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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">sue G&amp;#39;s blog </title><subtitle type="html">sue G&amp;#39;s blog </subtitle><id>https://community.macmillan.org.uk/cancer-blogs/b/sue_g/atom</id><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/sue_g" /><link rel="self" type="application/atom+xml" href="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/atom" /><generator uri="http://telligent.com" version="12.1.2.21912">Telligent Community (Build: 12.1.2.21912)</generator><updated>2009-04-11T12:54:16Z</updated><entry><title>Latest 02.04</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/posts/latest-02-04" /><id>https://community.macmillan.org.uk/cancer-blogs/b/sue_g/posts/latest-02-04</id><published>2010-04-02T19:18:22Z</published><updated>2010-04-02T19:18:22Z</updated><content type="html">&lt;p&gt;Had the op and recovering slowly. Still very tired and in pain. getting over initial post op problems tho. Hope to escape in a few days &lt;/p&gt;
&lt;p&gt;Sue&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=328578&amp;AppID=21420&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Sue G</name><uri>https://community.macmillan.org.uk/members/a0e56845c5e24bb7983b1c0cc1149ab2</uri></author></entry><entry><title>Result of bone scan </title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/posts/result-of-bone-scan" /><id>https://community.macmillan.org.uk/cancer-blogs/b/sue_g/posts/result-of-bone-scan</id><published>2009-04-30T18:52:56Z</published><updated>2009-04-30T18:52:56Z</updated><content type="html">Got the god news from my GP that my bone scan is clear. Still have a lot of pain in the arm and rib. Am told it is the effects from the radiotherapy which I finished last November. Seems I just have to take painkillers but at least my fears were unfounded.
I am lucky that I have a brilliant GP. The breast cancer nurse from the hospital has not phoned me with the results!!!!! &lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=226892&amp;AppID=21420&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Sue G</name><uri>https://community.macmillan.org.uk/members/a0e56845c5e24bb7983b1c0cc1149ab2</uri></author><category term="Hospital" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/Hospital" /><category term="bone scan" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/bone%2bscan" /><category term="Breast cancer" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/Breast%2bcancer" /><category term="painkillers" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/painkillers" /><category term="radiotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/radiotherapy" /></entry><entry><title>Reconstruction - choices</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/posts/reconstruction-choices" /><id>https://community.macmillan.org.uk/cancer-blogs/b/sue_g/posts/reconstruction-choices</id><published>2009-04-14T21:29:44Z</published><updated>2009-04-14T21:29:44Z</updated><content type="html">Hi 
I have an appointment on Thursday in Birmingham with my consultant plastic surgeon to discuss the reconstruction of my left breast after my mastectomy last April.
I have watched the DVD they kindly sent me and to be honest the Tram Flap is a no no for me. Would like to hear from ladies who have had implants and LD reconstruction.
I am 59 and a 36b cup so I have never been blessed with a big bust.
Am a coward too hence no to the TF option.
I have plenty of time to think about the options as I understand I have to wait 12 months from the end of radiotherapy before he will operate and that means November time.
Love
Sue&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=226891&amp;AppID=21420&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Sue G</name><uri>https://community.macmillan.org.uk/members/a0e56845c5e24bb7983b1c0cc1149ab2</uri></author><category term="reconstruction" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/reconstruction" /><category term="Operate" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/Operate" /><category term="surgeon" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/surgeon" /><category term="Breast cancer" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/Breast%2bcancer" /><category term="Removing the breast" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/Removing%2bthe%2bbreast" /><category term="implants" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/implants" /><category term="radiotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/radiotherapy" /><category term="mastectomy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/mastectomy" /></entry><entry><title>Effects of Radiotherapy</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/posts/effects-of-radiotherapy" /><id>https://community.macmillan.org.uk/cancer-blogs/b/sue_g/posts/effects-of-radiotherapy</id><published>2009-04-11T11:54:16Z</published><updated>2009-04-11T11:54:16Z</updated><content type="html">Hi
I am new to this but would welcome any thoughts on what I am going through at the mo.
I had a mastectomy and full anxillary clearance in April 08 followed by 6 sessions of chemo and 13 sessions of radiotherapy which finished Nov 08.
Except for the painful burning under my arm at first I have been feeling very well and in no pain.
In March this year I have been feeling incresingly tired and have been in pain in my left &amp;quot;breast&amp;quot; under my arms and in my top left rib.
My GP took a chest x ray and I am now waiting for a bone scan in the next couple of weeks.
Has anyone had the same effects.
Love
Sue x x&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=226886&amp;AppID=21420&amp;AppType=Weblog&amp;ContentType=0" width="1" height="1"&gt;</content><author><name>Sue G</name><uri>https://community.macmillan.org.uk/members/a0e56845c5e24bb7983b1c0cc1149ab2</uri></author><category term="bone scan" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/bone%2bscan" /><category term="Breast cancer" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/Breast%2bcancer" /><category term="chemotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/chemotherapy" /><category term="Removing the breast" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/Removing%2bthe%2bbreast" /><category term="radiotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/radiotherapy" /><category term="mastectomy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/sue_g/archive/tags/mastectomy" /></entry></feed>