Moylan Family Guest Book 2005 Guest Book Entries 2005
ambra kelly on Saturday December 17, 2005 at 8:57 PM
WS : Yes - Relation : Self
Found : Link from a WS site
Comments : Its good to see that i"m not alone.
rowe on Thursday December 8, 2005 at 7:30 PM
WS : No
Which : looking for my family tree
Comments : i wan't to make my own family tree up so my family in the past can see there family tree
S Barley on Thursday December 1, 2005 at 3:04 PM
WS : No
Found : Search for WS sites - Which : google
Comments : doing WS as part of my dissertation!
Kim Elgee on Sunday November 20, 2005 at 11:29 PM
WS : Yes - Relation : Parent
Found : Link from a WS site - Which : Google
Comments : My son William ironically has williams syndrome. We live here in Wasilla Alaska. He was diagnosed by Ieon Glass from Seattle Childrens Hospital at nine months of age. He was diagnosed with the fish test.
Rhonda Burriss on Tuesday November 15, 2005 at 12:37 AM
WS : Yes - Relation : Friend
Found : Search for WS sites - Which : ask jeeves.com
Betty Ann Austin-Lue on Friday November 11, 2005 at 4:09 PM
WS : No
Found : Link from a WS site - Which : yahoo.com
Comments : Researching WS for a paper for a class assignment. Enjoyed reading the information on your website.My son attended Presentation College in Trinidad,West Indies.
Ita Smyth on Thursday November 3, 2005 at 10:08 PM
WS : No
Which : Google
Comments : I got your name from the NAMHI Directory because we are running a Health Symposium for people with intellectual disability and I was searching for all the "syndromes". I did not know what Williams Syndrome was and searched for a definition when I came across the Moylan site. It was a very moving account of beautiful Patricia's development and required a response. I am the mother of a severely autistic daughter so understand some of the problems although our Kate would never reach the fantastic academic standards that Patricia has attained. Well done Patricia. I wish you and your lovely brother John and your parents every blessing and good wish that you wish for yourselves.
Ita Smyth
noreen collins on Thursday October 27, 2005 at 5:31 PM
WS : No
Found : Link from a WS site - Which : google
Comments : I'm a 2nd year intellectual disability nursing student and am doing a search on Williams Syndrome and came across your site which is very interesting. your children are beautiful. many thanks
Niamh Riddell on Wednesday October 19, 2005 at 5:01 PM
WS : Yes - Relation : Friend
Found : Search for WS sites - Which : GOOGLE
Comments : Hey to all the moylans,
you may remember me from wsai music camp.hope everyone is keeping fine and happy.glad to hear patricia is doing so well.hopefully if all goes well i'll be seeing ye this summer.im researching ws for a college presentation.lovely site, very helpfull.all my love and best wishes.
debi wootton on Friday October 14, 2005 at 4:33 PM
WS : Yes - Relation : Other relative
Found : Search for WS sites - Which : google
Comments : My neice has just been diagnosed with williams syndrome. When the pediatrician first told my sister to consider genetic testing I did a search on ws and found your site. I knew immediately this was what my neice had. Your site has been very helpful. Thank you!
sally on Friday October 7, 2005 at 2:39 PM
WS : No
Which : yahoo
Comments : i was just looking at websites as i have concerns about my son,trying to match symptoms etc.its been very usefull-thankyou.
misty on Thursday October 6, 2005 at 7:37 PM
WS : Yes - Relation : Parent
Found : Link from another site - Which : google
Comments : i am not sure that my son has this but he has alot of the symtoms of it and i was wonder do i just ask the doc to do the test and if so what kind of test is it . ty
Frank Murray on Monday October 3, 2005 at 9:59 PM
WS : No
Found : Other - Which : eircom.net
Comments : The name Murray caught my eye for obvious reasons. I live in Brasil and was picking up my email thru the Eircom .net site. Now my brother Diarmuid Murray GP in Knock has done a lot of work on the Murrays who were originally Scots Presbyterians who came from Aberdeen to Tubercurry in the mid 1800s and some of the sons married local girls and "turned"; some didn't. So I believe there are still the two branches. Our side (Taigs now from Belfast; my father from Tubbercurry finished the RIC in 1922 and joined the RUC)all emigrated to the States in 1912. My brother has tracked them all down fairly recently in California. don't know the family medical history but possibly Diarmuid might.
