<?xml version="1.0" encoding="UTF-8"?><rss xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns:atom="http://www.w3.org/2005/Atom" version="2.0"><channel><title><![CDATA[Children with Thalassemia?]]></title><description><![CDATA[<p>Hi do any parents here have children with Thalassemia. Is it a serious blood disorder? <img src="https://forum.kiasuparents.com/assets/plugins/nodebb-plugin-emoji/emoji/android/1f61e.png?v=f4f27f6278e" class="not-responsive emoji emoji-android emoji--disappointed" style="height:23px;width:auto;vertical-align:middle" title=":(" alt="😞" /></p>]]></description><link>https://forum.kiasuparents.com/topic/16056/children-with-thalassemia</link><generator>RSS for Node</generator><lastBuildDate>Sun, 03 May 2026 06:13:12 GMT</lastBuildDate><atom:link href="https://forum.kiasuparents.com/topic/16056.rss" rel="self" type="application/rss+xml"/><pubDate>Thu, 18 Nov 2010 08:26:24 GMT</pubDate><ttl>60</ttl><item><title><![CDATA[Reply to Children with Thalassemia? on Mon, 27 Dec 2010 18:15:49 GMT]]></title><description><![CDATA[<p dir="auto">I’m a Thal carrier, found out only when I was preg with my first child. Luckily my hubby is normal. Now with 3 kids only my first born is a carrier. There is a Thal registry at KK and according to the nurse only 3% of singaporean with Thal.</p>
]]></description><link>https://forum.kiasuparents.com/post/320721</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/320721</guid><dc:creator><![CDATA[Red_Snow]]></dc:creator><pubDate>Mon, 27 Dec 2010 18:15:49 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Tue, 21 Dec 2010 16:58:50 GMT]]></title><description><![CDATA[<p dir="auto">DW is a carrier (i.e. alpha T), detected at her gynae’s clinic. i was advised to take test too, and it was negative, so we were given green light to have kids.<br /><br /><br />Green light in that kids would be either normal, or at worst, carrier (like DW). If both parents are carriers, then there is a one-quarter chance that the kid will manifest thalessemia, which is a form of anemia, and often live threatening. <br /><br />Both DD and DS were tested after childbirth, and DD is also carrier and DS is normal.<br /><br />DW does have faint spell occasionally. when we went europe in winter, her hands were freezing cold (not like mine were still warm, but at least not so cold). Since blood keeps us warm, I assume that her being a carrier played a part.<br /><br />DW and DD are otherwise normal.</p>
]]></description><link>https://forum.kiasuparents.com/post/317076</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/317076</guid><dc:creator><![CDATA[atrecord]]></dc:creator><pubDate>Tue, 21 Dec 2010 16:58:50 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Fri, 19 Nov 2010 15:15:20 GMT]]></title><description><![CDATA[<p></p><blockquote><b>verykiasu2010:</b><blockquote style="border:1px solid black">thought there is a national register for Thalassemia ?</blockquote></blockquote><br />I have called up KK hospital nurse hotline to enquiry about thalassemia. The nurse advise me to bring my dd to their paediatrician to do a thalassemia blood test or I can choose to go to private paediatrician to do the test. She said is not life threatening ...so hope everything is fine... :scared:<p></p>]]></description><link>https://forum.kiasuparents.com/post/297897</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297897</guid><dc:creator><![CDATA[vlim]]></dc:creator><pubDate>Fri, 19 Nov 2010 15:15:20 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Fri, 19 Nov 2010 08:16:49 GMT]]></title><description><![CDATA[<p></p><blockquote><b>ZacK:</b><blockquote style="border:1px solid black">We went for blood test before trying for kids because DW has Thalassemia minor, does not affect her lifestyle other than she is anaemic and prone to fainting spells.<br /><br /><br />So far both my boys have G6PD, which I think was largely due to my wife Thalassemia condition. Wonder if this is the same for mothers with the same condition?