98 episodes

The Cycle is a podcast about Endometriosis stories from patients as well as helpful information about the disease and ways to cope with it. Our goal is to share endo stories from people all over the world to empower you.

Medical disclaimer
THIS PODCAST IS NOT INTENDED FOR THE PURPOSE OF PROVIDING MEDICAL ADVICE.
All information, content, and material of this podcast is for informational purposes only and is not intended to serve as a substitute for the consultation, diagnosis, and/or medical treatment of a qualified physician or healthcare provider.

The Cycle. Endometriosis Podcast The Cycle. Endometriosis podcast

    • Health & Fitness
    • 4.9 • 117 Ratings

The Cycle is a podcast about Endometriosis stories from patients as well as helpful information about the disease and ways to cope with it. Our goal is to share endo stories from people all over the world to empower you.

Medical disclaimer
THIS PODCAST IS NOT INTENDED FOR THE PURPOSE OF PROVIDING MEDICAL ADVICE.
All information, content, and material of this podcast is for informational purposes only and is not intended to serve as a substitute for the consultation, diagnosis, and/or medical treatment of a qualified physician or healthcare provider.

    95. Early education about Endo, hormones, health care delay & struggle in the UK.

    95. Early education about Endo, hormones, health care delay & struggle in the UK.

    Nikki is from the UK and is a mindset coach. She shares her journey with endometriosis, as well as how important hormones are. How her daughters rare condition helped her discover her passion for advocacy and fighting the the right medical care. We talk about so much more.



    Find the programs she mentioned here: https://www.ijustdontknow.org/



    Want to watch the show on YouTube? ⁠⁠⁠https://www.youtube.com/@MelissaBou⁠⁠⁠


    Follow for clips of the show:
    Instagram: ⁠⁠⁠⁠https://www.instagram.com/thecycle.endopodcast/⁠⁠⁠⁠
    TikTok: ⁠⁠⁠⁠https://www.tiktok.com/@thecycleendopodcast⁠⁠⁠⁠



    Thank you for listening to and supporting this podcast. We need awareness about this disease. If you want to be on the podcast or have feedback, please reach out via my website, ⁠⁠⁠www.melissaboudreau.com⁠⁠⁠ or DM me @⁠⁠⁠https://www.instagram.com/melisbou/⁠⁠⁠



    Thank you SO much for your support and time.


    Please consider subscribing and writing us a 5-star review on Apple or Spotify podcasts. It helps us get more awareness and with guests agreeing to come on!

    • 51 min
    94. Was it really her appendix or was it endo...UTI's..self diagnosis and more

    94. Was it really her appendix or was it endo...UTI's..self diagnosis and more

    Fenella joins us from the UK on today's show. We chat about how she thinks her appendix may have been endo, chronic UTI, and the shame around them, as well as how she was diagnosed from a podcast. And so much more!

    Things she mentioned to check out:

    Podcasts:

    ⁠28 days later ⁠⁠How Do You Cope?⁠

    ⁠Woman’s Hour (specific episode about appendix)⁠⁠Room 5: series 1 ep7⁠

    Books:

    Period (it’s about bloody time) - Emma Barnett

    You can have a better period - Le’Nise Brothers

    Invisible Women - Varoline Criado Perez

    Menopausing - Davina McCall

    Self-help for your Nerves - Dr Claire Weeks

    Another book I found amazing, talking more about mental health, very specifically postnatally, but still a remarkable read is - ‘What have I done? - Laura Dockrill 


    Want to watch the show on YouTube? ⁠⁠⁠⁠https://www.youtube.com/@MelissaBou⁠⁠⁠⁠
    Follow for clips of the show:
    Instagram: ⁠⁠⁠⁠⁠https://www.instagram.com/thecycle.endopodcast/⁠⁠⁠⁠⁠
    TikTok: ⁠⁠⁠⁠⁠https://www.tiktok.com/@thecycleendopodcast⁠⁠⁠⁠⁠

    Thank you for listening to and supporting this podcast. We need awareness about this disease. If you want to be on the podcast or have feedback, please reach out via my website, ⁠⁠⁠⁠www.melissaboudreau.com⁠⁠⁠⁠ or DM me @⁠⁠⁠⁠https://www.instagram.com/melisbou/⁠⁠⁠⁠

    Thank you SO much for your support and time.


    Please consider subscribing and writing us a 5-star review on Apple or Spotify podcasts. It helps us get more awareness and with guests agreeing to come on!

    • 1 hr 6 min
    93. 20 years to get diagnosed with endometriosis, what helped, and how it influenced a career path.

    93. 20 years to get diagnosed with endometriosis, what helped, and how it influenced a career path.

    *** please note we had some audio issues, I am so sorry about this****



    Join us today to chat with Samm, an endo, Lyme, and celiac warrior. She chats about how, even after being diagnosed with Lyme and Celiac, she still knew something was wrong and how her pain progressed daily. Learn what she did to help feel better and how it helped her in her current businesses.