Mary Jo Trail on Sunday October 2, 2005 at 5:39 PM
WS : Yes - Relation : Grandparent
Found : Link from a WS site
Comments : My 8 mo old grandson has recently been diagnosed. I am trying to learn all I can about the Syndrome.
Camelia on Tuesday September 27, 2005 at 2:19 PM
WS : Yes - Relation : Parent
Found : Link from a WS site
Comments : Patricia's story is quite similar with my Anna Maria's story (she only 10 months old) especially the colic and digestive problems during night. Good luck to all of you
LEONE Christophe on Monday September 26, 2005 at 5:32 PM
WS : Yes - Relation : Parent
Found : Link from a WS site
Comments : A new web site has just been born: the web site of the ASWB the Rhone-Alpes in French. It is still incomplete but we will try to improve it with the wire of time.
Its address:
http://perso.wanadoo.Fr/aswbrhonealpes/
and a forum : http://aswb-rhone-alpes.forumactif.com/
Thank you, in a friendly way. dad of a child reached of the syndrome and member of the ASWB the Rhone-Alpes.
Kelly on Wednesday September 14, 2005 at 3:22 PM
WS : No
Found : Other - Which : Google
Comments : Just thought I would let you know my MOYLAN family history page has been updated - new URL is www.whiba.com. Hope that your family is well and good luck with everything.
Zandra on Tuesday September 13, 2005 at 9:43 PM
WS : No
Which : Google
Carlo Di Donato on Thursday September 8, 2005 at 4:28 AM
WS : Yes - Relation : Parent
Found : Link from a WS site - Which : google
Comments : I have 4 year old daughter and non identical twin 15 month old boys. Ben the youngest (by 5 minutes) has recently been diagnosed with WS.
Familie Bursee on Wednesday September 7, 2005 at 12:10 PM
WS : Yes - Relation : Parent
Found : Link from a WS site - Which : www.wbs-bayern.de
Comments : very nice site.
Im afather of a 5 years old ws(in Germany WBS) boy.
We are living 50 miles from Hamburg.
Please visit our WBS Site www.familie.bursee.de
so long
Rolf Bursee
Rachna Uberoi on Tuesday September 6, 2005 at 7:35 PM
WS : Yes - Relation : Parent
Found : Link from a WS site
Comments : I pray your precious Patricia continues to do well in life. As a new parent it is very comforting to know that 'our' kids read, write and ultimately complete school/ college. They are different but still intelligent in their own way - am I right? I would be obliged if you can tell me if Patricia works/ lives independently, has friends her own age group and is accepted by normal people in all walks of life? Thank you in anticipation of your reply. By the way I and my little girl live in Canada and would love to hear from you or Patricia. Rachna
alan craughwell on Friday August 26, 2005 at 10:11 PM
WS : Yes - Relation : Friend
Found : Link from a WS site - Which : yahoo
Comments : Hello to all the Moylans just stumbled across your web site very impressive, had a great time at camp this year good to see you again Patricia looking forward to next year already. All best Alan PS up Galway
Sally Hawker on Friday August 26, 2005 at 1:38 AM
WS : Yes - Relation : Teacher
Found : Search for WS sites - Which : Yahoo oemji
Comments : I am a supervisor of a young man at a Sheltered Workshop in Missouri, USA. Want to do all I can to help him, so I must educate myself about WS. Thank you for your help.
Donna MacInnis on Wednesday August 24, 2005 at 4:38 PM
WS : Yes - Relation : Parent
Found : Search for WS sites - Which : microsoft exployer
Comments : Your site was very interesting and story so simular to mine. thank you
alison jane james on Wednesday August 24, 2005 at 9:44 AM
WS : Yes - Relation : Other relative
Found : Search for WS sites
vicki foster on Wednesday August 24, 2005 at 12:50 AM
WS : Yes - Relation : Parent
Found : Search for WS sites
Daniel J. Moylan on Tuesday August 23, 2005 at 3:45 AM
WS : No
Found : Search for a name - Which : Google
Comments : Best wishes to you and yours. Take care.
chela weitzel on Monday August 15, 2005 at 3:33 PM
WS : No
Found : Search for WS sites - Which : Google
Comments : I study psychology at the University of Sydney, Australia. It's great to read about Patricia and to get a small insight into what life is really like, living with the conditions that i study. Thanks!
roger on Friday August 12, 2005 at 6:59 AM
WS : No
Comments : Hi everyone greatsite weljob keep it up by.
