TheMagic5 Swimming Blog

Kyle Brown: Breaking the Rules of ALS

34 commentaires

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I’ve been living with Parkinson’s disease for quite some time, and for years, I struggled to find lasting relief. While medications offered some temporary help, the symptoms always returned and often worsened.Out of a mix of hope and hesitation, I decided to try an herbal treatment program from NaturePath Herbal Clinic. I’ll admit, I was skeptical at first. But around the fourth month, I began to notice real, steady progress.my tremors became less frequent the stiffness in my body eased My balance and coordination gradually improved It wasn’t an overnight transformation, but it was consistent and life changing. For the first time in years, I feel more in control of my body. I can move with greater freedom, sleep more peacefully, and enjoy daily activities without the constant discomfort I once accepted as normal.The improvement I’ve experienced physically, emotionally, and mentally has been nothing short of upliftings.If you're exploring natural options for managing Parkinson’s, I wholeheartedly recommend looking into NaturePath Herbal Clinic. Their approach has made a real difference in my life, and I’m truly grateful I gave it a chance. <www.naturepathherbalclinic.com> <info@naturepathherbalclinic.com>

William 24 juin 2025

After struggling with Parkinson’s disease and vertigo for 8 years…and my wife with ALS for 5 years, we had almost given up hope. We spent so much money on conventional treatments, but nothing truly worked. Then we found “www.earthcureherbalclinic,com”. After completing their treatment program, all our symptoms are completely gone. We are finally healthy again, and words can’t express how grateful we are.

Tariq Aarav 11 juin 2025

My first ALS  symptom occurred in 2016, but was diagnosed in 2018. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatiue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Aknni herbs centre, It has made a tremendous difference for me (Visit ww w. aknniherbscentre.c om). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others.

cory melon 10 juin 2025

My first ALS  symptom occurred in 2016, but was diagnosed in 2018. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatiue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Aknni herbs centre, It has made a tremendous difference for me (Visit ww w. aknniherbscentre.c om). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others.

cory 09 juin 2025

My first ALS  symptom occurred in 2016, but was diagnosed in 2018. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatiue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Aknni herbs centre, It has made a tremendous difference for me (Visit ww w. aknniherbscentre.c om). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others.

cory 09 juin 2025

My first ALS  symptom occurred in 2016, but was diagnosed in 2018. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatiue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Aknni herbs centre, It has made a tremendous difference for me (Visit ww w. aknniherbscentre.c om). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others.

cory 09 juin 2025

I was diagnosed in March 2017, but was running around from doctor to doctor before I finally got a result that I was free from MND ALS. Mine started on top and progressed into the bottom. I could walk very little but need assistance as I have no balance. It is sad all the time that we thought this disease had no cure with all the technology we have, while some formulas at there can relieve all symptoms and get this of ALS. I’m passing this information to anyone who needs it, because www. madibaherbalcenter. com has the right cure and caregiver for this disease.I took various supplements, medicine prescribed by a neurologist, massage, and physiotherapy, still the disease was progressing very fast until the ALS formula from that company.

Andrea 07 juin 2025

I was diagnosed in March 2017, but was running around from doctor to doctor before I finally got a result that I was free from MND ALS. Mine started on top and progressed into the bottom. I could walk very little but need assistance as I have no balance. It is sad all the time that we thought this disease had no cure with all the technology we have, while some formulas at there can relieve all symptoms and get this of ALS. I’m passing this information to anyone who needs it, because madibaherbalcenter. com has the right cure and caregiver for this disease.I took various supplements, medicine prescribed by a neurologist, massage, and physiotherapy, still the disease was progressing very fast until the ALS formula from that company.

