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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">sam</title><subtitle type="html" /><id>https://community.macmillan.org.uk/cancer-blogs/b/sam/atom</id><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/sam" /><link rel="self" type="application/atom+xml" href="https://community.macmillan.org.uk/cancer-blogs/b/sam/atom" /><generator uri="http://telligent.com" version="12.1.2.21912">Telligent Community (Build: 12.1.2.21912)</generator><updated>2011-02-24T08:16:08Z</updated><entry><title>my baby boy</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/my-baby-boy" /><id>https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/my-baby-boy</id><published>2011-07-02T13:40:16Z</published><updated>2011-07-02T13:40:16Z</updated><content type="html">&lt;p&gt;Manged to push enough drugs into the system to get to see my youngest son arrive at his prom.He knew how hard&amp;nbsp; it was for me to get there and how rough i must have been feeling, he immediatelt came over to me gave me a massive hug and said thaks mum for coming. I have no idea how i managed not to cry my eyes out i was so moved and emotional. Even more amazing is that they diagnosed him when he was 3 with Autusim and the prognosis was not good, 13 years on and he looks like to be getting 8 or so GCSE at b or above has a girlfriend and a really good set of friends. Its times like these that really give you the boost to fight the daily crap you endure with cancer and i was such a proud mummy last night, even though i am paying for it today. &lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=435401&amp;AppID=31551&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></entry><entry><title>COLLEGE</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/college" /><id>https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/college</id><published>2011-06-27T16:49:40Z</published><updated>2011-06-27T16:49:40Z</updated><content type="html">&lt;p&gt;Passed my college course in nvq 2 in hairdressing very pleased, being theeldest on course, having 2 operations and 3 lots of chemo am a very happy person.&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=434534&amp;AppID=31551&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/sam/archive/tags/chemotherapy" /></entry><entry><title>poor lad</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/poor-lad" /><id>https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/poor-lad</id><published>2011-06-13T17:14:05Z</published><updated>2011-06-13T17:14:05Z</updated><content type="html">&lt;p&gt;My poor son has to go back to Barts after 5 years in remission, i cant but help feel sad for him(we are not the closest of mums and sons) but having to go through this is awfull once but faced with it twice is tragic at such a young age. It seems his liver is an issue now as was before when he had testicular cancer, with stomach, lung an dliver secondries.Finding the strength to do the fight again must be so hard as i am ony half way through my chemo and have had enough allready, imagining knowing whats ahead of you?.&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;sam&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=430974&amp;AppID=31551&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/sam/archive/tags/chemotherapy" /><category term="remission" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sam/archive/tags/remission" /><category term="Testicular cancer" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sam/archive/tags/Testicular%2bcancer" /></entry><entry><title>3rd chemo</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/3rd-chemo" /><id>https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/3rd-chemo</id><published>2011-06-10T20:38:34Z</published><updated>2011-06-10T20:38:34Z</updated><content type="html">&lt;p&gt;3rd chemo woo hoo half way there thank god ..........bloody painfull getting canulated 3 times they tried ....................i swore like a navvy lol not to mention cut of the nurses blood supply in her hand. Feeling a bit sick but nothing major.Weekend of rest.&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=430404&amp;AppID=31551&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/sam/archive/tags/chemotherapy" /></entry><entry><title>HAIR</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/hair" /><id>https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/hair</id><published>2011-05-18T19:03:46Z</published><updated>2011-05-18T19:03:46Z</updated><content type="html">&lt;p&gt;13 Days in from 1st Chemo and started to loose hair, day 19 and hair amost gone allready am very shocked at how quickly it has gone. Have to say it was a bad day for me.&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=425364&amp;AppID=31551&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/sam/archive/tags/chemotherapy" /></entry><entry><title>omg</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/omg" /><id>https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/omg</id><published>2011-05-11T18:18:40Z</published><updated>2011-05-11T18:18:40Z</updated><content type="html">&lt;address&gt;OMG my bloody hair is falling out allready and its only been 13 days so not good :(&lt;/address&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=423792&amp;AppID=31551&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></entry><entry><title>ONE WEEK IN</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/one-week-in" /><id>https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/one-week-in</id><published>2011-05-05T18:04:35Z</published><updated>2011-05-05T18:04:35Z</updated><content type="html">&lt;p&gt;One week in and not so bad yet!!!!!!!&lt;/p&gt;
