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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">My daughter Stevie</title><subtitle type="html" /><id>https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/atom</id><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie" /><link rel="self" type="application/atom+xml" href="https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/atom" /><generator uri="http://telligent.com" version="12.1.2.21912">Telligent Community (Build: 12.1.2.21912)</generator><updated>2010-10-03T18:20:41Z</updated><entry><title>my beautiful daughter</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/posts/my-beautiful-daughter" /><id>https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/posts/my-beautiful-daughter</id><published>2011-12-09T18:34:18Z</published><updated>2011-12-09T18:34:18Z</updated><content type="html">&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=474445&amp;AppID=31179&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>what next</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/posts/what-next" /><id>https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/posts/what-next</id><published>2011-07-12T10:12:32Z</published><updated>2011-07-12T10:12:32Z</updated><content type="html">&lt;p&gt;After having her grade 3 Anaplastic Astrocytoma debulked again in January my beautiful daughter stevie had a stroke. After rehab she was able to walk and talk again, but unfortunately the poor wee soul caught pnuemonia and has spent the last 3 months in hospital. Before going into a rehabilitation unit we were told that she had swelling on her brain, that was 4 weeks ago and we are waiting for an appointment to start her Chemo. Stevie is coming home next weekend as they cant do anymore for her, she&amp;#39;s very weak and cant walk, her speaking has been affected and she shakes all the time. I cant wait to get her home but im scared as no one has told me what to expect next, i know she&amp;#39;s going to die but im not ready to loose her just yet. I dont know if palliative chemo will benefit her i dont know what to do..........&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=437235&amp;AppID=31179&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="swelling" scheme="https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/archive/tags/swelling" /><category term="stroke" scheme="https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/archive/tags/stroke" /><category term="Hospital" scheme="https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/archive/tags/Hospital" /><category term="chemotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/archive/tags/chemotherapy" /><category term="palliative" scheme="https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/archive/tags/palliative" /><category term="brain" scheme="https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/archive/tags/brain" /><category term="astrocytoma" scheme="https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/archive/tags/astrocytoma" /></entry><entry><title>Angry all the time</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/posts/angry-all-the-time" /><id>https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/posts/angry-all-the-time</id><published>2010-10-06T09:40:08Z</published><updated>2010-10-06T09:40:08Z</updated><content type="html">&lt;p&gt;I am getting so angry at everyone at work and all the moaning that they do. I want to scream at them and tell them to get a life. I know I am feeling like this because all I do is worry about my daughter. I am going to try Yoga and meditation to see if I can calm down a bit.&lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=373465&amp;AppID=31179&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>My daughters brain tumor</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/posts/my-daughters-brain-tumor" /><id>https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/posts/my-daughters-brain-tumor</id><published>2010-10-03T17:20:41Z</published><updated>2010-10-03T17:20:41Z</updated><content type="html">&lt;p&gt;My daughter Stevie was having funny turns for a number years and the doctors were not very helpful. 2 weeks before her 25th birthday she was send for a scan. This showed that she had a brain tumor. She had an operation one week after her birthday to de-bulk the tumor. She came through the operation really well the only side efect was she had lost part of her sight in one eye. The following year the grade 4 tumor had grown and she was sent for a 7 weeks course of radiotherapy. The poor we soul lost all her hair and despite having beautiful wigs she lost a lot of her confidence. She has been doing really well until we had a routine scan this September her tumor has grown again. Because she is feeling ok and has not had any fits the surgeon doesnt want to see her till January 2011. I dont know what the future holds for her but for the next 3 months I will make sure that she has a brilliant time. &lt;/p&gt;&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=372695&amp;AppID=31179&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/my_daughter_stevie/archive/tags/tumour" /><category term="surgeon" scheme="https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/archive/tags/surgeon" /><category term="brain" scheme="https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/archive/tags/brain" /><category term="operation" scheme="https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/archive/tags/operation" /><category term="radiotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/my_daughter_stevie/archive/tags/radiotherapy" /></entry></feed>