Andrea 07 juin 2025

I was diagnosed in March 2017, but was running around from doctor to doctor before I finally got a result that I was free from MND ALS. Mine started on top and progressed into the bottom. I could walk very little but need assistance as I have no balance. It is sad all the time that we thought this disease had no cure with all the technology we have, while some formulas at there can relieve all symptoms and get this of ALS. I’m passing this information to anyone who needs it, because www. madibaherbalcenter.com has the right cure and caregiver for this disease.I took various supplements, medicine prescribed by a neurologist, massage, and physiotherapy, still the disease was progressing very fast until the ALS formula from that company.

Andrea 07 juin 2025

My first ALS symptom occurred in 2016, but was diagnosed in 2018. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatiue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Aknni herbs centre, It has made a tremendous difference for me (Visit ww w. aknniherbscentre.c om). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others.

cory melon 31 mai 2025

My first ALS symptom occurred in 2016, but was diagnosed in 2018. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Aknni herbs centre, It has made a tremendous difference for me (Visit ww w. aknniherbscentre.c om). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others.

cory melon 08 mai 2025

I got cured from this traditionalist doctor who help me with his medicine to cure me totally from ALS which the scientist claim there is no care that is a death sentence, believe me there is no problem without a solution, the issue is that where can you get the solution, this man send me a herbal medication and oil , I drink the medicine 3 times daily and I use the oil every night after bathing before going to bed, I swear with the name of God in heaven, just a week I start seeing changes before I could finish the course I was already free from this deadly disease, he said is spiritual even the lab can’t get the cure now till 2 centuries, I will advise you suffering from ALS to try it, his email is <healthmedlab@gmail.com> but the medication is so expensive that is the only issue some people can't afford it and some are skeptical if it will work for them, as far you were diagnose of ALS , you will get cured I promise you with my life, I know what I went through how my life was flashing out of my face every day knowing I’m dying and getting close to my grave each and every seconds. MY Name is Grace I’m from Spain Madrid.  

kelly 07 avril 2025

I am a CALS. My husband is PALS. It was hard and I cry daily but not in front of him unless we cry together. He couldn’t find anything to give him happiness or hope. We have been focusing on our faith. He was only losing his voice before we made the decision to try different medications, which significantly enhanced his condition. He received treatment for ALS/MND at uine health centre . co m from Canada approximately four months ago; since then, he has stopped using a feeding tube, speech is getting better by the day, sleeps well, works out frequently, and has become very active.

Grace Nathan's 13 février 2025

This was great, I have been researching for a while now, and I think this has helped. Have you ever come across uine health centre ALS/MND Programme (just google it). It is a smashing one of a kind product for reversing Lou Gehrig’s disease completely. Ive heard some decent things about it and my husband got amazing success with it.

Grace Nathan's 13 février 2025

My husband was diagnosed with bulbar ALS. He started slurring his speech and clearing his throat constantly. He also started choking on food before we made the decision to try different medications, which significantly enhanced his condition. He received treatment for ALS/MND at uinehealth centre . com from Canada approximately four months ago; since then, he has stopped using a feeding tube, speech is getting better by the day, sleeps well, works out frequently, and has become very active. Although it doesn’t cure his ALS, it has improved his quality of life.

Grace Nathan 13 février 2025

Last year, my 68-year-old partner was diagnosed with Lou Gehrig’s disease also known as ALS. Speaking and swallowing were two of his challenges. His collapse was swift and catastrophic, and neither the riluzole nor the medical staff did much to aid him. He would not have survived if our primary care physician hadn’t given him attentive care and attention, as the hospital center didn’t provide any psychological support. His fall was abrupt and catastrophic. His hands and legs gave way to weakness in his arms. This year our family physician suggested using vinehealthcentre. com ALS/MND treatment, which my husband has been receiving for a few months now. I’m delighted to say that the treatment greatly reduced and reversed his symptoms of ALS, he no longer requires a feeding tube, sleeps soundly, works out frequently, and is now very active. In the hopes that it could be useful, I thought I would relate my husband’s tale; in the end, you have to do what suits you the best.