&lt;p&gt;A few mouth ulcers, a little bit of nausea and an overwhemlming feeling of tiredness but otherwise ok. Oh and the body rash from the antibiotics that makes me look like a 17th century pox victim lol, but if it keeps bugs at bay i can live with it. Adelaide is behaving herself rather well and even the teenage son is doing housework wihout being&amp;nbsp; asked, yes i must be ill lol.&lt;/p&gt;
&lt;p&gt;So in all not a bad start to chemo!!!!&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=422185&amp;AppID=31551&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="Ulcers" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sam/archive/tags/Ulcers" /><category term="nausea" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sam/archive/tags/nausea" /><category term="tiredness" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sam/archive/tags/tiredness" /><category term="chemotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sam/archive/tags/chemotherapy" /></entry><entry><title>1st Chemo</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/1st-chemo" /><id>https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/1st-chemo</id><published>2011-04-28T15:31:20Z</published><updated>2011-04-28T15:31:20Z</updated><content type="html">&lt;p&gt;1st one today of 6 feeling a bit woosy but ok, took the brave step to cut all my hair off.&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=420336&amp;AppID=31551&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/sam/archive/tags/chemotherapy" /></entry><entry><title>BAD PLACES</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/bad-places" /><id>https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/bad-places</id><published>2011-03-31T21:17:37Z</published><updated>2011-03-31T21:17:37Z</updated><content type="html">&lt;p&gt;Really in a bad place at the moment feeling very low and alone but still pushing everyone away completely fed up and dreading chemo.&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=414064&amp;AppID=31551&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/sam/archive/tags/chemotherapy" /></entry><entry><title>FIRST DAY BACK AT COLLEGE</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/first-day-back-at-college" /><id>https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/first-day-back-at-college</id><published>2011-03-01T06:36:34Z</published><updated>2011-03-01T06:36:34Z</updated><content type="html">&lt;p&gt;Had my first&amp;nbsp; full day back at college since the christmas break, after the operations to remove lump and lymph nodes.&lt;/p&gt;
&lt;p&gt;Was extremly tired at the end of the day but was truly happy and content to be back. I had an assessment which i passed and have 3 more this week.&lt;/p&gt;
&lt;p&gt;Hosp has given a breather of this half term to get my course as near completed as i can so when i am on Chemo i have very little to complete and can relax as much as you can whilst on Chemo!!!!&lt;/p&gt;
&lt;p&gt;Had many ask me how i was feeling and many said how much better i was looking. Think i had a very big smile on my face all day.&lt;/p&gt;
&lt;p&gt;Still could not sleep though.&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=407149&amp;AppID=31551&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="christmas" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sam/archive/tags/christmas" /><category term="chemotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sam/archive/tags/chemotherapy" /></entry><entry><title>excellent news</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/excellent-news" /><id>https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/excellent-news</id><published>2011-02-25T07:05:38Z</published><updated>2011-02-25T07:05:38Z</updated><content type="html">&lt;p&gt;Cancer has not spread. Chemo starts on 28th April managed to negoiate a reprive as i need to sort out so much prior to chemo and need my head to be in the right place. Radio therapy and Tamox tablets after as well.&lt;/p&gt;
&lt;p&gt;Also got a chance to tell oncology team how badly i felt i had been treated and the total lack of aftercare&amp;nbsp; that i have recieceved . I actually felt in control for the first time in months.&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=406115&amp;AppID=31551&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="oncology" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sam/archive/tags/oncology" /><category term="chemotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sam/archive/tags/chemotherapy" /><category term="therapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sam/archive/tags/therapy" /><category term="radiotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sam/archive/tags/radiotherapy" /></entry><entry><title>today isD day or more apt C day</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/today-isd-day-or-more-apt-c-day" /><id>https://community.macmillan.org.uk/cancer-blogs/b/sam/posts/today-isd-day-or-more-apt-c-day</id><published>2011-02-24T07:16:08Z</published><updated>2011-02-24T07:16:08Z</updated><content type="html">&lt;p&gt;will finally get my results of tumour analysis, bloods and scans etc. Its&amp;nbsp; DOUBLE EDGED KNIFE i want to know but i dont as i want my life to just carry on as normal.I have been coming up with all sorts off plans to evade the dreaded chemo for a variety of reasons deep down i dont think these are going to work and i will have to acceptt Cemo will happen just when it will is a negoiation. So much to juggle being a single mum to a 3 yr old for starters and sorting her needs out comes pretty high on the list.&lt;/p&gt;
&lt;p&gt;Well must stop watching Peppa PIg&amp;nbsp; sunuggled up on sofa and go get ready for hosp&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=405855&amp;AppID=31551&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="tumour" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sam/archive/tags/tumour" /><category term="chemotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sam/archive/tags/chemotherapy" /></entry></feed>