LITTLELAUREN.ORG
LittleLauren.org | Help Us Fight OMSLittle Lauren.org was created to raise awareness about opsoclonus-myoclonus syndrome (OMS), a very rare neurological autoimmune disease.
http://www.littlelauren.org/
Little Lauren.org was created to raise awareness about opsoclonus-myoclonus syndrome (OMS), a very rare neurological autoimmune disease.
http://www.littlelauren.org/
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LittleLauren.org | Help Us Fight OMS | littlelauren.org Reviews
https://littlelauren.org
Little Lauren.org was created to raise awareness about opsoclonus-myoclonus syndrome (OMS), a very rare neurological autoimmune disease.
littlelauren.org
LittleLauren.org | Help Us Fight OMS
http://www.littlelauren.org/index.php
Lauren keeps busy doing crafts while in the hospital. Lauren's "Home" for several months in 2012. Lauren and her wonderful surgeon, Dr. Chris Weldon. Lauren returns to school after a 5 month hospital stay. OMS Fundraiser Mother-Son Dance. Little Lauren.org was created to raise awareness about opsoclonus-myoclonus syndrome (OMS), a very rare neurological autoimmune disease that Lauren has been ill with and fighting since January 2009. THE 2015 MOTHER SON DANCE. HOW YOU CAN HELP.
LittleLauren.org | About OMS
http://www.littlelauren.org/aboutoms.php
About Opsoclonus-Myoclonus Syndrome (OMS). Resource: http:/ en.wikipedia.org/wiki/Opsoclonus myoclonus syndrome. Opsoclonus myoclonus is a syndrome in which the eyes dart involuntarily (opsoclonus or dancing eyes) and muscles throughout the body jerk or twitch involuntarily (myoclonus). About half of all cases of opsoclonus myoclonus are associated with neuroblastoma and most of the others are suspected to be associated with a low-grade neuroblastoma that spontaneously regressed before detection. It ...
LittleLauren.org | Donate Now
http://www.littlelauren.org/donate.php
The Lauren Mantz OMS Research Fund. The Lauren Mantz OMS Research Fund was created by the parents of Lauren Mantz at Boston Children’s Hospital to address some of the many shortcomings today in the diagnosis and treatment of OMS. After our daughter Lauren was diagnosed with OMS, we were very surprised to find such little information and research existed about OMS. This has improved the last few years, but still has a long ways to go. Who is behind this research? How can I help? We are putting together a ...
LittleLauren.org | Lauren's OMS Journey
http://www.littlelauren.org/journey.php
Lauren spent another week in the hospital in Orlando in May 2012 for another bout of pancreatitis. She recovered and remains on a strict low-fat diet. Luckily she has done well on it until October 2014 when she had a small relapse of OMS symptoms. She had grown quite a bit since stopping the prednisolone/steroid so they increased her evening dose of Cellcept. This has proven effective so far.
LittleLauren.org | The 2015 Mother Son Dance
http://www.littlelauren.org/msdance.php
The 2015 Mother-Son Dance. Mothers or mother-figures and sons (ages 3-12) are invited for an evening filled with jammin’ fun to include DJ, dancing, refreshments, and cherished memories. $5 professional photo opportunity available. All donations and proceeds from this event are put towards OMS research at Boston Childrens Hospital, one of a few facilities in the US to be actively studying OMS. BUY TICKETS IN PERSON. 106 SW 17th Street, Ocala, FL 34471. Hours: Mon Sat: 10 9; Sun 12-5.
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Recipes and Meal Plans. The $10 Food Challenge. Small bites and delights around Melbourne CBD. August 3, 2015 9:01 am. A good ad campaign can really kill a joint. I’m being serious. From watching Melbourne ads I expect every laneway to deliver the most exquisite bar/restaurant/cafe/shop. Unrealistically high expectations. NB this intro is laced with jokes that only make sense if you’ve seen the ads…. We stopped into this unassuming cafe to be surprised with one of the most delicious pork belly bahn mis a...
LittleLauren.org | Help Us Fight OMS
Lauren keeps busy doing crafts while in the hospital. Lauren's "Home" for several months in 2012. Lauren and her wonderful surgeon, Dr. Chris Weldon. Lauren returns to school after a 5 month hospital stay. OMS Fundraiser Mother-Son Dance. Little Lauren.org was created to raise awareness about opsoclonus-myoclonus syndrome (OMS), a very rare neurological autoimmune disease that Lauren has been ill with and fighting since January 2009. THE 2015 MOTHER SON DANCE. HOW YOU CAN HELP.
littlelauren17 (Lauren Martin) - DeviantArt
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littlelaurenbigworld.tumblr.com
Little Lauren, Big World
Little Lauren, Big World. Just Like John Keating. Today, I wrote a character monologue for my. Second City comedy writing class. Yay for free time! Actually, not yay for unemployment. If you know anyone looking for a copywriter, please send them my way, stat.). It’s also worth noting that this is a fictitious piece. So for my teacher friends out there: don’t go around trying to guess who this is about. Enjoy, and please let me know your thoughts! So let me get this straight. I’m. Me before, and I mean,.
littlelaurenbyrne.blogspot.com
LA BLOGOTHEQUE USA
Sunday, May 25, 2008. Various Musings of Mine Own (2006-present). Woody Allen wonders aloud, "What makes life worth living? I say: the scorched feeling of my body after a day in the sun. Before I realize that I am now, sunburnt. My hair and my skin are salty and dry, and all I want to do is to drive home with the windows down as the wind blows in my face. I say: love, the eternal kind. . The moonlight dancing atop the darkened waters. I miss the Atlantic and its billowing waves. . The wonder of these sig...
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More options ▼. Subscribe to my blog. Created: 20/01/2014 at 11:32 AM. Updated: 26/12/2014 at 7:46 AM. 12525;ーレンス。 Don't forget that insults, racism, etc. are forbidden by Skyrock's 'General Terms of Use' and that you can be identified by your IP address (66.160.134.3) if someone makes a complaint. Please enter the sequence of characters in the field below. Posted on Tuesday, 28 January 2014 at 5:58 PM. Edited on Friday, 26 December 2014 at 7:46 AM. Tue, January 28, 2014. Subscribe to my blog!
LittleLaurenCX (Lauren) - DeviantArt
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