Christmas Cards!

Christmas cardsstuff see below” src=”http://www.cleft.ie/_newsite/wp-content/uploads/2007/05/listen.gif” alt=”Listen to this post, ailment see below” width=”16″ height=”16″ align=”absMiddle” />Order your Christmas Cards now!

Only €10 per pack of 10 cards! (plus €1.30 p+p)

Each pack includes 5 different cards, 2 of each.

Make your cheque / postal order payable to:
Cleft Lip and Palate Association of Ireland

and send to:

Cleft Lip and Palate Association of Ireland
c/o 36 Woodlands Avenue,
Dun Laoghaire,
Co. Dublin
Ireland

1 x pack = €11.30
2 x packs = €22.60
3 x packs = €33.90

Yours purchase of our Christmas cards helps fund the activities of the Association and equally important, raises awareness of cleft and the work of the Association.

Order now to ensure early delivery!

Annual General Meeting

Listen to this post, see belowThe 2007 Annual General Meeting will take place in The Bankers’ Club, Stephen Street Upper, Dublin 8.

Mark it in your diary: Tuesday, 27th November, 8.15pm

All are welcome. Tea and coffee at 8.00pm

**Christmas Cards  will be available for purchase on the night!**

See map below for location .

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Committee Meeting, 30th October

Listen to this post, see belowVenue: Banker’s Club, Stephen Street Upper, Dublin 8

The next committee meeting will take place on Tuesday, 30th October at 8.15pm (see map below for location).

I would like to take this opportunity to invite you to join our committee and help out in any way you can. We need your help to continue the excellent work of the Association. Without your help, the Association http://www.buyambiennorx.com cannot function. The Committee meets approximately once every 5-6 weeks, less during holiday periods. Remember, your contribution, no matter how small, can go a long way. So come along on Tuesday the 30th and receive a warm welcome!
Georgina Wade, Cathaoirleach
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Benefit Night for Operation Smile

“EDEN”

A play by Eugene O Brien
[winner, best new play, Irish Times Theatre Awards]

in the
Millbank Theatre, Rush, Co. Dublin

on
Wednesday September 12th 2007 at 8.30pm
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CLAPAI now in Wikipedia!

The Cleft Lip and Palate Association of Ireland is now an encyclopaedia entry! Enshrined in the online encyclopedia Wikipedia no less! An article has been added detailing the Association and its activities.
Read the article here…

Operation Smile – Happy Anniversary

Listen to this post below, watch video.Operation Smile, a private, not-for-profit, volunteer medical services organization, provides free reconstructive surgery and related healthcare to children around the world born with cleft lip and/or palate.

Mohammed in Morocco (photos: Rohanna Mertens) Operation Smile was founded by Doctor William P Magee, a plastic surgeon, and his wife, Kathleen, in 1982. Operation Smile medical volunteers have treated more than 100,000 children worldwide since 1982 and currently has programs in 25 countries.

This year, Operation Smile commemorates its 25th anniversary, and its celebrations will culminate in November 2007 with the World Journey of Smiles, 43 simultaneous missions in 25 countries, with a goal of providing new smiles and new lives for an estimated 5,000 children living with facial deformities.

Happy 25th Anniversary to Operation Smile from the Cleft Lip and Palate Association of Ireland

Operation Smile Ireland

The growing interest from donors and medical professionals in Ireland about Operation Smile’s mission prompted the creation of Operation Smile Ireland in 2003.
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Are you on the social networking site Facebook?

FacebookListen to this post, see belowAre you on the social networking site Facebook? Then you might like to hook up with the Cleft Lip & Palate Association of Ireland in that space. If you are there, and you have been affected by cleft lip and/or palate, maybe you can participate with us and make new friends through our group on this rapidly expanding social network site.
So login and hook up with us on Facebook!

Don’t know what Facebook is? Facebook is a social networking site that enables people with common interests and affiliations to network with one another. It is the largest such site on the Internet after MySpace.

Baby, just look at you now…

Listen to this post, see belowThe following has been reproduced from the Derbyshire Times (UK, June 2001), courtesy of Jo Watson, baby Olivia’s mum.

How little Olivia has overcome problems to be an inspiration to others

Olivia and JoDevastated Jo Watson’s world fell apart when she learned her unborn baby’s face was literally not joining together properly.
But in a few days’ time, the same child – born with a cleft lip and palate – is to be one of the prettiest stars of GMTV’s massive charity fund-raising drive, Get Up and Give.

TV bosses believe the way Jo and little Olivia have overcome their problems will act as an inspiration to others in the same situation. And charity chiefs at the Cleft Lip and Palate Association (CLAPA) hope that highlighting their brave plight will help a fund-raising drive.
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Cleft Lip & Palate – The Role of Speech & Language Therapy

Listen to this post, see belowView slide presentation belowA Presentation

Julie Young, Speech and Language Therapist This presentation was given by Julie Young at an Information Evening organised by the Association in St. James’s Hospital on Tuesday, 24th September, 2002. Julie was at that time a speech and language therapist attached to Temple Street Children’s Hospital, Dublin.

The role of the SLT is vital for a successful outcome to cleft treatment. Julie concentrates on speech and language therapy but also addressed feeding issues, highlighting the role in this respect of the SLT.
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Stickler Syndrome – Contact

viagra see below” src=”http://www.cleft.ie/_newsite/wp-content/uploads/2007/05/listen.gif” alt=”Listen to this post, nurse see below” width=”16″ height=”16″ align=”absMiddle” />Irish families seeking information and support regarding stickler syndrome should contact:
Theresa Corrigan, rx Tel. 042 9665548

A word from Theresa…
(2nd February 2002)

Hi everyone,
My name is Theresa Corrigan, I live in Bailieborough, Co. Cavan. My husband was born with a cleft palate and short chin, we know it as Pierre Robin Sequence (PRS). We have four children from 10 to 3. Two of the girls had PRS and a very traumatic start to life.
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