In a world as connected as ours, friendship spanning across the globe is a simple evolution. This morning I saw that Facebook has surpassed 2 Billion users each month. Taking into account other Social Media platforms such as, Twitter, Instagram and Snapchat it is no wonder our modern society has developed into what we take... Continue Reading →


It’s okay to be in moments of vulnerability, it’s simply part of our shared life experience.

Meet The Admin Team

A fantastic group of people from around the world with a shared story of complexity and conquering life through adversely.

My Medical Musings

Medical Musings with Friends started in January 2017. I was resting one afternoon in my bedroom, contemplating the new year ahead & wondering what possible purpose my life could hold, as my body kept spectacularly attacking me from every angle.

I have a Rare Genetic Bone Disease with multiple bone breaks & ongoing surgeries, Rheumatoid Arthritis, Permanent Colostomy due to a bowel prolapse, Fibromyalgia, Sjogrens Syndrome, Trigeminal Neuralgia, an inflammatory nerve disease, Scoliosis & Severe Degenerative Disc Disease plus a few other issues. It can be slightly overwhelming when the list adds up.

I suddenly had an idea, a slightly crazy idea, that maybe if I set up a closed forum for people with chronic, complex & rare diseases it could be an extension of my blog. A place where a few people could gather to provide support & genuine understanding. A place where it was ok to “muse” about…

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No memory of the day that changed my life

My name is Michelle Munt and this is my story about surviving a brain injury and what I continue to learn about it. This is for other survivors and their loved ones, but also to raise awareness of what can happen to those in an accident. This invisible injury too often goes undiagnosed and it can be difficult to find information about it. I will talk about things that have helped me as I continue to recover and invite others to see if it works for them too.

my oms life

mum, psychologist, researcher & overcoming MS with a new way of living through Overcoming Multiple Sclerosis lifestyle approach (OMS)

Beautifully Raw

Cultivating Wholehearted Living

Pain Pals

My family & friends living with me.....and chronic illness

The Little Cripple That Could

Tales of my journey through chronic illness & pain.

OCD meets MS

The ultimate battle. . .


I am so glad you have chosen to visit my website and I hope you will continue to come back to read more! You will see that I do believe that a positive attitude can make a huge difference! I truly hope that my website will reassure others that they are not alone with their battles; my goal is to help others!


Swimming as hard as I can to stay afloat!

FibroFlutters - Chronic, Invisible and Rare Illness Support / Advice / Advocacy

FibroFlutters - Support Group for people with Fibromyalgia, Chronic Pain, EDS/Hypermobility, Mental health, Chronic fatigue/Me, Rare & others offering friendship, support & advice in Sunderland, NE UK and across the globe

Insideout Ostomy Life

Had your world turned inside out? Me too!

Tripping Through Treacle

Stumbling my way through life with Multiple Sclerosis

Thriving Under Pressure

Positive Psychology & Stress Resilience


Smile! You’re at the best site ever

Sparkle With UC

Leave a Little Sparkle Wherever You Go

Reflection & Renewal

Creative Writing by Mary Pettigrew


Leave a little sparkle wherever you go!