    Where to find Samm:
    @matchanude + @sammssimplelife on Instagram, FB @matchanude - LinkedIn Samantha Coffin + Matcha Nude. We also have a YouTube account and are @ilovematchanuse on TikTok

    Want to watch the show on YouTube? ⁠⁠https://www.youtube.com/@MelissaBou⁠⁠
    Follow for clips of the show:
    Instagram: ⁠⁠⁠https://www.instagram.com/thecycle.endopodcast/⁠⁠⁠
    TikTok: ⁠⁠⁠https://www.tiktok.com/@thecycleendopodcast⁠⁠⁠

    Thank you for listening to and supporting this podcast. We need awareness about this disease. If you want to be on the podcast or have feedback, please reach out via my website, ⁠⁠www.melissaboudreau.com⁠⁠ or DM me @⁠⁠https://www.instagram.com/melisbou/⁠⁠

    Thank you SO much for your support and time.


    Please consider subscribing and writing us a 5-star review on Apple or Spotify podcasts. It helps us get more awareness and with guests agreeing to come on!

    • 55 min
    92. After seeing 25 doctors, Margaret finally got some answers and developed an app to help endometrosis patients!

    92. After seeing 25 doctors, Margaret finally got some answers and developed an app to help endometrosis patients!

    In this episode, I chat with endometriosis patient, Margaret, who had pelvic pain and saw 25 doctors before she was diagnosed with endo. She worked in health technology before she was diagnosed and was working on an app to help others with pelvic pain- tracking and learning. She shares her endo story and why she started Lasa Health with her husband to help others with endo. Listen in to learn more about this great new resource for patients and it's FREE!



    Want to watch the show on YouTube? https://www.youtube.com/@MelissaBou

    Follow for clips of the show:

    Instagram: ⁠https://www.instagram.com/thecycle.endopodcast/⁠

    TikTok: ⁠https://www.tiktok.com/@thecycleendopodcast⁠

    Thank you for listening to and supporting this podcast. We need awareness about this disease. If you want to be on the podcast or have feedback, please reach out via my website, www.melissaboudreau.com or DM me @https://www.instagram.com/melisbou/

    Thank you SO much for your support and time.

    Please consider subscribing and writing us a 5-star review on Apple or Spotify podcasts. It helps us get more awareness and with guests agreeing to come on!

    • 37 min
    91. The Journey: Navigating Mental Health with Endometriosis

    91. The Journey: Navigating Mental Health with Endometriosis

    Katrina shares navigating mental health with endometriosis & emphasizes the years it takes to process the impact of Endometriosis on one's emotional well-being. Katrina shares her story and how working with a therapist helped her understand that "Endo is not rational." Many patients struggle with feeling well one day or hour to not feel well at all at the flip of a switch, as well as years of people not believing patients how challenging this disease is.



    Want to watch the show on YouTube? ⁠https://www.youtube.com/@MelissaBou⁠

    Follow for clips of the show:

    Instagram: ⁠⁠https://www.instagram.com/thecycle.endopodcast/⁠⁠

    TikTok: ⁠⁠https://www.tiktok.com/@thecycleendopodcast⁠⁠

    Thank you for listening to and supporting this podcast. We need awareness about this disease. If you want to be on the podcast or have feedback, please reach out via my website, ⁠www.melissaboudreau.com⁠ or DM me @⁠https://www.instagram.com/melisbou/⁠

    Thank you SO much for your support and time.

    Please consider subscribing and writing us a 5-star review on Apple or Spotify podcasts. It helps us get more awareness and with guests agreeing to come on!

    • 52 min
    90. How challenging it is to be taken seriously as teenager with Endometriosis, Melissa 20 years old shares her journey.

    90. How challenging it is to be taken seriously as teenager with Endometriosis, Melissa 20 years old shares her journey.

    Melissa joins us on today's show to walk us through her journey as a teen starting in 2015- how many doctors she saw and how long it took to hear that it may be endo. Join us today as we chat about her story.



    You can follow Melissa on IG at: https://www.instagram.com/melissaagagnee/?igshid=MzRlODBiNWFlZA%3D%3D



    Want to watch the show on YouTube? ⁠https://www.youtube.com/@MelissaBou⁠

    Follow for clips of the show:

    Instagram: ⁠⁠https://www.instagram.com/thecycle.endopodcast/⁠⁠

    TikTok: ⁠⁠https://www.tiktok.com/@thecycleendopodcast⁠⁠

    Thank you for listening to and supporting this podcast. We need awareness about this disease. If you want to be on the podcast or have feedback, please reach out via my website, ⁠www.melissaboudreau.com⁠ or DM me @⁠https://www.instagram.com/melisbou/⁠

    Thank you SO much for your support and time.

    Please consider subscribing and writing us a 5-star review on Apple or Spotify podcasts. It helps us get more awareness and with guests agreeing to come on!

    • 34 min

Customer Reviews

4.9 out of 5
117 Ratings

117 Ratings

___LB______________ ,

Thank you!

I’m 42 and feel I’m so late in receiving a diagnosis of endometriosis and having an expert excision surgery. This heartfelt podcast of personal stories has really helped me cope with my experience of the past 12 years leading up to this moment, xo

LiaBlair ,

thank you

I am 22 and have been diagnosed with endo, pcos, and interstitial cystitis. I was diagnosed back in december and was pretty clueless to what all this is. I thought I was going crazy and most of my symptoms might’ve been in my head. This podcast has brought me so much knowledge and comfort. thank you so much for doing this

VGC16 ,

Thank you

Dr Fenske brought me so much hope. Thank you from the bottom of my heart!

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