DCSIMG

Why register?

CloseX

If you have not signed up previously

It's free and only takes a minute!
Benefits to registering with us
comment on storiesComment on stories
Customise daily e-mail newslettersCustomise daily e-mail newsletters
Arrange your newspaper/digital subscriptions onlineArrange your newspaper/digital subscriptions online
Offers, promotions and deals from partnersOffers, promotions and deals from partners
Add/claim your business on Find itAdd/claim your business on Find it
true
  • 25/05/13
  • 7°C to 16°C Sunny spells
  • Portsmouth 5-day weather forecast

    CloseX

    Sunday 26 May

    Sunny

    Temp

    High17°c

    Low8°c

    Wind

    From West

    Speed23 mph

    Monday 27 May

    Sunny spells

    Temp

    High15°c

    Low9°c

    Wind

    From South west

    Speed25 mph

    Tuesday 28 May

    Light rain

    Temp

    High14°c

    Low8°c

    Wind

    From West

    Speed25 mph

    Wednesday 29 May

    Light showers

    Temp

    High14°c

    Low8°c

    Wind

    From West

    Speed17 mph

    Thursday 30 May

    Sunny spells

    Temp

    High18°c

    Low10°c

    Wind

    From North west

    Speed18 mph

  • Follow us
  • Place your Ad
  • Subscribe

Leigh Park youngsters’ diabetes funding row goes to parliament

ACTION Emma Bailey with her insulin pump.  Picture: Ian Hargreaves  (120711-4)

ACTION Emma Bailey with her insulin pump. Picture: Ian Hargreaves (120711-4)

 

BRAVE Emma Bailey is taking her fight for better care for diabetes sufferers all the way to the Houses of Parliament.

The eight-year-old has Type 1 diabetes which is a serious condition that causes the body’s own immune system to turn on itself and attack cells in the pancreas which produce insulin.

It means Emma, from Emsworth, must use a pump which feeds insulin into her system each day rather than having to inject herself.

But not every child with the disease is given the pump, turning it into a postcode lottery for those wanting to get hold of the life-saving medical equipment.

The schoolgirl will join members of research charity JDRF and dozens of other adults and children with the condition in London on April 25.

Emma’s mum Helen, 52, of Linkenholt Way, Leigh Park, said: ‘Emma has to have insulin all day, every day through a pump which is a little device that looks like a pager.

‘It’s administered via a cannular and she also has to do finger prick tests.

‘She will have to do this for the rest of her life unless a cure is found.

‘But not everyone is able to get one of these – it depends on funding and we will be raising that in parliament.’

Emma, a pupil at Bosmere Junior School in Havant, will meet MPs and NHS bosses to explain what life is like living with the disease.

She explained: ‘It’s a bit strange actually because I feel different to other people.

‘Some people think I look a bit odd because I have a pump.

‘Sometimes at lunchtime I don’t get to sit with my friends because I have my lunch early as I need to use my insulin pump before every meal.

‘I would really like to find a cure for diabetes.’

Type 1 diabetes affects about 350,000 adults in the UK, including over 26,000 children. In 2009 the government committed £51m to research but only £6m was for Type 1 diabetes.

JDRF is lobbying MPs to boost the amount given for research, claiming it will not only help find a cure but will bring significant benefits to the economy. To find out more about Type 1 diabetes or to make a donation go to jdrf.org.uk or call 020 7713 2030.

 

Comments

 
 

Back to the top of the page