Sotelo Family Tree

Sotelo Family Tree Our single mission... funding a cure... A CURE... not a treatment, or acceptance... but a CURE for Huntington's Disease. THIS IS JUST THE BEGINNING!!!

We will fund raise, sell donated goods and time, and collect any and all donations that we can to reach our $5million mark. We are currently working with Dr. Jan Nolta at UC Davis Medical Center to continue to fund her ongoing research for the cure for HD. This cure will in turn provide the building blocks for curing such diseases as Alzheimers, Parkinsons, and ALS. It's just the beginning, AND it

's so close. We have been to these research facilities and seen first hand that these doctors are confident in their knowledge that they CAN cure HD. What they need is FDA approval for clinical trials, and funding. They're estimate was that we could have a CURE in FIVE YEARS!!! FIVE YEARS!!! $5million sounds like a lot, but I think we can do it....

http://www.ipscell.com/2012/12/knoepfler-blog-stem-cell-person-of-the-year-finalists-time-to-vote/Jan Roberson has promi...
12/18/2012

http://www.ipscell.com/2012/12/knoepfler-blog-stem-cell-person-of-the-year-finalists-time-to-vote/

Jan Roberson has promised to donate her winnings to Dr. Jan Nolta at the Center for Excellence at UC Davis to help fight Huntington's Disease! Vote daily!!!

Knoepfler Blog Stem Cell Person of the Year Finalists: time to votePosted on December 17, 2012 by adminI’m giving out a Stem Cell Person of the Year award for 2012 along with all my other annual awards (e.g. best stem cell journal, paper, blog, comic, activist, etc).The Person of the Year winner wil...

Just in case you missed it on MY page...
10/05/2012

Just in case you missed it on MY page...

Meeting his family history head-on, Charles Sabine, center, participates in a clinical trial to shed light on Huntington's disease. Mr. Sabine's father, at

06/20/2012

Canada, Feb. 18 -- In a breakthrough study, researchers have identified a potential novel therapy for Huntington disease.

Experts revealed that Huntington disease is a neurodegenerative genetic disorder that affects muscle coordination and leads to cognitive decline and psychiatric problems. HD is the most common genetic cause of abnormal involuntary writhing movements called chorea. Physical symptoms of Huntington's disease can begin at any age from infancy to old age, but usually begin between 35 and 44 years of age.

Researchers from the University of Alberta revealed that people suffering from the disorder have faintly reduced amounts of a brain molecule called GM1. One of the researchers said that when GM1 levels were returned to normal among lab simulations suffering from the disorder, motor abilities were back to normal within some days.

The GM1 molecule treatment was provided to the lab models for about a month. Within the initial 14 days following completion of the therapy, the subjects had usual motor working, but after that, a decline in the working was observed. The researcher suggested that a promising therapy with the molecule would entail frequent treatments in the long run.

The findings were featured in Proceedings of the National Academy of Sciences journal.

Written by Ritika Berry Published by HT Syndication with permission from Health Daily Digest. For any query with respect to this article or any other content requirement, please contact Editor at [email protected]

05/27/2012

Raised another $100 with an in home "trunk show" with Norwex products. Remember, if you're hosting a show in your home, ask your consultant to donate the proceeds directly to SOTELO FAMILY TREE!!!!!

03/28/2012

Do you or someone you know have Huntington's Disease? We would love the opportunity to include your family tree on our website. Please let me know, and I'll send you the information for how to submit pictures and bits of info about your family!

xxoo

03/20/2012

Lesley's Digital Story for Dr. Boland's Neural Communications Class (Biol199) about Huntington's Disease

03/19/2012

I feel like I've lost my way in regards to promoting Sotelo Family Tree, and I apologize. I didn't realize it until my daughter said to me today, "mommy, what's Huntington's Disease?" I thought, dang it, she's forgotten!!! I've failed... then she started to slowly recollect Uncle Joe, who he was, what he looked like... and why we're fighting. Please remember to 'share' this page with your friends... we only have 64 'likes' and i'd like that to be 1064... =)

02/29/2012

Will be speaking to a panel of medical students at UC Davis Med Center next week regarding how HD has effected my family.

02/17/2012

Do you want your message/video/blog/pics/family story to be included on our new website raising funds to find a cure for Huntington's? LMK

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2091 Letterkenny Lane
Lincoln, CA
95648

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