Crohn’s Fitness Food Podcast is dedicated to raising awareness, sharing IBD stories, and offering support for those with Crohn’s & Colitis. If you’re going through your own IBD journey or are a family member supporting someone with this disease, I hope you find inspiration, confidence, and community through this podcast. Together we can share knowledge, experiences, and help show the world the many faces of IBD.
A lot has happened since my last episode so I'm giving you an update on my own IBD journey and sharing a big move that my husband and I are about to embark upon!
Topics covered:
#chronicillness #travel #crohns
Ashley Zuchelli shares her journey with Crohn's disease, from the onset of symptoms to her recent diagnosis. She discusses the challenges she faced in finding a doctor who would listen and the frustration of not knowing what was causing her symptoms. Ashley also talks about the impact of Crohn's on her work and how she manages anxiety. Finally, she shares her motivation for advocacy and raising awareness about IBD. In this conversation, Ashley Zuchelli shares her journey with IBD and the challenges she faced in getting a diagnosis. She emphasizes the importance of realizing when something is wrong and seeking help, even when faced with fears and uncertainties. The conversation also highlights the difficulties doctors face in diagnosing IBD and the need for patients to advocate for themselves. Ashley encourages listeners to not give up on their goals, to prioritize their health, and to listen to our bodies and not dismiss symptoms.
Takeaways
Topics covered in the interview
From the show
Stephanie: What have you done over the years to help manage anxiety?
Ashley: I would say meal prepping actually soothes me and it keeps my mind at ease because I know if I am hungry or if…I’m feeling good that day, I have food ready for me and it just makes me happy just cooking in the kitchen…And then I started doing the HelloFresh program, where I get ingredients sent to me and then I just cook. I don't have to think about the recipes. They have dietary restrictions on there of things you can and cannot eat, so that helps my anxiety—to make sure I have the food I need when I have a long day at work or if we go travel.
feeling so great today or, you know, I do have that type of job where if I wasn't feeling well, I can block that time and deal with what I need to deal with. If I had a flare or upset stomach from eating something or just.
Stephanie: How do you balance work and work in IBD?
Ashley: You know, Crohn's being Crohn's, acting up when it's not the best time, so I was just honest with my clients. Like if I didn't feel well, like I have to go to the bathroom, [saying] I'll be right back. We don't discuss what happens in the bathroom, but they know I need a moment to break away because of issues going on…I am grateful that I have the luxury to make my own schedule when a flare happens.
Links from the show:
* * * * *
Support the podcast ❤️ at https://www.crohnsfitnessfood.com
Want to share your story? Send me a message here or email [email protected]
#crohns #crohnsdisease #ulcerativecolitis #ibd #podcasthost #healthpodcast #chronicillness #chronicillnesspodcast #ostomy
Back on medication and mindset changes during my Crohn’s journey
It’s been over 20 years since my colon started bleeding and my inflammatory bowel disease (IBD) journey began. In 2003, I ignored the symptoms of blood, pain, and bloating for nearly three years. When I finally sought help in 2006 after a severe flare, it took another three years to reach a diagnosis. In those first six years, I was left to my own devices to try and stop the symptoms and find some way of living a normal life.
It’s been a long journey with Crohn’s disease and I know it’s far from over. As I reflect back to my first six years with IBD and being left on my own to manage symptoms, I now wonder if I would have been so determined to come off medications ten years ago if I would have received the help and diagnosis I needed at the very beginning. I don’t know the answer to that, but what I do know is that as life goes on, we evolve, we grow, and things change – including our perspectives and even beliefs we once held so tightly.
I’m ready now, and I’m grateful. Grateful to have a supportive gastroenterologist who listens and actually believes me, grateful to have access to medications I need, and grateful for a clear path ahead for this next chapter.
