I haven't forgotten...still trying to get answers for you!
Hi and welcome. I have another place that I network with others about CM. Today I saw someone is currently asking for recmdations for NM for a newly diagnosed Chiari sister. I will contact her and let her know that I would like any info and then pass it along to you....but, sometimes it takes days to get a response. Will keep my fingers crossed that they are near you!
Hugs, Jiggle
Thank you I will post more of my journey.
Thank you
Hi and welcome to the Chiari forum.
I know it can be difficult to deal with this alone...and that is y this forum is here, it may not be the same as meeting in person, but we do make life long friends here that feel and are as important as family....so I hope, u will share ur concerns and ur journey with us.
Know u r not alone.