</blockquote></blockquote>Not related. <br /><br />G6PD is an enzyme deficiency, and sex-linked --&gt; <a href="http://kidshealth.org/parent/general/aches/g6pd.html">http://kidshealth.org/parent/general/aches/g6pd.html</a><br /><br />Thal is due to abnormal haemoglobin formation, and occurs equally in males and females (autosomal recessive) --&gt; <a href="http://en.wikipedia.org/wiki/Thalassemia">http://en.wikipedia.org/wiki/Thalassemia</a><p></p>]]></description><link>https://forum.kiasuparents.com/post/297641</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297641</guid><dc:creator><![CDATA[3Boys]]></dc:creator><pubDate>Fri, 19 Nov 2010 08:16:49 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Fri, 19 Nov 2010 07:24:59 GMT]]></title><description><![CDATA[<p></p><blockquote><b>ZacK:</b><blockquote style="border:1px solid black">So far both my boys have G6PD</blockquote></blockquote><br />My boys do not hv this deficiency.<p></p>]]></description><link>https://forum.kiasuparents.com/post/297584</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297584</guid><dc:creator><![CDATA[Jennifer]]></dc:creator><pubDate>Fri, 19 Nov 2010 07:24:59 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Fri, 19 Nov 2010 02:33:31 GMT]]></title><description><![CDATA[<p dir="auto">thought there is a national register for Thalassemia ?</p>
]]></description><link>https://forum.kiasuparents.com/post/297381</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297381</guid><dc:creator><![CDATA[verykiasu2010]]></dc:creator><pubDate>Fri, 19 Nov 2010 02:33:31 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Fri, 19 Nov 2010 01:28:59 GMT]]></title><description><![CDATA[<p dir="auto">DH is Thalassemia minor, inherited from MIL.<br /><br /><br />I do not have that blood trait.<br /><br />DD had blood tests done after birth due to jaundice, I’d requested her PD to test for Thalassemia. Test came back negative. DD inherited my blood trait.<br /><br />DH gets tired easily but he keeps a fairly active lifestyle, jogging at least 3 times a week and swimming with DD, at least 3 times a week as well.<br /><br />Thalassemia cause the body to make fewer healthy red blood cells and less haemoglobin than normal. Haemoglobin is an iron-rich protein in red blood cells. It carries oxygen to all parts of the body. Haemoglobin also carries carbon dioxide from the body to the lungs, where it’s exhaled. <br /><br />People who have thalassemia can have mild or severe anaemia. This condition is caused by a lower than normal number of red blood cells or not enough hemoglobin in the red blood cells.</p>
]]></description><link>https://forum.kiasuparents.com/post/297326</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297326</guid><dc:creator><![CDATA[duriz]]></dc:creator><pubDate>Fri, 19 Nov 2010 01:28:59 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Fri, 19 Nov 2010 01:14:21 GMT]]></title><description><![CDATA[<p dir="auto">We went for blood test before trying for kids because DW has Thalassemia minor, does not affect her lifestyle other than she is anaemic and prone to fainting spells.<br /><br /><br />So far both my boys have G6PD, which I think was largely due to my wife Thalassemia condition. Wonder if this is the same for mothers with the same condition?</p>
]]></description><link>https://forum.kiasuparents.com/post/297313</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297313</guid><dc:creator><![CDATA[ZacK]]></dc:creator><pubDate>Fri, 19 Nov 2010 01:14:21 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Thu, 18 Nov 2010 14:04:16 GMT]]></title><description><![CDATA[<p></p><blockquote><b>3Boys:</b><blockquote style="border:1px solid black">Folks, Thal trait does not cause low blood pressure, it causes low red cell count. Yes, one may suffer increased fatigue and low effort tolerance, but it is on account of the cell count. Thal is hereditary, the majority have minor forms, but if 2 carriers have a child together, the child may end up with a severe form.</blockquote></blockquote><br />Yes, I also hv low red blood count.<br /><br />I only knew I am a carrier after I did a pre-martial blood test.<br /><br />My boys' PD also advised us to let them take the test when they are older.<p></p>]]></description><link>https://forum.kiasuparents.com/post/297153</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297153</guid><dc:creator><![CDATA[Jennifer]]></dc:creator><pubDate>Thu, 18 Nov 2010 14:04:16 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Thu, 18 Nov 2010 13:17:20 GMT]]></title><description><![CDATA[<p></p><blockquote><b>3Boys:</b><blockquote style="border:1px solid black">Folks, Thal trait does not cause low blood pressure, it causes low red cell count. Yes, one may suffer increased fatigue and low effort tolerance, but it is on account of the cell count. Thal is hereditary, the majority have minor forms, but if 2 carriers have a child together, the child may end up with a severe form.