Meyer Odette 08 août 2024

I am deeply sorry for all your condition, sending prayers and lots of love for your quick recovery from multivitamincare .org I strongly believe that this information I am about sharing with you will massively help you in all ramifications so Check out this amazing supporting page MULTIVITAMIN HERBAL CARE for Any information you seek and possible alternative treatments for Amyotrophic lateral sclerosis (ALS) that can help your situation. They really helped me and I trust them with my life. Godspeed and quick recovery.

Rebecca Callahan 06 novembre 2023

In December my health took a turn for the worse I became very weak fast and could not even eat When I say fast I mean going from eating a full plate of food to three days later not being able to drink a a sip of water I went to VA hospital emergency room for dehydration and figure they schedule me for a feeling tube placement They admitted me and two weeks later I woke up to my standing over me in the hospital room this occurred during my second or third drug holiday from Radicava Again no way to know if what I experienced was a side effect When I was discharged I was completely paralyzed So i started on Ayurvedic treatment from Natural Herbs Centre website As time went on movement returned to my legs and to my arms and hands Able to hold my head up and strength has returned I give credit to God and NHC for my recovery Almost forgot to mention I was on 24 hours ventilation Now only use vent at night and during naps Was diagnosed in 2021 with ALS, This Ayurvedic treatment is a breakthrough

Julie Hilditch 04 octobre 2023

My husband who had been diagnosed with Bulbar ALS disease for 2 years at the age of 63 had all his symptoms reversed with Ayurveda medicine from natural herbs centre after undergoing their ALS/MND natural protocol, he no longer requires a feeding tube. God Bless all Lou Gehrig’s disease Caregivers. Stay Strong, take small moments throughout the day to thank yourself, to love your self, and pray to whatever faith, star, spiritual force you believe in and ask for strength. I can personally vouch for these remedy but you would probably need to decide what works best for you.

Amy Larder 17 juin 2023

My first symptoms of ALS occurred in 2014, but was diagnosed in 2016. I had severe symptoms ranging from shortness of breath, balance problems, couldn’t walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Tree of Life Health clinic. It has made a tremendous difference for me (Visit w w w. healthcareherbalcentre .com I had improved walking balance, increased appetite, muscle strength, improved eyesight and others. ]

thato amelia 30 mai 2023

In July last year, I started on ALS/MND disease TREATMENT PROTOCOL from Natural Herbs Centre (ww w. Naturalherbscentre. com). One month into the treatment, I made a significant recovery. After I completed the recommended treatment, almost all my symptoms were gone, great improvement with my movement and balance. Its been a year, life has been amazing

Amy Larder 30 mai 2023

My husband who had been diagnosed with Bulbar ALS disease for 2 years at the age of 63 had all his symptoms reversed with Ayurveda medicine from naturalherbscentre. com after undergoing their ALS/MND natural protocol, he no longer requires a feeding tube. God Bless all Lou Gehrig’s disease Caregivers. Stay Strong, take small moments throughout the day to thank yourself, to love your self, and pray to whatever faith, star, spiritual force you believe in and ask for strength. I can personally vouch for these remedy but you would probably need to decide what works best for you.

Amy Larder 24 mai 2023

My husband who had been diagnosed with Bulbar ALS disease for 2 years at the age of 63 had all his symptoms reversed with Ayurveda medicine from naturalherbscentre. com after undergoing their ALS/MND natural protocol, he no longer requires a feeding tube. God Bless all Lou Gehrig’s disease Caregivers. Stay Strong, take small moments throughout the day to thank yourself, to love your self, and pray to whatever faith, star, spiritual force you believe in and ask for strength. I can personally vouch for these remedy but you would probably need to decide what works best for you.

Amy Larder 18 mai 2023

My spouse also used the www multivitamincare .org ALS, amyotrophic lateral sclerosisorganic herbal supplement ,2 times daily. The treatments are incredible and we have told so many people about it.

