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I'm NEW!
Hi everyone, I'm new and was diagnosed with CIDP in 2008, I'm struggling still with knowing who to deal with everything. My family and friends are also very confused and scared by not knowing how to support me during my relapse's. I'm currently struggling with a relapse :(
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Hello and Welcome!!
You have found a WONDERFUL place full of very kind and caring people! Here is a couple of links that you may find interesting... to get you started.
Please feel free to roam around all of the forums and join in any where! If you have any questions or need any assitance please don't hesitate to ask... someone will always be along shortly to assist in any way that we can. I look forward to seeing you around the board!! :) Abbie |
Hello and Welcome!!
Hello and welcome to NeuroTalk. Happy to see you have come to be with us. Just let us know if we can be of any help. Look likes Abbie has given you some links to get started. My thoughts and prayers are with you. Again welcome, looking forward to seeing you around. Darlene :hug: |
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Are you on IVIG? I know many people who have CIDP and they are helped tremendously by IVIG treatment. What kind of treatment have you done for your CIDP?? Melody P.S. You have been given the correct forums to go to. |
Please go to the PN site? And the Autoimmune Site.. READ
Posters and their comments and also the 'stickies' at the top of each forum.
It's scary, but also good that you've been diagnosed soo soon. Keep asking questions under these forums, and many will help you ....Once you've made *a few* posts? you can PM folks... feel free to ask ME. I have been thru the CIDP IVIG and a lot of other med complications issues. Around the block about 17 times? Couldn't even do it once! These days. HUGS AND HOPE! :hug::hug::hug:!!!! - j |
Here is the link to our Autoimmune Disease Forum:
http://neurotalk.psychcentral.com/forum44.html Hope this link helps too... :) Abbie |
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