* * * * *
Support the podcast ❤️ at https://www.crohnsfitnessfood.com
Want to share your story? Send me a message here or email [email protected]
#crohns #crohnsdisease #ulcerativecolitis #ibd #podcasthost #healthpodcast #chronicillness #chronicillnesspodcast #ostomy
Dr. Natalie Scheeler, a naturopathic doctor specializing in integrative treatments for gastrointestinal conditions, shares her perspective and valuable insights on gut health. She discusses the difference between naturopathic doctors and traditional MDs, the use of fecal microbiota transplant (FMT) and Helminthic therapies in treating inflammatory bowel disease (IBD), the impact of food and probiotics on IBD, and trends in flare management and remission. Dr. Scheeler also provides information about her practice, Modrn Med, and offers a final message of hope and encouragement for patients seeking alternative or complementary treatment options.
Takeaways
Topics covered in the interview
Links and studies from the show
Support the podcast ❤️ at https://www.crohnsfitnessfood.com
Want to share your story? Send me a message here or email [email protected]
#crohns #crohnsdisease #ulcerativecolitis #ibd #podcasthost #healthpodcast #chronicillness #chronicillnesspodcast #ostomy
Enjoy this interview with Megan Starshak, an ulcerative colitis warrior, adventurer, runner, cyclist, patient advocate and co-founder of The Great Bowel Movement.
In this conversation, Megan shares her journey with inflammatory bowel disease (IBD), her advocacy work, and how she balances life with chronic illness. She discusses her diagnosis of ulcerative colitis and the challenges she faced in finding effective treatments. Megan emphasizes the importance of finding a supportive community and offers advice for young adults with IBD. She also talks about her involvement with The Great Bowel Movement, an organization that aims to decrease the stigma surrounding IBD. Megan shares her career in marketing and how she uses her skills to support other patient advocates. She closes this interview with a message of empowerment and the importance of not wasting the challenges we face.
Takeaways
Topics covered in the interview
Links from the show:
The Great Bowel Movement:
Megan:
* * * * *
Support the podcast ❤️ at https://www.crohnsfitnessfood.com
Want to share your story? Send me a message here or email [email protected]
#crohns #crohnsdisease #ulcerativecolitis #ibd #podcasthost #healthpodcast #chronicillness #chronicillnesspodcast #ostomy
Enjoy this interview with Leah Crumrine, a businesswoman, mother, and wife of IBD Warrior Logan Crumrine. Logan has been on the show to share his story with Crohn’s disease, but today, his wife Leah shares from her perspective about what it’s been like to walk along IBD with her husband. She shares her experience, insights, and tips for supporting those in your life with IBD.
Summary
Leah Crumrine shares her experience as a caregiver to her husband, Logan, who has Crohn's disease. She discusses the challenges they faced during Logan's flare-up, the changes in roles and responsibilities, and the importance of communication in their relationship. Leah also talks about managing food and family meal planning, communicating with their children about the disease, and the support system they had throughout their journey. She emphasizes the need for caregivers to prioritize self-care and balance, and offers advice for managing day-to-day flare-ups. Leah concludes by discussing the therapeutic aspect of advocacy and sharing their journey with others. This conversation explores the journey of Logan and Leah Crumrine as they navigate life with inflammatory bowel disease (IBD). It highlights their journey to recovery, reaching remission, finding balance, and hope and perseverance. Leah also offers support to others facing similar challenges and emphasizes the importance of continuous learning and love.
Takeaways
Topics covered in the interview
Links from the show:
* * * * *
Support the podcast ❤️ at https://www.crohnsfitnessfood.com
Want to share your story? Send me a message here or email [email protected]
#crohns #crohnsdisease #ulcerativecolitis #ibd #podcasthost #healthpodcast #chronicillness #chronicillnesspodcast #caregiver
Enjoy this interview with Steve Carver, an IBD warrior, a personal trainer with over 30 years of experience, and the business and product development director at JumpSport. He shares his journey with colitis and dives deep into one of my favorite topics and activities: rebounding!
Summary
Steve Carver shares his journey with colitis and how he found recovery through a holistic approach. He discusses the benefits of rebounding and how it has helped him maintain his health. Steve also provides advice on getting started with rebounding and emphasizes the importance of consistency and discipline in managing IBD. In this conversation, Steve discusses the benefits of rebounding. He shares options for trying rebounding, including gyms and online platforms. Steve emphasizes the fun and versatility of rebounding, highlighting that it is not a boring workout! Steve encourages listeners to put in the work to overcome health challenges and live a peaceful lifestyle. He emphasizes the importance of maintaining a positive attitude and learning from setbacks. Steve provides information about JumpSport and invites listeners to reach out with any questions.
