[an error occurred while processing this directive]
BBC News
Launch consoleBBC News in video and audio
Last Updated: Wednesday, 18 July 2007, 12:42 GMT 13:42 UK
Baby cells hope for sick brother
Joanna Stanley and Mike Emms, her partner's son
Joanna Stanley and Michael Emms, her partner's son
A Monmouthshire couple plan to use the umbilical cord of the baby they are expecting for stem cell treatment for the unborn child's 20-year-old brother.

Joanna Stanley, 27, is pregnant by partner Julian Emms, 41, whose other son, Michael, has been diagnosed with motor neurone disease.

It is hoped the baby due in September, a boy, already named Rhys, will be a match for the younger Mr Emms, 20.

The treatment will be performed in America as it is illegal in the UK.

Experts believe the cells could reverse the muscle wastage Mr Emms has suffered since the illness was diagnosed.

The plan is to freeze stem cells from baby Rhys's umbilical cord and fly them to a clinic at the Institute of Cellular Medicine, in Boston, where they will be implanted into Mr Emms' spinal cord.

Mr Emms, of Caerwent near Newport, has been told he will not see his 21st birthday without the treatment.

Ms Stanley said she was six-weeks pregnant when she read on the internet about stem cell treatment for motor neurone disease.

She said: "Mike's best chance is to have cells from a donor who is a close genetic match. The best he is going to get is from his own brother even though he is not born yet.

Julian Emms and Joanna Stanley
Julian Emms and Joanna Stanley admit it's a 'long shot'

"To get a match otherwise could take three or four years and Michael doesn't have years, he only has months.

"It's a race against time but Rhys will have a DNA link. We know it's a long shot and we are all hoping against hope."

Julian Emms said: "This disease is meant to affect old people. Not my young and healthy son."

Michael Emms is losing the mobility in his limbs, especially in his hands and suffers from extreme fatigue.

The Motor Neurone Disease Association (MNDA) say most sufferers die within two to five years of diagnosis - with half dying within 14 months.

Julian said: "When doctors first diagnosed Mike, none of us knew what it was.

Nerve cells

"Then when we did some research, we couldn't get our heads round it. This disease is meant to affect old people. Not my young and healthy son.

"It would be just amazing if little Rhys saved Michael. Rhys will be our miracle baby."

Motor neurone disease affects about 5,000 people in the UK. It is most common among people aged 50 to 70, and tends to affect men slightly more than women.

It is a progressive disorder caused by the breakdown of the nerve cells which control muscle activity.

People with the condition suffer muscle-wasting, loss of mobility, and difficulties with speech, swallowing and breathing.

Stem cell research has been condemned by pro-life campaigners and church groups as it often involves harvesting cells from human embryos.


Stem cell therapy is being used to treat motor neurone disease patients in the US and Canada.

But it has yet to be approved by UK health authorities because doctors are split on its effectiveness.

A spokeswoman for the MNDA said: "We are not for or against the treatment but it is at very early stages and not proven that it can have any effect on motor neurone disease."

The family talk about their hopes for Michael

Q&A: Stem cells
19 May 05 |  Health
Motor neurone disease
20 Aug 01 |  Medical notes
Stem cells: Hope or hype?
09 Nov 06 |  Health
Bush vetoes stem-cell funds bill
20 Jun 07 |  Americas

The BBC is not responsible for the content of external internet sites

Has China's housing bubble burst?
How the world's oldest clove tree defied an empire
Why Royal Ballet principal Sergei Polunin quit


Americas Africa Europe Middle East South Asia Asia Pacific