Another instalment from a day in my life of living with dysautonomia and EDS!
This week is an anniversary of sorts. An anniversary that coincides with a famous horse race, The Melbourne Cup.
It marks the time I last skipped in front of the TV!
Here’s a recap from that memorable day in November 2015….
Continue reading Living with Dysautonomia and EDS – Chapter 14 “My Last Flutter with Too Much Fun”
Introducing you to Kami Lingren from Living Grace who is a truly beautiful soul. Kami has been diagnosed with Lyme and a handful of other diagnoses, with dizziness, head pain, bone and joint pain as the most debilitating symptoms. At its worst, her list of symptoms from her illness had grown to nearly 80, which she know so many others can relate to. Thankfully she’s been finally improving this year and her symptom list has become much smaller! Find out how she is living well with chronic illness by reading more…
Continue reading Kami Lingren: Living well with chronic illness
Change isn’t easy, especially when it’s foisted on you and the future is unknown – Here’s “How to Manage Change when the Future is Unknown”
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.
Continue reading How to Manage Change when the Future is Unknown
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.
Continue reading Kamilah Howard: Living well with chronic illness
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
Are you running around on adrenaline, much like ‘roadrunner’ just running non stop? Living on too much adrenaline?
Following my own rather large run in with adrenaline and the diagnosis of having dysautonomia and being hyperadrenergic (a-dren-err-gic – I still have problems saying it) I’ve become somewhat interested in the role it plays on the body and thought I would share some of what I know. So here goes…. Continue reading What is the Impact of Living on Too Much Adrenaline?