EP is a community where members connect through shared life experiences-- like MS--and so much more. You are not defined by any one thing, so be your true self and find others just like you at
Experience Project.
Posted: Mon May 12, 2008 9:12 am Post subject: hi, new here and scared
Hi all, I'm hoping to get some answers and info from people who have gone through this.
some background...
There are 3 cases of ms on my mother's side of the family. So naturally when I started getting some weird symptoms a couple years ago, I was worried and did some research. But all the feelings I had were so vague that I never went to the doctor's with my concerns. Then I got pregnant with my 4th child and I felt MUCH better.
Then these last couple months the symptoms returned, but still vague. Achiness in the legs, feeling of spaciness, inner trembling. So I took a wait and see appraoch. Now last week I got pain in my face. Again, I was worried about ms, but stillthinking it was in my haed or unrelated, as the symptoms were atypical. Instead of the sharp, short bursts of pain that I read about in the articles, my cheeks are constantly achy, feels like someone is pinching me.
Not a month ago, I had a physical, and he checked my reflexes, they were all normal. Again, from the online research I did, I read about the Babinsky reflex, and decided to try it out on myself last night. I have no reflexes at all. I discovered my feet are numb and I can't feel anything. Yet I can walk no problem? I even tried to get the kids to tickle my feet this morning, and I felt nothing.
Of course this convinced me to call the doctor, finally. I have an appointment on Wednesday. In the meantime, I am petrified of these new sensations. And also still in denial. I don't have Babinski's reflex after all.
Have others felt atypical symptoms? It seems everything I read baout, mine case is different. What can I expact the doctor will do wednesday?
It must be a very scary time for you. I've not long been dx myself. I would expect that the doctor will do a round of reflexes, strength and resistance & co-ordination tests.
I would recommend taking the time to write down everything that has happened / you've felt so that you can tell the doctor (i always forget otherwise).
If the doc thinks there's something to be worried about / to rule out he will probably refer you to a nuero who most likely would do some blood tests, possibly an MRI and a lumbar puncture. But that's a way off.
If I've learnt anything about MS it's that it's never the same for 2 people. If you are concerned you are doing the right thing to check it out. I hope it goes well for you and that it's not MS.
You cannot post new topics in this forum You cannot reply to topics in this forum You cannot edit your posts in this forum You cannot delete your posts in this forum You cannot vote in polls in this forum
We encourage you to also visit our Multiple Sclerosis story and support community on Experience Project.
Experience Project is a vast and powerful community where people connect anonymously through life experiences. It's made by the same people who built This is MS,
on the premise that no one life experience-- like having MS-- defines a person. It now covers over 2 million life stories. Find and share yours!