neurological disorders

A Chronic Spoonful
Thoughts and stories from the world of chronic pain, illness, and disability.
Abridged The Blog
Life. (With chronic illness). In smallish bits.
AS I Live & Breathe
A Woman’s Journey With Rare Disease
Chronic Mom Life
A spoonie lifestyle blog to help women find wholeness on the journey.
Chronically Something
Writing about life with chronic illness, the good, the bad, the ugly and all the realities that come with these.
Feasting On Joy
At Feasting On Joy, we help people navigate their personal path to healing and live out their God-given purpose! Our mission is to educate, bring awareness and provide sustainable, multi-disciplinary solutions to be well long term. Through cultivating an intentional, holistic lifestyle in the areas of faith, health and home as well as purposing to conquer autoimmunity, we guide our clients and readers to thrive in life rather than just survive.
Grace Quantock Trailblazing Wellness
I want to live in a world where you are loved, accepted & supported & when illness, disability, trauma or grief throws your life off track you can blaze a new trail to the true you & I write, podcast & vlog about doing just that.
Happy Tired Mummy
Inspiring Mother’s with chronic illness to live with positivity, purpose and love.
My name is Victoria and I have Charcot Marie Tooth Disease.
Inflamed & Untamed
I’m Sara and I have Crohn’s disease and a rare disease called, Chronic Intestinal Pseudo Obstruction. I also had my entire large intestine removed and live with a J-pouch but prior to that lived with a temporary ileostomy.
Inkblots of Hope
Hope is an option, even in chronic illness and other seasons of pain.
Jess’ ME/CFS Blog
A young adult battling multiple debilitating chronic illnesses
Laughing while you’re crying
A blog about trying to live a positive life, with a rare brain condition called IIH and writing to raise awareness that migraine is more than just a headache. My aim is to help just one person with my story, if I achieve that, then I have done what I set out to do.
Memoirs of a Strong Woman; A Frightening Look Inside the US Healthcare System
A trip to the local Emergency room culminates in profiling, medical neglect, and then gaslighting, and ultimately physical abuse by a sadistic on-call neurologist and then his female resident. Little does the patient know this is just the beginning of a horror story that never seems to end.
Moving Naturally with Hypermobility
Education for patients and healthcare providers on proper physical therapy techniques, natural movement, and restorative exercise for Hypermobility Syndromes, such as Ehlers-Danlos syndrome (EDS), including the complexities often caused by overlapping conditions.

Living with chronic pain is one of the hardest things that many of us have to endure on a daily basis. Living with pain while also coping with the multi-systemic effects of joint hypermobility, commonly diagnosed as Ehlers-Danlos syndrome (EDS), is even more challenging. One of the best treatments for chronic pain due to Hypermobility Syndromes/EDS is learning how to move and exercise properly — our muscles do what our connective tissues cannot.

Move More. Move Better.
My Medical Musings
My musings of living a medically retired life with a rare genetic bone disease, permanent colostomy & Rheumatoid Arthritis
Not So Average Mama
Not So Average Mama blog is a blog about life in general. I write about many topics including Chronic illness and alternative ways of treating. We are also an unschooling family. I work as a professional photographer and spend my spare time with my kids at roller derby as well as fostering puppies.
Overcome Lupus
OVERCOME LUPUS exposes realities of Lupus with insightful posts, to make it as known as cancer. This unique Instagram blog motivates with advice to overcome it & other chronic illnesses.

Peering Through the Fog
A means of creating a community where those of us with chronic illness/pain will be able to forge friendships and give support to each other as we deal with chronic illness and our day-to-day lives.
Read Between the Lyme
This is a personal journey about living with Chronic Lyme disease.
The Enigma – Wrapped in a DNA Encoded Riddle
Single, empty nester, living with chronic Illness who in 2016 was struck with yet another illness that left the rural Doctors of the small Midwest town she was living stumped. This is her journey through a silent home, a long road trip and clinging to the hope for answers.