familiesofangelmansyndrome : Messages : 1-30 of 2802

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30	We will have to check that restaurant out. Ya if you are ever here let me know.......I know how our angels are so cute and you can't help but love them. I can...	sweetemma2	Jun 6, 2001 12:13 am
29	Do we have ato come to this site every time we want to post to this club? I have tried to post to an email address and have yet to see them show...	angelmum01	Jun 5, 2001 11:30 pm
28	Hi, Im Frifoley. I have a daughter with AS who is 6yrs. old her best friend who is 5yrs. old has an extra chromosome #15 her parents were told she could have...	frifoley	Jun 5, 2001 4:25 pm
27	Bonnie - Just wanted to say Hi and to let you know that I am from Indiana - 2 hrs. away. My son does live in Louisville at the present time. He just graduated...	bwilson_46173	Jun 5, 2001 2:57 pm
26	Susan - Sure you do have a lot of info for those of us who have contact with younger angels. The angel in my life is Ali who will be 3 June 16th. Just leaving...	bwilson_46173	Jun 5, 2001 2:43 pm
25	By the way. I know I have a strange user name. It is my Star Wars name. My name is Susan....	fersu_jobai	Jun 5, 2001 10:02 am
24	Hi Lori ,<br>We also have a son with AS del+. Kris will be 17 next week. I like talking to other Angelman Parents too. We have a lot to offer those parents ...	fersu_jobai	Jun 5, 2001 10:00 am
23	Hi everyone! My name is Bonnie and I am the proud mom of two great kids. AJ is my angel and he is 8 and deletion positive and Emily is 4 going on 20 LOL. Winna...	sweetemma2	Jun 4, 2001 9:01 pm
22	Hi, my name is Lori. My husband Mark and I live in Fancy Farm, Kentucky with our 2 sons, Jonathan (AS, del+) will be 16 this month, and Matthew is 4 1/2....	lorilou1966	Jun 4, 2001 2:44 pm
21	Barbara~Good luck with your move. Keep us updated as to how things are going. I am glad that you did get attent one of the conferences. I'm hoping that ...	wsj88	Jun 4, 2001 7:01 am
20	Hi Wendy,<br>We won't be going to the conference this year either. We are moving from Maryland to New Jersey in a couple of weeks. We did attend when it was ...	bwieckowski2001	Jun 4, 2001 2:21 am
19	Hi Barb~ I live in Portage, Indiana(NW~close to Chicago). I wish I could say that I was going to the comference on July, but finances won't allow it this time....	wsj88	Jun 3, 2001 4:41 am
18	Hi Winna,<br><br>My son Stephen who is also 7 was diagnosed at the<br>age of 31/2 years. He is a clinical dianogsis.<br>So I know what a relief it is to...	bwieckowski2001	Jun 2, 2001 4:34 pm
17	I have heard the term UPD and that very well is the case. We have not gone throw the blood work yet on myself or my husband though. Do you know of other ...	Flash_NC	Jun 2, 2001 11:28 am
16	Wendy -<br><br>My name is Barb Wilson. I also live in Indiana - Rushville (which is 45 min se of Indy). I have an adopted granddaughter who will be 3 June 16th...	bwilson_46173	Jun 2, 2001 5:10 am
15	Would duplication mean possibly that there are two paternal 15's. If that is the case I would call that UPD? That testing would require both parents blood...	angelmum01	Jun 1, 2001 8:59 pm
14	I was wondering how Don got my email address.<br>I was also wondering how many of you guys are on the listserv. <br>My daughter is 7 clinically dxed and seven...	angelmum01	Jun 1, 2001 8:54 pm
13	Thanks Don for the invite! Hi Penny! Hi everyone!! I am looking forward to getting to know everyone in here.<br><br>A little about me and my family:<br>I'm...	wsj88	May 31, 2001 3:46 am
12	My Name is Andrea Glossenger and i think this Club is a great Idea. My sons name is Dean, he was diagnosed with AS 4 Years ago. He is 7 now.We live in N.C . He...	nine_27239	May 27, 2001 12:22 pm
11	HI Flash,,, dont know much about PWS but i know lots about angelmans, we thought our little granddaughter had it but the test was normal so we are stil ...	starr5959	Mar 21, 2001 4:01 pm
10	My daughter is 14yo. We knew at 2 months she had delays but didn't know why. We've had and MRI, EEG, Fragile X testing, and a few years ago cytogenetics ...	Flash_NC	Mar 20, 2001 2:12 pm
9	HI! Did i read your posr right? it only tooktwo weeks to get the results back? wnder why they told us it would be months before we got anything back??? Maybe...	starr5959	Feb 10, 2001 2:21 pm
8	It was two weeks later after our son William was tested for Angelman Syndrome that they sent us a letter and a packet of info on Angelman Syndrome telling us ...	donaldtyrrel	Feb 9, 2001 5:55 pm
7	HELLO! I POSTED SOME PICTURES FOR YOU TO SEE, HOPE THEY MAKE YOU SMILE TODAY, WE WILL WAIT FOR THE TEST RESULTS AND THEN SEE WHAT HAPPENS,,,,<br>ALEXIS WILL...	starr5959	Feb 9, 2001 2:26 pm
6	HELLO , <br>OUR LITTLE GRANDDAUGHTER ALEXIS-MARIE WAS GIVEN THE BLOOD TEST YESTERDAY TO CHECK FOR ANGELMANS, NOW WE WAIT.....HOW LONG DID ANY OF YOU WAIT TO ...	starr5959	Feb 9, 2001 2:16 pm
5	HI , thanks for writing back, I had added you to my pager, I am starr5959 on the yahoo pager. We have been thru most of the stages so far, awaiting the ...	starr5959	Jan 24, 2001 7:48 pm
4	Welcome to this club starr5959. I know how the testing stages can be tough & not knowing a diagnosis can be. We knew when our son was three months old that ...	donaldtyrrel	Jan 24, 2001 7:08 pm
3	we are still in the testing stage, so far everything has come back normal, even the EEG , but with all the seaching I have done, Anglemans fits the criteria,...	starr5959	Jan 24, 2001 1:58 pm
2	The two photo albums that I've added were taken at the Drury Inn's swimming pool the night before the 1999 Angelman Syndrome Family Picnic at Danville, ...	donaldtyrrel	Jun 30, 2000 3:01 am
1	Welcome to the Yahoo! Message Board for Families of Angelman Syndrome...	donaldtyrrel	Jun 28, 2000 4:33 pm

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