I am going to finish now, because although I could go on for hours on this matter, I am sure that even Sir Alan would not bat at the crease at Essex for as long as this.
What fires me up about this issue is the letters that some of us receive. I know that the following letter is anecdotal and it is only one letter, but we receive lots of these. This person writes that they have"““a 42 year old daughter who is COMPLETELY disabled with multiple sclerosis. The only…movement my daughter has is to blink for yes and move her head from side to side for no.””"
A famous movie that is out shows the same thing involving a very autistic Frenchman.
The letter continues:"““She cannot speak, see very well, eat, except for tiny amounts of food…Her husband is her main carer and she is dependent…on him…She spends 20 hours each day in bed as M.S. is extremely fatiguing…There is no cure at present. The only hope is stem cell research. Please, when you are voting on the…Bill think of my daughter and what this research could do for her and for others like her, please do not deny them a possible cure.””"
I am inspired by people writing to me out of the blue like that. I receive lots of letters like that, and I would be the last person to prevent our scientific and medical community from trying to develop the kind of cures that help people just like that.
Human Fertilisation and Embryology Bill [Lords]
Proceeding contribution from
Ian Gibson
(Labour)
in the House of Commons on Monday, 19 May 2008.
It occurred during Debate on bills
and
Committee of the Whole House (HC) on Human Fertilisation and Embryology Bill [Lords].
Type
Proceeding contribution
Reference
476 c41-2 
Session
2007-08
Chamber / Committee
House of Commons chamber
Subjects
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Timestamp
2023-12-15 23:14:40 +0000
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