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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">teakbank12&amp;#39;s blog </title><subtitle type="html">teakbank12&amp;#39;s blog </subtitle><id>https://community.macmillan.org.uk/cancer-blogs/b/teakbank1201/atom</id><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/teakbank1201" /><link rel="self" type="application/atom+xml" href="https://community.macmillan.org.uk/cancer-blogs/b/teakbank1201/atom" /><generator uri="http://telligent.com" version="12.1.2.21912">Telligent Community (Build: 12.1.2.21912)</generator><updated>2009-09-01T14:16:22Z</updated><entry><title>First visit to the Consultant</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/teakbank1201/posts/first-visit-to-the-consultant" /><id>https://community.macmillan.org.uk/cancer-blogs/b/teakbank1201/posts/first-visit-to-the-consultant</id><published>2009-09-01T13:16:22Z</published><updated>2009-09-01T13:16:22Z</updated><content type="html">Hi all
Just returned from my first visit to the consultant. Had bloods done again for him to look at.
He took details &amp;amp; we discussed options (i had said what i knew &amp;amp; had read about)...
He believes i&amp;#39;ve probably had CLL undiagnosed for a couple years.
As with most its watch and wait initially with a CT scan booked to check my lymph nodes in the next 2-3 weeks.
I have to return in 2 months  (late October) for another bloodtest &amp;amp; chat with him &amp;amp; obviously discuss CT scan results.
He doesn&amp;#39;t think at present anything will be done for a couple years but did ask about brothers/sisters for Bone Marrow matching.
I discussed the extreme tiredness &amp;amp; night sweats &amp;amp; how hot i often feel &amp;amp; said maybe i should listen to my body a bit more &amp;amp; refrain from work when i&amp;#39;m too exhausted. I&amp;#39;ve always put this down to the Crohn&amp;#39;s disease i have (certain days i go into work &amp;amp; struggle to stay awake at my keyboard).
All i&amp;#39;ve to do now is tell my family still :( then i guess i can rest easy &amp;amp; learn to live with it like i&amp;#39;ve done with my Crohn&amp;#39;s for 25 odd years. 

Dave&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=251384&amp;AppID=29831&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="sweats" scheme="https://community.macmillan.org.uk/cancer-blogs/b/teakbank1201/archive/tags/sweats" /><category term="disease" scheme="https://community.macmillan.org.uk/cancer-blogs/b/teakbank1201/archive/tags/disease" /><category term="tiredness" scheme="https://community.macmillan.org.uk/cancer-blogs/b/teakbank1201/archive/tags/tiredness" /><category term="CT Scan" scheme="https://community.macmillan.org.uk/cancer-blogs/b/teakbank1201/archive/tags/CT%2bScan" /><category term="Leukaemia, chronic lymphocytic" scheme="https://community.macmillan.org.uk/cancer-blogs/b/teakbank1201/archive/tags/Leukaemia_2C00_%2bchronic%2blymphocytic" /></entry></feed>