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> <channel><title>Comments on: About me</title> <atom:link href="http://after-cancer.com/about-me/feed/" rel="self" type="application/rss+xml" /><link>http://after-cancer.com</link> <description>Verite Reily Collins writes about Cancer Side Effects</description> <lastBuildDate>Wed, 08 Sep 2010 13:09:07 +0000</lastBuildDate> <generator>http://wordpress.org/?v=2.9.2</generator> <sy:updatePeriod>hourly</sy:updatePeriod> <sy:updateFrequency>1</sy:updateFrequency> <item><title>By: Verite Reily Collins</title><link>http://after-cancer.com/about-me/comment-page-1/#comment-14330</link> <dc:creator>Verite Reily Collins</dc:creator> <pubDate>Wed, 02 Jun 2010 09:50:51 +0000</pubDate> <guid
isPermaLink="false">http://after-cancer.com/?page_id=2647#comment-14330</guid> <description>Sylvie,  Thank you for writing, which I take as a great compliment.  As you say, what about those afraid to ask - I fear that many of those just get discouraged, and eventually fade away.  The statistic that  60% of UK patients come off hormonal drugs because of side effects shocks me - but doesn&#039;t seem to worry the doctors!   But they are one of the reasons why I started the web site, to try and reach out to them and say there ARE solutions.
As you say, I know that the French system isn&#039;t all roses, but overall I am very impressed.  I did find one person who complained bitterly though.  He had had to wait six hours in A &amp; E to be seen when he broke his leg.  Afterwards his wife told me (and you will understand this) he broke it on August 1st!
Do go and see the latest story I have posted on NHS Watch - re doctor-speak ! www.after-cancer.com/NHS-watch.  Best wishes, and if OK with you I will put you on my list to let you know when I have more stories up.  Verite.</description> <content:encoded><![CDATA[<p>Sylvie,  Thank you for writing, which I take as a great compliment.  As you say, what about those afraid to ask &#8211; I fear that many of those just get discouraged, and eventually fade away.  The statistic that  60% of UK patients come off hormonal drugs because of side effects shocks me &#8211; but doesn&#8217;t seem to worry the doctors!   But they are one of the reasons why I started the web site, to try and reach out to them and say there ARE solutions.<br
/> As you say, I know that the French system isn&#8217;t all roses, but overall I am very impressed.  I did find one person who complained bitterly though.  He had had to wait six hours in A &amp; E to be seen when he broke his leg.  Afterwards his wife told me (and you will understand this) he broke it on August 1st!<br
/> Do go and see the latest story I have posted on NHS Watch &#8211; re doctor-speak ! <a
href="http://www.after-cancer.com/NHS-watch" rel="nofollow">http://www.after-cancer.com/NHS-watch</a>.  Best wishes, and if OK with you I will put you on my list to let you know when I have more stories up.  Verite.</p> ]]></content:encoded> </item> <item><title>By: sylvie</title><link>http://after-cancer.com/about-me/comment-page-1/#comment-14319</link> <dc:creator>sylvie</dc:creator> <pubDate>Tue, 01 Jun 2010 12:34:17 +0000</pubDate> <guid
isPermaLink="false">http://after-cancer.com/?page_id=2647#comment-14319</guid> <description>Hello Verite
your name in French means truth as you probably know it. I also had a cancer journey, not for breast cancer but for lymphoma and I am just finishing chemo. I happen to be French and a doctor who has worked for the NHS for the last 9 years after my husband was transferred in London. I couldn&#039;t agree more with your comments about doctors listening. I had various side effects during my chemo and almost every time was dismissed as it wasn&#039;t life threatening. Serious infections would have been dealt with but various pains, loss of voice or other &quot;unusual&quot; effects were qualified as either not bothersome or impossible to have (was I faking it? you don&#039;t get pain in your chemo arm that wakes you up just for the fun of it!). I was lucky because as a doctor I was able to monitor myself most of the time and to search the internet for information. I came across most of the help you mention, acupuncture, massage, diet and they helped me tremendously. I do not live far from a Maggie centre and they were great but what about those afraid to ask, too tired to move or unaware. Where do they find the support?
By the way, I like your enthusiasm about the French medical care but we also have our non listeners.
Thanks for all the info on your website, I wish I had found it when I started my journey, it would have saved me time.</description> <content:encoded><![CDATA[<p>Hello Verite<br
/> your name in French means truth as you probably know it. I also had a cancer journey, not for breast cancer but for lymphoma and I am just finishing chemo. I happen to be French and a doctor who has worked for the NHS for the last 9 years after my husband was transferred in London. I couldn&#8217;t agree more with your comments about doctors listening. I had various side effects during my chemo and almost every time was dismissed as it wasn&#8217;t life threatening. Serious infections would have been dealt with but various pains, loss of voice or other &#8220;unusual&#8221; effects were qualified as either not bothersome or impossible to have (was I faking it? you don&#8217;t get pain in your chemo arm that wakes you up just for the fun of it!). I was lucky because as a doctor I was able to monitor myself most of the time and to search the internet for information. I came across most of the help you mention, acupuncture, massage, diet and they helped me tremendously. I do not live far from a Maggie centre and they were great but what about those afraid to ask, too tired to move or unaware. Where do they find the support?<br
/> By the way, I like your enthusiasm about the French medical care but we also have our non listeners.<br
/> Thanks for all the info on your website, I wish I had found it when I started my journey, it would have saved me time.</p> ]]></content:encoded> </item> </channel> </rss>
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