Endometriosis: A Supporter’s Perspective

Guest post: Endometriosis: A Supporter’s Perspective by Lucjan Living with Endometriosis There is really nothing more miserable than seeing your loved one in pain day by day and knowing, you can do nothing about it! Hi, I’m Lucjan B. and this is my story. A few words from a man who supports someone suffering from […]

Living with Dystonia: Tom’s Story

Guest post: What It’s like Living with Dystonia by Tom Seaman I have lived with chronic pain from dystonia for almost 20 years. Since it is often very difficult for others to understand what it feels like, I want to provide some information about what it is, how it feels, and how living with dystonia […]

Researching, Reusing and Recounting

In this month’s linkup party hosted by A Chronic Voice, I’m talking about researching, reusing and recounting when you have a chronic illness. This means being your own investigator, attempting (and failing) to count meds and the oh-so-controversial plastic straws. You can read A Chronic Voice’s post for this linkup here. The prompts for this […]

Living with Trigeminal Neuralgia: Liz’s Story

Guest post: What It’s like Living with Trigeminal Neuralgia by Liz I live with a facial pain condition called trigeminal neuralgia. I have other pain issues too including a back problem which resulted in me having to take early retirement when I was twenty-eight. My back pain is extremely debilitating, but trigeminal neuralgia is just […]

Living with Hereditary Lymphedema: Jordyn’s Story

Guest post: What It’s like Living with Hereditary Lymphedema by Jordyn. You can find Jordyn’s previous guest post on Erythromelalgia here. Hello again! My name is Jordyn and I’m chronically ill. I actually have many different chronic illnesses, but I thought that today we would talk about one of the rarer ones. I am living […]

Living with Mitochondrial Disease: Kelcie’s Story

Guest post: What It’s like Living with Mitochondrial Disease by Kelcie Miller-Anderson My name is Kelcie Miller-Anderson, a twenty-something social entrepreneur and scientist from Canada. I also have several rare diseases. 3 to be exact, but the one that is most significant and impacts my life daily is called Mitochondrial Disease. What Is Mitochondrial Disease? […]

Living with Functional Neurological Disorder (FND): My Story

After so many guest posts for my What It’s Like Living With series, I thought I’d contribute myself and share what it’s like living with Functional Neurological Disorder (FND). It’s been 2.5 years but I finally know what’s wrong with me (part of it, at least) and why it happened. I have a chronic illness […]

A Chronic Voice Linkup Party: July 2019

I’ve decided that I’ll be participating in A Chronic Voice’s monthly chronic illness linkups. I’ve already taken part in May and June’s linkups, which means it’s now time for A Chronic Voice’s July 2019 linkup party! You can see A Chronic Voice’s linkup post for this month here. A Chronic Voice’s July 2019 Prompts The […]

Living with Erythromelalgia: Jordyn’s Story

Guest post: What It’s like Living with Erythromelalgia by Jordyn Hi, my name is Jordyn and I have many different chronic illnesses. However today, I want to talk about one of the rarer ones in hopes of bringing awareness to it. I am living with Erythromelalgia and no, I don’t know how to pronounce it […]

A Chronic Voice Linkup Party: June 2019

I really enjoyed writing a post for A Chronic Voice’s May Linkup so I decided I’d participate in A Chronic Voice’s Linkup Party June 2019! This month I’ll be writing about wondering, turning and desiring when you have a chronic voice. I feel these are very fitting, as recently I’ve been wondering what my life […]