MRS SARAH MCPHILBIN on Wednesday August 10, 2005 at 11:00 PM
WS : Yes - Relation : Other relative
Found : Link from a WS site - Which : WILLIAMS SYNDROME FOUNDATION KENT UK
Comments : Very interesting to read the different abilities of each individual who has williams. Our 4 month old has just been diagnosed and we want to find out as much information as possible so it helps to learn about others.
Thankyou
Kim Shively on Monday August 8, 2005 at 6:25 PM
WS : Yes - Relation : Parent
Found : Link from a WS site
Comments : The pictures of Ireland are beautiful. I will bookmark the page and pretend I live there. I live in Richmond, IN, USA
joe Meehan on Sunday July 31, 2005 at 7:58 PM
WS : No
Found : Search for a name - Which : google
Comments : I have an extensive list of Moylan family members on my website. homepage.mac.com/trochujoe/Meehan/index.htm Click on the web cards go to Moylan & Milan in the Surnames.
stephanie moylan on Monday July 18, 2005 at 9:48 PM
WS : No
Found : Search for a name
Comments : Are you related to me?
Mary Carrig on Saturday July 16, 2005 at 1:04 PM
WS : Yes - Relation : Friend
Found : Other - Which : External links
Comments : Hello,
Thank you for sharing your story. I am a non-traditional Graduate student studying Special Education in Massachusetts. I hail from Dublin but have spent most of my adult life in the States. Your site is listed by my professor. I am taking an on-line Language Development class. I am always curious to know how Special Ed. works in Ireland. My memories of school do not include any mainstreaming, I am glad that things have changed. Patricia sounds like a beautiful child, she is so lucky to have been exposed to so much opportunity, music, family traditions, etc. Although your diagnosis came late, she seems to have flourished. I am familiar with all the place names, Cabinteely, Churchtown, Rathmines. Seems like you do a fair amount of driving around. Anyway, good luck, thanks again.
Mary Carrig
Janet Chaytor on Saturday July 2, 2005 at 2:49 AM
WS : No
Found : Search for WS sites
Comments : We watched a wonderful program tonight (an American TV show, "60 Minutes") covering gifted children including the amazing musical talents on some with Williams Syndrome. I had never heard of this syndrome and hoped to find out more via web research. Thanks for your informative web site and as an added bonus, the links to the beautiful photos of Ireland! We live in beautiful Stonington, Maine USA. There are similarities to the coastal landscape and the descriptions of the late spring in your brother's site! Thanks. And love to Patricia.
kelly on Thursday June 30, 2005 at 2:48 AM
WS : No
Which : google
Comments : where's sheffield? i might be related to you but i don't know
Bernadette Roberts on Wednesday June 29, 2005 at 8:52 AM
WS : Yes - Relation : Parent
Found : Link from a WS site
Comments : i have a son with williams syndrome we found when he was about four months old he is called william williams he is now one would like to hear from any one with a williams child or any one with williams syndrome as i do not know any one with williams
email chickencrisps@tiscali.co.uk
Erica on Thursday June 23, 2005 at 4:24 AM
WS : No
Found : Search for WS sites - Which : askjeeves.com
Comments : I was looking for some info on WS for a nursing class and came across your site.I have to do a oral report on WS.Before getting assigned this project I had never heard of the syndrome before.Thank you for the great infomation and a look at you family and life.
Alison on Tuesday June 21, 2005 at 6:19 AM
WS : No
Found : Link from a WS site - Which : MSN
Comments : I am looking for someone to answer some questions for me about WS.
tina rowe on Friday June 10, 2005 at 7:00 AM
WS : No
Found : Other - Which : Rowe
Comments : I am looking for my grandfathers daughter from 1957 we don't know much about. i saw your site and have very similar Rowe named relatives?
amanda on Monday June 6, 2005 at 7:43 PM
WS : No - Relation : Friend
Found : Yahoo! WS club
Comments : Hope the information on your site will help parents who have just found out their baby has WS.
