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Hope for MS sufferers as city scientist nears breakthrough

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Published Date: 28 July 2008
AN Edinburgh scientist is nearing a breakthrough that will revolutionise the treatment of Multiple Sclerosis and change the lives of generations of future sufferers.
Edinburgh University's Professor Charles ffrench-Constant, whose work has largely been funded with £2 million from the author JK Rowling, below, is working on a way of using stem cells to halt the deterioration of sufferers.

He is carrying out tes
ts on mice and rats to try to find a way of using the cells to repair damage to the brain.

Combined with the earliest possible detection of MS in patients, Prof ffrench-Constant's work offers the best hope of eradicating its devastating effect on patients.

He recently appeared in a documentary made by journalist and MS sufferer Elizabeth Quigley, who sees his tests as a possible "cure", although sadly for future generations rather than herself.

Prof ffrench-Constant, head of the Edinburgh University Centre for Translational Research, is reluctant to talk so boldly, but is confident that progress can be made in combating the disease which affects about 10,000 Scots.

He said: "We need to identify targets – molecules that contribute to the repair process in the brain. We have identified one interesting new candidate and are progressing with that, as well as trying to identify others.

"Once we have a positive target we have to see if it is present in patients with MS, we can't assume that just because it's worked on rats and mice.

"The MS Society has a brain bank with lots of tissues from people who have died from MS. If it is present we would run tests to see whether manipulating the target would have the result we hope. Then we would have the long, complicated process of developing the drug."

This means a treatment being available to patients in the UK is likely to be ten or 15 years away, although, for many people living with a history of MS in their family that will be a comforting thought.

Where MS comes from and what triggers it remains a mystery, but it is believed to be at least partly hereditary.

It is sometimes known as the "Scottish disease" as this country has the highest concentration in the world. It can also be found abroad in areas which have a large Scottish community.

Countries with a similar latitude to Scotland also have high rates of MS, suggesting that temperature or sunlight could be a factor, and childhood illnesses are also common among sufferers who develop MS in later life.

About 85,000 people in the UK suffer from MS, the result of damage to myelin, which blocks signals from the brain, prohibiting things like movement and speech.

A drug that could undo that damage remains the stuff of science fiction, but Prof ffrench-Constant believes something that could stop further degeneration is within reach.

This combined with early detection to ensure sufferers are treated when their health is still relatively good, could seriously limit the effect MS will have on future generations.

Ms Rowling, whose mother died in 1990 from respiratory problems linked to MS, has said: "It would mean everything to me if I thought that as a result even one person did not have to go through what my mother did."

Mark Hazelwood, director of MS Society Scotland, said: "The MS Society Scotland was delighted to be able to provide £2 million funding to help establish this important and groundbreaking centre in Edinburgh."





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  • Last Updated: 28 July 2008 10:55 AM
  • Source: Edinburgh Evening News
  • Location: Edinburgh
 
1

Jenny MacArthur,

28/07/2008 13:39:15
This is the sort of vital work that Christian nutters want to stop, in their quest to bring love and compassion to the world. It's a case study in why fundamentalist megapixie worshippers should be kept safe in their asylum-churches, and well away from public policy.
2

Joe Smith.,

Moscow 28/07/2008 14:10:26

#1 Jenny - well said.
3

LUVMACITY,

IN THE LOBBY 28/07/2008 14:20:25
As someone who saw his dad with this terrible disease I pray the Proffesor succeeds. Well said again Jenny.
4

alex paterson,

edinburgh 28/07/2008 14:26:12
Good luck Prof.and well said Jenny.
5

Dr Avoido,

28/07/2008 14:32:34
#3 I lost my Dad to MS last year after a long and cruel illness. He was 58.

I sincerely hope that a breakthrough can be made to offer some hope to MS victims and their families.

6

mac77,

Edinburgh 28/07/2008 15:31:47
Jenny; resorting to abuse like that helps no-one. Most religions believe that life starts at conception. Can you prove otherwise? That is why they don't like embryo research. You'll note I said 'they'. I have no religion, but they have the right to their views in a democracy.
7

antifa,

28/07/2008 17:13:28
# 6. Nobody's saying they don't have a right to their views, but Jenny has every right to make the point that those views are ridiculous. Unfortunately, those views are often pandered to, with very damaging results.
8

S. A. C.,

Edinburgh 28/07/2008 19:24:34
I was diagnosed with MS 5 years ago, it came as a total surprise to me, but when I started to get to know all the different symptoms I was shocked to noticed I have had and still get nearly all of them. I'm not in a wheelchair yet, I do have a stick but prefer not to use it as I see that as a sign of defeat, but it hurts and angers me when people say "why you no in a wheelchair then if its that bad" and "you look alright today, you just suit yourself when you want it to come, get you oot the hoosework does it?", I am sick of it, I have cried myself to sleep over my condition not being taken seriously.

Good luck, in your research, it will probably be a bit late to help me, but not for the future generations of sufferers.
9

Fanling,

Switzerland 28/07/2008 22:51:39
#1 Jenny MacArthur

Good sense. You echo what most non-worshippers think on scientific investigation. Responsible medical science should be allowed to take its natural course for the benefit of society, unhindered by truly selfish, emotive nutjobs. Meantime, if the fundamentalists want to bellyache then let them pray to their personal sky-fairy that they never fall foul of a seriously debilitating condition such as MS.

#8 SAC

Good luck. Hopefully, progress is around the corner. The news, as reported above, is looking better all the time.
10

DrA,

USA 28/07/2008 23:44:27
Jenny, of course, has every right to her opinion and many who would oppose her viewpoint have given their lives so that she can continue to exercise that right. Others have the same right to comment on her apparent disdain for those who believe even a not-yet-born life is worth fighting to save.

To the point, it is unclear from this article whether or not the primary scope of this research involves the use of embryonic stem cells. As a practicing neurologist I support this research regardless, but will also say that it has been my experience that these news reports are all too often premature for public consumption - we need a few more basic discoveries to be made before that 10-15 year prediction can be considered plausible.
11

survivrgirl66,

USA 29/07/2008 00:09:24
Once again, people don't "get it" until they get it. Unless you have been afflicted with this horrible disease, you could never fully understand what it's like, even the most compassionate caregivers.

I applaud Jenny for her comment.
12

davale61,

UK, Leicester 29/07/2008 11:35:14
I'm sure the "do gooders" would soon change their opinions if they had to put up with the symptoms on a daily basis. Although my MS is not visible on the outside anyone with MS will tell you it's a different story on the inside. I have had MS for 10 years and would welcome any improvement to my health, whatever the cost !!
13

Babs1,

Livingston 29/07/2008 12:09:50
I agree that everyone that has this devastating disease has their own opinions of what is acceptable and/or ethical. I have had MS for 8 years and have seen and felt how it has destroyed by body and abilities and by the time this treatment is found there's a good chance it'll be too late for me. There are times I have felt utter despair, and one thing to stop me taking it further. This is because I am one of these so called "Christian nutters" as Jenny puts it and believe that all life (embryonic or not) is sacrosanct. I can also hold my head up high knowing that I have not stooped so low as to devaluate other peoples right to their opinion without feeling the need to name call. As DrA pointed out we don't know if the stem cells used for this treatment are embryonic or not, so lets not start jumping up and down just now and keep an open mind on this until more information is known.

 

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