Posts Tagged ‘child of the year award’

Schoolboy’s petition prompts move on MS link to vitamin D

Saturday, February 13th, 2010 | Tags: , , , , , , , , , , , , , , , , , , , , , , , ,
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ryantimesonline

An international conference is to be held in Scotland to discuss the health effects of vitamin D — thanks to the efforts of a 14-year-old schoolboy.

Ryan McLaughlin, from Glasgow, petitioned the Scottish Parliament questioning possible links between vitamin D and multiple sclerosis after discovering that the disease — from which his mother suffers — could be prevalent in Scotland because of vitamin D deficiency caused by a lack of sunlight.

The petition called on ministers to produce guidelines on vitamin D supplements for children and pregnant women, and launch an awareness campaign. As a result of his efforts, the Scottish government recognised “an urgent need” to provide information to health professionals and mothers, and is to launch a campaign.

Ministers also agreed to host a conference on April 27 to discuss the role of vitamin D. The event, to take place in Glasgow, will be opened by Nicola Sturgeon, the Health Secretary. Leading researchers into links between vitamin D deficiency and multiple sclerosis are expected to attend.

Yesterday, as the Public Petitions Committee agreed to close Ryan’s petition, members congratulated him for his achievement. Bill Butler, Ryan’s local MSP, hailed the schoolboy’s effort, saying that “a very great deal of progress” had been made.

The Glasgow Anniesland representative praised the way “Ryan and the McLaughlin family have persuaded the government; and the government has listened to the very sensible suggestions contained in the petition.

“The government has agreed to a co-ordinated programme of action with NHS Scotland to produce guidance on vitamin D, to educate women on its importance, to consider different messages for different groups of people, and to ensure that health professionals are giving correct and consistent advice to pregnant women and new mothers. Not only should the McLaughlin family be congratulated, but also the government for listening.”

He described that as a significant success. An image of Ryan is now featured on promotional literature for the petitions committee. Speaking about the campaign, Ryan said: “After an amazing year in raising both vitamin D and MS awareness, I now have the commitments that I wanted from the Scottish government.

“I applaud the positive action taken by the Scottish government and the support from Deputy First Minister Nicola Sturgeon and Shona Robison, Health and Sports Minister.”

A spokeswoman for the Scottish government said: “We’re keen to learn all we can about any possible links between vitamin D and multiple sclerosis and are keeping a very close eye on all the emerging evidence.”

• Breast cancer is diagnosed more often in the spring and autumn, and less often in the summer, leading researchers to suggest that its season-ality may be connected to vitamin D deficiency. Researchers at the University of South Carolina, who examined 2,921,714 breast cancer cases, also found that the seasonality was increasingly prominent the further away from the equator that the women lived. This implies that lack of sunshine, and therefore vitamin D, was a factor.

http://www.timesonline.co.uk/tol/news/uk/scotland/article7021318.ece

Ryan Mclaughlin will take the plunge for Glasgow MS Charity

Monday, February 1st, 2010 | Tags: , , , , , , , , , , , , , , , , , , ,
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big zip

14 year old Ryan McLaughlin will do a Zip slide from Forth Road bridge to raise money for Glasgow MS Charity!

Ryan McLaughlin from the Shine on Scotland campaign has offered his support and help to the Glasgow based charity Revive MS Support. Ryan McLaughlin will be taking part in ‘Revive MS support’s ” zip line event and he is gathering people from all over Scotland to help him.

Ryan said – I’ve been working very hard on the campaign for the prevention of MS with vitamin D that I just haven’t had any free time to do anything lately for Revive MS support, but when my mum had  a big relapse a couple of weeks ago Revive MS support was right there for us offering support and treatments.

I know its very important that I don’t forget this amazing charity that looks after my mum and i am honored to help, they have been there for our family right from the day she was diagnosed and I can not and will not let them down.

