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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">alleyh97&amp;#39;s blog </title><subtitle type="html">alleyh97&amp;#39;s blog </subtitle><id>https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701/atom</id><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701" /><link rel="self" type="application/atom+xml" href="https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701/atom" /><generator uri="http://telligent.com" version="12.1.2.21912">Telligent Community (Build: 12.1.2.21912)</generator><updated>2009-09-01T00:28:15Z</updated><entry><title>SHOULD I BE HAVING YEARLY SCANS!</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701/posts/should-i-be-having-yearly-scans" /><id>https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701/posts/should-i-be-having-yearly-scans</id><published>2009-09-10T22:43:14Z</published><updated>2009-09-10T22:43:14Z</updated><content type="html">I&amp;#39;M ALMOST 20 MONTHS IN REMISSION AND AFTER READING VARIOUS BLOGS ON SITE ,  IT&amp;#39;S ONLY DAWNING ON ME (DOH!)
SHOULD I NOT BE HAVING A YEARLY MRI OR SOMETHING,STARTING TO GET WORRIED AS THERE WERE QUITE A FEW TIMES THAT I&amp;#39;VE HAD TO CHASE UP RESULTS AND STUFF MYSELF, OMG!
HOW CAN THEY KNOW FOR SURE THAT I&amp;#39;M STILL IN REMISSION BY FEELING AROUND MY NECK AND STICKING A CAMERA UP MY NOSE TO SEE DOWN MY THROAT!

DOESN&amp;#39;T PAY TO BE OF A QUIET NATURE!&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=251467&amp;AppID=29867&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="nasopharyngeal cancer" scheme="https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701/archive/tags/nasopharyngeal%2bcancer" /><category term="Head and neck cancer" scheme="https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701/archive/tags/Head%2band%2bneck%2bcancer" /><category term="remission" scheme="https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701/archive/tags/remission" /></entry><entry><title>michael, my brightness on dark days</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701/posts/michael-my-brightness-on-dark-days" /><id>https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701/posts/michael-my-brightness-on-dark-days</id><published>2009-09-07T23:58:11Z</published><updated>2009-09-07T23:58:11Z</updated><content type="html">Although I&amp;#39;ve been remission for 19months now, the fear of the cancer returning often comes back to bite me on the bum, big time!
When it does I think of my nephew Michael and it comforts me so much!
He was diagnosed with a rare form of brain cancer and his outlook was not good, 15years old, his parents were devastated!
Michael under went an 8 hour operation were the surgeons managed to remove just over 90 percent of the tumor, he then spent weeks in intensive care very very poorly!
Chemotheraphy does not work on Michael&amp;#39;s type of cancer,his parents were told, radiotheraphy is our only hope, the doctor
said!
Eventually michael&amp;#39;s parents were told to 
take him home, time was precious!!
Fast forward to 2009,
Michael is now 29 years old and a strapping big man!!!
I hope that Michael&amp;#39;s story can bring someone else some comfort too!
                                             Alison x
&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=251459&amp;AppID=29867&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/alleyh9701/archive/tags/tumour" /><category term="nasopharyngeal cancer" scheme="https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701/archive/tags/nasopharyngeal%2bcancer" /><category term="Head and neck cancer" scheme="https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701/archive/tags/Head%2band%2bneck%2bcancer" /><category term="remission" scheme="https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701/archive/tags/remission" /><category term="brain" scheme="https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701/archive/tags/brain" /><category term="operation" scheme="https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701/archive/tags/operation" /></entry><entry><title>NO SPIT AFTER TREATMENT</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701/posts/no-spit-after-treatment" /><id>https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701/posts/no-spit-after-treatment</id><published>2009-08-31T23:28:15Z</published><updated>2009-08-31T23:28:15Z</updated><content type="html">HI, I&amp;#39;VE BEEN 19 MONTHS IN REMISSION AND I HAVE LITTLE  TO NO SALVIA,(STILL!)
HAS ANYONE ELSE THIS PROBLEM AS I WOULD LOVE TO KNOW  HOW THEY ARE  COPING!&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=251450&amp;AppID=29867&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="Head and neck cancer" scheme="https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701/archive/tags/Head%2band%2bneck%2bcancer" /><category term="remission" scheme="https://community.macmillan.org.uk/cancer-blogs/b/alleyh9701/archive/tags/remission" /></entry></feed>