</blockquote></blockquote><br />Major thalassemia is no joke. By right, any couple planning to get married should go for blood test to to make sure both parties are not carriers. I have a friend who suffered from major thalassemia did not live pass his teenage yrs. Not to frighten readers here but such pain can be avoided with knowledge and precaution.<br /><br />JMHO<p></p>]]></description><link>https://forum.kiasuparents.com/post/297134</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297134</guid><dc:creator><![CDATA[pecalis]]></dc:creator><pubDate>Thu, 18 Nov 2010 13:17:20 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Thu, 18 Nov 2010 12:32:36 GMT]]></title><description><![CDATA[<p dir="auto">Folks, Thal trait does not cause low blood pressure, it causes low red cell count. Yes, one may suffer increased fatigue and low effort tolerance, but it is on account of the cell count. Thal is hereditary, the majority have minor forms, but if 2 carriers have a child together, the child may end up with a severe form.</p>
]]></description><link>https://forum.kiasuparents.com/post/297117</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297117</guid><dc:creator><![CDATA[3Boys]]></dc:creator><pubDate>Thu, 18 Nov 2010 12:32:36 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Thu, 18 Nov 2010 12:09:22 GMT]]></title><description><![CDATA[<p dir="auto">Anyway thanks piccolo and Jennifer for the reply … I will consider go for the test myself also …</p>
]]></description><link>https://forum.kiasuparents.com/post/297108</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297108</guid><dc:creator><![CDATA[vlim]]></dc:creator><pubDate>Thu, 18 Nov 2010 12:09:22 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Thu, 18 Nov 2010 12:04:49 GMT]]></title><description><![CDATA[<p>Only purpose is to know whose family line has the genetic defect, if you care about it.  Most likely your dd has  thalassemia minor which does not need any treatment.  For more info: <br /><br /><br /><a href="http://en.wikipedia.org/wiki/Thalassemia">http://en.wikipedia.org/wiki/Thalassemia</a></p>]]></description><link>https://forum.kiasuparents.com/post/297105</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297105</guid><dc:creator><![CDATA[Picolo]]></dc:creator><pubDate>Thu, 18 Nov 2010 12:04:49 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Thu, 18 Nov 2010 11:54:34 GMT]]></title><description><![CDATA[<p dir="auto">But what is the purpose for my dh or me  to go for the test ??? Does it help in some way?</p>
]]></description><link>https://forum.kiasuparents.com/post/297100</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297100</guid><dc:creator><![CDATA[vlim]]></dc:creator><pubDate>Thu, 18 Nov 2010 11:54:34 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Thu, 18 Nov 2010 11:53:31 GMT]]></title><description><![CDATA[<p dir="auto">vlim,  you can go to any polyclinic - lab section to ask specifically for a test for thalassemia.  It’s quite cheap.</p>
]]></description><link>https://forum.kiasuparents.com/post/297099</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297099</guid><dc:creator><![CDATA[Picolo]]></dc:creator><pubDate>Thu, 18 Nov 2010 11:53:31 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Thu, 18 Nov 2010 11:50:49 GMT]]></title><description><![CDATA[<p dir="auto">Neither my dh or I have went for thalassemia test. The test which I have taken so far didn’t state specifically that I have thalassemia. But red blood count was pretty low once. I also get tired easily. So I suppose I also have thalassemia?? My dd have been looking pale since young. My elder also look pale but as he grow he looks better. So hope it will Not affect her from giving birth in future …</p>