I have asked all the people on my Facebook  group to help me and I’m proud to say that I’ve now got 14 people that offered to come along do the zip slide and raise at least £100 each which will go towards my target of raising £1500.

A lovely couple who have followed my campaign and have became online friends with my mum have even offered to come all the way from the Isle of Man and take part because they have been so inspired by what the ‘Shine on Scotland’ campaign has achieved in raising awareness of MS.

http://www.revivescotland.org.uk/get-involved/26-adrenaline-events/276-davidrevivemssupportorguk.html

Ryan Mclaughlin launches ‘Fortify Scotland’s school milk’ campaign

Sunday, January 3rd, 2010 | Tags: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,
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Ryan McLaughlin launches ‘Fortify Scotland’s school milk’ campaign

14 year old Ryan McLaughlin of the Shine on Scotland campaign has launched a new social networking campaign to gain public support for his Idea of adding vitamin D to all school milk in Scotland. The 14 year old campaigner believes that vitamin D is so important to improving the health of scottish kids and wants to ascertain how many parents agree with him, using the social platform Facebook.

Ryan is asking scottish parents to join the group and have their say on the subject.

Figures compiled by Oxford University for a national supplementation program of vitamin D in scotland suggest 2000 cases of MS could be prevented over the next 10 years and save the UK economy £4 billion over 25 years.

The World Health Organisation have said that Scotland should start a national supplementation program.

The campaigner says ‘much work still has to be done to get the RDA of vitamin D raised significantly and I will work with the Scottish Government, SACN and the FSA to get that done, but I am positive that fortifying school milk with vitamin D offers the best solution to offering protection to all kids in Scotland’

I am proud to say that the Scottish Government have been amazing in supporting my goals, they have really listened and acted on the current evidence in support of vitamin D, as more evidence is put in place I believe that the case for fortification of school milk will increase, the Scottish government have not ruled out my proposal for fortified school milk they have said “Following advice from the FSA Scotland, the Scottish Government believes that it would not be appropriate to introduce fortified milk (or other fortified drinks) at school until such time as the evidence base is more conclusive about the impact on the population.

However this was said before new research released by the scottish government and the announcement that NHS Scotland said there was now an ‘urgent need to educate women and that all pregnant mothers and all children up to the age of 4 should be taking vitamin D everyday’ .

Now that BUPA have said that they believe vitamin D could prevent cancer and Israel announced all 3% milk is to be fortified I think we need to ask the Scottish Government to look at this again as the evidence is certainly more conclusive and it can only have a healthy impact on the population .

We are now aware that it will cost  £2.7 million if every pregnant mother and child takes up the Health Start vitamin’s on offer but what would it cost to fortify the school milk, I think some political will and some help with financial costs to the dairies could see this happen sooner rather than later.

Almost all milk in the US is fortified with vitamin D, Israel has just decided to fortify all 3% milk and we have heard rumors that both France and Ireland are also considering such a move.

http://www.facebook.com/group.php?gid=150104079977&ref=nf

You’re 10 times more likely to get MS in Rhyl than you are in Rio !

