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Old 02-19-2013, 07:55 AM #1
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Default Spine Tingling "Fun"

I am so very frustrated and not sure what to do. I have my 1st neuro appt on Friday (4 more days!).

I don't have a dx...other then a rhemy telling me all my sx are consistent with MS and her referring me on to the neuro.

The last week i've had a tingling (off and on) that goes down my spine. It feels like sand trickling down the inside of my spinal column. I had the sensation for what felt like ALL night last night. I barely slept. I'm really just freaked out and sad and overwhelmed. I've read that others have had the same spine sensation.(have I mentioned how much I love this group!?!?)

I just don't know what I should do. 4 days doesn't seem like a long time to wait...but it also seems like a freaking lifetime!

I had to leave work yesterday because of a dizzy spell. i just feel so horrible all the time...before I felt very hopeful ("ok, if this is ms this is just an exacerbation...I'll get through this and be fine. and deal with whatever comes next"). NOW i just want to cry all the time. I feel like a shell of myself. I tried to go shopping over the weekend. I was so off balance, I had to grab a cart just to help steady myself. I feel like i'm shrinking away inside. No one around me can begin to understand what I feel. One "friend" has basically accused me of making stuff up...and even suggested that "maybe it's JUST a brain tumor!" (needless to say, I've quickly decided that is not the type of person I need in my life right now!)

I''m sorry for sounding like such a Negative Nellie...I'm just really scared and lost and not sure what I should be doing.

Thanks for allowing me to vent. Any suggestions you have are truly appreciated.

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Old 02-19-2013, 11:54 AM #2
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Hi sam71,

Abnormal sensations are known as Paresthesias (tingling, numbness) . A few causes of Paresthesias: back problems, B-12 deficiency, Diabetes, Thyroid and of course, MS (there are more causes).

http://www.nlm.nih.gov/medlineplus/e...cle/003206.htm
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Old 02-19-2013, 12:30 PM #3
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Hang on Sam-

Just a few days to go and you will have treatment of symptoms at the very least.

I wish you well and will be looking for your follow up.
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Old 02-19-2013, 12:53 PM #4
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Thank you for the responses.

The rheumy did a bunch of blood work to rule out the vit-D, thyroid and other things.

I called the neuro. They moved my appointment to Thursday. (it was the best they could do). The receptionist told me that everything I told her was consistent with what "other" MS patients say. That makes me feel some what better. However, it's just more than a little freaky to have all these strange new things going on with my body.

I know I may not have any more answers come Thursday...but at least I'll have seen a doctor and will hopefully gain more understanding on what's happening.
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Old 02-19-2013, 01:49 PM #5
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Good luck Thursday Sam!!
Please let us know what the Neuro says.
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Old 02-19-2013, 01:59 PM #6
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It's all very scary at first. It was for all of us (I feel comfortable grouping us all together for that!). And it's hard to wait....and wait.....and wait. I'm so glad they moved your appointment up so you can get some answers.

MS isn't easy to diagnose. It's more of an elimination of other conditions to narrow it down to MS. And that can take some time. It sounds like you've got a good doctor who's working to figure this out. It's still hard to wait, though.

When I was waiting for my diagnosis I actually thought I had a brain tumor. My most prevalent symptom was severe double vision. And it lasted for about six months! I did alot of self-diagnosing on the Internet and let me just say that is NOT a good idea! By the time I heard the Neuro say "you have MS" I was thrilled! He was a little taken aback by my reaction but when you're convinced you have a brain tumor hearing "you have MS" was music to my ears!

I hope you'll post again after your appointment and let us know what the doctor said. You're going to be fine......
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Old 02-19-2013, 09:49 PM #7
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Quote:
Originally Posted by Kitty View Post
It's all very scary at first. It was for all of us (I feel comfortable grouping us all together for that!). And it's hard to wait....and wait.....and wait. I'm so glad they moved your appointment up so you can get some answers.

MS isn't easy to diagnose. It's more of an elimination of other conditions to narrow it down to MS. And that can take some time. It sounds like you've got a good doctor who's working to figure this out. It's still hard to wait, though.

When I was waiting for my diagnosis I actually thought I had a brain tumor. My most prevalent symptom was severe double vision. And it lasted for about six months! I did alot of self-diagnosing on the Internet and let me just say that is NOT a good idea! By the time I heard the Neuro say "you have MS" I was thrilled! He was a little taken aback by my reaction but when you're convinced you have a brain tumor hearing "you have MS" was music to my ears!

I hope you'll post again after your appointment and let us know what the doctor said. You're going to be fine......
Thank you SO much! I will most certainly let you know what the doctor says. I have a pretty extensive history of symptoms and I have them all complied and written up for the neuro to see. I'm hoping that will help her narrow things down a bit. I also had a bunch of labs done at the beginning of the month and also at the end of the summer...(again, hoping it will speed things along).

Also, A HUGE THANK YOU for the reassurance that it's going to be ok!!
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