Takeaways:
Rebounding on a trampoline can provide numerous health benefits, including increased lymphatic flow, improved mental health, and enhanced balance and stability.
Getting started with rebounding can be as simple as purchasing a personal fitness trampoline or finding a gym that offers rebounding classes. You can use the JumpSport club finder to find a gym near you with classes: www.jumpsport.com/jumpsport-club-studio-locator/
Rebounding is a fun and versatile workout.
Consistency and discipline are keys in maintaining a healthy lifestyle.
Putting in the work and having a positive attitude can help overcome health challenges.
Topics covered in the interview:
Steve Carver's Journey
Holistic Approach to Treatment
Transition to Rebounding
Health Benefits of Rebounding
Time Spent on the Trampoline
Getting Started with Rebounding
Options for Trying Rebounding
The Fun and Versatility of Rebounding
Accessing Rebounding Programming
Maintaining a Positive Attitude
Finding Information about JumpSport
Additional Questions and Contact Information
Links from the show:
JumpSport - www.jumpsport.com
Rebounding Benefits - www.jumpsport.com/fitness/benefits-of-rebounding/
ACE Study - www.jumpsport.com/blog/ace-study-proves-exercise-trampoline-benefits/
YouTube Channel - www.youtube.com/@JumpSportFitness/videos
Instagram JumpSport - www.instagram.com/jumpsportfitness
Instagram Steve Carver - www.instagram.com/carvercompletefitness
* * * * *
Support the podcast ❤️ at https://www.crohnsfitnessfood.com
Get your copy of Crohn's Fitness Food and My Rocky Road to Health,
Shop my favorite products,
Read my favorite books,
Subscribe to the podcast,
Send a little love/coffee 😉
More at crohnsfitnessfood.com
Want to share your story? Send me a message here or email [email protected]
#crohns #crohnsdisease #ulcerativecolitis #colitis #ibd #podcasthost #healthpodcast #chronicillness #chronicillnesspodcast #jumpsport
Enjoy this interview with Logan Crumrine, a Crohn’s disease warrior of more than 30 years, advocate, and writer.
Logan was first diagnosed in 1990. For years he fluctuated between states of flares, semi-remission, clinical trials and surgeries, and then went into complete remission for over 15 years! But remission came to an end in 2012 and he spent the next few years fighting for his life and eventually filed for disability. Today, he’s now in his second year of remission and living life to the fullest.
Some of you will remember Logan as one of my repeat guests. He shared the first part of his story in episode 29 of this podcast in July 2019, and came back a year later in 2020 to talk about his experience and knowledge about going through the process of filing for disability.
Today, he’s back to update us on his journey and share what it’s like to now live in remission.
From the show:
Stephanie: What kind of tips do you have for other people who are finding themselves newly in remission and still afraid to let go of the habits that they've held onto for so many years as their safety net?
Logan: I think the best advice would be that you've kind of got to do your own walk in that. You've got to kind of let go of those things as you feel comfortable. I still carry supplies in my backpack, but I don't carry as many. I don't carry an extra change of clothes, so my backpack has gotten down to just some undergarments in there and some stuff to clean up if I need to.
It's a much smaller kit, but again, I'm still learning. It's still automatic for me to put all that stuff on when I'm going out. And I think it's just, you just kind of have to challenge yourself and push yourself. It helps too that I have Leah with me, who's an incredible partner who reminds me, ‘hey, you know, you made this trip a couple of times without anything. Why don't you try it again?’
Or I'll be able to share with her that I didn't even get ready like I normally do for a trip. And then it's kind of an epiphany almost to say, ‘oh wow, we don't need that stuff all the time anymore.’
Stephanie: You've shared on social media a few times about struggling with Crohn's and depression. Can you talk about how you've coped through some of the hardest times and how has remission affected your overall mental health?
