Darlene is a beautiful 28 year old warrior from Norway that has been managing a diagnosis of endometriosis and osteoporosis since 2009. Before she was diagnosed, Darlene explains how she was told it was normal for women to be in pain when they had their period. Darlene was in so much pain at times she would pass out. When Darlene got to high school she started questioning that her body was normal. Darlene spent many visits to the hospital for severe pain. We have a conversation about how she would have to get injections in her knee because she was unable to walk. Darlene tells me how her diagnosis affected her mental health especially when she was told she had to have children immediately because she needed a hysterectomy at 25 and she wasn't even dating anyone at the time. With everything that Darlene had going on in her life she was also diagnosed with depression and PTSD. Darlene began to research in order to advocate for herself and found ways to manage her symptoms through natural remedies and acupuncture. We also have an awesome conversation about how she found an amazing guy online that has accepted her medical conditions after she thought she would never find love because no one understood her struggles. Darlene is such an amazing and courageous lady for sharing her journey with me so others can understand endometriosis and osteoporosis a little better. Darlene you are such a strong, intelligent and caring person the way you want to help others so they don't feel alone!

Follow Darlene on TikTok @darlene_mughole

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Holly is an MSer from the state of Wisconsin who was working in the healthcare field as an RN when she started experiencing dizzy spells when she was out in the heat. That feeling became more frequent and she started dropping things. Holly then went in for a regular physical and her doctor and friend told her that she needed to see a neurologist because something wasn't right with her eyes. Holly then went to see a neurologist and after an MRI she was diagnosed with MS in 2012.

Holly and I have an amazing discussion about how we both hid our diagnosis from our work our employers because of fear of being mistreated because we witnessed it in our work environments. Holly explains how she was pushed out of her profession by the leadership of her hospital. We discuss how employers can attempt to terminate you even though you received perfect evaluations if they consider you a liability. Holly explains how she advocated for her rights and settled with her employer to keep her quiet.

Holly talks to me about her DMT journey and how she didn't want to go on a DMT but tried Copaxone because her neurologist talked her into it. Holly didn't like anything about the treatment so Holly made the decision to quit her DMT. Holly explains how her neurologist was actually not going to see her anymore if she did but he backed down and continues to see her. Holly then explains how after years of doing well she crashed and decided to go back on a DMT.

Holly and I also have a discussion about the mental health part of the disease and how we have had to change the way we thought before MS and how we think about things today. We talk about how we want people to understand the disease and not pity us. Holly shares how important family support is and how it helps our mental health having there support.

Holly and I also talk about an incredible Facebook group called the Multiple Sclerosis Rebels (MSR) that is lead by a beautiful Columbian Liliana (Episode 30). We talk about the importance of finding a community that has people you can speak with.

Thank you so much for sharing your journey Holly! You are an amazing person and a badass MS Warrior!

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Mike is a US Navy veteran and an MS Warrior from the state of Maryland. When Mike was 29 he explains how he was working two jobs that were high stress and a lot of hours. He started having eye issues and was prescribed eyedrops to treat. He also said he was starting to get numbness and went to doctors and it was dismissed. A couple years later Mike began to experience cognitive issues and vertigo causing him to fall and go to ER. Mike even had two MRI's that didn't show any lesions. Then two years later in 2007 Mike had a fourth MRI in a year and a half that finally showed multiple lesions to officially diagnose Mike with MS.

We discuss how the diagnose at 29 affected his life from a mental standpoint. Mike explains how he had very little knowledge of MS. Mike said he was actually relieved when he was diagnosed because now he had answer to why he felt like he did. Mike also talks about the struggles he had with his diagnosis because of the fact it was chronic and would be there the rest of his life. Mike talks about how he attacked his disease with diet changes and exercise. Mike started getting into Bike MS events and found that to be his therapy and motivation in 2010 to fight and not let MS control him. Mike biked his first 100 mile event (century) in 2011 and his Mike Bikes for MS journey began.

Mike and I have an awesome conversation about his relationship with his wife and how his diagnosis made them stronger because his wife battles fibromyalgia so they understand each others struggles. Mike also goes through his DMT journey and how he had issues finding one because of crones disease and various infections. Mike explains the importance of doing your own research when choosing your DMT.

Mike is now an ambassador for the MS Society and an advocate for MS awareness. He continues to bike and if you want to follow him and his journey check his Facebook out @MikeBikesforMS. Thank you Mike for sharing your journey to help people understand what it's like living with MS.

