Episode 10 — Depression and Suicidality

This month we’re going to talk about some heavy stuff that a lot of us experience, especially during the holiday season: we’re going to talk with musician Amy McNally about ways she copes with depression and suicidal ideation, both with formal medical and psychological treatment and in ways she deals with it apart from that. Click through for links to resources on dealing with depression and suicidal thoughts. Musical excerpts copyright Amy McNally, used with permission.

Hello and welcome to episode 10 of the podcast Tips and Tricks on How to be Sick.

I’m Eirenne and I will be your host as we talk about navigating the world as people with chronic illnesses, both physical and mental, disabilities, and the ways in which the world isn’t necessarily designed for us.

This month we’re going to talk about some heavy stuff that a lot of us experience, especially during the holiday season: depression and suicidal thoughts. We’re going to talk with musician Amy McNally about ways she copes with depression and suicidal ideation, both with formal medical and psychological treatment and in ways she deals with it apart from that. If you need to skip this episode for now, you should absolutely do what you need to in order to take care of yourself. This podcast will still be here later, when and if you feel up to listening to it.

After the interview, I will have some numbers, links, and resources for coping with depression and suicidal thoughts, and direct links to them included in the transcript, so stick around for that, as well as information about the different music you’re hearing this month. And now, let’s get to the interview.

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Episode 09 — We’re back for Season 2! Administrative notes on our hiatus and then we talk dysautonomia

In honor of Dysautonomia Awareness Month, we’re going to discuss dysautonomia and the ways it can present in different people, both on its own and in conjunction with other disorders.

What is dysautonomia, anyway? Well, it’s a dysfunction of the autonomic nervous system, which tells you nothing unless you know a little bit about how the autonomic nervous system functions and what it does in the body. So let’s take this in two parts – what the autonomic nervous system does, and what things happen when it doesn’t do its job correctly.

Hello and welcome to episode 1 of season 2 of the podcast Tips and Tricks on How to be Sick.

I’m Eirenne and I will be your host as we talk about navigating the world as people with chronic illnesses, both physical and mental, disabilities, and the ways in which the world isn’t necessarily designed for us.

Before we begin, some administrative housekeeping and some thank yous are in order. Content note for the next bit: discussion of animal illness and death. Skip forward about 2 minutes if you need to avoid that.

Continue reading “Episode 09 — We’re back for Season 2! Administrative notes on our hiatus and then we talk dysautonomia”

Episode 08 — TBI and everything after – a conversation with Cheryl Green

What I would like to see is, at the same time that you’re going through rehab, that you’re getting constant reinforcement that it is OK to be a person with a disability or with an impairment.

It is not embarrassing to ask for help. You are not a burden if you need something, ever. And what disabled people need is not special. You don’t have special needs, you’re not a ‘special person’ – you are a person who has a specific need around your disability, and maybe that need will change, maybe you’ll continue to rehab and you won’t need that thing anymore. … Like, we hate these signs of impairment so much, and even mobility aids, and we lust for normalcy to this degree that if you’re not getting better at a really fast trajectory, it’s easy to hate yourself.


Hello and welcome to episode 8 of the podcast Tips and Tricks on How to Be Sick.

I’m Eirenne and I will be your host as we talk about navigating the world as people with chronic illnesses, both physical and mental, disabilities, and the ways in which the world isn’t necessarily designed for us.

In this episode, we are having a conversation with documentary filmmaker Cheryl Green. Cheryl has a traumatic brain injury, or TBI, and she thinks that the TBI community and the wider disability community could learn from each other if they connect and share experiences. So today, Cheryl is going to share her experiences before and after acquiring her disability, the ableism she has found in the process, and how we can make things just a little bit better for people with intellectual disabilities, TBIs, and really, any disability that causes temporary or permanent cognitive impairment.

A few content notes for this episode:

  • This episode was originally intended to go up in August. It is now the very end of December. My bad!
  • There are some frank discussions of ableist language in this episode, including some specific examples.

And now let’s get to the conversation.

Continue reading “Episode 08 — TBI and everything after – a conversation with Cheryl Green”

Episode 04 — Autism – including interviews with an #ActuallyAutistic adult and a licensed therapist

In this episode, we are going to be talking about autism, also called Autism Spectrum Disorder (ASD), and what it’s like to realize, as an adult, that not only are you non-neurotypical but that you are, in fact, autistic.

http://traffic.libsyn.com/tipsandtricksonhowtobesick/04_autism_-_including_interviews_with_an_actuallyautistic_adult_and_a_licensed_therapist.mp3 autoplay=0

Hello and welcome to episode 4 of the podcast Tips and Tricks on How to Be Sick.