]]></description><link>https://forum.kiasuparents.com/post/297097</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297097</guid><dc:creator><![CDATA[vlim]]></dc:creator><pubDate>Thu, 18 Nov 2010 11:50:49 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Thu, 18 Nov 2010 11:45:51 GMT]]></title><description><![CDATA[<p>BTW, if your dd has it, you and your hubby should go for the Thalassamia test (easily done at Polyclinic)  to find out who is the carrier. I found out my dad is the 'culprit'.   <img src="https://forum.kiasuparents.com/assets/plugins/nodebb-plugin-emoji/emoji/android/1f609.png?v=f4f27f6278e" class="not-responsive emoji emoji-android emoji--wink" style="height:23px;width:auto;vertical-align:middle" title=":wink:" alt="😉" />  And guess what, he didn't know until he went for the test in his sixties.</p>]]></description><link>https://forum.kiasuparents.com/post/297094</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297094</guid><dc:creator><![CDATA[Picolo]]></dc:creator><pubDate>Thu, 18 Nov 2010 11:45:51 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Thu, 18 Nov 2010 11:41:42 GMT]]></title><description><![CDATA[<p dir="auto">Think I have Thalassamia K-traits. Like what Jennifer shared, other than being tired more easily than the rest of the people, and blood pressure on the low side of normal range, life is very normal.  I don’t even know that I have this until I was tested during pregnancy.  So long as your partner does not have Thalassamia, it should be fine.  No worries…</p>
]]></description><link>https://forum.kiasuparents.com/post/297093</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297093</guid><dc:creator><![CDATA[Picolo]]></dc:creator><pubDate>Thu, 18 Nov 2010 11:41:42 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Thu, 18 Nov 2010 10:50:46 GMT]]></title><description><![CDATA[<p></p><blockquote><b>vlim:</b><blockquote style="border:1px solid black">ok..my dd last blood test findings is suggestive of thalassamia..so going for a detail test next week. Hope is mild.. <img src="https://forum.kiasuparents.com/assets/plugins/nodebb-plugin-emoji/emoji/android/1f61e.png?v=f4f27f6278e" class="not-responsive emoji emoji-android emoji--disappointed" style="height:23px;width:auto;vertical-align:middle" title=":(" alt="😞" /></blockquote></blockquote><br />Are u or your hubby a carrier?  If only one of u is a carrier, then the child is likely to be a carrier too (like my case).<br /><br />I know there are two types- Beta and Alpha.  Beta carriers are more common than Alpha carrier.  I did not bother to check the difference between the two, just need to confirm my then-boyfriend (now hubby) is not a carrier.<br /><br />Dun worry too much.  A child who has the serious Thalassamia disorder wld hv bn uncovered long ago since babyhood.<p></p>]]></description><link>https://forum.kiasuparents.com/post/297075</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297075</guid><dc:creator><![CDATA[Jennifer]]></dc:creator><pubDate>Thu, 18 Nov 2010 10:50:46 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Thu, 18 Nov 2010 10:27:22 GMT]]></title><description><![CDATA[<p>ok..my dd last blood test findings is suggestive of thalassamia..so going for a detail test next week. Hope is mild.. <img src="https://forum.kiasuparents.com/assets/plugins/nodebb-plugin-emoji/emoji/android/1f61e.png?v=f4f27f6278e" class="not-responsive emoji emoji-android emoji--disappointed" style="height:23px;width:auto;vertical-align:middle" title=":(" alt="😞" /></p>]]></description><link>https://forum.kiasuparents.com/post/297055</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297055</guid><dc:creator><![CDATA[vlim]]></dc:creator><pubDate>Thu, 18 Nov 2010 10:27:22 GMT</pubDate></item><item><title><![CDATA[Reply to Children with Thalassemia? on Thu, 18 Nov 2010 10:05:16 GMT]]></title><description><![CDATA[<p dir="auto">I myself have Alpha Thalassemia which explained for my low blood pressure n fainting spells during my teens.  After a mth of prolonged menses, I was seen by a TCM physician.  After which I no longer experienced fainting spells.<br /><br /><br />Other than blood pressure still on the low side and been easily tired, I lead a normal life.  <br /><br />My hubby does not hv Thalassemia, hence we dare to hv children.</p>
]]></description><link>https://forum.kiasuparents.com/post/297032</link><guid isPermaLink="true">https://forum.kiasuparents.com/post/297032</guid><dc:creator><![CDATA[Jennifer]]></dc:creator><pubDate>Thu, 18 Nov 2010 10:05:16 GMT</pubDate></item></channel></rss>