Wood Jones 18 mai 2023

My husband who had been diagnosed with Lou Gehrig’s disease for 2 years at the age of 63 had all his symptoms reversed with Ayurveda medicine from naturalherbscentre. com after undergoing their ALS/MND natural protocol. God Bless all Lou Gehrig’s disease Caregivers. Stay Strong, take small moments throughout the day to thank yourself, to love your self, and pray to whatever faith, star, spiritual force you believe in and ask for strength. I can personally vouch for these remedy but you would probably need to decide what works best for you.

Amy Larder 11 mai 2023

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I’m a rule breaker,” Kyle Brown says. “I think bending the rules is a good thing.” A successful age group triathlete and lifelong cyclist, Brown was diagnosed with Amyotrophic Lateral Sclerosis (ALS) in July 2021 at the age of 51. The terminal diagnosis gave him a mere 6-18 months to live but Brown has never been a rule follower and his way of living with ALS included qualifying and competing at the Ironman 70.3 World Championships.

Brown, who was a domestic professional cyclist in the United States, first found triathlon thanks to an ex-girlfriend. “One relationship lasted, one didn’t,” he jokes. He had the cycling down, running was a “natural” movement, but swimming was more of a challenge. “I have never swam before so it was comical when I started. It was more me drinking pool water,” he says. Nevertheless, Brown won his first triathlon, a local sprint, and within a year, he had progressed to
longer distances.

A decade in the sport later, while training for his first Ironman 70.3, Brown felt like his speech was slurred. Although no one else seemed to notice, Brown began to investigate. A few months later, a diagnosis of ALS was confirmed and with it a lifestyle change. Affecting the motor neurons of the brain and spinal cord, ALS causes the progressive loss of muscle control including the ability to speak, walk, and breathe. “ALS and triathlon, they don’t fit together,” Brown says frankly.  But he wasn’t resigned to give up sports or anything else for that matter. His lifestyle
change was to hit the accelerator and a few months later he qualified for the Ironman 70.3 World Championship.

“I don’t have time to cry too much. I have shit to do.”

In September 2021, wearing retired bib number 179 in honor of Jon Blais (the first ALS triathlete to complete an Ironman), Brown rolled across the world championship line, breaking every rule in the book when it comes to what is expected from someone with ALS.

Brown is still actively training and continues to work. There is no cure for ALS but Brown takes a cocktail of around twenty medicines and supplements everyday— “anything that might help a little bit.” The side effects of the drugs along with the physical symptoms of the disease make training difficult but it’s the realities that he and his wife face as they watch his body deteriorate that makes Brown reach for triathlon or anything else that makes him feel alive and a sense of normality.

“Triathlon has given me a great life, you know, meeting people that have helped me in this journey. It’s how I met my wife and many of my best friends,” Brown explains. Without his support system, especially his wife, Brown says “it would be a whole different story.” Despite the constant heavy presence of his disease, Brown says they always try to stay positive. “I don’t have time to cry too much. I have shit to do.”

Now as the face of ALS in the triathlon community and beyond, Brown is creating a life that not only raises awareness but continues to push boundaries, and not just in the realm of ALS. Still hopeful for the future, even if it’s beyond his own, Brown says his goal is to become “number 57.”  

“In the last 10-15 years there have 56 full ALS reversals. It’s documented. It’s not some internet story or dude with a beard in his car talking about it. It’s Duke university and a few other hospitals that have documented it. Our goal is to become number 57 or 58.”

Along with his foundation and work with other ALS support and watchdog groups, Brown’s choices challenges everyone to live beyond the accepted rules. “My diagnosis allowed me to take a step back,” he explains. “I never realized how fortunate, lucky, or blessed I am. With these people, living where I do, this country, this state, the people
I get to hang around every day, my job. I’m not wealthy by any means but I just feel like it couldn’t be any better.”

Photo: Patrick McDermott/Getty Images for Ironman

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