This week, I would like to introduce you to Donna Grant who lives with Fibromyalgia and Chronic Lyme Disease and writes about her experiences on her February Stars blog. Here she talks about her experiences and living well with her chronic illness.
I have written the following post in collaboration with Sam Moss of My Medical Musings and I have referenced some of the posts that Sam has written there. It makes for powerful reading in terms of what you can do to better manage your personal circumstances when you find yourself in a place of despair. Her learnings will also help anyone undergoing change when that change is occurring through choice.
Here’s some of her story.
This week I would like to introduce you to Kamilah Howard from Anchoredinhealth.com.
Kamilah has asthma and gluten intolerance. Her asthma symptoms are mostly exercise-induced, which is something she does almost every day. Her gluten intolerance really affects what she eats day to day, but it’s very manageable through a gluten free diet.
I’ve been meaning to write about Kayla for some time. We connected a few months back but it’s taken me some time to sit down and do her justice! Kayla has lived with Chronic Fatigue Syndrome (CFS)/ME since she was 12 years old. Continue reading Kayla Kurin: Living well with chronic illness
To look at me is to look at anyone else.
I look like a typical 40 something with the confidence you would expect of someone who has been in her profession for 25 years. If you are talking with me, you would likely also make the assumption that I hold down a full time job. Like everyone else who looks and sounds a bit like me.
Except, I can’t.To look at me is to look at anyone else. Or is it? Click To Tweet
I share my life with a chronic illness.
My last post in this new series about living well with chronic illness was about Brittany and her love of coffee. This week I would like to introduce Linda, another chronic illness blogger, who lives in a most beautiful part of the world and gets to work with my favourite sweet treat – chocolate!
Life with ME/CFS and Fibromyalgia
This is me. The dreamer. The hungover. The fatigued. Daily specials on my menu of life. Here’s a taste…
Every morning, to varying degrees depending on how busy my day was previously, I wake in a fog. A pea soup kind of fog. Feeling like I’ve been somewhere half the night.
In another mad dream. With people I don’t know, writing the story as I go. Continue reading My daily specials of dreams, hangovers and fatigue