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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">Ian</title><subtitle type="html" /><id>https://community.macmillan.org.uk/cancer-blogs/b/ian/atom</id><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/ian" /><link rel="self" type="application/atom+xml" href="https://community.macmillan.org.uk/cancer-blogs/b/ian/atom" /><generator uri="http://telligent.com" version="12.1.2.21912">Telligent Community (Build: 12.1.2.21912)</generator><updated>2010-03-19T19:31:02Z</updated><entry><title>Non Hodgkins Lymphoma v's Tattoo</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/ian/posts/non-hodgkins-lymphoma-v-s-tattoo" /><id>https://community.macmillan.org.uk/cancer-blogs/b/ian/posts/non-hodgkins-lymphoma-v-s-tattoo</id><published>2010-07-20T18:19:52Z</published><updated>2010-07-20T18:19:52Z</updated><content type="html">&lt;p&gt;Could anyone give me advice.&lt;/p&gt;
&lt;p&gt;I Have NHL, diagnosed in 2005. Finished R-CVP treatment on Hogmany 2009, now on Rituximab maintenance therapy every 12 weeks. I&amp;#39;d quite like to get a new tattoo but don&amp;#39;t know if there are complications with treatment. &lt;/p&gt;
&lt;p&gt;Thanks&lt;/p&gt;
&lt;p&gt;Ian&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=353980&amp;AppID=30556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author><category term="Rituximab" scheme="https://community.macmillan.org.uk/cancer-blogs/b/ian/archive/tags/Rituximab" /><category term="Lymphoma" scheme="https://community.macmillan.org.uk/cancer-blogs/b/ian/archive/tags/Lymphoma" /><category term="Hodgkins" scheme="https://community.macmillan.org.uk/cancer-blogs/b/ian/archive/tags/Hodgkins" /><category term="therapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/ian/archive/tags/therapy" /></entry><entry><title>Can R-CVP chemo cause eyesight problems.</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/ian/posts/can-r-cvp-chemo-cause-eyesight-problems" /><id>https://community.macmillan.org.uk/cancer-blogs/b/ian/posts/can-r-cvp-chemo-cause-eyesight-problems</id><published>2010-07-20T09:11:07Z</published><updated>2010-07-20T09:11:07Z</updated><content type="html">&lt;p&gt;Hi everyone&lt;/p&gt;
&lt;p&gt;I finished my chemo on Hogmany and started on maintenance therapy in March. I have noticed a deterioration in my eyesight, blurred vision when reading. My friend in Canada who is also going through chemo told me his Oncologist mentioned this was a possible side effect. Anyone any ideas or experiencing the same?&lt;/p&gt;
&lt;p&gt;Ian&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=353855&amp;AppID=30556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author><category term="chemotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/ian/archive/tags/chemotherapy" /><category term="therapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/ian/archive/tags/therapy" /><category term="Oncologist" scheme="https://community.macmillan.org.uk/cancer-blogs/b/ian/archive/tags/Oncologist" /><category term="vision" scheme="https://community.macmillan.org.uk/cancer-blogs/b/ian/archive/tags/vision" /></entry><entry><title>Realistic Travel Insurance Quotes</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/ian/posts/realistic-travel-insurance-quotes" /><id>https://community.macmillan.org.uk/cancer-blogs/b/ian/posts/realistic-travel-insurance-quotes</id><published>2010-05-28T10:58:16Z</published><updated>2010-05-28T10:58:16Z</updated><content type="html">&lt;p&gt;Hi My name is Ian. I was diagnosed with non-hodgkins lymphoma in 2005 and have had various treatments since. I am due to fly out to Turkey 2 weeks today for a much needed break with my wife and 2 children. The stumbling block was finding travel insurance at a realistic price.&lt;/p&gt;
&lt;p&gt;I tried all the companies that were listed on the Macmillan website and they all seemed to be plucking figures out of the sky. The quotes I was receiving ranged from &amp;pound;224 to &amp;pound;560, unbelievable.&lt;/p&gt;
&lt;p&gt;What a relief,the very last company on the list quoted me a realistic &amp;pound;44.95. So I just wanted to share this with anyone else having similar problems. The company is called &lt;strong&gt;&lt;span style="text-decoration:underline;"&gt;&lt;em&gt;&amp;nbsp;&lt;/em&gt;Insure Blue.&lt;/span&gt;&lt;/strong&gt; I hope this information comes in handy to many.&lt;/p&gt;
&lt;p&gt;Ian&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=341230&amp;AppID=30556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author><category term="Lymphoma" scheme="https://community.macmillan.org.uk/cancer-blogs/b/ian/archive/tags/Lymphoma" /><category term="travel" scheme="https://community.macmillan.org.uk/cancer-blogs/b/ian/archive/tags/travel" /><category term="insurance" scheme="https://community.macmillan.org.uk/cancer-blogs/b/ian/archive/tags/insurance" /></entry><entry><title>St Johns Wort advice</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/ian/posts/st-johns-wort-advice" /><id>https://community.macmillan.org.uk/cancer-blogs/b/ian/posts/st-johns-wort-advice</id><published>2010-03-19T18:31:02Z</published><updated>2010-03-19T18:31:02Z</updated><content type="html">&lt;p&gt;Hi everyone. I&amp;#39;m looking for some advice if anyone can help. I am due to start maintenance therapy next week. I&amp;#39;ve to have IV Rituximab every 3 months. I&amp;#39;m feeling a bit down as I thought I had finished my treatment for a bit. I was thinking of trying St Johns Wort. Anyone know of any side effects or reasons why I shouldn&amp;#39;t?&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=325320&amp;AppID=30556&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Former Member</name><uri>https://community.macmillan.org.uk/members/formermember</uri></author><category term="Rituximab" scheme="https://community.macmillan.org.uk/cancer-blogs/b/ian/archive/tags/Rituximab" /><category term="side effects" scheme="https://community.macmillan.org.uk/cancer-blogs/b/ian/archive/tags/side%2beffects" /><category term="therapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/ian/archive/tags/therapy" /></entry></feed>