Shirley Moylan Garypie on Thursday May 26, 2005 at 4:58 PM
WS : No
Found : Search for a name - Which : google
Comments : I was searching for Moylan relatives. I was born in Sag Harbor N.Y. and have no Idea where my family came from in Ireland. They emmigrated to Manchester, England during the potato famine and later to the USA.
michele dillon on Tuesday May 24, 2005 at 7:20 PM
WS : Yes - Relation : Music Therapist
Found : Link from a WS site - Which : google
Comments : I work with a delightful 14 yr. old young lady by the name of "Kelle"(Kelly)She has many interests',very skilled in music , very social--- would love to communicate with other young people with WS.Thank you,Michele Dillon
kelly moylan on Monday May 23, 2005 at 2:36 PM
WS : No
Found : Search for a name
Comments : my name is kelly moylan and i read about kelly moylan from sdney i live in sheffield i am 13 i wonderd if i was related to any one out there
Vools Isabelle on Friday May 6, 2005 at 8:46 AM
WS : Yes - Relation : Parent
Found : Link from a WS site - Which : Google
Comments : We have a beautiful son who is almost 2 years old and is diagnosed with WS about 2 months ago. We are very glad to have internet and have access to all this information. It's nice to know that you are not alone and it's a big support for us. The story of your daughter is very recognizable. There are many people who have never heard of the syndrome, and sites like this help to make it more known. All the best for your daughter and family. PS: we are from Belgium.
Kelly Moylan on Wednesday May 4, 2005 at 2:52 AM
WS : No
Found : Search for a name - Which : google
Comments : Hello i am Kelly Moylan and i was trying to find some family. My Dad is Allan Moylan and his dad is John Moylan, and he is from somewhere in Ireland. Is anyone related to him because he doesn't communicate with family left in England and Ireland. I was born here in Sydney Australia and have lived here my whole life and never been overseas so i don't know anything about the Moylan family. I'm 15 and would like to know anything about this family i have because i don't know them. Lots of love Kelly
Colette on Wednesday April 27, 2005 at 4:22 PM
WS : No
Found : Link from a WS site - Which : www.williams-syndrome.org.uk
Comments : I am studying to be a speech and language therapist in the UK and was looking for more information on WS. It is essential to get parents' views, so I found your sight really useful. I'm pleased to report that we, at least, cover quite a bit about WS in our course, so hopefully issues around diagnosis and support for families will not be dealt with so badly in the future! Good luck to all of you.
For others looking for information, I found www.williams-syndrome.org.uk useful.
Shannon on Wednesday April 27, 2005 at 4:22 PM
WS : Yes - Relation : Parent
Found : Search for WS sites - Which : yahoo
wendy averett on Tuesday April 19, 2005 at 7:44 PM
WS : Yes - Relation : Parent
Found : Search for WS sites - Which : ask jeeves
Comments : my daughter is now 9 years old and was diagnosed at 2 months old and is having problems in school and i don't know what to do.im now a single parent raising a ws child but she's very special to us
Sanja on Sunday April 17, 2005 at 8:36 PM
WS : Yes - Relation : Parent
Found : Search for WS sites
nicole johnston on Saturday April 9, 2005 at 10:39 PM
WS : Yes - Relation : Parent
Found : Search for WS sites - Which : ask
Comments : just wanted to tell you all about my little boy was digonsed with WS at 8mths old he has the heart condition that goes with WS it was corrected at 17mths and he goes from strenght to strenght he is 3yrs old now and has been attending nursery since he was 4mths now in a state nursey(mainstream) and he is coping beautifully he is very out going and loveable sometimes he is a real horror but he is a real joy to us and everyone who meets him.
alex on Saturday April 9, 2005 at 8:24 AM
WS : Yes - Relation : Self
Found : Yahoo! WS club - Which : yahoo
Comments : i wave ws and ive not recived any kinda of help nor do i know any one else with the disorder so ever fee like ur a lone in the world i am and im not too happy please contact me through my email
Elizabeth Prez on Saturday April 2, 2005 at 3:42 PM
WS : Yes - Relation : Parent
Found : Link from a WS site
Comments : I live in Mxico city, I am starting a WS mexican assosiation, unfortunately medical and educatioinal workers know nothing or very litle about this condition ( in Mexico) after an intensive research me and other families found no services or support groups at all regarding our kids condition, therefore, "Im getting my hans to work", Ill love to be in touch with you, I have two sons, the oldest one is Omar, hes 12 and my "musical genius" is Jose-Carlos, hes 10, Im a music teacher, at the present time Im attending to univerity, Im studing Education, my husband has a MBA and likes to sing, he also studied "Belle canto"
Joan Lalor on Thursday March 31, 2005 at 1:30 AM
WS : No
Found : Link from another site - Which : Ireland
Comments : Fascinating reasearch. I am teacher and am very interested in the education of children with special needs. Keep up the great efforts!