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Madylyn is my beautiful 26 year old step daughter that was diagnosed on the autism spectrum when she was four. Madylyn and I talk about what she remembers from her childhood and how she perceived things different from atypical kids. We talk about sensory issues she had growing up and how she was in a fight or flight mode to stop simple situations because of being on the spectrum. Madylyn talks about how she remembers a lot of therapy when she was young with her mom and how she was always pushed outside her comfort zone as therapy. Madylyn talks about stemming tools and how she learned how to use them to manage her autism. We talk about how why doctors would tell her mom she would never graduate high school because of her autism because of the wide range of the spectrum and how we just don't know early in diagnosis. Madylyn is currently studying to be a pharmacists at the University of Toledo and we get into an amazing conversation about what she is being taught about patient care and also about the pharmacy industry. We talk about everything from costs and research to where medicine is going to look like in the future with AI. We also talk about kickbacks from pharmaceutical companies and taking supplements. Incredible discussion with a brilliant young mind about the pharmacy industry from a pharmacy student. Thank you so much Madylyn for telling your story about what it's like being on the autism spectrum and sharing your knowledge about medicine and pharmaceuticals. You are a warrior and I am so proud to be your step dad!

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I sit down with my beautiful wife, Sharon, who is the mom of an Autistic Warrior and my step daughter Madylyn. We have an incredible conversation about her journey raising a child on the autism spectrum. Sharon explains how she had to fight doctors for four years telling them that her daughter wasn't atypical. Doctors actually were blaming Sharon for her daughter's symptoms as "bad parenting". Finally Madylyn was diagnosed as being autistic and Sharon's journey just started. Sharon then explains how she worked with her daughter every day and how she learned different therapies to use with Madylyn. Sharon tells me how she was on a mission to prove the doctor wrong that said Madylyn would never make it out of high school. We talk about the importance of early recognition of autism signs and diagnosis to get on best therapy path. Sharon also goes into her reasoning why she never told any of her daughter's teachers about Madylyn's diagnosis all the way until she graduated high school because she didn't want her daughter "labeled" by the system. Sharon and I have a great conversation about how people on the spectrum are special and gifted individuals, We talk about how there can be high functioning and low functioning but doesn't mean they don't deserve respect. Sharon talks about how Madylyn was perceived when young by teachers and how she handled the situation. We get into a great discussion about how kids are perceived as being uncontrollable because of sensory issues. There are many people that are on autism spectrum that go to school, work and live throughout society and people need to learn and try to under a little better. Its easy if we just take the time to learn. Thank you so much for sharing your journey of raising a daughter on the autism spectrum.

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Tilly is a return MSer from British Columbia Canada that joined me in Episode 4 to talk about her diagnosis in 2020, We get into a great discussion about how much she has learned about her MS. We talk about how her children have been on board with her fight and how much more they have learned. Tilly discusses how she has learned to adjust her diet because she has figured out that some foods are symptom triggers, We also talk about her employment situation and how she has been fighting every day to get back to work and she is due to start back up in May. Tilly explains how she attacks the weight room daily to improve leg strength. We also talk about the affect that being off work has on our mental health. Tilly says that she is understanding her disease more each day and it is so important to pay attention to your body and the symptoms it presents. Tilly and I discuss how we are goal driven people and how we never give up even if we have a bad day. Tilly is so inspirational with how she attacks this disease and continues to learn and never give up. Tilly is an MS badass that understands the fight and how she has to stay focused on her mission of getting back to work and running a 2K again because that is her passion! Tilly also explains her experience with "crap gap" which she is experiencing right now as she is due to have her next DMT infusion in May.

Tilly thank you so much for sitting down with me to update us on you're journey! I absolutely love talking with you to hear how you fight MS and watching you work towards your goals!

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Karen is an MSer from the state of Washington that was diagnosed with MS 31 years ago in 1994. Karen started her journey right after the birth of her child. She explains how she didn't feel right and it was blamed on post pardon depression and shortly after developed a severe fever after witch her MS symptoms started with her hands tingling. She was rapidly diagnosed with RRMS in 1994 and had to enter a lottery to see if she could receive medication. Karen goes into great detail about her31 year DMT journey and we also get into an awesome discussion about her mental health part of her journey. Karen talks about her experience of being very vocal early on because she wanted to learn and help other people deal with their diagnosis. She also explains how she has learned so much from listening to other people's journey's and has lead support groups. Karen and I have a conversation how she went a four year period symptom from with no DMT and ate super pure and she felt amazing until she had to go on her latest DMT.

