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<?xml-stylesheet type="text/xsl" href="https://community.macmillan.org.uk/cfs-file/__key/system/syndication/atom.xsl" media="screen"?><feed xmlns="http://www.w3.org/2005/Atom" xml:lang="en-US"><title type="html">Life&amp;#39;s adventures </title><subtitle type="html" /><id>https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/atom</id><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures" /><link rel="self" type="application/atom+xml" href="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/atom" /><generator uri="http://telligent.com" version="12.1.2.21912">Telligent Community (Build: 12.1.2.21912)</generator><updated>2024-11-11T17:55:20Z</updated><entry><title>Waiting</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/posts/waiting" /><id>https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/posts/waiting</id><published>2025-03-02T09:36:05Z</published><updated>2025-03-02T09:36:05Z</updated><content type="html">&amp;nbsp;02.03.25 This has been the most difficult week yet. Rod was admitted to the oncology ward for rehydration and to have a stent fitted. That was on Monday and he&amp;#39;s still there today, Sunday. He was put on blood infusions because his counts we...(&lt;a href="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/posts/waiting"&gt;read more&lt;/a&gt;)&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=721982&amp;AppID=42042&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>LozzaT</name><uri>https://community.macmillan.org.uk/members/a6d073d35df341e4a2d8941f1be6f418</uri></author></entry><entry><title>Pleasure, pain</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/posts/pleasure-pain" /><id>https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/posts/pleasure-pain</id><published>2025-02-23T11:34:41Z</published><updated>2025-02-23T11:34:41Z</updated><content type="html">The cancer is spreading and growing at an incredible rate. Difficult to believe that, in one month, we&amp;#39;ve driven to the Alps and back for a skiing holiday, had an overnight theatre break and have flown to Krakow for a city break; then we got the ...(&lt;a href="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/posts/pleasure-pain"&gt;read more&lt;/a&gt;)&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=721971&amp;AppID=42042&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>LozzaT</name><uri>https://community.macmillan.org.uk/members/a6d073d35df341e4a2d8941f1be6f418</uri></author></entry><entry><title>Highs and lows</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/posts/highs-and-lows" /><id>https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/posts/highs-and-lows</id><published>2025-02-13T21:54:23Z</published><updated>2025-02-13T21:54:23Z</updated><content type="html">So, 1st follow up CT scan had shown a 50% reduction in all tumours. The next showed continued improvement and we were feeling very optimistic. The Christmas period was a struggle for Rod because the mouth soreness caused by the mucositis made eating ...(&lt;a href="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/posts/highs-and-lows"&gt;read more&lt;/a&gt;)&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=721961&amp;AppID=42042&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>LozzaT</name><uri>https://community.macmillan.org.uk/members/a6d073d35df341e4a2d8941f1be6f418</uri></author><category term="tumour" scheme="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/archive/tags/tumour" /><category term="Paclitaxel" scheme="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/archive/tags/Paclitaxel" /><category term="side effects" scheme="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/archive/tags/side%2beffects" /><category term="chemotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/archive/tags/chemotherapy" /><category term="CT Scan" scheme="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/archive/tags/CT%2bScan" /><category term="Oncologist" scheme="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/archive/tags/Oncologist" /></entry><entry><title>Results!</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/posts/results" /><id>https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/posts/results</id><published>2024-11-18T17:18:18Z</published><updated>2024-11-18T17:18:18Z</updated><content type="html">Follow up appointment with the oncologist today.
Great news. The tumour and lymph nodes have been shrunk by 50%. The MDT told Rod this is the best outcome they could hope for at this stage. He thought he was getting a whole cycle off but, because his...(&lt;a href="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/posts/results"&gt;read more&lt;/a&gt;)&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=721798&amp;AppID=42042&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>LozzaT</name><uri>https://community.macmillan.org.uk/members/a6d073d35df341e4a2d8941f1be6f418</uri></author></entry><entry><title>Pit stop</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/posts/pit-stop" /><id>https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/posts/pit-stop</id><published>2024-11-11T17:55:20Z</published><updated>2024-11-11T17:55:20Z</updated><content type="html">After the wtf moment back in August, when the gastrointestinal surgeon apologetically informed my husband that his cancer was inoperable, he is 4 cycles into palliative treatment. This is FOLFOX and Nivolumab, fortnightly. He also has an infusion of ...(&lt;a href="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/posts/pit-stop"&gt;read more&lt;/a&gt;)&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=721792&amp;AppID=42042&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>LozzaT</name><uri>https://community.macmillan.org.uk/members/a6d073d35df341e4a2d8941f1be6f418</uri></author><category term="side effects" scheme="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/archive/tags/side%2beffects" /><category term="FOLFOX" scheme="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/archive/tags/FOLFOX" /><category term="nivolumab" scheme="https://community.macmillan.org.uk/cancer-blogs/b/life-s-adventures/archive/tags/nivolumab" /></entry></feed>