Monday, December 21st, 2009 | Tags: , , , , , , , , , , , , , , , , , ,
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A CHARITY has called on the Welsh Assembly Government to fund a campaign about vitamin D deficiency and multiple sclerosis.
The MS Society Cymru is calling for ministers to follow Scotland’s lead and raise awareness about the links between the two.
Such a campaign would encourage pregnant women and children under four to take a regular vitamin D supplement.
Scientists recently discovered that MS could be prevented through daily vitamin D supplements.
There is a clear link between vitamin D – known as the sunshine vitamin – and a gene that increases the risk of MS, raising the possibility that the debilitating auto-immune condition could be eradicated.
The prevalence of MS is far higher in typically wet and cold countries such as Wales, where 110 people in every 100,000 are living with the condition.
In a country with lots of sunshine – such as Brazil – only 18 people in every 100,000 have MS.
The NHS in Scotland said it would raise awareness about the links between vitamin D deficiency and MS this month, after being spurred into acting by Glasgow teenager Ryan McLaughlin.
Ryan’s mother, Kirsten, has had MS for three years, and Ryan, 14, has shown some symptoms of the disease but the family only discovered the link earlier this year after a family holiday.
The teenager said: “I was shocked there had not been publicity around this before. We wanted there to be more awareness of the link and more research into how much of a problem it is in Scotland.
“These actions will make a big difference – it will go a long way to giving children some protection against the disease and give parents proper advice.”
Joseph Carter, spokesperson for MS Society Cymru, said: “We are delighted by this announcement by the Scottish Government and are now calling on the Welsh Assembly Government to do the same.
“You are 10 times more likely to develop MS in Rhyl than you are Rio de Janeiro, and new research suggests this is due to vitamin D deficiency.”
Vitamin D, obtained from foods and through the action of sunlight on skin, is essential for maintaining healthy bones.
It is unclear exactly what causes MS but it has become increasingly evident that environmental and genetic factors play a role.
Previous research has shown that populations from Northern Europe have an increased MS risk if they live in areas receiving less sunshine.
This supports a direct link between deficiency in vitamin D, which is produced in the body through the action of sunlight, and increased risk of developing the condition.
Researchers at the University of Oxford and the University of British Columbia this year discovered a direct relationship between the genetic variant DRB1*1501, which is associated with MS, and vitamin D.
Dr Julian Knight, a co-author of the research, said: “In people with the DRB1 variant associated with MS, it seems that vitamin D may play a critical role.
“If too little of the vitamin is available, the gene may not function properly.”
And the study’s lead author Dr Sreeram Ramagopalan said: “Our study implies that taking vitamin D supplements during pregnancy and the early years may reduce the risk of a child developing MS in later life.”
A spokeswoman for the Welsh Assembly Government said: “We are working closely with the MS Society to raise awareness of multiple sclerosis.
“Earlier this year, we produced a leaflet, Multiple Sclerosis – living with a long term condition. This includes information on the condition, its symptoms and the people affected.”

A CHARITY has called on the Welsh Assembly Government to fund a campaign about vitamin D deficiency and multiple sclerosis.

The MS Society Cymru is calling for ministers to follow Scotland’s lead and raise awareness about the links between the two.

Such a campaign would encourage pregnant women and children under four to take a regular vitamin D supplement.

Scientists recently discovered that MS could be prevented through daily vitamin D supplements.

There is a clear link between vitamin D – known as the sunshine vitamin – and a gene that increases the risk of MS, raising the possibility that the debilitating auto-immune condition could be eradicated.

The prevalence of MS is far higher in typically wet and cold countries such as Wales, where 110 people in every 100,000 are living with the condition.

In a country with lots of sunshine – such as Brazil – only 18 people in every 100,000 have MS.

The NHS in Scotland said it would raise awareness about the links between vitamin D deficiency and MS this month, after being spurred into acting by Glasgow teenager Ryan McLaughlin.

Ryan’s mother, Kirsten, has had MS for three years, and Ryan, 14, has shown some symptoms of the disease but the family only discovered the link earlier this year after a family holiday.

The teenager said: “I was shocked there had not been publicity around this before. We wanted there to be more awareness of the link and more research into how much of a problem it is in Scotland.

“These actions will make a big difference – it will go a long way to giving children some protection against the disease and give parents proper advice.”

Joseph Carter, spokesperson for MS Society Cymru, said: “We are delighted by this announcement by the Scottish Government and are now calling on the Welsh Assembly Government to do the same.

“You are 10 times more likely to develop MS in Rhyl than you are Rio de Janeiro, and new research suggests this is due to vitamin D deficiency.”

Vitamin D, obtained from foods and through the action of sunlight on skin, is essential for maintaining healthy bones.

It is unclear exactly what causes MS but it has become increasingly evident that environmental and genetic factors play a role.

