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New to MS Forum
Hi,
I am new to the MS forum. I had an initial diagnosis, and then, my Neuro retracted it, because he didn't want to "label" me with MS. So, I have been through a multitude of tests and continue to live in pain. Chelle |
Welcome Chelle, so glad you found us. Yeah , my Doc said the same thing, when he DXed me...35 years ago...LOL!
Come on in and join us, won't you? :):hug: |
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I'm glad I found you, too. :) I'll definitely come on in and join you, although, I will be away from Monday until late Thursday. My D.O. just continues to medicate me for the severe nerve pain in my spine, and my DH decided, "Enough is enough", and made an appt. for me with a Spine Specialist, whom I saw on June 14th, had a new spine MRI, which we will see him on Friday to get the results. Chelle I'm praying to God he can help me. I've been through so many tests, seen so many doctors. |
Welcome Chelle. After reading a bit more about your story it sounds similar to mine. My very first MS sx was in my GI tract! not in my head! I explained it in the bathroom thread you started. Its important to get your MS MD and your GI MD to be on the same page.
I am glad you are finding answers. :hug: |
Hi Chelle and welcome to NT! I hope your MRI explains some of your symptoms. It's awful being in pain but not being able to have a reason for it. Let us know how your results turn out. :hug:
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And thank you for all of your input. I didn't know there was anyone out there with my exact problem. I'll chat with you on Thursday. :hug: Chelle |
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Thank you so much for the warm welcome. I am so happy to have found this forum family. I will definitely let you know the results of my MRI. We are going away for a few days, but I will be back Thursday. :hug: Chelle |
Hi Yorkieville,
Enjoy your vacation and be sure to come back here. We welcome you to NT and hope you find the answers to your symptoms. We all need a name to what is bothering us. Eventually they find out. Nice to meet you and see you soon. |
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Than you for the welcome. Trip wasn't great. I was tired, and in pain, but it is always nice to be away. I've been this way since 2005, so I hope you are right, and they figure it out. It is very nice to "meet" you, too. Chelle |
Hello Everyone!
My name is Frana (Salmone on here) and I', a new member. Was diagnosed 7 years ago with relapsing/remitting MS and have been on Copaxone for six years. I haven't been ab;e to see a neurologist in two years due to my insurance and my health has really taken a turn for the worse. I can't sleep, having trouble eating, very week and my doctor just will not listen or dosen't care. I don't know where to turn. Thank you for listening.
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