vcfs22q11.blogspot.com

VCFS 22q11 Foundation

I am dedicated to raising the profile of VCFS or Deletion 22q11.2 Syndrome. My lovely Charli has this syndrome and i want to help and support others. VCFS 22q11 Foundation Australia. The VCFS and 22q11 Foundation supports families and persons affected by VCFS or Deletion 22q11. THe VCFS 22q11 Foundation. View my complete profile. Sunday, August 21, 2011. VCFS 22q11 Awareness Week. VCFS affects approx. 1 in 2000 - 3000 persons making it the second most prevalent genetic syndrome after Down syndrome. It do...

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VCFS 22q11 Foundation | vcfs22q11.blogspot.com Reviews

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I am dedicated to raising the profile of VCFS or Deletion 22q11.2 Syndrome. My lovely Charli has this syndrome and i want to help and support others. VCFS 22q11 Foundation Australia. The VCFS and 22q11 Foundation supports families and persons affected by VCFS or Deletion 22q11. THe VCFS 22q11 Foundation. View my complete profile. Sunday, August 21, 2011. VCFS 22q11 Awareness Week. VCFS affects approx. 1 in 2000 - 3000 persons making it the second most prevalent genetic syndrome after Down syndrome. It do...

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1 vcfs 22q11 foundation

2 vcfsef

3 the dempster foundation

4 mind institute ca

5 donna cutler landsman

6 cheri

7 child development institute

8 welcome

9 supporters of vcfs

10 storage king

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VCFS 22q11 Foundation | vcfs22q11.blogspot.com Reviews

https://vcfs22q11.blogspot.com

I am dedicated to raising the profile of VCFS or Deletion 22q11.2 Syndrome. My lovely Charli has this syndrome and i want to help and support others. VCFS 22q11 Foundation Australia. The VCFS and 22q11 Foundation supports families and persons affected by VCFS or Deletion 22q11. THe VCFS 22q11 Foundation. View my complete profile. Sunday, August 21, 2011. VCFS 22q11 Awareness Week. VCFS affects approx. 1 in 2000 - 3000 persons making it the second most prevalent genetic syndrome after Down syndrome. It do...

INTERNAL PAGES

vcfs22q11.blogspot.com

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VCFS 22q11 Foundation: VCFS 22q11 Foundation: 1/2 Marathon for kids with VCFS

http://vcfs22q11.blogspot.com/2011/04/vcfs-22q11-foundation-12-marathon-for.html

I am dedicated to raising the profile of VCFS or Deletion 22q11.2 Syndrome. My lovely Charli has this syndrome and i want to help and support others. VCFS 22q11 Foundation Australia. The VCFS and 22q11 Foundation supports families and persons affected by VCFS or Deletion 22q11. THe VCFS 22q11 Foundation. View my complete profile. Friday, April 8, 2011. VCFS 22q11 Foundation: 1/2 Marathon for kids with VCFS. VCFS 22q11 Foundation: 1/2 Marathon for kids with VCFS. Subscribe to: Post Comments (Atom). The fo...

2

VCFS 22q11 Foundation: May 2011

http://vcfs22q11.blogspot.com/2011_05_01_archive.html

I am dedicated to raising the profile of VCFS or Deletion 22q11.2 Syndrome. My lovely Charli has this syndrome and i want to help and support others. VCFS 22q11 Foundation Australia. The VCFS and 22q11 Foundation supports families and persons affected by VCFS or Deletion 22q11. THe VCFS 22q11 Foundation. View my complete profile. Sunday, May 29, 2011. Our website http:/ www.vcfsfa.org.au/. We will also soon have wrist bands to support this cause as well. Rare disease. vcfs. Vcfs 22q 22q11.2 syndrome.

3

VCFS 22q11 Foundation: February 2011

http://vcfs22q11.blogspot.com/2011_02_01_archive.html

I am dedicated to raising the profile of VCFS or Deletion 22q11.2 Syndrome. My lovely Charli has this syndrome and i want to help and support others. VCFS 22q11 Foundation Australia. The VCFS and 22q11 Foundation supports families and persons affected by VCFS or Deletion 22q11. THe VCFS 22q11 Foundation. View my complete profile. Tuesday, February 15, 2011. Parenting - Its a hard Job - Looking after yourself is harder! Rare disease. vcfs. Wednesday, February 2, 2011. World Rare Disease Day. Or book onlin...

