Cherry
Active member
- Joined
- Oct 14, 2009
- Messages
- 37
- Reason
- Loved one DX
- Diagnosis
- 09/2009
- Country
- UK
- State
- Nottinghamshire
- City
- Nottingham
Hi, just read this, always looking for some good news.
Best wishes to all, Cherry.
Another breakthrough on the horizon -- one for ALS. People who get the devastating diagnosis are often told they only have a few years to live. Now, gene therapy could add years to their life.
"We hope to slow disease progression and, in our wildest dreams, we hope to dramatically to slow disease progression," added Don Cleveland, Ph.D., a neuroscientist at the University of California, San Diego.
Researchers have tested a molecular therapy in rats that turns off the bad gene in ALS. The drug is infused right into the spinal cord. It could be the first really effective treatment for the disease, and the first gene-silencing therapy used in people for a neurological disorder. The therapy could also be applied to diseases like Parkinson's and Alzheimer's.
"That will be quite different -- if we are successful -- quite different from therapies available," Dr. Cleveland said.
These two different solutions are helping researchers get one step closer to a cure. The diabetes and ALS trials in people will start around 2008. They've already proven effective in animals with virtually no side effects.
For more information:
org
ALS, or Lou Gehrig's Disease:
Neurosciences Department University of California San Diego ranks first NIH grant funding committed Excellence in Research, Teaching, Clinical Care
Best wishes to all, Cherry.
Another breakthrough on the horizon -- one for ALS. People who get the devastating diagnosis are often told they only have a few years to live. Now, gene therapy could add years to their life.
"We hope to slow disease progression and, in our wildest dreams, we hope to dramatically to slow disease progression," added Don Cleveland, Ph.D., a neuroscientist at the University of California, San Diego.
Researchers have tested a molecular therapy in rats that turns off the bad gene in ALS. The drug is infused right into the spinal cord. It could be the first really effective treatment for the disease, and the first gene-silencing therapy used in people for a neurological disorder. The therapy could also be applied to diseases like Parkinson's and Alzheimer's.
"That will be quite different -- if we are successful -- quite different from therapies available," Dr. Cleveland said.
These two different solutions are helping researchers get one step closer to a cure. The diabetes and ALS trials in people will start around 2008. They've already proven effective in animals with virtually no side effects.
For more information:
org
ALS, or Lou Gehrig's Disease:
Neurosciences Department University of California San Diego ranks first NIH grant funding committed Excellence in Research, Teaching, Clinical Care