Logan: I think remission has helped my mental health and has benefited it. I still struggle with depression and sometimes, some days, it's absolutely debilitating. Right now, my depression seems to be presenting itself with insomnia. So I can be tired at seven o'clock and think, okay, I'm going to head to bed around nine and then I'm up till two. So it seems to be presenting that way.
I think being in a place with more sunlight has helped. Seasonal depression affected me really bad in Washington because where I lived in Washington, from about October to March, it's very dark and very gray. It's nice to be able to look out the window and see blue skies and sun, I'm trying to get back to exercising because that's so vital to mental health.
Stephanie: You have shared on social media about your fitness journey and just getting to a place of better overall health, what were some of the baby steps or the ways that you started to get back into that as you were feeling better?
Logan: I think that, and for the record, my hiking and walking come and go, like any kind of fitness thing, I do really good for a while and kind of back off for a little while. I think that one thing that I had to do is realize that I have to start with what I can do, even if it's five minutes of getting outside and taking a walk. I started when I was starting to get my health back. I was just literally doing laps around the cul-de-sac. And that's all I could do, just walk around the cul-de-sac very slow with a cane. It was very difficult for me to even get out and do anything. And now, I mean, where I was at the height that's kind of dropped off since we moved, but I'm trying to get back into it. I think I was doing three or four miles a day walking. I was lifting regularly because again, medications that you get on Crohn's and colitis, steroids, sometimes those things play havoc on your bones.
Links from the show:
Social Media
Studies on steroids and blood sugar:
What if the Monsters are Afraid of Me (Book)
Previous episodes with Logan:
* * * * *
Support the podcast ❤️ at https://www.crohnsfitnessfood.com
Get your copy of Crohn's Fitness Food and My Rocky Road to Health,
Want to share your story? Send me a message here or email [email protected]
#crohns #crohnsdisease #ulcerativecolitis #ibd #podcasthost #healthpodcast #chronicillness #chronicillnesspodcast #ostomy
Enjoy this interview with Abigail Marie the Chef With IBD. She was diagnosed with ulcerative colitis in 2014, halfway through culinary school. Throughout her journey, she’s navigated various medications, been hospitalized during severe flares, and even adjusted her career path as chronic illness was consuming her life.
Unable to find relief, she began experimenting with diet and eventually found the Specific Carbohydrate Diet (SCD). Since then, she’s improved her health and discovered a new dream: to help others with inflammatory bowel disease (IBD) live better lives through healing and flavorful foods.
In this podcast episode, she share’s her story, perspective, and tips for fellow IBD patients.
From the show:
Stephanie: What advice would you give to other IBD patients who might be in a similar position where they're having to face making a career change?
Abigail: You know, I was so set on my dream of being a chef, but that's not the path that life took. And you know, you'll find another dream. Now my dream is working on my blog, doing SCD recipes and sharing with the community — sharing my story and advocating and raising awareness.
You will find something else. I know it seems so devastating, but just trust that you're on the right path and that you'll find a new dream.
Stephanie: What are some of the things you've found in your life to help manage stress?
Abigail: I keep a gratitude journal. I do that first thing in the morning and right before I go to bed, and it really helps me get the right mindset for the day. I also do a daily meditation. It's not long, it's 10 to 12 minutes, but just having those 10 to 12 minutes to myself in the morning before my day starts has been really helpful for me.
And then just practicing mindfulness, just trying to be in the moment. Chronic illness can be really scary, you don't always know what's around the corner, but you have this moment right now. So just trying to take yourself out of that worrying about the big picture. I also practice Qigong, it’s similar to Tai Chi, it's like mindfulness movement.
I do that a few times a week for 15 or 20 minutes and that really helps me move stress through my body. Whereas the meditation and the gratitude journal are more for my mind. The mindfulness movement is more for the body. So balancing both of those, mind and body.
Links from the show:
* * * * *
Support the podcast ❤️ at www.crohnsfitnessfood.com
Want to share your story? Send me a message here or email [email protected]
#crohns #crohnsdisease #ulcerativecolitis #ibd #podcasthost #healthpodcast #chronicillness #chronicillnesspodcast #ostomy
Enjoy this interview with Amber J Tresca, health content creator, writer, speaker, advocate, and host of the About IBD podcast.
