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lgsfoundation.org

LGS Foundation | Lennox-Gastaut Syndrome

The LGSF is a nonprofit organization dedicated to improving the lives of individuals with Lennox-Gastaut Syndrome through research, programs and education

http://www.lgsfoundation.org/

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CONTACTS AT LGSFOUNDATION.ORG

Christina SanInocencio

PO b●●●●6948

New●●●ork , New York, 10150

US

1.71●●●●3800
ch●●●●●●●@lgsfoundation.org

View this contact

Christina SanInocencio

PO b●●●●6948

New●●●ork , New York, 10150

US

1.71●●●●3800
ch●●●●●●●@lgsfoundation.org

View this contact

Christina SanInocencio

PO b●●●●6948

New●●●ork , New York, 10150

US

1.71●●●●3800
ch●●●●●●●@lgsfoundation.org

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LGS Foundation | Lennox-Gastaut Syndrome | lgsfoundation.org Reviews

https://lgsfoundation.org

The LGSF is a nonprofit organization dedicated to improving the lives of individuals with Lennox-Gastaut Syndrome through research, programs and education

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As a social responsible company, it is our pleasure to give back. For every T-Shirt that The Family T-Shirt. Sells, we give back $1. Lennox Gastaut Syndrome Fundation. Is a non-profit organization dedicated to providing information about Lennox-Gastout Syndrome (LGS). Hile raising funds to pursue research, services and programs for patients living with LGS and their families. Big Little JC Association. Pics of The Day.

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The life and adventures of a little girl with epilepsy. About us (the short version). Keeping everyone on their toes. She is into another period where she is babbling more. I really enjoy hearing her “talk”. Her mood has been much better too, ever since we added Zoloft. It seems I made a good choice. Normally a patent (or in Becca’s case, a caregiver) would “swipe” the magnet over the VNS implant in her chest to case it to activate an extra pulse in addition to the normal cycle. The very fabulous Nurse P...

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Resources – North American SUDEP Registry (NASR)

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North American SUDEP Registry (NASR). Please forgive our site's appearance. We are currently undergoing site maintenance. Research & Tissue Donation. Coordinated by the Epilepsy Foundation of America, the SUDEP Institute is a collaboration of nonprofit organizations, medical professionals, parent advocates, and government agencies. It offers SUDEP education for families and doctors; counseling for bereaved families; and supports research into the causes of and ways to prevent SUDEP. PAME is a four-day le...

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eterryhistory.com – About

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Elizabeth Terry, M.A. Elizabeth Terry was raised on a cattle ranch on the Wyoming/Nebraska line. There she developed her love of history, from walking along old wagon ruts on the wind-blown prairie to working cattle in log corrals as her ancestors had. After graduating with a history degree from the University of Nebraska at Kearney, Elizabeth earned her Masters in Public History from James Madison University in Virginia. And the Missouri Methodist Journal. Her second book, Ethnic St. Louis,. 8220;When S...

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Cat's in the Bronx: February 2013

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Cat's in the Bronx. Sunday, February 10, 2013. Feeding Tube Awareness Week. Sunday, February 10, 2013. Subscribe to: Posts (Atom). Bronx, New York, United States. I am a wife and mother to 3 beautiful children. Eoghan my oldest has Eosinophilic Eosghagitis,Maura my girl talks too much and Finnian my youngest who battles the seizure monster everyday as well as his other disabilities. View my complete profile. Http:/ picasaweb.google.com/geraldinecat. Keeping up with the Cosgroves. Keto Diet (seizures)stil...

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Cat's in the Bronx: Control????????

http://bronxcataldos.blogspot.com/2014/06/control.html

Cat's in the Bronx. Thursday, June 19, 2014. Finnian might have Epilepsy/ Dystonia/CP and other issues but we try not to let them control our lives. Thursday, June 19, 2014. Subscribe to: Post Comments (Atom). Bronx, New York, United States. I am a wife and mother to 3 beautiful children. Eoghan my oldest has Eosinophilic Eosghagitis,Maura my girl talks too much and Finnian my youngest who battles the seizure monster everyday as well as his other disabilities. View my complete profile. Why do we do the t...

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Cat's in the Bronx: Its been awhile

http://bronxcataldos.blogspot.com/2014/04/its-been-awhile.html

Cat's in the Bronx. Monday, April 14, 2014. A collage of his hospital stay we have to have fun. Not too impressed with the snow on his face. StPatrick's Day yup she put a skirt on me. Citi Field Spartan Race. Finnian and his HERO Steve-o. See the cheeky grin on him he is having fun. Me and the 2 kids. That's it for now. Monday, April 14, 2014. Subscribe to: Post Comments (Atom). Bronx, New York, United States. View my complete profile. Http:/ picasaweb.google.com/geraldinecat. Http:/ dutchcosgroves.b...

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Cat's in the Bronx: June 2014

http://bronxcataldos.blogspot.com/2014_06_01_archive.html

Cat's in the Bronx. Thursday, June 19, 2014. Finnian might have Epilepsy/ Dystonia/CP and other issues but we try not to let them control our lives. Thursday, June 19, 2014. Why do we do the things we do with Finnian? Some people are amazed and some are shocked. Yes shocked. We know some people talk about us that we are great and then we hear from other via the grapevine that we need out heads examined we shouldn't be doing those things with our disabled child. What if he is scared? Tuesday, June 10, 2014.

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Cat's in the Bronx: August 2012

http://bronxcataldos.blogspot.com/2012_08_01_archive.html

Cat's in the Bronx. Thursday, August 2, 2012. Thursday, August 02, 2012. Subscribe to: Posts (Atom). Bronx, New York, United States. I am a wife and mother to 3 beautiful children. Eoghan my oldest has Eosinophilic Eosghagitis,Maura my girl talks too much and Finnian my youngest who battles the seizure monster everyday as well as his other disabilities. View my complete profile. Http:/ picasaweb.google.com/geraldinecat. Keeping up with the Cosgroves. Http:/ cosgroves.blogspot.com. Banzel (seizures) still...

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LGS Foundation | Lennox-Gastaut Syndrome

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