Karen is incredible with her experience and wisdom with how to manage her MS with the tools she has developed along the way. Thank you so much Karen for talking with me about your journey! You are a Warrior!

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Jeanene is an MSer from New Jersey that was living her dream in the corporate world when she was diagnosed with MS at 27 years old. Jeanene explains how she experienced numbness in her right leg which she was referred to a chiropractor to treat eventually leading to a neurologist and her diagnosis. Jeanene rebounded and ignored her diagnosis without a DMT and had two children. She explains how after her second child she had vision issues and was recommended a DMT so Jeanene complied because she didn't understand what was happening. While on her DMT Jeanene declined rapidly and she was told by her neurologist there was nothing that could be done. Jeanene and I discuss how she was at her lowest point when she decided to stop her DMT and take control of her MS.

Jeanene shares how her then husband left her because he couldn't handle the diagnosis and she had two young kids to raise and how she fought back. Jeanene started researching and tried to figure out why MS attacks our body and how we can repair our body through diet and nutrition as well as mind and attitude. Jeanene experimented with different diets to see the affect on her body and she started experiencing huge improvements with cognitive and motor function. Jeanene also began researching Epstein-Barr and the correlation with MS.

Jeanene, after 20 years since being diagnosed, is now living a symptom free life with her MS. She explains the tools she has developed and shares with anyone who wants to listen. Jeanene and I discuss how important the mind is battling MS and how we need to have an attitude attacking this disease. Jeanene is absolutely amazing to talk to about her journey kicking MS's ass. Thank you so much sharing your journey Jeanene!

Check out Jeanene's website: https://www.mindingyoursoul.com/

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Adam is an MSer from Michigan that was living the great life at 36 years old. He was working as a supervisor with UPS for 12 years when he started experiencing pain in his feet and numbness. Adam spent the next few months trying to figure out the reason. He explains how he was very athletic and a workaholic putting in 16 hour days so he figured it was work related. Adam declined very rapidly in the next few months and was diagnosed with PPMS at the age of 37 in 2019. Adam explains how he had no knowledge of MS and needed to figure out how he was going to live the rest of his life with new diagnosis.

Adam and I have a great discussion about how stress triggers our MS and how he figured that out very quick in his journey after his insurance was cut off because of a doctor's mistake in documentation. We talk about how his diagnosis affected him mentally because of the loss of independence. We also discuss how both of us were always the person helping and now we are the one that needs help. Adam explains how he had to move back in with his parents because he was not able to take care of himself independently.

MS took Adam's ability to walk and drive but Adam never quit. He explains how he worked hard in a gym every day for a year to regain his ability to walk and how he invested in hand controls for his car so he can keep his independence and drive again after 1 1/2 years of relying on his parents and friends to drive him to appointments.

Adam goes by the brand "MS'd with the Wrong MF'r" that he created and now he is an advocate for MS awareness. Adam is in his 4th year organizing a bike run in Flint Michigan to raise money for the MS Society. His bike run is May 4 2025 and I am going to be driving up to Michigan to join Adam. If anyone would like to join us please check Adam's Facebook and TikTok out for details. Also if you want one of his T-shirts message Adam directly through social media.

Thank you so much Adam for helping to spread awareness about what it's like living with MS!

Follow Adam on TikTok and Facebook @ms'dwiththewrongmf'r

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Maggie is a beautiful lady from the UK that was diagnosed with POTS (Postural Orthostatic Tachycardia Syndrome) in 2021 after getting covid. Maggie goes into great detail what POTS is and the different types that a person can be diagnosed with. Maggie explains how her heartrate was getting into the 200 bpm range when she first started her symptoms and how it took 2 1/2 years to get a diagnoses. Maggie talks about when trying to get answers how she was gas lit by doctors with them blaming her symptoms on anxiety and long covid. Maggie advocated for herself until she could find a doctor that was willing to listen to her. Maggie went through testing that included heart monitors, electrocardiogram and a tilt table test. Maggie explains the validation feeling of the diagnosis after finally being told what she already knew because she knows her body.

Maggie and I have an awesome discussion about how she has learned to manage her symptoms with a beta blocker and also by learning her limitations now with POTS. We talk about how we have to change our lifestyle to live the best quality life we can and sometimes that means losing friends and family along the way. Maggie also talks about the importance of finding a community so you can communicate with other people that can relate to you and your diagnosis.

Maggie is a true warrior with her positivity and never give up hope attitude! Thank you so much Maggie for teaching me so much about POTS! Ignorance is a choice!

Follow Maggie on TikTok @PotsieBotsie

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