A final note: One of the parents of an MOPD II child has set up a charitable foundation to help out the families who are struggling financially because of the medical bills associated with the syndrome. It can be found on the web at http://www.potentialsfoundation.org/
Thanks again!
]]>I was in Montreal this past weekend and saw this documentary for the first time. I was immediatly inspired by their stories and could not be happier for these children as they seem to be marhcing on full force in life, not limiting their own abaillities. I was so sad to hear Hannah say that she felt like nothing. I am a singer songwirter and I have written a song for Hanna. Does anyone know how I could possible get into contact with her and her family, so I can share it with her?? Your help would be greatly appreciated.
Denise
]]>There children, adults and their families are so inspirational. What we take for granted these children and adults take in their stride albeit it can be a hurdle for them and they do it with dignity!
Over the last couple of months I have serached the web for information about the condition and whilst the medical information is limited and confusing, there are some remarkable sites out there about the chIldren themsleves.
www.ourlittlemiracle.com
ww.tinybraveheart.com
www.alex-connerty.co.uk
www.walkingwithgiants.org
These children and families are truly marvellous
Dave
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