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Is A Cure For ALS Around the Corner?

November 11, 2009 - 1:25 PM | by: Reena Ninan

When New York Yankee Hall of Famer Lou Gehrig died from ALS (Amyotrophic Lateral Sclerosis also known as Lou Gehrig's disease) in 1941 there was no cure. Sixty-eight years later there is still no cure. The disease affects nerve cells in the brain and spinal cord, eventually paralyzing the body.

BrainStorm Cell Therapeutics Inc, a public U.S.-Israeli company that develops adult stem cell therapeutic products, may be on the verge of a significant breakthrough in ALS treatment. Fox's Middle East Correspondent Reena Ninan sat down with the company's chief scientist Prof. Daniel Offen, here are excerpts from the interview:

NINAN: What's the ALS breakthrough you're working on?

OFFEN: In our previous studies we have shown that our newly developed bone marrow derived stem cells can protect neurons in tissue cultures and in animal models. Recently, we found, in several experiments, that these unique cell populations can rescue motor neurons which are the cells that degenerate in ALS, as well.

NINAN: What makes you optimistic this will work with ALS patients?

OFFEN: Instead of using embryonic stem cells, which have ethical and safety issues, we take adult stem cells, differentiate them and transplant them into the patient. Our focus is to change the environment of the cells at the site of damage in the body. We also use cells taken from the actual patient with the disease, which greatly reduces the chance of rejection. We know of no other company that is doing this. We are extremely optimistic about our approach and its chances of success in helping ALS patients.

NINAN: If this research proves affective how will this change how we treat ALS patients?

OFFEN: We believe that within a year, if not sooner, our cell-based approach will be proven to be safe. Then, after controlled studies and FDA approval, ALS patients, both in early and late stages of the disease, will be able to enjoy alleviation of the symptoms and have the benefit of a better quality of life.

NINAN: Why has finding a cure for ALS been so difficult?

OFFEN: Because the exact cause of the disease is not known. Today there is no effective drug that is able to slow down the progression of the disease. Our new approach bypasses our lack of understanding and utilizes the patient's own cells to secrete high doses of natural protective factors to the cells affected by the disease.

NINAN: You've also had success with neurodegenerative diseases like Parkinson's disease and Huntington disease. What's new there?

OFFEN: In studies we have shown that neurodegenerative diseases share the same damage pattern. Therefore, a specific therapeutic agent can potentially ameliorate the symptoms of several distinct neurodegenerative diseases. We used our unique stem cells in animal models of Parkinson's disease and Multiple Sclerosis and found that indeed, the transplanted cells rescue the degenerated neurons. Brainstorm plans to continue to study how our stem cell technology and methodology can be further utilized in the treatment of other neurodegenerative diseases.

Mike Roach

Brainstorm, Neuralstem, and TCA Cellular Therapy are three companies who have received or are vying for FDA approval for stem cell treatment of ALS. They are LEGITIMATE research companies. Shame on those who are making them out to be shams, those days are coming to an end in the new era of credible stem cell research.

November 14, 2009 at 6:08 AM
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Diane L.

My husband was diagnosed with ALS 3 years ago and I have seen a very athletic man go to a man with braces and a cane. We read and educate ourselves constantly and pray and pray, for a cure. His is very slow moving and I am thankful for that because we have been married 33yrs and he is my life. Please, everyone, keep praying for a cure for this horrible disease. God is in the miracle business and we pray for one every day.

November 13, 2009 at 10:38 PM
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roger

There is a fine line between hope and denial. Careful of anyone / any for-profit business or entity that indicates they have a cure or potential for ALS. I have lived with ALS for 10+ years and have not had any expensive procedures done as some deperate folks have pursued. Why have I lived so long? Don't know the answer to that one, but if I did, I would definitely share the secret. My heart goes out to everyone with ALS and their family members. It is a devastating disease in so many ways.

November 13, 2009 at 5:17 PM
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Dan Reed

A cure for ALS around the Corner? More like "Sensational Reporting Over to Top and Around the Bend". Inaccurate, incompetent reporting here borders on criminal. This report shows a lack of understanding by the interviewer and slightly misleading statements by the interviewee. ALS is a disease of the brain, that effects the motor neurons. Those are muscle neurons that slowly atrophy because the brain stops sending and receiving signals to them and from them. This "Cure Story" is a curel hoax.

November 13, 2009 at 2:46 PM
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Ray Mumme

My thoughts and prayers go out to anyone dealing with ALS. Please take a look at a product that releases your own adult stem cells which can renew rebuild and rejuvenate any tissue cell or organ in the body. We have the science to back it up. This is an all natural supplement that when taking two capsules you trigger the release of 3 to 4 million adult stem cells into your blood stream. Your body knows what to do with them google search (ALS adult stem cells)and find over a million studies with success when using ASC www.raymumme.com or www.asultstemcellsrelease.com

November 13, 2009 at 2:25 PM
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Harrison Hannover

Please be wary of this man. He lurks on ALS sites and makes claims which are outlandish and unproveable. This term "solving ALS" is as absurd as it sounds. Mr. Murray is yet to show any proof of his claims. Patients beware!

