ms limbo land
 

I have been in limbo land for 4 years. I have many of the symtoms and even been on Copaxone, yet I don't have the lesions to make it offical. I saw an MS specialist who agreed in me coming off the meds. I am quite frustrated. The symptoms have taken over a large bit of the quality with walking, pain, and energy. The doc wants to see me every 3-4 months to monitor. He beleives it might be 'temporary' or it could be MS. 4 years of symptoms and still no answers.

Where can I go to find people like me who have gone through similar struggles.

Hi 13 monka and welcome to Neuro Talk...here is the link to our very active MS forum....http://neurotalk.psychcentral.com/forum17.html

You find lots of information there and they have a lot of fun in the Stumble Inn. http://neurotalk.psychcentral.com/forum102.html

I hope you find some answers soon. :hug:

Hi, 13monka, and welcome! You will find there a lot of people in your situation and many open ears to listen to your story. Look forward to seeing you on the MS board!

Hey 13! Many of us, if not close to all of us MSers were in limbo for years. Unfortunately, it's the nature of the beast of MS. I hope you find your medical answers, meanwhile we would love you to hang out with us.

Peace.

Hello and welcome to NeuroTalk. It is great to see you have come to be with our hugh and loving family. There is a great group here to assist in how they can. I am so sorry to hear of you lost. My thoughts and prayers are with you.

Looking forward to seeing you around.

Darlene:hug:

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Hi Monka, and welcome to NeuroTalk. We have a great MS forum, that's where I hang out most of the time. Looking forward to seeing more of your posts and getting to know you.

There are lots of friendly and helpful people here. :)

welcome to neurotalk ... there are lots of friendly and supportive people here so jump right in and start posting ... should you need help, don't hesitate to ask someone ... we are here to help ... again ...
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