Guest guest Posted August 20, 2009 Report Share Posted August 20, 2009 Hi Celeste heart conditions are a concern, but they are congenital, so they are born with a heart condition or they aren't. They don't get a heart condition later. But, if her heart has not been checked, then it needs to be done, because as Darlene here can tell you, sometimes heart conditions can be left unnoticed for years if they aren't checked properly. The other thing that needs to be checked is the thyroid. This is done by an annual blood test and if it is underactive then they would give your daughter meds to keep it level. (my son had this problem for half his childhood before it was found out and treated) Digestion problems can sometimes be present, but if you are not having problems with constipation then I wouldn't worry about it. Your doctor should be following the Health Care guidelines for Down syndrome because your daughter has a percentage of cells with the extra 21st chromosome so it is possible for her to have medical problems associated with Ds. This does not mean she WILL get these problems. It just means that it is possible, so these health care guidelines will help keep her healthy. If you would like to view this guidelines we do have them posted on our site with other information that you may find helpful as well. Just go to http://www.imdsa.org/Information/infopack.htm Kristy Colvin IMDSA President ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ International Mosaic Down Syndrome Association PH: Toll Free: 1-888-MDS-LINK http://www.imdsa.org http://www.mosaicmoments.today.com Subject: MDS health issues To: MosaicDS Date: Thursday, August 20, 2009, 9:58 AM Hi there...along the lines of health issues, it seems like heart issues are a concern with MDS also, right? I have read a few things about digestive problems but what else is a concern? Ava sees an audiologist regularly for her hearing loss and the geneticist wants her heart checked. I am just wondering what else would be a concern. From the time Ava was born, she had acid reflux but out grew that by the time she was 18 months (thank goodness!!). Thanks!! Celeste (mom to a 7, Dylan 4 and Ava 2) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 21, 2009 Report Share Posted August 21, 2009 Well we finally went to see a genticist and I do find it a waste of my $40.oo copay(lol). I really didn't get any more info than I already new. They only tested 23 cells and she told me there really is no reason to test anymore, because each child is different and reguardless if they have mds or ds is varies so different in each individual. I explained to them these were so sure he had mds instead of ds at birth because he only had a few features of ds9???). The the cells they tested came of all t21 but he most likey is at least 75% ds in his cells. So she said he's progressing very well so far(but what can you really tell at 6 months). Also he is babbling alot and saying da da. Is this a good sign. He is starting to sit up alittle by himself , although he does have some muscle weekness. Anyway such is life He does need heart surgery I found out my the pediatric cardo. But he has a very small hole in is upper left chamber and he dr said it's a very easy procedure the kind that heart surgeon's love to do????????? > > Hi there...along the lines of health issues, it seems like heart issues are a concern with MDS also, right? I have read a few things about digestive problems but what else is a concern? Ava sees an audiologist regularly for her hearing loss and the geneticist wants her heart checked. I am just wondering what else would be a concern. From the time Ava was born, she had acid reflux but out grew that by the time she was 18 months (thank goodness!!). > Thanks!! > Celeste (mom to a 7, Dylan 4 and Ava 2) > > > > > Quote Link to comment Share on other sites More sharing options...
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