nicola on Friday March 18, 2005 at 12:23 PM
WS : Yes - Relation : Parent
Found : Search for WS sites - Which : google
Comments : im a mother of 3 kids and my oldest boy has williams syndrome and lots of heart defects! and i was just browsing to find ways to help him go foward as he seems to hav stoped still for some time,wish you well for future x
Tahnee Bird on Thursday March 17, 2005 at 9:24 PM
WS : Yes - Relation : Other relative
Found : Link from a WS site - Which : The WSF site
Comments : My son Tyler is 8. He still can't walk or talk and his eating is slowly getting better. We don't know of any other WS person who has the condition so bad so feel quite alone. Tyler is very smiley and can be loving but only on his terms! We wouldn't change him for the world and we love him dearly. His sister and brother are great with him and know how special he is. Thank god there is such a great website to come to when need be. Take care bye
pam berg on Saturday March 12, 2005 at 8:06 PM
WS : No
Found : Search for WS sites - Which : goggle
Comments : beautiful site
Jeannie on Friday March 11, 2005 at 7:00 PM
WS : Yes - Relation : Self
Found : Link from a WS site
Comments : hi!
i am 63. i have ws.i am happy your dauter is well.
myra mulvay on Monday March 7, 2005 at 12:10 AM
WS : Yes - Relation : Parent
Found : Link from a WS site - Which : aol
Comments : could our name be linked in some way? I know my husbands' family is from irland greatgrandfather John mulvey, just a thought great web site for parents like me. my son is now 15
Julia on Thursday March 3, 2005 at 11:23 AM
WS : No
Found : Search for WS sites - Which : google
Comments : My name is Julia, I'm from Russia. I'm a mother of a 6y.o. boy, his name's Dima. He suffers from atopical dermatitis, food allergy, bronchial asthma, chronical allergical rhinitis & conjunctivitis, neurological problems(night fears), natal brain injury, connective tissue disorder (or MASS phenotype,Marfan related syndrome, and the affection of it: rotation of right side kidney, additional chord on average of third of left ventricle of heart, sinusoid tachycardia, arthralgy, V-deformation of chest, joint hypermobility, eye myopia, palsy of the upper nerve of the left eye). I'm looking for any kind of help,either any info on MASS or any other kind of help like used clothes, toys or vitamins, soy products, medicine. If there's someone who doesn't need boy's clothes anymore, would it be possible to donate it to my son? I'd be so much thankful!. I'd accept used boy's clothes, shoes, things, toys. Sizes: clothes 122-128 cm (6-7 years), shoes 29-31(European size). Thank you very much in advance. I'm also looking for people with MASS or people having children with MASS, to exchnage experience. Julia Katkova, POB 276, St. Petersburg-332, 198332 RUSSIA, e-mail: yuk246@yandex.ru
Lorena Rodriguez on Friday February 25, 2005 at 12:59 AM
WS : Yes - Relation : Other relative
Found : Link from a WS site - Which : Altavista
Comments : My sister is a WS girl, shes 28, and I interesting for information for for help her. We Mexican on this country the information is poor. Congratulations for your website. Greeting to all Family and Patricia.
Tina Barker on Thursday February 24, 2005 at 2:44 AM
WS : Yes - Relation : Other
Found : Link from a WS site - Which : WSFSG Victoria Australia
Comments : I've been a Family Day Care Provider for a little girl now aged 4yrs 3mths since she was 19mths. She's a joy to have in my home & is much loved by the other children in my care
Art Schicatano on Sunday February 20, 2005 at 5:22 PM
WS : Yes - Relation : Parent
Found : Link from a WS site - Which : WS.org
Comments : Just signed on as Regional Co-chairperson for our Region (great Plains) in the USA. Very interested in meeting parents/children from around the Globe. We have a 6 yr. old son (Angelo) with WS. He is our precious little "Gift".