Previous research has shown that populations from Northern Europe have an increased MS risk if they live in areas receiving less sunshine.

This supports a direct link between deficiency in vitamin D, which is produced in the body through the action of sunlight, and increased risk of developing the condition.

Researchers at the University of Oxford and the University of British Columbia this year discovered a direct relationship between the genetic variant DRB1*1501, which is associated with MS, and vitamin D.

Dr Julian Knight, a co-author of the research, said: “In people with the DRB1 variant associated with MS, it seems that vitamin D may play a critical role.

“If too little of the vitamin is available, the gene may not function properly.”

And the study’s lead author Dr Sreeram Ramagopalan said: “Our study implies that taking vitamin D supplements during pregnancy and the early years may reduce the risk of a child developing MS in later life.”

A spokeswoman for the Welsh Assembly Government said: “We are working closely with the MS Society to raise awareness of multiple sclerosis.

“Earlier this year, we produced a leaflet, Multiple Sclerosis – living with a long term condition. This includes information on the condition, its symptoms and the people affected.”

Schoolboy Ryan McLaughlin wins vitamin D campaign

Saturday, December 5th, 2009 | Tags: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,
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Pregnant women are to be educated about the importance of taking vitamin D supplements thanks to a campaign by a 14-year-old Glasgow schoolboy.

Ryan McLaughlin, whose mother Kirsten has the incurable disease, took his case to the Scottish Parliament’s petitions committee earlier this year.

He believes taking vitamin D can help prevent the condition.

In a written response, the Scottish government said it would put in place an action plan to increase awareness.

It said recent research had found there was an “urgent need” to provide information to all health professionals who work with pregnant women and young children about current guidance on vitamin D.

“There is also a need to educate women about the importance of taking vitamin D supplement when pregnant and the importance of giving their children a vitamin D supplement until the age of four,” the response added.

The Scottish government will now agree a co-ordinated programme of action with NHS Health Scotland, and has pledged to keep the McLaughlins informed of developments.

Mrs McLaughlin, a former European Taekwondo champion, was diagnosed with MS two years ago.

Ryan, from Drumchapel, said: “I am so happy to hear that the Scottish government are being so proactive and really getting behind my campaign.

“These actions will make a big difference to the health of generations of Scots, and it will go a long way to giving Scots children some protection against disease caused by vitamin D deficiency and gives parents proper advice.

“I am now looking forward to the summit next year when we’ll hopefully be able to tackle the recommended levels but this is such great news.”

Fortified milk

Ryan became the face of a YouTube campaign to publicise the use of vitamin D, and led hundreds of supporters down Edinburgh’s Royal Mile to Holyrood before he put his proposals to the petitions committee in June.

He told MSPs research into the genetic effect of vitamin D deficiency showed a link to the development of MS. Vitamin D, which the body needs for healthy, strong bones is largely gained through sunlight and food.

The Scottish government has already ruled out free vitamin D supplements for all pregnant and breastfeeding women, and said there were no plans to introduce the supplements in the form of fortified milk or other drinks at school.

Scotland is thought to have the highest rate of MS in the world.

Husband’s studies lead to clinical trial

Tuesday, December 1st, 2009 | Tags: , , , , , , , , , , , , , , , ,
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News reports this week have detailed the research of Italian scientist Dr Paolo Zamboni, who is a professor of medicine at the University of Ferrara in Italy and whose wife has multiple sclerosis (MS).

Dr Zamboni claims from his studies of MS literature to have discovered what he believes could be a revolution for the treatment and diagnosis of the life-long condition.

Now, researchers at Buffalo University in New York are recruiting 1,700 adults and children from the United States and Canada to test his hypothesis.

His theory centres around the repeated references in research text books to deposits of iron in the blood vessels and a link to MS.

Excess deposits of the heavy metal have been proven to lead to inflammation and cell death in the laboratory. These are both characteristics of MS.

