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There are 9 comments on Head Trauma Linked to ALS-Like Disease

  1. Adam Heidingsfelder D.C. Healing Hands Chiropractic, Gulfport MS
    As football season is upon us, we are likely to see some rough hits coming from on the field. Almost all of the resulting incident is a little soreness to the body and ego. But research is beginning to shed some disturbing light on what may really be going on inside the brains of these athletes.
    A brain autopsy of a University of Pennsylvania football player who killed himself last April has revealed the same trauma-induced disease found in more than 20 deceased National Football League players. This player had never been diagnosed with even a mild concussion.
    How could this affect young football players, especially since their brains are still developing? Chronic traumatic encephalopathy occurs from repeated traumas to the head. These traumas can seem minor to the parent or coach, but the effects are cumulative over time. Each hit essentially adding to the damage of the brain. One quick youtube search and you will see what I mean.
    To understand what happens to a player, we need to understand the forces and the anatomy. As two child football players approach each other, they have hard plastic protective helmets on their heads. As the helmets contact, they immediately stop. The head continues to travel within the helmet until the padding of the helmet becomes compressed. The skull is then stopped. With the skull stopped, the brain continues to move forward until it meets the skull, or small, specialized ligaments stop it. If the brain hits the skull with enough force, it becomes bruised, or damaged directly.
    What can be done? At the age of 13 I took one serious hit, and decided to remove myself from something that may not be worth the toll it may take on my body. There are only 1,900 active NFL players each season. There are more than 3 million children playing football at the youth level and 1.2 million more playing at high school level. This doesn’t even begin to count the number of kids playing other contact sports. There needs to be changes to the rules, equipment, and culture. The most important is to properly train the coaches and trainers, in order to avoid these injuries in the first place.
    http://www.healinghandsms.com/

  2. I’m wondering, as a result of reading your article, about my wife’s situation. She is a 66 year old women who has recently been diagnosed with ALS. Three years ago she received significant he’d trauma. She was out cold for 2 minutes, then had no short term memory for the next 6 hours.
    My concern is that her condition, as it is developing, might be the result of the head trama. This becomes more of a consideration when we include the mental effects I’m noticing which are in addition to the normal ALS symptoms. In addition to speak slurring, increased saliva production, and EMG results, she is having recall issues, mostly with nouns. Any thoughts?

  3. I am in a state of shock. i just watched a program on PBS. and my wheels began to spin. My father died from ALS(probably CTEM) 3yrs ago.He played football all of his life,he played college ball,and was the head football coach at many prominent Universities.So hits to the head were part of his every day life. However, sometime after his retirement. While attending The Kentucky derby he fell and hit his head. he was out cold for almost a minute. About a year later he was diagnosed w/ parkinsenns disease. two years later after completely loosing the use of his arms. We were given the news that he’d been mis-diagnosed and that he had ALS. Two years later he was gone. there is no doubt that because of football he is no longer with us. thank you Dr McKee for your dedication and making this a subject that is in the publics eye. i just wish more people would pay attention. i miss you pops.

  4. Our son played hockey all his life up herein Canada. No problems. He is an electrian and about 4 years ago received a horrible neck injury while holding a large drill overhead. HE was off work and into one doctor after another and after about two years with problems was diagnosed with ALS. We wonder if this injury could be a big part of the onset of his disease. We live in London Ont and thru a Dr Strong at Western University and the research centre have worked on this disease. HIs doctor doesn’t know.

  5. My mother was diognised with ALS one week before her death,This dilled in the reason for her death.She and her mother were driving in the wintertime and hit a patch opf ice aweninto a skid and upon hiting dry pavement rolled over multible times and both ended up in hospital. 3years later her foot dropped and it was all downhill for a year and a half and she lost her ability to breathe amd passesd. Lou Gerig after playing footnall without the orop[er head protection. So in my humble opinion als BAH HUMBUG. RFegards. J,R.PS Iwonder about Stephen Hockimg

  6. 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. treeoflifeherbalclinic .com ). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others. ]

  7. 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 difficultyswallowing 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. treeoflifeherbalclinic .com ). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others. ]

  8. My husband has Bulbar ALS, he is about 63 years old it was diagnosed 2 years ago. It was getting more difficult to live for him, because of stiff muscles he couldn’t even move. Riluzole and tofersen medicines were given, but didn’t give much relief. He couldn’t eat food without choking. I thought this might be the last stage and the medications he was given did not help at all, so I started to do alot of research on Ayurveda treatments, I was introduced to Natural Herbs Centre and their ALS/MND Ayurveda Protocol. He started on the Ayurveda Treatment last year, his symptoms gradually diminished including his vocal cord spasm, Muscle Weakness, speech and Difficulty with swallowing. Reach them at natural herbs centre , he is getting active again since starting this treatment, he is able to walk again ( down the street and back ) he has also resumed exercising to strengthen muscles and lo longer require a feeding tube!! God Bless all ALS 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.

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