4

VCFS 22q11 Foundation: VCFS 22q11 Foundation Conference Sydney 2011

http://vcfs22q11.blogspot.com/2011/08/vcfs-22q11-foundation-conference-sydney.html

I am dedicated to raising the profile of VCFS or Deletion 22q11.2 Syndrome. My lovely Charli has this syndrome and i want to help and support others. VCFS 22q11 Foundation Australia. The VCFS and 22q11 Foundation supports families and persons affected by VCFS or Deletion 22q11. THe VCFS 22q11 Foundation. View my complete profile. Tuesday, August 9, 2011. VCFS 22q11 Foundation Conference Sydney 2011. 28th August 2011 , 9.00am. The Children’s Hospital Westmead. Registration / Morning Tea. Sibling Workshop ...

5

VCFS 22q11 Foundation: November 2010

http://vcfs22q11.blogspot.com/2010_11_01_archive.html

I am dedicated to raising the profile of VCFS or Deletion 22q11.2 Syndrome. My lovely Charli has this syndrome and i want to help and support others. VCFS 22q11 Foundation Australia. The VCFS and 22q11 Foundation supports families and persons affected by VCFS or Deletion 22q11. THe VCFS 22q11 Foundation. View my complete profile. Sunday, November 28, 2010. VCFS Supports World Rare Disease Day. World Rare Disease Day. 388 George Street, Sydney NSW. 630pm to 8.30pm. Only 70 tickets available). The first pa...

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vcfsfa.org.au

VCFS 22q11 Foundation - Home

http://www.vcfsfa.org.au/index.php

Fact Sheets and Conferences. 22q at the Zoo. The VCFS and 22q11 Foundation supports families and persons affected by VCFS or Deletion 22q11. Membership is now Free. Membership is now free! VCFS 22q11 Foundation is on Social Media @vcfs22q11 and Hashtag #22qAwarenesss. Welcome to New Zealand. We are pleased to announce that New Zealand is now also represented by the VCFS22q11 Foundation! 22q at the Zoo - which zoo for you? Organized and developed by The International 22q11.2 Foundation. 22q at the Zoo!

liontamar.wordpress.com

liontamar | Tamar's art lounge

https://liontamar.wordpress.com/author/liontamar

Tamar's art lounge. Adventure's of a cafe journalist! Weekly Photo Challenge: Earth. May 8, 2016. What a great topic for this weeks challenge. For me earth is something to be kind to whether it’s creating soil, creating micro climates or enjoying the land through all of our senses. Blessed are the meek,. For they will inherit the earth. Weekly Photo Challenge: Dance. March 19, 2016. Some say that boxing is a dance. Why don’t you have a dance with a flag. The dance of the light sabre. March 12, 2016.

liontamar.wordpress.com

Tamar's art lounge | adventure's of a cafe journalist!!!! | Page 2

https://liontamar.wordpress.com/page/2

Tamar's art lounge. Adventure's of a cafe journalist! Newer posts →. A Fun Family Day. January 10, 2016. Yesterday our little family decided to take a train to the Gong and check out the Toy Brick Fair. This adventure really had everything going for it and could be classified as a win win as our son loves a train ride, Lego and Starwars. There was a designated spot to make your own creation……Zach didn’t make anything but guess who did? Had really paid off. Macquarie Pass National Park. January 3, 2016.

liontamar.wordpress.com

A tourist in my own home town | Tamar's art lounge

https://liontamar.wordpress.com/2011/05/27/a-tourist-in-my-own-home-town

Tamar's art lounge. Adventure's of a cafe journalist! Amaki Cottage Cafe →. A tourist in my own home town. May 27, 2011. When I was planning my getaway destination all I could think of was Kiama. My home town where I was born and bred. Well technically I was bred in Kiama Downs but we wont let details get in the way. I believe that it was the best choice as I was relaxed and enjoyed every moment of my getaway. I booked a lovely cottage. For two nights that was walking distance to everything. You are comm...

liontamar.wordpress.com

My Getaway 2015 | Tamar's art lounge

https://liontamar.wordpress.com/2015/08/01/my-getaway-2015

Tamar's art lounge. Adventure's of a cafe journalist! Weekly Photo Challenge: Muse. Weekly Photo Challenge: Grid →. August 1, 2015. Another year and another getaway at the same place. This time I got to meet the owner and she is lovely. Going back to the same place feels like I’m building a relationship with the place, house, owner and myself. It’s a special thing and even though some things are the same, many things are different. My art was still there. What an amazing walk. My favourite part is th...

liontamar.wordpress.com

Weekly Photo Challenge: Muse | Tamar's art lounge

https://liontamar.wordpress.com/2015/07/02/weekly-photo-challenge-muse

Tamar's art lounge. Adventure's of a cafe journalist! Weekly Photo Challenge: ROY G. BIV (rainbow colours). My Getaway 2015 →. Weekly Photo Challenge: Muse. July 2, 2015. I grew up by this river and I often dream about it. This space, The Barrack Heights Community Garden. I am forever taking pictures every time I go there. The Lake is always inspirational. And I can’t stop taking pictures of my garden and chooks. And of course, these two. This entry was posted in weekly photo challenge. Sorry, your blog ...