Using ultrasound to examine the vessels leading in and out of the brain, Dr. Zamboni tested his theory in people and found that in a majority, including his spouse who he also experimented upon, the veins draining blood from the brain were malformed or blocked. In people without MS, they were not.

He further suggested that iron was damaging the blood vessels and allowing the heavy metal, along with other unwelcome cells, to cross the crucial brain-blood barrier, a process termed Chronic Cerebrospinal Venous Insufficiency (CCSVI).

Commenting on his theories, Dr Susan Kohlhaas, Research Communications Officer at the MS Society, said: “The MS Society supports evidence-based information concerning MS and welcomes new avenues of research into the causes and possible treatments.

“More research is needed to pin down any relationship between CCSVI and MS and in that respect we welcome the trial currently recruiting in New York.”

Story by MS Society UK

Kano is going home!

Sunday, November 29th, 2009 | Tags: , , , , , , , , , , , , , ,
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http://www.dailyrecord.co.uk/news/scottish-news/2009/11/16/man-crippled-by-devastating-rare-illness-set-to-come-home-thanks-to-generosity-of-scottish-football-fans-86908-21825707/

A SCOTS family man whose life has been devastated by a crippling illness is on his way home, thanks to an incredible fundraising effort by Scottish football fans.

Martin Kane, 41, was hospitalised a year ago when he was left paralysed by the rare disease Devic’s Syndrome and suffered a lifetime of multiple sclerosis symptoms in one night.

The devastating illness has left the Glasgow-born expat almost entirely paralysed, and he has spent more than a year in hospital because his family house in Perth, Australia, could not meet his medical needs and needed a refit costing £50,000.

But earlier this year, a group of kind-hearted fellow Celtic fans, whom he had only ever chatted to on the internet, launched a huge fundraising effort to get him back home with his family in time for Christmas and, after six months of hard work, reached the target this weekend with a charity night at Celtic Park.

And with the funds in place to renovate and refit the house to accommodate his special needs, Martin, nicknamed Kano by pals, is now on target to get home for Christmas.

Martin’s wife Carolyn, 49, said the entire family were amazed and grateful for the incredible effort from the fans.

She said: “I can’t find the words to express how grateful I am or how amazed I am at what so many people have done for us, and the efforts people have gone to for Martin even though they have never met or even spoken to him in real life.

“The support we have had from the Celtic fans around the world is what has kept us both going over the last year, and it has made all the difference to Martin while he has been stuck in hospital.

“But now we can get the work done on the house in time, and with help from the hospital, should have him home for a proper family Christmas.”

Martin was struck by the disease on the night of November 5, last year, when a tingling sensation quickly developed into a loss of feeling right across his body.

He was rushed to hospital in Perth, where doctors feared the worst and Carolyn was told his situation could not be more serious.

Although a heart attack or stroke were initially suspected, he was later diagnosed with Devic’s, which is a very rare and extreme neurological condition, similar to suffering a lifetime’s worth of MS symptoms in a matter of minutes.

The condition is an extreme form of multiple sclerosis. It causes the immune system to attack the protective material that covers the nerves, and is so rare there is not even a statistic covering its incidence per head of population.

Like many neurological conditions, the cause is unknown, and it is impossible to know how long it might take Martin to recover.

Hours after his first symptom, Martin became paralysed from the neck down and breathes through a ventilator.

He has been living in a rehab centre in Perth ever since, unable to move or speak, and can only mouth words or smile to communicate to his wife and children Sean, 16, and Alanna, 13.

His story was first told in an Australian news broadcast this summer when star player Scott Brown and former manager Gordon Strachan sent him messages of support.

And when his friends on popular Celtic fans blog Celticquicknews.co.uk found out, they launched a worldwide campaign to raise the funds needed.

