Hey everyone. My name is Renee (Nay) and I turned 26 last Tuesday. I was diagnosed with MS yesterday. Happy Birthday to me!
I don't really have symptoms per say. Its all very strange the way it happened. My mom has had MS for many years and was properly diagnosed 8 years ago. I on the other hand, had my first (and only) exacerbation about 1 year ago. Both of my feet were tingling and numb for a few days. I chalked it up to being a new runner, but just in case saw my primary physician who ordered a lumbar MRI because of my family history. Negative, moved on.
Well, this April I had a minor car accident (rear ended, still some neck pain.) Since the pain wasn't going away with therapy, that doctor ordered a cervical spine MRI. Surprise, surprise...1 inactive MS lesion. Followed by a brain and thoracic spine MRI...2 more on the brain and one more on the spine.
Next was the blood work, which showed high ANA cells...yay, "it may be Lupus." More blood work, appointment with Rheumo...not Lupus but don't know why your ANA cells are high.
Then, the lumbar puncture. "It won't really hurt, just a little sting and then some pressure"...HA. Not for me! Pain all through, muscle spasms for days after along with the wonderful spinal headache (which wasn't bad long as I was lying down, but lying down hurt my back so it was a pain...)
VEP was negative which was a blessing, but MS specialist pretty much confirmed that all signs point to MS and that he recommended starting treatment. So i will be starting Copaxone shortly.
I am planning a bowling fundraiser to benefit the National MS Society in October, and plan to run the Philly Half Marathon in November for I Run to Stop MS. However, I am not sure whether these issues are all mental (which everyone tells me they are) or I am beginning to have physical problems but my running has been suffering lately. I was up to running 7-8 miles at a time and lately am exhausted by the time I hit mile 1. Please don't let me be falling apart already...
I don't really have symptoms per say. Its all very strange the way it happened. My mom has had MS for many years and was properly diagnosed 8 years ago. I on the other hand, had my first (and only) exacerbation about 1 year ago. Both of my feet were tingling and numb for a few days. I chalked it up to being a new runner, but just in case saw my primary physician who ordered a lumbar MRI because of my family history. Negative, moved on.
Well, this April I had a minor car accident (rear ended, still some neck pain.) Since the pain wasn't going away with therapy, that doctor ordered a cervical spine MRI. Surprise, surprise...1 inactive MS lesion. Followed by a brain and thoracic spine MRI...2 more on the brain and one more on the spine.
Next was the blood work, which showed high ANA cells...yay, "it may be Lupus." More blood work, appointment with Rheumo...not Lupus but don't know why your ANA cells are high.
Then, the lumbar puncture. "It won't really hurt, just a little sting and then some pressure"...HA. Not for me! Pain all through, muscle spasms for days after along with the wonderful spinal headache (which wasn't bad long as I was lying down, but lying down hurt my back so it was a pain...)
VEP was negative which was a blessing, but MS specialist pretty much confirmed that all signs point to MS and that he recommended starting treatment. So i will be starting Copaxone shortly.
I am planning a bowling fundraiser to benefit the National MS Society in October, and plan to run the Philly Half Marathon in November for I Run to Stop MS. However, I am not sure whether these issues are all mental (which everyone tells me they are) or I am beginning to have physical problems but my running has been suffering lately. I was up to running 7-8 miles at a time and lately am exhausted by the time I hit mile 1. Please don't let me be falling apart already...
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