November 12, 2009 at 8:50 PM
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Philippe

Marty Murray, if you can't provide details then please either get your head out of the clouds or just stop spreading false hopes. Everyone, stem cell treatments aren't new: http://www.xcell-center.com/treatments/diseases-treated/als.aspx (about $10k). I think Fox News should have done a little more fact-finding regarding this company's claims. Also check out the US-based organization for all types of ALS info, including past/present/future trials & drugs: http://www.alsa.org/patient/drug.cfm

November 12, 2009 at 3:29 PM
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Debbie Harrod

The figure was $30,000 for the two stem cell treatments received in Europe. Tag this with my previous comment.

November 12, 2009 at 3:07 PM
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Jeff

I was diagnosed with PLS (primary lateral Sclerosis) early in 2009 at SW Medical Center in Dallas. I am 70. It was slow progressing starting about 5-6 years ago and wasn't recognized by doctors. It affects my left arm (aboout 80% strength) and left leg from knee to hip. I am on a walker. I was a runner and very active until 3 1/2 years ago when I had to start slowing down. Let's pray this will be a cure

November 12, 2009 at 2:39 PM
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Debbie Harrod

My husband was diagnosed with ALS in October 2008. He is very close to death. If this stem cell treatment works for ALS patients, I would be happy for others. We made two trips to Europe for this very same procedure, adult stem cell replacement taken from his bone marrow. 30,00 dollars wasted, but we woild have tried anything. I don't believe this is a new procedure. The are many locations throughout the world doing it already. Whst a shame that we had to leave the US to seek help.

November 12, 2009 at 2:03 PM
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Gina

Susan, I am interested in how long you have been taking this and what is your disease? My dad was diagnosed in October with ALS and it has progressed rapidly and we want to fight hard. Thanks for the comment and please let me know if this is what you have and where are you in the progression stage if you don't mind. THANK YOU

November 12, 2009 at 10:17 AM
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Jeff

I have Multiple Sclerosis. At the time I was diagnosed, I was traveling around the world training the world's fiercest fighting men and women of todays US Air Force. My diagnosis put an end to all of that. These brain, spinal cord nerve diseases are the absolute worse outcome a man of 40 years could possibly receive, yes worse than AIDS, cancer or being hit by a train. My daily meds are about $200, thank GOD for insurance. But not being able to talk, find words that came second nature, being numb and most of all the Pain is unbearable. Please those of you reading this, contact your represenatives and lets gets Stem Cell therapy on the agenda. Thanks from the bottom of my numb heart.

November 12, 2009 at 9:55 AM
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Neil Gordon

It turns out that adult stem cells are about the only stem cell therapies around that are producing real results in numerous diseases. Fetal or embryonic stem cells, however have produced nothing but tumors in patients and have actually killed at least one person involved in a clinical trial.

November 12, 2009 at 9:46 AM
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mrpristine

Kory just get her to hang in there another year or two..Im betting help is right arounf the corner with stem cell research.

November 12, 2009 at 9:43 AM
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Joey

US company Neuralstem is already doing human trials in China for this using adult stem cells.

November 12, 2009 at 8:46 AM
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Bobby Ross

I lost a cousin that I had not seen since my childhood. We were reaquainted at my grandmothers funeral & at that time he was 6 months into the disease. He was young & left one son. I can only hope that their work can prevent another child from losing a parent.

November 12, 2009 at 8:25 AM
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dave

Hopefully this works, but too late for our friend, Ron K.

November 12, 2009 at 8:00 AM
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DMR

My aunt just passed away on Easter Sunday with an associated rare disease called PLS. PLS is post-lateral syndrome. It is affiliated with ALS as they are distant cousins. My concern is the same with anybody else's when it comes to these rare diseases. Don't give up and don't let your family member(s) or yourself quit living and doing what they or you can for self. It is important to have support from family and friends. My aunt was bed rested for about 5 or 6 years. It started when she was losing her voice. It was thought that she had a stroke though there was no evidence of any stroke and she also saw a cancer doctor but there was no cancer. There is also no real cure for this disease. I guess the only cure for any disease or disorder is prayer. Prayer is very strong and can work with belief. Please take care of your family member or self and let them know that you love them. If it's you suffering from something, just remember there are support groups and always somebody somewhere welling to help. God Bless...

November 12, 2009 at 2:51 AM
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Gary C, Berliner, MD

Will this technique work as well in anoxic brain damage, and spinal cord injury?

November 12, 2009 at 2:31 AM
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Lilly

Hope is a great thing, and naysayers should be ashamed! In 01 I was given no hope for my 17 year old with colon cancer stage 4, she was given less than 1%survival rate, so I went with experimental treatment for her, what choice did I have? After 50 weeks of chemo she has ben cancer free even though we were told that she would not be "cured" that it will come back! She was treated at St jude. At the time embryonic was really the :hot" ticket but they were more into using a persons own stem cells. All cancer or catastrophic treatments were experiments at one time or another.At the time I think 1 in 4 survived the treatment, but it was adjusted for the individual and she is in school today. So please let these people hope.

November 12, 2009 at 2:16 AM
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