They have since staged sponsored slims, bike rides, sponsored 10k entries, quiz and music nights, and also raised £10,000 from a bucket collection outside Celtic Park last month, but the target was reached on Saturday at a special charity race night in the stadium.

The campaign was boosted by a £3000 donation from the Celtic Charity Fund, while old firm rivals Rangers donated a signed Ally McCoist print for auction.

Vitamin D might be just as important as vaccine to prevent effects of H1N1 swine flu, say researchers

Thursday, November 26th, 2009 | Tags: , , , , , , , , , , , , , , , , ,
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TORONTO, Nov. 26

The world’s leading vitamin D experts say that raising your levels of “the sunshine vitamin” this winter might be the best way to help your body naturally raise its resistance to all forms of the flu virus – including the H1N1 swine flu virus.

That’s the message vitamin D advocate Dr. William Grant wants you to take to the bank.

“I’m a little hesitant to say it will reduce your risk of being infected, but it certainly will reduce your risk of dying from the complications, such as pneumonia, if you are infected,” says Grant, founder of the Sunlight, Nutrition and Health Research Center – a vitamin D research and advocacy group.

Grant is concerned that epidemic vitamin D deficiency in Canada — 97 percent of Canadians are vitamin D deficient in the winter due to Canada’s northerly latitudes and relatively weak sunlight 4-6 months of the year — means that Canadians could be more susceptible to flu virus in the winter.

Grant points to research suggesting:

    -  Higher vitamin D levels assist the body's innate immune system. Some
       studies suggest taking 2,000 IU of vitamin D/day will decrease your
       risk of seasonal flu.
    -  The groups most affected by the H1N1 swine flu virus have been those
       most likely to be vitamin D deficient: pregnant women, obese people,
       those with Type II diabetes and children with neurological disorders.
    -  Many of the deaths associated with the H1N1 virus have been pneumonia
       related, which means anything that would assist your body's innate
       immune system would make you less likely to be affected.
The worldwide vitamin D research community now recommends getting your vitamin D levels checked with a calcidiol test and maintaining vitamin D levels of 40-60 ng/ml.

 

November is Vitamin D Awareness Month in Canada.

Vitamin D – the missing link for multiple sclerosis sufferers

Monday, November 23rd, 2009 | Tags: , , , , , , , , , , , , , , , , , , ,
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Vitamin D – the missing link for multiple sclerosis sufferers

By Hilary Freeman

Sunlight provides Vitamin D – but is weaker in northern countries like Iceland.

Scientists have uncovered increasing evidence of the significance of Vitamin D in the development of multiple sclerosis. Now, Australian researchers have found that Vitamin D may actually reduce its symptoms.

Professor Bruce Taylor, a principal research fellow at the Menzies Institute in Hobart, studied 145 patients in southern Tasmania and tracked their seasonal susceptibility to the disease. He looked at how Vitamin D levels influenced their risk of having an attack of MS.

‘We found that the higher your Vitamin D level, the lower your chance of relapse, and for each ten nanomole [a standard measure of concentration of Vitamin D in the blood] increase in Vitamin D, you can reduce your risk of having an attack of MS by about ten per cent. Doubling your Vitamin D will reduce your risk by up to 50 per cent – a major result.’

Helen Yates, the Multiple Sclerosis Resource Centre’s chief executive, says: ‘It has long been believed that Vitamin D has a role to play in the risk of developing MS but this new research opens up the strong possibility that this vitamin could impact on relapse rates.’

The MS Society’s research communications officer, Dr Susan Kohlhaas, says: ‘These results are very early-stage and need to be reviewed and validated before we draw any firm conclusions.’

It has been known for many years that the further you live from the Equator, the more likely you are to develop MS. For example, Malaysia has hardly any sufferers but in Scotland and Scandinavia MS is relatively common.

It is believed this is due to a shortage of Vitamin D; countries far from the Equator, such as those in Northern Europe, enjoy less sunshine, the main source of Vitamin D.