Eno on Saturday February 19, 2005 at 12:39 PM
WS : No
Found : Told about it
Comments : I am a medical student. I really love to learn about anything. Actually, i really apreciate if you want to describe for me about this genetic disease. That's make me want to study harder than before, to make the people with this disease life normally. i'm so sorry if my english bad (i'm Indonesian :) )
JACKIE ZBIEGIEN on Friday February 18, 2005 at 4:49 PM
WS : Yes - Relation : Sibling
Found : Link from a WS site
Comments : MY HUSBAND MIKE AND I HAVE A CHILD WITH WS, HIS NAME IS RYAN AND HE IS 10YRS OLD.
garry on Friday February 18, 2005 at 1:54 AM
WS : Yes - Relation : Sibling
Found : Link from another site - Which : www.geocities.com/williamssyndrome
Comments : Nice site
Cormier on Friday February 18, 2005 at 12:17 AM
WS : No
Found : Told about it
Sharon Ullman on Thursday February 17, 2005 at 1:45 AM
WS : Yes - Relation : Parent
Found : Link from another site - Which : ? not sure at this point.. was following a series.
Sue on Tuesday February 15, 2005 at 5:00 AM
WS : Yes - Relation : Other relative
Found : Link from a WS site
Comments : Thank you for providing Patricia's story, I hope she continues to grow and develop to her full potential. My niece has just had her daughter at age 7 months diagnosed with WS, it is so helpful to learn what to expect and interesting to read the wonderful comments in your guest book from parents of much loved children.
Pam on Friday February 11, 2005 at 5:56 PM
WS : No - Relation : Parent
Found : Link from a WS site - Which : williams syndrome
Comments : We've had foster child for 5 years. I want his blood tested for williams syndrome ?
James on Wednesday February 9, 2005 at 2:48 AM
WS : No
Found : Other - Which : Google
Comments : My Great Grandfather David Moylan 1860-1889(son of another David)from Cork, came to America and Married Bridget Sullivan from Glenbeigh, Kerry. They settled in Omaha.
Estelle on Monday February 7, 2005 at 12:40 AM
WS : No
Found : Search for a name - Which : Google
Comments : hi, I have been doing research into the Moylan family, I am connected to James and Margret Moylan from Ireland both born in 1837, they moved to the uk from ireland
ieda on Sunday February 6, 2005 at 1:42 PM
WS : Yes - Relation : Other relative
Found : Search for WS sites
Comments : My name is Ieda. My oldest brother is SW.He's 50 years old.
sorry my english.I wiuld like receive information SW. I love my brother
Kathryn Simpson on Sunday February 6, 2005 at 5:13 AM
WS : Yes - Relation : Parent
Found : Link from a WS site - Which : yahoo
Comments : My Daughter beth is 7 & has williams syndrome.She is waiting on an answer from doctors for pulmonary artery grafting. So i was checking out the site for some info.
Irene Philips on Friday February 4, 2005 at 10:55 PM
WS : Yes - Relation : Teacher
Found : Link from another site - Which : Yahoo
Comments : I wanted to learn more about Williams Syndrome because it was so unfamilair to me. I worked with a student who has benn diagnosed with this syndrome. I was browsing the internet and came across your website. God Bless you and your family.
David on Monday January 24, 2005 at 5:38 AM
WS : No
Found : Search for a name - Which : Google
Comments : Nice site. I'd like to know how you got the private/public option on your guestbook. Thanks for letting me visit. :) david@schildfamily.org / http://schildfamily.org
MaryAnn Moylan on Friday January 21, 2005 at 4:39 PM
WS : No
Found : Search for a name - Which : google
Comments : Grandfathers name:Keyran Joseph Moylan m Anne Barton left Queens County, Garryduff about 1920 came to Greenfield,Ma. His fathers name was Keyran Patrick Moylan m Anne Magher. Some of the names we are connected with are: Maguire,Dolan, Duggan. I think we are from the Port Laoise area.
Caitlyn Tipton on Saturday January 15, 2005 at 3:06 AM
WS : No
Found : Link from a WS site - Which : google
Comments : I found your website extremely interesting. I am doing a research project on Williams Snydrome at school for my Biology class and your website was not only beneficial for my report, but also beneficial for my own personal use.

Moylan Family Website