Welcome to my website

Welcome to my website

My name is Sarah Spencer. I am a mother of a Cystic Fibrosis sufferer.
I have set up this website to raise money and awareness in Spain.
Although the doctors and hospitals are fantastic here, there is not a lot of information given out about the disease to the public. So unless you are a CFer or have a child who is then you would not know much about this life threatening disease.
To the best of my knowledge everything on this site is true.
I will be adding events as and when they are organised.
Thank you for taking the time to look at my website.

Welcome to my website

This website will include:
Information about Cystic Fibrosis.
Fundraising events.
Articles from Cystic Fibrosis sufferer Becky.
Ways you can help.
How to donate to Cystic Fibrosis Research.
Updates on Research.

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Latest comments

24.01 | 21:45

Have you heard of the Gerson Institute? I believe they can help Becky. If you havent heard of it check their web site, www. gerson.org You can email them.

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15.04 | 00:09

You are so brave. I admire you. This is an amazing story and I am glad that you have been able to come through fighting. Much love.

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18.06 | 00:27

Dear Becky, Sarah and Ken
Congratulations for all that you do for CF

Kisss

Merche

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22.07 | 18:46
Cystic Fibrosis Has received 17
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