There’s been a lot of media buzz surrounding the recent Ice Bucket Challenge. From the average Joe to Donatella Versace, everyone has been uploading their videos online to raise awareness for ALS (Amyotrophic lateral sclerosis), or Lou Gehrig’s disease. But what about those working behind the scenes? Scientists like Dr. Teepu Siddique at Northwestern University have donated their life’s work to ALS research – and today, he is excited to say that they may have found the root cause of each type of ALS.
“ALS has a very tragic outcome…It’s like being jailed in your own body. It’s an example of the overall human condition of futility and helplessness. That is the philosophic and humanistic underpinning of my interest in this disease.”
— Dr. Teepu Siddique
There are three kinds of ALS: sporadic, hereditary and that which targets the human brain. Dr. Siddique and other researchers at Northwestern’s Davee Department of Neurology and Clinical Neurosciences believe the underlying problem with each has to do with something called “the breakdown of protein recycling.”
Essentially, says their study, “[the] basis of ALS is a malfunctioning protein recycling system in the neurons of the brain and spinal cord. Efficient recycling of the protein building blocks in the neurons are critical for optimal functioning of the neurons. They become severely damaged when they can’t repair or maintain themselves.” This, say researchers, is a problem prevalent in all cases of Lou Gehrig’s.
What does this mean for the future of ALS research? Well, now Dr. Siddique says scientists can start focusing their energy on drugs that could regulate these protein “pathways,” altering them to the patient’s benefit. It’s an exciting discovery for a disease that has changed the lives of around half a million people worldwide.
You may enjoy:
- Reading Health magazine’s article on the above topic here
- Visiting the ALS Association website here.
- Reading our article, “Before It’s “Too Late”: Seniors Share Fears Before Death The fears and regrets of the dying expressed through an honest photo series by Steve Rosenfield”here
There are only two types of ALS – sporadic and hereditary. Both types affect the brain.
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This was great, I have been researching for a while now, and I think this has helped. Have you ever come across Healthherbsclinic Amyotrophic Lateral Sclerosis HERBAL FORMULA (just google it). It is a smashing one of a kind product for reversing ALS completely. Ive heard some decent things about it and my buddy got amazing success with it.
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I was diagnosed last July. I was wheelchair bound. My feet hurt horribly on the foot petals. I started ALS/MND programme about 4 months ago. I’m now able to walk down the street and back at least I couldn’t do that prior to the ALS treatment. It doesn’t make the ALS go away but it did give me better quality of life.
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I am a CALS of my 68 year old Husband who suffered from muscle tiredness brought on by chronic fatigue in its early stages. Neurologists first had difficulty diagnosing it until multiple examinations indicated ALS, for which there was no known cure other than the prescription of riluzole medications, vitamins, and therapies. More advancements in breathing difficulties, difficulty pronouncing words, and difficulties eating occurred before we made the decision to try different medications, which significantly enhanced his condition. He received treatment for ALS/MND at vinehealthcentre. com from the U.S approximately four months ago; since then, he has stopped using a feeding tube, sleeps well, works out frequently, and has become very active. Although it doesn’t cure his ALS, it has improved his quality of life. .
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Thank you for your personal experience. It’s always special when a person’s kind heart seeks to help others. 💜
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