Research has shown that babies born in May – who developed in the womb during the Vitamin D-scarce winter months – are the most likely to get MS in later life, while those born in November are at much lower risk.

Another study this year found evidence that Vitamin D deficiency during pregnancy and infancy could increase a child’s risk of developing MS in later life. The researchers concluded that taking Vitamin D supplements during these times could reduce the risk, although this has yet to be proven.

Schoolboy campaigner backs vitamin D summit

Wednesday, November 4th, 2009 | Tags: , , , , , , , , , , , , ,
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A major international summit on the links between multiple sclerosis and vitamin D deficiency, supported by the Scottish government, is to take place in Scotland early next year thanks to the efforts of a campaigning schoolboy.

Ryan McLaughlin, 14, whose mother suffers from the disease, said yesterday he was delighted that that Ministers were backing an opportunity to explore the growing evidence that lack of the vitamin could be implicated in the high incidence of the disease.

The summit will bring together government health advisers as well as researchers from Britain and countries such as Canada, where much work has been done on MS, and where supplementation of vitamin D is officially advocated in the general population.

The Scottish conference will be organised by the MS Society and Shine on Scotland, Ryan’s group. News of the event follows a long campaign by The Times to highlight evidence that shortage of vitamin D, caused by Scotland’s lack of sunshine, could be linked to the country’s record for chronic ill health, including cancer, diabetes and heart disease.

Yesterday, the petitions committee at Holyrood supported Ryan’s call for new guidelines on vitamin D supplements for pregnant women and young children, and agreed to take the issue forward.

Alan McLaughlin, Ryan’s father, said he was “a little disappointed” the matter had not been referred to the health committee, but said the family was still confident that Parliament would carry out the inquiries into the disease which they sought.

He said the family had had a meeting with Nicola Sturgeon, the Health Secretary, and Shona Robison, Minister for Public Health, and had been told that the government would also support a clinical trial in one of Scotland’s major cities to test pregnant women for their levels of vitamin D.

The Scottish government told the campaigners in September that an awareness campaign highlighting the importance of vitamin D was under “active consideration,” and promised new guidelines on the use of the vitamin by children, pregnant and breastfeeding women.

However, it ruled out free vitamin D supplements for all pregnant and breastfeeding women, and said there were no plans to introduce the supplements in the form of fortified milk or other drinks at school.Link

In its response to Ryan’s petition, the government said it was fully committed to improving the understanding and treatment of MS, although it said much of the evidence of a link between vitamin D and the disease was at an early stage and further work was needed before any definitive clonclusions be drawn.

Alan McLaughlin described the Government response as “very supportive” of their broad aims. He said that Ms Sturgeon had also been supportive of the idea of government funding for a clinical trial in a major Scottish city in which thousands of pregnant women would have their vitamin D levels taken, in order to determine the prevalence of deficiency. The research would be carried out by the University of Edinburgh.

Mr McLaughlin pointed out that American scientists, meeting in Boston two weeks ago, have evaluated the feasibility of conducting what would be the largest clinical study ever undertaken to explore the role that vitamin D may play in MS.

David McNiven, director of MS Society Scotland, said: “We have been asked to deliver the summit but we haven’t yet sat down and worked out the logistics of it. It will be early next year in Edinburgh.”

A spokesman for the Scottish government said: “We’re keen to learn all we can about any possible links between Vitamin D and Multiple Sclerosis and are keeping a very close eye on all the emerging evidence.

“During a very positive meeting with Shine On Scotland the Cabinet Secretary for Health and Wellbeing Nicola Sturgeon supported proposals to organise a summit on MS and its links to Vitamin D, details on this will be made available once plans are finalised.

“Shine On Scotland also raised the possibility of applying for funding for a research project involving women who are pregnant. These proposals, once submitted, will be considered in the normal manner.”

Story by Melanie Reid The Times

http://www.timesonline.co.uk/tol/news/uk/scotland/article6902010.ece