season in history. It become the 12 months of hurricanes: Dennis, Emily, Katrina, Rita, and Wilma.
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i was running lengthy hours and turned into feeling overwhelmingly tired, harassed, and depressed from all of the devastation we had been seeing on television.
Little did I realize my body become managing its very own neurological hurricane, one that had been forming for years.
I determined to take some day off and get a few rest. the first day of my excursion, I woke up to numbness in my toes and parts of my legs. I felt like I couldn’t get away from bed. I had no idea what was wrong.
the first health practitioner I went to turned into blunt and sincere. “this could be whatever from a slipped disc to more than one sclerosis. You need to see a neurologist,” he said.
"MS? Isn’t that the wheelchair disease?" I concept. So I did as i was instructed and were given in to see a neurologist who gave me MRIs and a most unpleasant spinal tap.
The result: I had lesions on both my brain and backbone. The spinal faucet fluid had also proven the protein they look for in MS sufferers.
related: AINSLEY EARHARDT: 'MY journey TO becoming A mother began WITH A MISCARRIAGE'
The physician gave me steroids to help with the numbness and tingling and told me I more than probably had multiple sclerosis: an unpredictable, persistent, incurable, and probable disabling disorder of the crucial fearful gadget that interrupts the go with the flow of records within the mind and among the brain and the body.
At that moment I thought my life become over. My profession would be completed. the man that i used to be relationship could likely leave me. How would I assist myself?
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I began learning and reading as lots as I should on MS even as trying to stay constructive. i used to be capable of find a wonderful, type MS medical doctor, and his nurse Jennifer changed into an angel in a white coat. She might calm my fears at the same time as holding my hand—sharing tales of perseverance and how someday we might find a cure for this contamination. Jen was a brilliant light in a prognosis that appeared so darkish.
in the course of that time, I also located people to talk to who were residing with MS, and who had been no longer just functioning, but thriving.
inside the thirteen years considering that my first MS episode, I’ve attempted no longer to strain about matters that used to trouble me for the duration of my existence. Weight and body-photo issues are something i have had in view that a totally young age. i used to be teased approximately my “curvy” determine in my teenage years and throughout my profession on tv.
related: WHAT it is want to BE recognized WITH multiple SCLEROSIS AT AGE 25
however on the grounds that my diagnosis, i've tried to remind myself to be appreciative of the frame that has supported me for 47 years. It allowed me to stroll down the aisle with the affection of my existence who stood with the aid of me while i was first identified. This brilliant frame that brought stunning kids and has taken me to so many places.
however when i used to be looking through my fb page ultimate week for no specific purpose, I came across a remark that made me pause:
“dear Janice please prevent permitting fox to dress you in those quick skirts. they're not flattering on you. Your an attractive female, love the eighty's hair, however your legs are distracting each time you walk on display screen.”
i used to be greatly surprised at how merciless it became. This character who had in no way met me, but felt compelled to comment on my body. I decided to reply:
"hello JoAnn,
Fox would not get dressed me. I get dressed myself. i am sorry in case you do not like my legs. i'm thankful i have them to walk with. you are proper. I don't appear to be the typical man or woman on television, and i'm proud to be a length 10. consider that! you can constantly turn the channel in case you're offended through my large legs. hope you do not thoughts. I may additionally share your post with every body on my facebook web page. all of the best, Janice”
approximately 15 minutes later a familiar call came up on my facebook web page. It turned into from my MS nurse Jen. The angel in a white coat. She wrote:
“dear Janice, i really like the ones robust legs. i like that you stand tall, stroll, run, squat, lunge, bypass, bounce and hop on the ones legs. you're blessed and a blessing to have strong legs!!! wear skirts proudly and display your robust legs!!! Love you!”That’s when tears began falling down my face.
living with MS there'll constantly be are reminders that my immune device isn’t the finest, and this contamination remains unpredictable (just like the climate I forecast), putting while you least expect it.
but my MS has also given me power in methods I in no way imagined. So this too is a reminder. Be happy with this frame. There’s so much greater I want to do with it. And i'm able to. With my head held high. On my big strong legs.
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