40. Diagnosed herself at 26, via Google, then yearly surgeries, adenomyosis symptoms, 10 years to finally found a doctor who helped.

40. Diagnosed herself at 26, via Google, then yearly surgeries, adenomyosis symptoms, 10 years to finally found a doctor who helped.

Mara is 36 years old from WI. She had heavy and long periods starting at 15 years old, at 17 years old she had her first GYN appointment where she was put on Birth Control which helped reduce her cramps, but as years went on in her twenties she began to have increased symptoms such as large blot clots, back pain, pain that felt like contractions and GI symptoms. At 26 she was googling and self-diagnosed with endo... about 6 weeks out from her wedding, 3 weeks before she got married she had surgery! She had back surgery and post-surgery she had bladder retention one month after surgery due to the inflammation of her uterus. Over the next 10 years, she had surgery, changed her diet, and was diagnosed with Adeno. Listen to the rest of her journey on the show. Want to keep the conversation going? Join our Facebook Group: tiny.cc/7mpbnz Thank you for listening 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. Thank you for your support and time. Please consider subscribing and writing us a review on Apple podcasts it really helps us get more awareness and with guests agreeing to come on! You can do that here! http://tiny.cc/f74onz

Avsnitt(119)

59. Former competitive Ice Dancer for USA. She could skate through anything except the extreme pain from endometriosis.

59. Former competitive Ice Dancer for USA. She could skate through anything except the extreme pain from endometriosis.

Alissandra, a professional athlete, Ice Dancer for the United States was on birth control from 16 to 22 years old to help control her cycle, she did not have a period in these years. She knew she really wanted to have children and she became nervous about being on BC so she stopped taking it. After she stopped taking it she was in excruciating pain, she found out she had a cyst rupture. She talks about how she could skate through anything but this extreme pain. After several months of cyst ruptures her doctor mentioned endometriosis. She talks about the challenges of being an athlete with endo and how it can be difficult for others to understand what people with endo may be going through. We chat about the taboos of talking about periods. Listen to the rest of her story here. Want to keep the conversation going? Join our Facebook Group: tiny.cc/7mpbnz Want to watch it on YouTube? http://tiny.cc/6cx6tz Thank you for listening 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. Thank you for your support and time. Please consider subscribing and writing us a review on Apple podcasts it really helps us get more awareness and with guests agreeing to come on! You can do that here! http://tiny.cc/f74onz

17 Juli 202140min

58. The ups and downs of endometriosis and trying to start a family.

58. The ups and downs of endometriosis and trying to start a family.

**trigger warning we talk about pregnancy, adoption, & miscarriage. *** hysterectomy is not a cure for endo. Jana felt period before it started, but at 18 years old she knew something was off. She began to have pain all the time, and the pain became increasingly worse. At 19 years old she went to her first gynecologist appointment. She went on BC but she had plenty of side effects like anxiety from it for 5 years. She reflects back on symptoms, acne, constipation, painful sex, and more, now that she knows she had endo. Listen to the rest of her story here. Want to keep the conversation going? Join our Facebook Group: tiny.cc/7mpbnz Want to watch it on YouTube? http://tiny.cc/6cx6tz Thank you for listening 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. Thank you for your support and time. Please consider subscribing and writing us a review on Apple podcasts it really helps us get more awareness and with guests agreeing to come on! You can do that here! http://tiny.cc/f74onz

9 Juli 202155min

57. Endo Warrior and Founder of Hormone University.

57. Endo Warrior and Founder of Hormone University.

Ana is from Spain, but living in New York City. She talks about stress and how her pain increased during extreme stress in her life, multiple surgeries, IVF treatments, fertility, and how important it is for us to take care of ourselves. She founded Hormone University in 2020 as an educational platform with the mission to improve hormone health through widely accessible knowledge and advocate for social impact in our communities. Listen to the rest of her story here. Want to keep the conversation going? Join our Facebook Group: tiny.cc/7mpbnz Want to watch it on YouTube? http://tiny.cc/6cx6tz Thank you for listening 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. Thank you for your support and time. Please consider subscribing and writing us a review on Apple podcasts it really helps us get more awareness and with guests agreeing to come on! You can do that here! http://tiny.cc/f74onz

