Guestbook
If you would like to make a comment about any matter related to the Association, your own experiences with a heart child or comments about our website, you may do so in this Guestbook. Note: Latest entry is now at the bottom of the last page.Page: < 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16
17 18 19 20 21 22 23 24 25 26 27 28 29 >
Linda Johansen, Chelmsford, Essex
Sent: 2002-01-12 at 21:54:45 GMT
Homepage : www.geocities.com/noahsmummy2001
I am the mum of a 5 month old boy who was born with Left Pulmonary Artery Sling and PDA. His sling was repaired at 4 weeks old at the same time as they ligated the PDA.
I have searched and searched to try and find other children/adults with a pulmonary artery sling, but I have yet to succeed. Please if you know anyone with this defect, could you get in touch on < ... >
Linda
Click here to contact 'Linda Johansen'.
Elizabeth Evans, BALA, NORTH WALES, UK
Sent: 2002-02-02 at 22:56:28 GMT
My son Mathew (who is now 8 yrs old) was diagnosed with
CONGENITALLY CORRECTED TRANSPOSITION , EBSTEINS'S ANOMALY AND 2 VSD when he was 6 months old. He had surgery at Birmigham's Childrens Hospital. He has yearly check ups and is doing well.
Sorry, 'Elizabeth Evans' did not leave an email address.
Pauline Mclennan, Ayrshire, Scotland
Sent: 2002-02-03 at 21:25:41 GMT
My daughter Jaymee has SVT which has been corrected by surgery. This all happened in 1996 and i was wondering if anyone who was at Yorkhill at that time remembers us if so i would like to know how you are?
Click here to contact 'Pauline Mclennan'.
Kerri Greene, Edinburgh, Scotland
Sent: 2002-02-13 at 19:45:22 GMT
Hi,my name is Kerri and i am 17 years old, i was diagnosed as having SVT when i was 3 years old and would like to hear from anyone else who has SVT. My email address is < ... >
thanks :-)
Click here to contact 'Kerri Greene'.
Tanya Herbert, Carshalton, Surrey, England
Sent: 2002-02-14 at 20:52:59 GMT
Hi,my name's Tanya.In Sept'99,my son,Nathan died at 32 days old from congenital heart disease(it was not detected).If anybody else has been in a similar situation and would like to talk about it,let me know.I am also holding a LADIES NITE in June 2002 to raise money for TACHD.If you would like more information or would like to buy tickets,please e-mail me.
Nathan will always be in a special place in my heart!
This website has been an eye opener and I would like to wish everybody all the best in the future - you're not alone!
Click here to contact 'Tanya Herbert'.
Belinda A. Bassett, United Kingdom
Sent: 2002-02-27 at 14:47:17 GMT
Homepage : http://www.thereishope.freeservers.com
I think your site is very helpful,please check out mine.
Click here to contact 'Belinda A. Bassett'.
samantha shaw, lincoln, england
Sent: 2002-02-28 at 21:43:17 GMT
i am a 12yr old girl with complete heart block, and i need to have a pacemaker fitted this year at Great Ormond Street Hospital. Does anyone have any experiences of this procedure? If so could you send to E-mail address above.
Click here to contact 'samantha shaw'.
victoria gavin, america
Sent: 2002-03-17 at 05:51:04 GMT
Hello! I have a 2 yr old daughter with Ivemark Syndrome. Is there anybody out there also with this condition?
Click here to contact 'victoria gavin'.
17 18 19 20 21 22 23 24 25 26 27 28 29 >
Where the poster has left an email address, a 'Contact' link will appear.
Please use this if you wish to get in touch with the poster.
