THE HAELTHY AF PODCAST: Recent Episodes

Aprille Lim

Hosted by former beauty queen, actress, model, and lawyer, turned entrepreneur, Aprille Love, explores the world of Hereditary Angioedema (HAE), a condition she herself has been diagnosed with, in order to understand it better and raise awareness for it.

The podcast shares real life stories and wisdom from people around the globe as well as interviews with thought leaders in the space.

The purpose of this podcast is to help those with HAE feel supported and to let them know: We are in this together. #HaelthyAF

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Welcome to Episode 7 of the HAELTHY AF Podcast.

For this episode, I am joined by Professor Connie Katelaris, Professor of Allergy and Immunology at Western Sydney University. She is also the head of unit at Campbelltown Hospital and has a private practice in Westmead.

Professor Connie and I discuss preparing for pregnancy, delivery and post pregnancy care.

Please don't forget to subscribe via Spotify, Apple Podcasts, Castbox and Google Podcasts.

Please follow:

Haelthy AF Podcast: @HaelthyAF

Aprille Love: @aprillelove

Professor Connie Katelaris: https://www.allergy.org.au/patients/locate-a-specialist/nsw/item/prof-connie-katelaris

About HAELTHY AF:

HAELTHY AF is a podcast that explores what it's like living with Hereditary angioedema or HAE, a rare, chronic, and potentially life-threatening condition resulting in swelling in various body parts internally and externally.

Being a sufferer of this condition myself, I wanted to raise awareness for this condition and also educate myself and others on how best to live with it.

This podcast will share stories from others around the globe living with HAE, share interviews with professionals and thought leaders in the space and provide some tips and pearls of wisdom on what it is like living with it.

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Welcome to Episode 6 of the HAELTHY AF Podcast.

For this episode, I am joined by my partner in love and life, Pier. ❤️

Pier and I discuss what it is like from his perspective and being in a relationship with someone with HAE.

Please don't forget to subscribe via Spotify, Apple Podcasts, Castbox and Google Podcasts.

Please follow:

Haelthy AF Podcast: @HaelthyAF

Aprille Love: @aprillelove

About HAELTHY AF:

HAELTHY AF is a podcast that explores what it's like living with Hereditary angioedema or HAE, a rare, chronic, and potentially life-threatening condition resulting in swelling in various body parts internally and externally.

Being a sufferer of this condition myself, I wanted to raise awareness for this condition and also educate myself and others on how best to live with it.

This podcast will share stories from others around the globe living with HAE, share interviews with professionals and thought leaders in the space and provide some tips and pearls of wisdom on what it is like living with it.

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Welcome to Episode 5 of the HAELTHY AF Podcast.

For this episode, I am joined by Henrik Boysen, Executive Vice President and COO at HAE International (HAEI).

Henrik and I discuss his HAE story, life with a family who have HAE, establishing HAE International, what services they offer to patients globally and tip and tricks for everyday living.

Please don't forget to subscribe via Spotify, Apple Podcasts, Castbox and Google Podcasts.

Please follow:

Haelthy AF Podcast: @HaelthyAF

Aprille Love: @aprillelove

HAEi: https://haei.org/

Download the HAEi Tracker App here.

HAEi Companion App here.

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Welcome to Episode 4 of the HAELTHY AF Podcast.

For this episode, I am joined by Fiona Wardman, HAE Australasia Co-founder and CEO, HAE International Director, Treasurer and Chief Regional Patient Advocate, and Regional Patient Advocate – Asia Pacific.

Fiona and I discuss her HAE story, living a normal life with HAE, establishing HAE Australasia, what services they offer to patients with HAE in Australia and much more.

Please don't forget to subscribe via Spotify, Apple Podcasts, Castbox and Google Podcasts.

Please follow:

Haelthy AF Podcast: @HaelthyAF

Aprille Love: @aprillelove

HAE Australasia: https://haeaustralasia.org.au/

HAE Australasia Facebook Support page: https://www.facebook.com/www.haeaustralasia.org.au

About HAELTHY AF:

HAELTHY AF is a podcast that explores what it's like living with Hereditary angioedema or HAE, a rare, chronic, and potentially life-threatening condition resulting in swelling in various body parts internally and externally.

