karensfshjourney.blogspot.com
Karen's FSH JourneyOn going story of life with Facioscapulohumeral Muscular Dystrophy(FSH-MD).
http://karensfshjourney.blogspot.com/
On going story of life with Facioscapulohumeral Muscular Dystrophy(FSH-MD).
http://karensfshjourney.blogspot.com/
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Karen's FSH Journey | karensfshjourney.blogspot.com Reviews
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On going story of life with Facioscapulohumeral Muscular Dystrophy(FSH-MD).
Karen's FSH Journey
http://karensfshjourney.blogspot.com/2008/04/karens-fsh-journey.html
On going story of life with Facioscapulohumeral Muscular Dystrophy(FSH-MD). Monday, 21 April 2008. Karen’s FSH Journey. An everyday account of living with Fasio Scapulo Humeral Muscular Dystrophy. the ups and the downs the frustrations and the positives.oh yes there are positives. I’ve had FSH all my life. I was born with a defective gene passed on from my Dad. There’s a 50-50 chance of it being passed on. Even now I can still hear my mums voice “Will you turn that leg in when you walk no wonder yo...
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Pacific Northwest Friends of FSH Research: March 2008
http://blog.fshfriends.org/2008_03_01_archive.html
Pacific Northwest Friends of FSH Research. Supporting research into Facioscapulohumeral Muscular Dystrophy. Friends of FSH Research Official Site. Wednesday, March 26, 2008. Deena Tannous Will Be Missed. Deena Tannous sitting with her friend Amanda. Age 26, passed away peacefully in. March 24, 2008. Dearly beloved daughter of Peter and Basma. Loving sister of Speero, Annie and William. She will be greatly missed by her numerous aunts and uncles, cousins, relatives from the. March 25, 2008. Was the Friend...
Pacific Northwest Friends of FSH Research: Platform development for candidate drug screening for FSHD
http://blog.fshfriends.org/2012/07/platform-development-for-candidate-drug.html
Pacific Northwest Friends of FSH Research. Supporting research into Facioscapulohumeral Muscular Dystrophy. Friends of FSH Research Official Site. Thursday, July 26, 2012. Platform development for candidate drug screening for FSHD. Platform development for candidate drug screening for FSHD. Miller Lab News Story. Subscribe to: Post Comments (Atom). FiSHing for a Cure with HeART. There was an error in this gadget. Pacific Northwest Friends of FSH Research. Chris Carrino FSHD Foundation.
Pacific Northwest Friends of FSH Research: April 2009
http://blog.fshfriends.org/2009_04_01_archive.html
Pacific Northwest Friends of FSH Research. Supporting research into Facioscapulohumeral Muscular Dystrophy. Friends of FSH Research Official Site. Thursday, April 23, 2009. Assumptions - Living with FSHD. My friend Anne has allowed me to share her story here on my blog. Please take a moment to learn more about living with Facioscapulohumeral Muscular Dystrophy. We all make assumptions about others based on our own life experiences. Sometimes assumptions are helpful. Many times they are not. April 9, 2009.
Pacific Northwest Friends of FSH Research: New "DNA Combing" Test for FSHD
http://blog.fshfriends.org/2012/04/genomic-vision-launches-innovative-new.html
Pacific Northwest Friends of FSH Research. Supporting research into Facioscapulohumeral Muscular Dystrophy. Friends of FSH Research Official Site. Monday, April 16, 2012. New "DNA Combing" Test for FSHD. Biotech company Genomic Vision. Just announced the release to market of a new method of testing for FSHD. The test uses molecular combing technology that stretches DNA and affixes it to a treated glass surface. The DNA can then be analyzed using FSHD-specific software. Subscribe to: Post Comments (Atom).
Pacific Northwest Friends of FSH Research: January 2010
http://blog.fshfriends.org/2010_01_01_archive.html
Pacific Northwest Friends of FSH Research. Supporting research into Facioscapulohumeral Muscular Dystrophy. Friends of FSH Research Official Site. Tuesday, January 26, 2010. Maarel, S.M. van der; Frants, R.R. Padberg, G.W.am. Http:/ repository.ubn.ru.nl/handle/2066/51789. Biochimica et biophysica acta. Molecular basis of disease, Vol. vol. 1772, p.p. 186-p. 194. Wednesday, January 20, 2010. Sleep disordered breathing in facioscapulohumeral muscular dystrophy. Pietro A. Tonali. Received 20 March 2009.
Pacific Northwest Friends of FSH Research: September 2009
http://blog.fshfriends.org/2009_09_01_archive.html
Pacific Northwest Friends of FSH Research. Supporting research into Facioscapulohumeral Muscular Dystrophy. Friends of FSH Research Official Site. Wednesday, September 30, 2009. Standing In Line for Vodka for FSH research? Yep, Dan Akroyd was in Seattle promoting his "Crystal Head" triple filtered vodka. I stood in line (among other fans) to have a bottle signed. Go see the Youtube video. Tells his story, or the story of the head. Friends of FSH Research. Tuesday, September 29, 2009. So What is FSHD?