I’m Eirenne and I will be your host as we talk about navigating the world as people with chronic illnesses, both physical and mental, disabilities, and the ways in which the world isn’t necessarily designed for us.

In this episode, we are going to be talking about autism, also called Autism Spectrum Disorder (ASD), and what it’s like to realize, as an adult, that not only are you non-neurotypical but that you are, in fact, autistic. I’m going to take a moment here and give you some definitions before we get started, just so we’re all on the same page and speaking the same language. I, myself, am not autistic, so I’m drawing my information from published articles on the subject, taking care to prioritize actually autistic voices and views whenever possible.

Coined by Judy Singer, an Australian social scientist, the word ‘neurodiversity’ is a non-judgmental, non-medicalized way to talk about and talk to folks who aren’t neurologically typical, or neurotypical. Neurological diversity, or neurodiversity, covers a huge range of things, from anxiety and depression to ADHD and dyslexia and epilepsy and autism and so much more. Essentially, people with some form of neurodivergence are just wired differently than those who are neurotypical. One person can have multiple kinds of neurodivergence, and indeed that happens frequently.

We used to think of being neurotypical as being “normal” and so any deviation from that was bad or wrong or something to be fixed. And yes, in some cases, the neurodivergent person might still want some things to be ‘fixed’ or otherwise made different or better than they are, and seek treatment for them. But, by shifting to thinking in terms of neurodiversity, we give that power and agency back to the people who should have it: the people who are neurodivergent themselves.

Autism is one type of neurodivergence, and one that the autistic community largely does not want to be ‘fixed’ or removed from them. Autism is something people either are or are not born with; nothing “causes” autism, and nothing “cures” autism, either. There could be a whole podcast on just the ways autism can present in people, but I’ll simplify it down here to save time.

Autism is typically noticed in kids around age 2 or so, but some people don’t realize that they are autistic until they’re much older, even into adulthood, perhaps because people around them didn’t notice or pursue the differences in them, maybe because they had a mild presentation as a child, or because they were just trained to hide those differences and act like other children. Regardless of the reason, some folks realize their own specifically-autistic neurodivergence as adults when they realize that they:

  1. Have trouble with social skills and communication in general; trouble with eye contact and other non-verbal communication, or making emotional connections to other people, or not understanding verbal cues in conversation. And
  2. That they perform repetitive, restrictive motions or actions; repetitive body movements like rocking or flapping hands, repeating the same words or sounds (this is called echolalia), or repetitively lining up or stacking objects.

Again, this is remarkably simplified here. There are million different ways autism can manifest, and there are resources out there written by people much more knowledgeable than me about it. I’ll include links to some of those in the transcript for this episode.

Now that we’ve got the language sorted, we can get on to talking with our guests this month. We’re going to talk with Tobias, an autistic man in his 20s who knew he was neurodivergent already, but figured out the autistic piece of the puzzle later, and who will now share his tips with us on adjusting to that realization as an adult. We’ll also chat with Dani Higgins, a Licensed Professional Counselor, about the mental health aspect of being autistic, and what it’s like to pursue a formal diagnosis. We’ll discuss self-diagnosis vs formal diagnosis, and the reasons someone may choose, or not, to seek a formal diagnosis from a mental health professional, and we’ll talk about the importance of having an understanding community and support system as an autistic person.

Without further ado, let’s get to the interviews.


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Episode 03 — ME/CFS and an interview with filmmaker Jen Brea

In this episode, we have a special guest: we are going to be talking with filmmaker Jen Brea. Jen has ME/CFS, and while making a documentary about the progress of her condition from first symptoms through diagnosis and beyond, she did most of that work from her bed.

http://traffic.libsyn.com/tipsandtricksonhowtobesick/03_me-cfs_and_an_interview_with_filmmaker_jen_brea.mp3 autoplay=0

Hello and welcome to episode 3 of the podcast Tips and Tricks on How to Be Sick.

I’m Eirenne and I will be your host as we talk about navigating the world as people with chronic illnesses, both physical and mental, disabilities, and the ways in which the world isn’t necessarily designed for us.

In this episode, we have a special guest: we are going to be talking with filmmaker Jen Brea. Jen has ME/CFS, and while making a documentary about the progress of her condition from first symptoms through diagnosis and beyond, she did most of that work from her bed.

Without further ado, let’s go to the interview.

Continue reading “Episode 03 — ME/CFS and an interview with filmmaker Jen Brea”