<?xml version="1.0" encoding="UTF-8" ?>
<?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">cornishmaid&amp;#39;s blog </title><subtitle type="html">cornishmaid&amp;#39;s blog </subtitle><id>https://community.macmillan.org.uk/cancer-blogs/b/cornishmaid/atom</id><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/cornishmaid" /><link rel="self" type="application/atom+xml" href="https://community.macmillan.org.uk/cancer-blogs/b/cornishmaid/atom" /><generator uri="http://telligent.com" version="12.1.2.21912">Telligent Community (Build: 12.1.2.21912)</generator><updated>2009-06-23T11:51:09Z</updated><entry><title>Where we are now</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/cornishmaid/posts/where-we-are-now" /><id>https://community.macmillan.org.uk/cancer-blogs/b/cornishmaid/posts/where-we-are-now</id><published>2009-06-23T10:51:09Z</published><updated>2009-06-23T10:51:09Z</updated><content type="html">Well its been a while since I joined this group, since then Fran has started his chemo 2 out of 6 so far, his third was put off as his blood was low so he&amp;#39;s back in this week. He also starts his Radiotheraphy as well

 Life is now very strange, up and down like a rollercoaster. 

Fran is still in denial, talking about doing things , moving house so we can have our dream house with a bit of land. Buying more equipment for the garage . Its great he&amp;#39;s so positive, but thats because he  does not know anything or want to know anything about what he has. Who am I to burst that bubble, he&amp;#39;s happy.
 
Me, I feel on a razor edge, I don&amp;#39;t let him see me cry,  I go out to walk the dog or go in the shower.  i can&amp;#39;t sleep, or think straight. My work is suffering as my mind is not in it and find it hard to concentrate on the most simple tasks these days. 
I just hope he stays well as he is for a long time.I scare myself rigid when I read up on the pack the hospital has given us, I just have to be strong for him. 


&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=227669&amp;AppID=22230&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="Mesothelioma" scheme="https://community.macmillan.org.uk/cancer-blogs/b/cornishmaid/archive/tags/Mesothelioma" /><category term="Hospital" scheme="https://community.macmillan.org.uk/cancer-blogs/b/cornishmaid/archive/tags/Hospital" /><category term="chemotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/cornishmaid/archive/tags/chemotherapy" /><category term="Equipment" scheme="https://community.macmillan.org.uk/cancer-blogs/b/cornishmaid/archive/tags/Equipment" /><category term="shower" scheme="https://community.macmillan.org.uk/cancer-blogs/b/cornishmaid/archive/tags/shower" /></entry></feed>