When most people hear “Sjögren’s syndrome,” they think of dry eyes and dry mouth. That’s the face...
Janet Ellis
Patient advocate and neuropathy support group leader with over a decade of personal experience managing peripheral neuropathy. I started Neuropathy Resource to create the resource I wish had existed when I was first diagnosed — honest, accessible information written by someone who actually lives with this condition. Everything here comes from personal experience, published medical research, and conversations with healthcare providers. I am not a medical professional — I'm someone who has walked this road and wants to help others navigate it.
A member of our neuropathy support group first mentioned lion’s mane mushroom to me about two years...
How common is neuropathy, really? It’s a question I get asked constantly — both from people newly...
One of the most common questions I hear from people in my support group is some version...
The first time I stayed in a hotel after my neuropathy diagnosis, I was unprepared in every...
There is a particular kind of dread that healthy people do not understand. It is the moment...
There’s a particular kind of frustration I didn’t expect neuropathy to bring, and it’s a small one...
A woman in my support group — I’ll call her Carol — stopped taking the bus for...
For a lot of us, a worship service isn’t just an item on the calendar. It’s where...
The first time I flew after my neuropathy got significantly worse, I cried in the security line....