Ever wondered what it's like to work on the frontline of scientific discovery? We're taking you on a journey behind the scenes of a cutting edge medical research laboratory, exploring how stem cells are used to find treatments for neurological disease, as well as showing you the highs and lows of what life is like as a research scientist.
At the Patani Stem Cell Lab at University College London (UCL) our goal is to discover treatments for Motor Neuron Disease (MND) using stem cells. MND is a debilitating condition that causes patients' muscles to waste away and eventually to die. Its effect on patients with the disease and on their carers is devastating but sadly there's no known cure for the condition.
This is an exciting time in the field of stem cell research and we're looking forward to sharing it with you, as well as hearing your thoughts on what we're doing in the hope that it can guide our own research.
Produced by Orinoco Media - www.orinocomedia.co.uk
i agree with you. I have heretary C9 and ALs 2 gene. When i was diagnosed i went on Thc and hemp gummies. I was put on a bi pap . i have done this for now entering my 8th year of ALs. started this every 4 to 6 hours after diagnosis. I think this is why i can stil walk talk and eat and take care of myself. it stopped the bad protiens . NOw i am diagnosed wtih breast cancer. Which my mother died of and i took progesteron . So probably one of those caused it . But amazing thing i discovered after the biopsy was I Had fast moving cancer cells but this makes no sense.I was htr2 neg. So my thc and hemp togethers has been keeping this entact and not feeding it. the Thc and hemp kills the bad cells and dont harm the good ones. something to look into
A drug called WF10 was patented by the NIH headed by the evil Dr. Fauci who worked with big pharma to suppress the drug and sat on the Patent No.: US 8,029,826 B2 (45) Date of Patent: Oct. 4, 2011. Clinical human trials allowed reversal of stage 4 intubation so that patients could eat on their own. Why was this drug research terminated? GREEDY PHARMA KNOW The active ingredient is Sodium Chlorite a dirt cheap molecule commonly used in the food and agriculture as well as water sterilization industries. NASA also has a patent on this same molecule. Why is this being suppressed?
This came a year or two too late for my late father who lived into his 90,s. He often went to the local hospital for training purposes. Swallowing was a problem. I did not have children and it is hereditary.
I know this is a old vid but I was wondering if anyone with it lost muscles at a fast rate. I am trying to get the VA to listen to civilian Neurologist. I am awaiting further testing.
Сan tell you about my experience. Muscle loss is slow, but muscle fatigue is very high. Because of this, the quality of life decreases, because simple things become complicated. For example, I cannot hold a cat in my arms for a long time, because the muscles of my hands tire quickly. And this is only the least of all inconveniences
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the xylophone music behind this awesome presentation of very valuable information actually prevents the delivery of the message! please allow him to speak without stupid xylophone!!
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Was this reaction of TDP-43 protiens because of toxins and chemicals that a individual has been exposed to or is it genetically passed down with in the cells? How does the toxic protiens get there?
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My father Gorgio 56 died in one year in 1986 From this horrible disease he was found on the floor of the hospital because they took his breathing machine away from him thinking he was OK to breathe on his own he suffocated to death that goes to show you how much people don’t know about this disease please help find a cure
TDP-43 clumping is not the cause, it's a result of a very slow triggering process of certain "suicidal mitochondria" that all sporadic ALS patients have had since birth inside their brains. We know this now, and the actual cellular death process is called "microautophagy". This is what causes the TDP-43 to clump, and become toxic. As more cells "pop" from this apoptosis process, the toxicity is released 1000x over and thus becomes overwhelming, and this "swamp" is fatal to the environment the motor neurons live in. In order to "fix" ALS, we are going to have to find a way to "clean up" the environment for the upper motor neurons. Stem Cells procedures like NurOwn can modulate this death process just enough to tip the balance and stop progression in many people. BTW, Dr. Hande Ozdinler just confirmed suicidal mitochondria at Northwestern. ALS is the most complex malfunction of the human body known right now, much more complex than Cancer.
My ALS (amyotrophic lateral sclerosis) symptoms started out with muscle weakness, stiffness and slurred speech. My primary physician prescribed riluzole and radicava to reduce symptoms and slow down the disease progress, I could not take them for long because of the terrible side effects. So i adopted a more natural approach and started on ALS Herbal formula from RICH HERBAL GARDENS, the ALS natural formula immensely helped my condition, i had a total recovery from ALS with this formula treatment. Their official web-site ww w. richherbalgardens. co m I feel so much alive again!
My husband was diagnosed with ALS in July of 2018. We live in Brazil, in the state of Paraná. My husband is 50 years old and as of two years ago started having fasciculations anda afther some consults with neurologists and underwent several tests, the results made his neurologist conclude that it was ALS. Then, the doctor indicated some medications. They are: methylcobalamin 50mg, riluzole, vitamin E 400 IU and continuous pulmonary physical therapy. Facing these facts, we would like to know about the researchs that you made there. Is it possible for my husband to be a volunteer patient in an ongoing trial?