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VCFS Dubai,vcfs,DiGeorge syndrome (DGS), velo-cardio-facial syndrome (VCFS), conotruncal anomaly face syndrome (CTAF), Opitz G/BBB syndrome,

Https:/ www.facebook.com/pages/VCFS22q112-deletion-awareness-Dubai-UAE/150462005055355. Https:/ www.facebook.com/groups/120247201099/.

vcfs.nl

22q11DS | Alle informatie over dit syndroom

Meldt u aan als lid! Over (het Netwerk) 22q11DS-VCFS. Het netwerk 22q11DS-VCFS bestaat uit ouders van kinderen met VCFS, (jong)volwassenen met VCFS en belangstellenden in VCFS. Ouders leren van elkaar en vinden (h)erkenning bij elkaar. Het netwerk zorgt dat hun ervaring behouden blijft, zodat ‘nieuwe’ ouders niet alles opnieuw hoeven te ontdekken. Het netwerk houdt nauw contact met onderzoekers en deskundigen. Op deze website vindt u veel informatie over VCFS en het netwerk. Op het forum. At The Zoo 2012.

vcfs.no

VCFS - DiGeorge - 22Q11 - syndrom

Under et VFCS-kurs på Frambu i 2011 besluttet noen av foreldrene å danne en Facebook gruppe for vår diagnosegruppe. Facebookgruppen heter: Velo Cardio Facial Syndrom Norge. Gruppen har ca 160 medlemmer (oktober 2014), og vi har plass til mange flere! Gruppen gjør det lettere å holde kontakt med de man har møtt på treff tidligere, samt andre i samme situasjon. Fordelene er mange. Raquo; Innkalling til årsmøte. Publisert: 10. May 2015. Agenda for årsmøtet vil være som følger:. Gjennomgang av årsmelding 2014.

vcfs.org.uk

VCFS, Information and Communication Technology Support for Voluntary, Community and Faith Sectors.

Is an organization who, through our Problem Resolution Service. Offer reduced cost Information and Communication Technology Support for Voluntary, Community and Faith Sectors - VCFS. We cover North Lancashire. And offer more than just a Problem Resolution Service. We provide a support service for all sizes of voluntary organizations which consists of consultancy, development and implementation of new technologies. Please see our services page.

vcfs22q11.blogspot.com

VCFS 22q11 Foundation

I am dedicated to raising the profile of VCFS or Deletion 22q11.2 Syndrome. My lovely Charli has this syndrome and i want to help and support others. VCFS 22q11 Foundation Australia. The VCFS and 22q11 Foundation supports families and persons affected by VCFS or Deletion 22q11. THe VCFS 22q11 Foundation. View my complete profile. Sunday, August 21, 2011. VCFS 22q11 Awareness Week. VCFS affects approx. 1 in 2000 - 3000 persons making it the second most prevalent genetic syndrome after Down syndrome. It do...

vcfsa.com

VCF, S.A. – Válvulas y Control de Fluidos, S.A.

Teléfono: 34 91 300 00 29. VCF, S.A. Fabricantes de reconocido prestigio. VCF, S.A. Más de 25 años de experiencia. Válvulas y Control de Fluidos S.A. es una compañía constituida con la clara vocación de velar por el cliente para el suministro de válvulas industriales. VCF está constituida por un equipo humano de profesionales de amplia experiencia, de más de 25 años, en el campo de la distribución de válvulas y la gestión de abastecimientos. VCF cuenta con un soporte técnico y comercial. VCF Certificado ...

vcfsantaynez.org

Valley Christian Fellowship / I'm New / Home

Websites made for ministries. QUEST 6th Grade Ministry. Paradigm - High School. Velocity - Middle School.

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Bi-Laws and Public Filings. Visionary Center for Sustainable Communities. Our mission and vision is to build sustainable communities by promoting and cultivating successful small businesses. Our focus is specifically to help minority, woman-owned, and veteran owned businesses; as well as minority individuals throughout the United States. We customize our services to provide viable, vetted, and validated businesses and individuals to pursue those opportunities. Needs assessments for community ecosystems.

vcfscenter.com

The Virtual Center for Velo-Cardio-Facial Syndrome

The Virtual Center for Velo-Cardio-Facial Syndrome. The Virtual Center for Velo-Cardio-Facial Syndrome, Inc. is an open-access 501(c)3, internet-based charitable organization that provides personalized information to people whose lives have been touched by VCFS and who are seeking applicable research and clinical expertise regarding the management of the syndrome. There is no charge for this service, which is funded by voluntary donations. Page, you may download growth charts specific to VCFS. Carefully ...