<?xml version="1.0" encoding="utf-8"?>
<rss version="2.0" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:atom="http://www.w3.org/2005/Atom">
	<channel>
		<title>CMPA - The Real Story! </title>
		<description>Discuss CMPA - The Real Story! </description>
		<link>https://intolerantgourmand.com/bg/allergies/728-cmpa-the-real-story.html</link>
		<lastBuildDate>Tue, 07 Apr 2026 01:41:47 +0000</lastBuildDate>
		<generator>JComments</generator>
		<atom:link href="https://intolerantgourmand.com/component/jcomments/feed/com_content/728.html" rel="self" type="application/rss+xml" />
		<item>
			<title>dairyfreebabyandme says:</title>
			<link>https://intolerantgourmand.com/bg/allergies/728-cmpa-the-real-story.html#comment-10841</link>
			<description><![CDATA[Very well put Natalie! I don't suppose Dr Chris considered his own 'sponsorship' by the BBC as clouding his judgement - he has to make programmes in order to keep the BBC pay check rolling in. Being controversial perhaps helps with that??]]></description>
			<dc:creator>dairyfreebabyandme</dc:creator>
			<pubDate>Wed, 06 Jun 2018 08:45:21 +0000</pubDate>
			<guid>https://intolerantgourmand.com/bg/allergies/728-cmpa-the-real-story.html#comment-10841</guid>
		</item>
		<item>
			<title>Matt says:</title>
			<link>https://intolerantgourmand.com/bg/allergies/728-cmpa-the-real-story.html#comment-10831</link>
			<description><![CDATA[There is an obvious reason why companies are happy to fund these education events. Maybe if the NHS funded their own events and research, they’d save money in the medium-long term in overdiagnosing unnecessary medicines.]]></description>
			<dc:creator>Matt</dc:creator>
			<pubDate>Tue, 05 Jun 2018 10:09:14 +0000</pubDate>
			<guid>https://intolerantgourmand.com/bg/allergies/728-cmpa-the-real-story.html#comment-10831</guid>
		</item>
		<item>
			<title>Shabnam Ahsan says:</title>
			<link>https://intolerantgourmand.com/bg/allergies/728-cmpa-the-real-story.html#comment-10635</link>
			<description><![CDATA[While I agree that pharmaceutical business interests should not be influencing patient care, I would be interested to know what Dr Chris suggests as alternative sources of funding for research and education into food allergies, as it is clear that this is a growing need which isn't being filled in other ways. Neocate was a lifesaver for my son when he was failure to thrive at 3 1/2 months - he is now a happy, healthy 8 year old. It doesn't look like the "missing nutrients" have had a massive impact on him - he'd have been missing a lot more without the formula. If I had continued to breastfeed he might have been ill for much longer as we later found out he was also allergic to wheat, oats and legumes. I wonder if Dr Chris could tell us an alternative formula that doesn't cost money to the NHS and isn't pushed by big pharma.]]></description>
			<dc:creator>Shabnam Ahsan</dc:creator>
			<pubDate>Fri, 01 Jun 2018 09:38:28 +0000</pubDate>
			<guid>https://intolerantgourmand.com/bg/allergies/728-cmpa-the-real-story.html#comment-10635</guid>
		</item>
		<item>
			<title>Adventures with J says:</title>
			<link>https://intolerantgourmand.com/bg/allergies/728-cmpa-the-real-story.html#comment-10621</link>
			<description><![CDATA[Well done for writing such a composed response. How dare he suggest that Neocate isn't needed. He should be talking to parents of children who suffered if he wants to make a good programme. Let's be fair there is enough drama and outrage in the truth so why go to all the effort of making a programme like this. Poor journalism at its best.]]></description>
			<dc:creator>Adventures with J</dc:creator>
			<pubDate>Thu, 31 May 2018 19:39:08 +0000</pubDate>
			<guid>https://intolerantgourmand.com/bg/allergies/728-cmpa-the-real-story.html#comment-10621</guid>
		</item>
	</channel>
</rss>