Being a sufferer of this condition myself, I wanted to raise awareness for this condition and also educate myself and others on how best to live with it.

This podcast will share stories from others around the globe living with HAE, share interviews with professionals and thought leaders in the space and provide some tips and pearls of wisdom on what it is like living with it.

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Welcome to Episode 3 of the HAELTHY AF Podcast.

For this episode, I am joined by special guest, Janice Strydom, Chairman of HAE South Africa and Patient Voices Ambassador at Rare Diseases South Africa.

Janice and I discuss her HAE story, HAE triggers, patterns and markers, finding support through Facebook and much more.

Please don't forget to subscribe via Spotify, Apple Podcasts, Castbox and Google Podcasts.

Please follow:

Haelthy AF Podcast: @HaelthyAF

Aprille Love: @aprillelove

HAE South Africa: https://southafrica.haei.org/

HAE South Africa Facebook Page: https://www.facebook.com/haesouthafrica

About HAELTHY AF:

HAELTHY AF is a podcast that explores what it's like living with Hereditary angioedema or HAE, a rare, chronic, and potentially life-threatening condition resulting in swelling in various body parts internally and externally.

Being a sufferer of this condition myself, I wanted to raise awareness for this condition and also educate myself and others on how best to live with it.

This podcast will share stories from others around the globe living with HAE, share interviews with professionals and thought leaders in the space and provide some tips and pearls of wisdom on what it is like living with it.

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Welcome to Episode 2 of the HAELTHY AF Podcast.

For this episode, I am joined by Professor Connie Katelaris, Professor of Allergy and Immunology at Western Sydney University. She is also the head of unit at Campbelltown Hospital and has a private practice in Westmead.

Professor Connie and I discuss what HAE is, how it manifests in patients, the average lifecycle for attacks, how it is diagnosed, the treatment options available in Australia and much more.

Please don't forget to subscribe via Spotify, Apple Podcasts, Castbox and Google Podcasts.

Please follow:

Haelthy AF Podcast: @HaelthyAF

Aprille Love: @aprillelove

Professor Connie Katelaris: https://www.allergy.org.au/patients/locate-a-specialist/nsw/item/prof-connie-katelaris

About HAELTHY AF:

HAELTHY AF is a podcast that explores what it's like living with Hereditary angioedema or HAE, a rare, chronic, and potentially life-threatening condition resulting in swelling in various body parts internally and externally.

Being a sufferer of this condition myself, I wanted to raise awareness for this condition and also educate myself and others on how best to live with it.

This podcast will share stories from others around the globe living with HAE, share interviews with professionals and thought leaders in the space and provide some tips and pearls of wisdom on what it is like living with it.

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Welcome to Episode 1 of the HAELTHY AF Podcast. 

For this episode, I am joined by a very special guest and also my best friend of over 10 years, Sammy D to help me tell my HAE Story. 

Apologies, the audio cuts out in some parts. 

Please don't forget to subscribe via Spotify, Apple Podcasts, Castbox and Google Podcasts. 

Please follow:

Haelthy AF Podcast: @HaelthyAF

Aprille Love: @aprillelove 

Sammy D: @hey_sammy.d

About HAELTHY AF:

HAELTHY AF is a podcast that explores what it's like living with Hereditary angioedema or HAE, a rare, chronic, and potentially life-threatening condition resulting in swelling in various body parts internally and externally.

Being a sufferer of this condition myself, I wanted to raise awareness for this condition and also educate myself and others on how best to live with it.

This podcast will share stories from others around the globe living with HAE, share interviews with professionals and thought leaders in the space and provide some tips and pearls of wisdom on what it is like living with it.

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Welcome to the HAELTHY AF podcast hosted by Aprille Love!

I'm Aprille Love, former beauty queen, model, and lawyer turned startup entrepreneur.

This podcast is a passion project of mine to raise awareness for this rare condition and explore what it is like living with Hereditary Angioedema or HAE - A condition which I myself have been diagnosed with. 

I created this podcast as a safe space to learn about this condition and better understand it - not only for myself but for my friends, family, and loved ones. 

Each episode will share stories from myself and others and interviews with health professionals and thought leaders in the space. 

I want to help those living with this condition know... they are not alone.

I look forward to going on this journey together!

If you know someone who could be a great guest for this show, please reach out. 

HaelthyAF