IMPORTANT NOTICE ABOUT COMMENTS

Because of spam, I personally moderate all comments left on my blog. That means you will not see your comment when you post it. It will instead show up within 48 hours, along with my response if one is appropriate.

All comments are welcome and will be posted, even if they are negative. You just can't promote other sites or products in them.

If you have a personal question about LI or any related topic you can send me an email at stevecarper@cs.com.

Otherwise, this blog and my Lactose Intolerance Clearinghouse are now legacy sites, meaning that I am not updating them any longer. The basic information about LI is still sound. However, product information and weblinks may be out of date.

My old website can be found at www.stevecarper.com/li

For quick offline reference, you can purchase Planet Lactose: The Best of the Blog as an ebook on Smashwords.com or Amazon.com or BarnesandNoble.com or a whole lot of other places that Smashwords is suppose to distribute the book to. Almost 100,000 words on LI, allergies, milk products, milk-free products, and the genetics of intolerance, along with large helpings of the weirdness that is the Net.

Sunday, September 13, 2009

Running Toward a Cure to Galactosemia

Galactosemia is that very rare congenital disease in which lactose is successfully digested into glucose and galactose but the galactose is never metabolized into more glucose. Instead it remains in the bloodstream and can eventually cause liver failure. The only remedy is to place the child on a strict lactose-free diet for life.

One such child is Sarah Southard of Wichita Falls, TX, whose parents have started an annual fundraiser toward research called Sarah's Cure.

This year all proceeds from the Wise Tri Triathlon will go to Sarah's Cure. You can read about it in an article by Jessica Langdon in the Wichita Falls TimesRecordNews.

For more about Sarah's Cure and about galactosemia, check out Parents of Galactosemic Children, Inc. (PGC).

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