Lost #FND soul searching for answers and ways to heal. It's left a wreckage in our lives; it started a chapter we never wanted to enter. #FNDHealing#FNDaware
The borderland of Multiple sclerosis and Functional Neurological Disorder: a call for clinical research and vigilance.
Here's the latest commentary on the overlap between functional neurological disorders & multiple sclerosis by @SelmaAybek & Andrew Chan https://t.co/qXMmvMoiwA
One thing I want chronically ill people to know is no matter what you choose to improve your situation: mobility aids, painkillers, surgery, psychotherapy, exercise, online community, spiritual practice, acceptance: someone will criticize you.
Ignore them and live your life.
We are very interested in the attendee experience of the past FNDS conference, so here's some experiences described by attendees based in Australia.
Missed this conference and are looking forward to the next one? Become a member today to stay up to date: https://t.co/LiJkDxrfsG
@SassyFNDLife I support this question. My NES's often tend are as described by FND sites, but other times are more complex or have consequences like physical damage or code blue situations. In my case, I know my daughter has a genetic form of epilepsy, so I'm surprised at a short EEG, too.
@FND_Together Nelson and tail are the closest. South surrey, white rock, Vancouver is ok because we have friends we can stay with of we can afford gas.
@FND_Together Hi Robin, I have just found a psychologist who is absolutely ready to do everything she can to help with my FND symptoms. She wonders what are the most up to date, best place(s) to go for exercises or therapeutic guidelines she can read about to work with me on?