This ill Only Hurt A Little

Aimee Bird is a mom and wife working full time as a HR manger. With 3 daughters, a bunch of dogs, and birds her life is bustling and full. When not watching and cheering on her daughters at their many sport events you can find Aimee and her husband on the golf course. You can count on Aimee to be the first to lend a helping hand or encourage/support/motivate/ her friends and family. Aimee's daughter Marlee has an eating disorder called Anorexia Nervosa. Anorexia is a psychological disorder characterized by abnormal eating habits, and an obsessive need to lose weight by not eating. Recognizing the signs of anorexia is not always easy, but a diagnosis is extremely crucial and can be life saving. These signs can be different and subtle but things to look out for include: fatigue, insomnia, yellow or blotchy skin, thinning hair, constipation, irregular or absent periods in women, dry skin, excessive exercise, irritability and low blood pressure. Although an eating disorder can look different for anyone who suffers from it, it is important to reach out and seek help. If you or someone you know Is suffering from an eating disorder you can call or text the national eating disorder association hotline at (800) 931-2237 And like Marlee said in the episode “nothing lasts forever” you can fight for a better life. --- Support this podcast: https://podcasters.spotify.com/pod/show/claire-scattini/support

Sal Lucatero (@thatoneguysal on Instagram) is, in every sense of the word, a community builder. He is an Events Manager for a tech company and works to build strong community networks through experiential events that help drive change and create a workforce in underdog communities. Using this same logic, he has found ways to bring together young people diagnosed with T1D and create a strong support system using real-life meetups and social media networks. He is currently obsessed with remodeling his home with his 130 pound, adopted Great Pyrenees, Clifford, and looking for ways to travel to some of the most exotic places on earth. When he's not at home or working in the community, you can find him hanging out with his friends at a music festival or finding ways to build a new music festival from scratch. Sal was diagnosed with Type 1 Diabetes at 19 years old and since then, has taken control of how to manage living with a chronic illness, especially as a young adult. Type 1, an autoimmune disorder, which occurs because of antibodies that destroy your pancreatic beta cells. Without these pancreatic cells, the body can no longer produce insulin. --- Support this podcast: https://podcasters.spotify.com/pod/show/claire-scattini/support

This week we interviewed our own brother Jordan! In his free time he paints, plays video games, cooks, travels the world, and works on his home renovations. He enjoys watching gaming streams on YouTube and Twitch, and is always dreaming up new business ideas. Jordan has obsessive compulsive disorder. OCD is a mental health disorder defined as Excessive thoughts (obsessions) that lead to repetitive behaviors (compulsions). Obsessive-compulsive disorder is characterized by unreasonable thoughts and fears (obsessions) that lead to compulsive behaviors. There are more than 20,000 cases of ocd in the United States each year, and although treatment can help there is no cure. This ill only hurt a little links: Instagram Facebook Twitter TikTok Music by: Alexis Tenney --- Support this podcast: https://podcasters.spotify.com/pod/show/claire-scattini/support

Gabby is a 24 year old future educator. She is currently getting her math education degree while working with students for the past 6 years. She has a strong passion for working with the youth and her goal in life is to make a difference in kids lives all throughout the community. While pursuing this passion, she has also been fighting cystic fibrosis. Her life consisted of countless hospital stays for 10 days minimum, lots of medications and breathing treatments. In 2018, her life was completely changed for the better when she started a gene modulator medication. Along with her CF, she became mostly deaf throughout her late high school & early college years. Her hearing loss came from an IV medication she would go on while in the hospital. Since losing 85% of her hearing, she has received a cochlear implant in her right ear and has a new way she looks at life. Cystic Fibrosis is an inherited disorder that damages the lungs and digestive system. Cystic fibrosis affects the cells that produce mucus, sweat, and digestive juices. It causes these fluids to become thick and sticky. They then plug up tubes, ducts, and passageways. This ill only hurt a little links: Instagram Facebook Twitter TikTok Music by: Alexis Tenney --- Support this podcast: https://podcasters.spotify.com/pod/show/claire-scattini/support

In this episode its just the two of us! We are going down the list of all our symptoms, the bad and the ugly. Let's start talking about how we actually feel and end the "I'm fine" stigma. You are doing great sweetie, with chronic illness there are good days and bad, so let's break it down and talk about what living with a chronic illness is truly like. This ill only hurt a little links: Instagram Facebook Twitter TikTok Music by: Alexis Tenney --- Support this podcast: https://podcasters.spotify.com/pod/show/claire-scattini/support