9 Juli 202139min

56. Does it run in the family? Her Mother & Aunt both had Endometriosis.

56. Does it run in the family? Her Mother & Aunt both had Endometriosis.

Jessica who had painful cramps early on would miss school and functions, she felt shame with this as she would cancel on her friends. As the years went on her pain increased as well. She knows how to prepare for her cycle and even carried a kit. She adjusted her diet and felt best on Paleo. She knows now she has endo and she had decided to go back to school to learn more about natural health. Listen to the rest of her story here. Want to keep the conversation going? Join our Facebook Group: tiny.cc/7mpbnz Want to watch it on YouTube? http://tiny.cc/6cx6tz Thank you for listening 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. Thank you for your support and time. Please consider subscribing and writing us a review on Apple podcasts it really helps us get more awareness and with guests agreeing to come on! You can do that here! http://tiny.cc/f74onz

9 Juli 202151min

55. Jessica Murnane, Endo Warrior & Author of Know Your Endo.

55. Jessica Murnane, Endo Warrior & Author of Know Your Endo.

Jessica chats with me about her endo story, what inspired her to write Know Your Endo as well as tips and tactics from the book. We talk about diet, movement and so much more. Grab a copy of the book here and find Jessica on social media: https://knowyourendo.com/ Listen in now! Want to keep the conversation going? Join our Facebook Group: tiny.cc/7mpbnz Want to watch it on YouTube? http://tiny.cc/6cx6tz Thank you for listening 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. Thank you for your support and time. Please consider subscribing and writing us a review on Apple podcasts it really helps us get more awareness and with guests agreeing to come on! You can do that here! http://tiny.cc/f74onz

9 Juli 202148min

54. Mini Show: Across the pond w. Elva. How to talk to your doctor about Endometriosis.

54. Mini Show: Across the pond w. Elva. How to talk to your doctor about Endometriosis.

Join Elva and Melissa as they chat about how to chat with your doctor about endo in this mini show. Listen in now! Want to keep the conversation going? Join our Facebook Group: tiny.cc/7mpbnz Want to watch it on YouTube? http://tiny.cc/6cx6tz Thank you for listening 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. Thank you for your support and time. Please consider subscribing and writing us a review on Apple podcasts it really helps us get more awareness and with guests agreeing to come on! You can do that here! http://tiny.cc/f74onz

9 Juli 202139min

53. Mini Show: Across the pond..where Elva & Melissa chat about endo, tips of the month and current news headlines about endo.

53. Mini Show: Across the pond..where Elva & Melissa chat about endo, tips of the month and current news headlines about endo.

Join Elva and Melissa in this new mini-episode show within the cycle podcast. They will chat monthly about all things endo, the differences between words in the US vs Ireland, and so much more. This month shows we talk about food, self-care, Jessica Murnane's book, and athletes chatting about endometriosis. Listen in now! Want to keep the conversation going? Join our Facebook Group: tiny.cc/7mpbnz Want to watch it on YouTube? http://tiny.cc/6cx6tz Thank you for listening 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. Thank you for your support and time. Please consider subscribing and writing us a review on Apple podcasts it really helps us get more awareness and with guests agreeing to come on! You can do that here! http://tiny.cc/f74onz

2 Juni 202130min

52. Ignored, laughed at & misdiagnosed with PCOS. Now awaits surgery which is delayed due to COVID-19 in the UK.

52. Ignored, laughed at & misdiagnosed with PCOS. Now awaits surgery which is delayed due to COVID-19 in the UK.

**trigger warning we talk about pregnancy, ectopic pregnancy & miscarriage. Lauren now 29, from Hampshire, UK began to have heavy periods and pain at age 11, her Mum did as well. She thought this was normal. At 14 years old she began birth control and remained on it for 14 years. (changes pills often and not tolerating it well) Her sister has PCOS. She was in and out of A & E with pain over the past 7 years. Where nothing was found to be wrong with her. We chat about NHS, the medical system in the UK, and how a doctor laughed in her face, which provoked her to demand the correct referrals and treatment. Listen to the rest of her story here. Want to keep the conversation going? Join our Facebook Group: tiny.cc/7mpbnz Want to watch it on YouTube? http://tiny.cc/6cx6tz Thank you for listening 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. Thank you for your support and time. Please consider subscribing and writing us a review on Apple podcasts it really helps us get more awareness and with guests agreeing to come on! You can do that here! http://tiny.cc/f74onz

23 Apr 202137min

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