TheMagic5 Swimming Blog

Kyle Brown: Breaking the Rules of ALS

45 commentaires

I was diagnosed with ALS (Amyotrophic Lateral Sclerosis) four years ago. For over two years, I relied on prescription medications and therapies, but unfortunately, the symptoms continued to worsen. I experienced increasing muscle weakness, fatigue, and difficulty with daily activities. Last year, out of desperation and hope, I decided to try an herbal treatment program from NaturePath Herbal Clinic. Honestly, I was skeptical at first, but within a few months of starting the treatment, I began to notice real changes. My energy improved, muscle coordination felt better, and I felt more capable in my daily life. Incredibly, I also regained some confidence and hope. It’s been a life-changing experience—I feel more like myself again, better than I’ve felt in years. If you or a loved one is struggling with ALS, I truly recommend looking into their natural approach.
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You said:

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>

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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

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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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