Alicia Quinn owns and operates Moonrise Aesthetics, a waxing and skincare studio in California. She relocated to back home from Northern California to raise her young daughter closer to family. When she isn't balancing work and mommy duty she can be found snuggling with her fur baby, reading tarot, gardening, or remodeling their 1960s house with her fiancé, Zephan. Today we will discuss her journey with Sjogren's Syndrome. With this disorder, the body's immune system attacks its own healthy cells that produce saliva and tears. Sjögren's often occurs with other such disorders, such as rheumatoid arthritis and lupus. This ill only hurt a little links: Instagram Facebook Twitter TikTok Music by: Alexis Tenney --- Support this podcast: https://podcasters.spotify.com/pod/show/claire-scattini/support

Jenni Stagis is a 35 year old pediatric RN, cop wifey and boy mama to 4 year old twins! You can find her and her family camping in the mountains any chance they get! She loves coffee, yoga and a good glass of wine. Her absolute favorite thing of all time are sunflowers... she just can't get enough of them! Jenni will be telling us about her journey with ovarian cancer. Ovarian cancer often has no symptoms in the early stages. Later stages are associated with symptoms, but they can be non-specific, such as loss of appetite and weight loss. Ovarian cancer often goes undetected until it has spread within the pelvis and abdomen. The American Cancer Society estimates for ovarian cancer in the United States for 2021 about 21,410 women will receive a new diagnosis of ovarian cancer. This ill only hurt a little links: Instagram Facebook Twitter TikTok Music by: Alexis Tenney --- Support this podcast: https://podcasters.spotify.com/pod/show/claire-scattini/support

Danica McCall is a wife and mom of two amazing kids, plus a few fur babies

Hannah Hawkins spends her days working as a personal assistant solving problems and creating order out of chaos. When she has free time, you can find her reading, listening to music, or sitting by the water in San Francisco after work. Her simple pleasures are ordering Uber Eats and anything with next day delivery on Amazon Prime. Hannah will be discussing endometriosis, a disorder in which tissue that normally lines the uterus grows outside the uterus. With endometriosis, the tissue can be found on the ovaries, fallopian tubes or the intestines causing excruciating pain. Endometriosis affects an estimated 1 in 10 women between the ages of 15 to 49, which is approximately 200 million women in the world. Endometriosis can mimic the symptoms of a urinary track infection and the condition can be found in adolescents and even in girls as young as 8 years old.This ill only hurt a little links: Instagram Facebook Twitter TikTok Music by: Alexis Tenney --- Support this podcast: https://podcasters.spotify.com/pod/show/claire-scattini/support

Ashley is a filmmaker, artist, and chronic illness advocate. She is also the director and producer of Behind the Visible, an upcoming documentary about living with POTS (postural orthostatic tachycardia syndrome). Over the last three years, she and her husband embarked on a journey to create this film to raise awareness for the little-known condition. When she's not advocating for POTS, she loves to explore the US National Parks, paint, sing, and tend to her garden. On this episode we will discuss all things related to filming a documentary about chronic illness while also having chronic illness. Behind the Visible premieres May 21, 2021 at 7pm CST. To register for the Virtual Premiere Night, @behindthevisiblefilm or visit www.behindthevisiblefilm.com This ill only hurt a little links: Instagram Facebook Twitter TikTok Music by: Alexis Tenney --- Support this podcast: https://podcasters.spotify.com/pod/show/claire-scattini/support

Matthew Prieto, while he's not busy working at a suspension shop he loves watching the raiders, going on runs and exercising with his brother. He recently made a best friend with a dog named Fen. Although he never was a fan of dogs, Fen stole his heart when his girlfriend brought the puppy home and they've been inseparable ever since. Today he will tell us about his health journey with ulcerative colitis, which is part of a group of diseases called inflammatory bowel disease (IBD). We will discuss his three surgeries, recovery, and how he is managing the disease today. This ill only hurt a little links: Instagram Facebook Twitter TikTok Music by: Alexis Tenney --- Support this podcast: https://podcasters.spotify.com/pod/show/claire-scattini/support

Jennie Schuh is a mom and a wife with a passion for all things creative. When she's not playing with her kids, her favorite thing to do is combine her love of travel and other cultures with her love of photography. One of her life goals is to visit every continent. On this episode we will discuss with Jennie her experience with Huntington's disease. Her moms diagnosis, genetic testing resulting in both she and her brother being diagnosed and her brother being diagnosed and her children's potential diagnosis. Symptoms of Huntington's disease usually develop between ages 30 and 50, but they can appear as early as age 2 or as late as age 80. The hallmark symptom of Huntington's disease is unctrolled movement of the arms, legs, head, face and upper body. HDSA link This ill only hurt a little links: Instagram Facebook Twitter TikTok Music by: Alexis Tenney --- Support this podcast: https://podcasters.spotify.com/pod/show/claire-scattini/support