Pacific Northwest Friends of FSH Research: January 2009
http://blog.fshfriends.org/2009_01_01_archive.html
Pacific Northwest Friends of FSH Research. Supporting research into Facioscapulohumeral Muscular Dystrophy. Friends of FSH Research Official Site. Friday, January 30, 2009. On the Road to Finding a Treatment. The journey toward a cure or treatment is made by the help of many - here is a note from one of the researchers funded by the Friends of FSH Research. Why Conduct an Auction? So the next question was "How close are we to developing a treatment? What are researchers doing for those with FSHD? In 2003...
Pacific Northwest Friends of FSH Research: May 2009
http://blog.fshfriends.org/2009_05_01_archive.html
Pacific Northwest Friends of FSH Research. Supporting research into Facioscapulohumeral Muscular Dystrophy. Friends of FSH Research Official Site. Wednesday, May 20, 2009. In the News - Researchers Recognized. March of Dimes Awards $250,000 Prize to Scientists Unraveling the Causes of Muscular Dystrophy. BALTIMORE, May 6 /PRNewswire-USNewswire/ - Two scientists whose work. Has led to new and better ways to diagnose and potentially treat muscular. To read the complete press release. FiSHing for a Cure wit...
Pacific Northwest Friends of FSH Research: February 2009
http://blog.fshfriends.org/2009_02_01_archive.html
Pacific Northwest Friends of FSH Research. Supporting research into Facioscapulohumeral Muscular Dystrophy. Friends of FSH Research Official Site. Thursday, February 26, 2009. The Promise of their Work. The impact you, the donor, has made is clearly stated in this excerpt from a letter, dated Feb. 26th, which we received. The complete letter written by Dr. Paul G. Ramsey, the Executive Vice President for Medical Affairs and the Dean of the School of Medicine is available on-line. Living with FSH has many...
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karensforayintoteaching.wordpress.com
Technology Safari | My ED554 Blog – Summer 2011
My ED554 Blog – Summer 2011. Apologies, but no results were found for the requested archive. Perhaps searching will help find a related post. Blog at WordPress.com. Blog at WordPress.com.
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Items in your cart. The New Website Will Be Complete Soon. Art by Karen Tribett. Art by Karen Tribett. Art by Karen Tribett. Art by Karen Tribett. Art by Karen Tribett. Art by Karen Tribett. KT088 Enjoy The Little Things. KT222A Be Still. 20x8. KT221A Rather Be On My Farm 20x8. KT217A Faith Family Farming 20x8. KT213A 8th Day Farmer Barn 20x8. MAZ5012 - Home - 12 x 12. Our Beautiful Art work will add peace and warmth to your home. This is one of our newest items that has been selling very well. Your stor...
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Just another WordPress.com site. When pain is a gift. September 18, 2014. A day or two later and the pain had gotten worse so I went to my doctor, got prescribed a metric f*ck tonne of painkillers and referred to a specialist. I kept relatively cheery, the pain killers made me feel like things were definitely getting better. And then two weeks in I came off them to find out there was only a tiny amount of progress. The trad season seems never ending! March 18, 2014. A guy in work asked me the other day a...
Karen's FSH Journey
On going story of life with Facioscapulohumeral Muscular Dystrophy(FSH-MD). Monday, 21 April 2008. Karen’s FSH Journey. An everyday account of living with Fasio Scapulo Humeral Muscular Dystrophy. the ups and the downs the frustrations and the positives.oh yes there are positives. I’ve had FSH all my life. I was born with a defective gene passed on from my Dad. There’s a 50-50 chance of it being passed on. Even now I can still hear my mums voice “Will you turn that leg in when you walk no wonder yo...
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Karen's Journey at Fuller Theological Seminary | Processing through my personal and spiritual journey in Grad School.
Karen's Journey at Fuller Theological Seminary. September 15, 2011 · 4:45 pm. Not that I wouldn’t be a cool professor, because I think I would – but being a cool staff member is much more fun right now! The list goes on and on. So as the fall season approaches, the fall season of my career also is upon me, and I am pretty sure I am ready for both. September 8, 2011 · 5:18 pm. I hate that feeling. And for the record, no, I am not pregnant,. Out of africa missions. August 1, 2011 · 9:45 am. Sudafed is a mu...
Karen's Fun Blog
Tuesday, March 27, 2018. Tilda in Mint Green. Tuesday, March 20, 2018. Today I have a get well card. I used the Thing-a-ma-jing to help position the step and Tilda stamps and it worked soooo great! It's so fun to stamp right the first time. lol I added the Band-Aid and Tilda tag die cuts along with lace and flowers from Wild Orchid Crafts. Thanks for stopping by! Monday, March 19, 2018. Today's card has Tilda all ready for spring! Sunday, March 18, 2018. Saturday, March 17, 2018. Friday, March 16, 2018.