Amber was diagnosed with ulcerative colitis at the age of 16, had a colectomy at age 26, and started writing about inflammatory bowel disease (IBD) and other health conditions one year later! She’s been writing ever since, sharing both about her own journey and writing for a variety of health publications giving insight and technical information about IBD.
In this podcast episode, she share’s her story, perspective, and tips for fellow IBD patients.
From the show:
SG: How important it is to get care, and the right care, right away?
AT: …it’s so important. And it's important also to not get into that fatalistic state of mind that I was in, that I still don't know where it came from, but that I could only expect so much improvement and that it wasn't going to go further than that. I should have expected, I should have demanded more, but I didn't know what I didn't know.
Today we have better treatments, we have a lot more understanding, there's better testing, etc. But you still, as the patient, have to be the one (or as a parent or a caregiver) you have to be the one to make sure that all of this is happening and you have to be the one to advocate for yourself or your loved one to make sure that you're getting what you need. And I've heard lots of stories about how people advocate for themselves and the ways in which they make changes…There’s always a workaround. There's always a way that you can make the situation work for your life, but you have to explain what that is to your healthcare providers and help them help you get to where it is that you want to be.
SG: What are some of the top resources that you would recommend to people listening to go to for information?
AT: …my first place to go is PubMed, but I know that's not for everybody. Not everybody wants to wade through all of that stuff to find what they're looking for. But I do often give talks or write about how you can find good sources of information.
…government sites, educational sites, and patient advocacy group sites, so .gov, .org, .edu, is usually a good place to start and to find information.
The second thing that I would look for in information is who wrote it. And I just told you that I write all kinds of stuff without a byline. But when you read something, there should be an identifiable entity, at least. Even if it says staff writer. It shouldn't just be a bunch of very clinical advice-sounding type stuff on a page and you don't know who wrote it. You should know who wrote it and how to get in contact with them.
Three, would be looking at what the site that you are interacting with, or the app, I guess I should say, what they're getting out of it. Are they selling you something? And I'm not saying that someone who has something for sale is always off the table. I mean, if you sign up for my newsletter, I have discount codes in there too that you can go and purchase some of the things that I have vetted and that I use in my own life…But I will say it should be clear and you should have a clear understanding of if that person is selling something and then what they are selling.
…So the fourth thing is, is that you want to see that the information that you are looking at, receiving, interacting with, goes back to some primary sources. So that's where it gets back to that PubMed thing…Did they get it from a source that is, for instance, someone interviewed a clinician, which is something that you and I do, you interview someone like that, they're a source. They link back to a clinical trial. Okay, they're talking about a medication. So they link to maybe a trial on that medication. That's great. Or they link back to, for instance, a patient advocacy group or an educational resource like an IBD center, which there are several across the country. That's good to know. Whenever I see something that says like 10% of people XYZ, I want to know where that 10% came from. Where'd that come from? There's got to be something behind that for me. So that's another thing that I usually say that people should look for when they're looking for good sources of information.
…number five is your own healthcare team. Ask them for the resources, okay, because we all want to go online and look for things because it's easy and convenient and works out really well. But there are also sources that are offline, another patient that they might suggest for you to be a sort of a mentor for you, or someone else on the healthcare team, like a dietician, like a mental health specialist. Those people are great sources, primary sources, of information for you, and then they can also tell you what it is that they think would be helpful for you.
Links from the show:
* * * * *
Support the podcast ❤️
Want to share your story? Send me a message here.
Enjoy this interview with Tim Parsons, a Crohn’s disease warrior, ambulance service chaplain, and author of the children’s book series Paramedic Chris.
Through the Paramedic Chris children’s books, Tim aims to help develop children's reading skills and also offers support for important subjects such as anxiety, fear, and working together as a community.
In today’s episode, he shares his story with IBD and how he balances life with Crohn’s.
Social media & links from the show:
Books:
* * * * *
Support the podcast ❤️
Want to share your story? Send me a message here.