Nicole is a wife, mother of 2 boys, RN, enjoys: spending time with family and friends, watching sports(not playing sports), weekend getaways to the central coast, wine tasting(haven't been able to tolerate that right now-but hopeful that will change). We will discuss Nicole's experience with Covid-19, her lingering symptoms and being hospitalized after recovery from COVID-19. She pushed for answers, a diagnosis and treatment with her medical knowledge but it has not been easy. Imagine you can't meet your responsibilities at home or at work: no energy, dizziness, chest pains and severe brain fog. Tens of thousands of people in the United States have lingering illness following COVID-19. “Long-haulers,” defined as individuals who have had COVID-19 symptoms for six or more weeks. A common long-hauler diagnosis is ME/CFS can be triggered by other infectious illnesses — such as mononucleosis, Lyme disease, or severe acute respiratory syndrome(SARS). This ill only hurt a little links: Instagram Facebook Twitter TikTok Music by: Alexis Tenney --- Support this podcast: https://podcasters.spotify.com/pod/show/claire-scattini/support

Crystal is a wife, dog mom, and avid plant lover filling her garden and home with beautiful greenery. While she is not being the karaoke Qween she can be found creating art and custom prints. Crystal will be discussing her journey with Polycystic ovary syndrome, or PCOS, which is an endocrine disorder in women. We will learn how she is navigating multiple ovarian cysts and infertility. She will be telling us how she has found joy in the #ttc community and advice on being a supportive spouse, family member or friend. PCOS is most common among women between the ages of 18 and 44. It affects approximately 2% to 20% of this age group depending on how it is defined. The earliest known description of what is now recognized as PCOS dates from 1721 in Italy and still PCOS has no cure. This ill only hurt a little links: Instagram Facebook Twitter TikTok Music by: Alexis Tenney --- Support this podcast: https://podcasters.spotify.com/pod/show/claire-scattini/support

Paige Willis is a full time student, barista at Starbucks while also pursuing a career as a musician and released her very first single “Does She Know Me” last fall. As well as pursuing music she is working towards a degree in theater with a minor in psychology. She's had a some great accomplishments but the most recent one she can check off her list is surviving brain surgery! We will discuss her diagnosis of Chiari Malformation, a condition in which brain tissue extends into your spinal canal. It occurs when part of your skull is abnormally small or misshapen, pressing on your brain and forcing it downward. How she discovered through genetics that she had the CM type l. And her experience and recovery from decompression surgery. Paiges instagram Paiges new single This ill only hurt a little links: Facebook Twitter TikTok Music by: Alexis Tenney --- Support this podcast: https://podcasters.spotify.com/pod/show/claire-scattini/support

Matty Penner is a talented artist, mental health advocate, and a published author. His memoir “Hide Your Shoes” is currently in the process for publication. You can view his art at therollawayart.com or follow him on Instagram @therollawayart Today we will discuss his journey and experiences with mental health and his diagnosis of bipolar disorder/manic depression. We'll explore what he's learned, how his life has changed, and the advice he would give someone experiencing similar symptoms. In addition, we'll reflect on how a friend or family member can help a loved one in a time of need. Ten percent of Matty's art sales are donated to the International Bipolar Foundation. For more information follow @intlbipolar and click the link. If you need to speak to someone immediately, please call the National Suicide Prevention Lifeline, available 24 hours at 800-273-8255 This ill only hurt a little: Instagram Facebook Twitter TikTok Music by: Alexis Tenney --- Support this podcast: https://podcasters.spotify.com/pod/show/claire-scattini/support

Armond Vance is an orchestra director, tedx speaker, music educator, artistic activist, yogi and so much more! In this episode we will discuss his health journey as he fought for answers and a diagnosis. And how he navigates life with Postural Orthostatic Tachycardia Syndrome. All while roller skating and playing violin at the same time people! This genius man plays FIVE instruments not including his beautiful voice! Armonds instagram This ill only hurt a little: Instagram Facebook Twitter TikTok Music by: Alexis Tenney Episode sponsored by Anchor.fm --- Support this podcast: https://podcasters.spotify.com/pod/show/claire-scattini/support

Chronic illness advocates, creating a community of acceptance. Welcome to our first ever episode! We are so excited to share our story and health journey, along with many others. In this episode we talk about our journey with diagnosis and life with chronic illness. Navigating Ehlers Danlos syndrome, Postular Orthostatic Tachycardia, Hydronephrosis, Mast Cell Activation disorder, Chronic active Epstein Barr virus, ME/CFS, cystitis, sleep apnea, and Acute Disseminated Encephallmyelitis. Chronic illness warriors.  Music by Alexis Tenney  Instagram: thisillonlyhurtalittle  facebook: thisillonlyhurtalittle  Twitter: candjthepod --- Support this podcast: https://podcasters.spotify.com/pod/show/claire-scattini/support