ALS News & Research For postings of news or research links and articles related to ALS


advertisement
Reply
 
Thread Tools Display Modes
Old 05-20-2008, 06:59 AM #1
BobbyB's Avatar
BobbyB BobbyB is offline
In Remembrance
 
Join Date: Aug 2006
Location: North Carolina
Posts: 4,609
15 yr Member
BobbyB BobbyB is offline
In Remembrance
BobbyB's Avatar
 
Join Date: Aug 2006
Location: North Carolina
Posts: 4,609
15 yr Member
Thumbs Up 'It gives me hope of a cure'

'It gives me hope of a cure'

video
Liz Shipley believes the research may lead to future treatment
http://news.bbc.co.uk/1/hi/health/7406660.stm

MND takes away a little piece of you, bit by bit

Liz Shipley

Legislation permitting controversial research which uses animal eggs to help make human cells for research is to be debated in the House of Commons.

The process takes virtually all the animal's genetic material out of the egg and replaces it with human DNA.

Critics say it is wrong to combine animal and human genetic material in admixed embryos, which then produce stem cells, in this way.

But Liz Shipley, who has Motor Neurone Disease (MND), says such research gives her hope there will one day be a cure.

MND is a muscle wasting disease. As the motor neurone cells in the brain and spine die and stop sending messages to muscles, the muscles gradually die.

But the person's brain is unaffected.



Most people with MND have the sporadic form of the disease, which appears for no apparent reason.

But, in about 5- 10% of cases, there is a family history.

In Liz's case, her grandfather, mother, two uncles, her sister and a cousin have all died from the disease.

She has watched them deteriorate, and knows what lies ahead for her.

"It ends up leaving you totally paralysed and unable to do anything, but the brain's unaffected."

She added: "I have cared for someone with MND. I've been on both sides of the fence. I know what the outcome is going to be, and I can't change that."

Death sentence

The family risk was only established after Liz had had her two children, and it is possible that they too could develop MND.


Liz Shipley with her family before she became ill

Liz, 46, from Newcastle, was diagnosed 10 years ago. Her legs and arms are now very weak, and she needs a wheelchair to get around.

She said: "MND takes away a little piece of you, bit by bit."

"I can't go out without someone being with me. Even something like making a cup of tea is very difficult on my own."

She added: "This technique should be able to be used in the hope it can find a treatment for MND. I hope MPs let it go ahead.

"They're not creating any human beings. They just need the cells in order to hopefully find a treatment and a cure."

"It would be brilliant if, one day, neurologists could say 'well you've got MND, but we can do something about it'.At the moment, there isn't anything.

"It wouldn't be in my lifetime, but if my children are unfortunate to develop MND, hopefully in their lifetime there will be a cure, and they won't have to face the consequences of MND.

"It would mean that people wouldn't live with a death sentence".



http://news.bbc.co.uk:80/1/hi/health/7405050.stm
__________________

.

ALS/MND Registry

.
BobbyB is offline   Reply With QuoteReply With Quote

advertisement
Old 05-20-2008, 07:04 AM #2
BobbyB's Avatar
BobbyB BobbyB is offline
In Remembrance
 
Join Date: Aug 2006
Location: North Carolina
Posts: 4,609
15 yr Member
BobbyB BobbyB is offline
In Remembrance
BobbyB's Avatar
 
Join Date: Aug 2006
Location: North Carolina
Posts: 4,609
15 yr Member
Post

A Wellcome debate
Embryo bill: An embryonic cell has little or no consciousness, so killing it may be no harsher than killing a plant for food
Anil Bhanot



About Webfeeds May 19, 2008 3:00 PM | Printable version
A debate was hosted by the Wellcome Trust last Friday on the ethics of the embryonic stem cell research (video here). http://commentisfree.guardian.co.uk:...me_debate.html

It was prefaced by speakers on both sides of the argument with some prominent scientists making the case for it and the Catholic ethicists - including a Catholic archbishop - expressing their concerns about the slippery slope towards playing God with human life. The debate was chaired by Edward Stourton and the audience comprised of a small number of distinguished scientists, medics, philosophers and some faith leaders who were also invited to comment.

Stem cell research under the existing Human Fertilisation and Embryology (HFE) Act 1990 is currently regulated by the HFE Authority (HFEA) and this has allowed research on adult stem cells where, for example, bone marrow cells have been transformed into nerve cells. However the regenerative potential of adult stem cells is far more restricted than that of the embryonic stem cells. Hence the new HFE bill proposes a new type of research on the human embryos relating to human reproduction.

The regenerative qualities of the embryo cells are so great that they can be transformed into any cell in the body, thus qualifying as pluripotent cells. This breakthrough gives a radical shift towards treating illnesses that we currently do not have a cure for. The scientists involved in the research are passionate about the benefits their research may lead to curing motor neurone disease, stroke, heart disease, multiple sclerosis and cancers of various sorts.

The ethical problem comes, however, in the way the embryonic cell is used and then destroyed. Although the embryonic cell is used from five to 14 days, ie at its very early stages, it is nonetheless life, potentially developing to a full human.

The embryonic cell is donated by the couples who undergo IVF treatment and 70% of such cells die anyway in that early process to fertilisation. Also one significant fact is that at this early state of the embryonic cell of 14 days, it does not feel any pain when it is finally destroyed.

Nonetheless the Catholic church feels that we would be killing a life, potentially a human being, and would like alternatives to be looked at, such as the umbilical cord blood cells (though scientists claim that the embryonic cell research is of much wider benefit). The Anglican church's position is softer in that it argues there should be a moratorium on this research for say, five years, after which it should be reviewed again.

From a Hindu position, I argued that although nonviolence is a central tenet of our faith we must also sacrifice for the greater good. Since the embryonic cell does not suffer pain at this stage the Hindu tenet of nonviolence, ahimsa, is not breached. Further, in Hinduism all life is sacred: humans, animals, plants and so on. However to Hindus what matters is not just "life" but also the different levels of "consciousness". In the case of this embryonic cell one may present a theological argument that at its early stage of life it has little or no level of consciousness and therefore killing it could be no harsher than killing a plant for food. The embryonic cell likewise seems to be used for a similar, if not nobler, reason for the survival of "other" human beings.

Moreover, according to the doctrine of reincarnation shared by all Indogenic faiths, we do not consider death as the end and if we were to extend the argument to an embryonic cell dying for a good cause, for helping others, one may say that the same cell may well get its just rewards and later incarnate into a better life.

Last week's debate was intense, not least regarding the hybrid embryos and transgenic embryos where animals and human cells and proteins are mixed to culture cells for use in humans. We do need more discussion but piecemeal legislation, with enforceable regulation through the HFEA body, is of the greatest importance in ensuring that the research stays on track. Perhaps the most sensible way forward is to give a green light for embryonic stem cell research but to take up the Anglican suggestion of a review in five years.

http://commentisfree.guardian.co.uk:...me_debate.html
__________________

.

ALS/MND Registry

.
BobbyB is offline   Reply With QuoteReply With Quote
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
cure? maryfrances Parkinson's Disease 14 03-25-2008 05:45 AM
No Cure dealingwithtos Reflex Sympathetic Dystrophy (RSD and CRPS) 15 07-06-2007 05:37 PM
The Venom Cure: hope for the future Wing42 Peripheral Neuropathy 2 07-06-2007 09:57 AM


All times are GMT -5. The time now is 08:13 AM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.