<?xml version="1.0" encoding="UTF-8" ?>
<?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">marie millie&amp;#39;s blog </title><subtitle type="html">marie millie&amp;#39;s blog </subtitle><id>https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/atom</id><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie" /><link rel="self" type="application/atom+xml" href="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/atom" /><generator uri="http://telligent.com" version="12.1.2.21912">Telligent Community (Build: 12.1.2.21912)</generator><updated>2009-03-12T22:11:20Z</updated><entry><title>c.t.scan</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/c-t-scan" /><id>https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/c-t-scan</id><published>2009-05-28T11:40:49Z</published><updated>2009-05-28T11:40:49Z</updated><content type="html">hi there,just had another c.t.scan this is my last for awhile i hope as i was on a choras trial so that is for them to put onto my records,next will be my first outpatients check up since finishing my chemo,you know i feel as if you have to live on a knife edge for ever more how to you get use to this can anyone tell me,i feel myself i have done very well coping with cancer,its just the thought this is my way of life now how do you cope,in a lot of ways it has made me feel very bitter,yes i know there are people lots worse off than myself but its getting my head around it.any ideas.&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=223152&amp;AppID=18342&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="Ovarian cancer" scheme="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/archive/tags/Ovarian%2bcancer" /><category term="chemotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/archive/tags/chemotherapy" /></entry><entry><title>paswords</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/paswords" /><id>https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/paswords</id><published>2009-05-09T14:00:37Z</published><updated>2009-05-09T14:00:37Z</updated><content type="html">just a small thought is there anyone else that has been having problems with there password to login onto this site everytime i try to use this site my password will not be accepted so yes i have to keep changing it does anyone else have this problem thanks.&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=223149&amp;AppID=18342&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>just a hello</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/just-a-hello" /><id>https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/just-a-hello</id><published>2009-05-04T10:37:49Z</published><updated>2009-05-04T10:37:49Z</updated><content type="html">just a quick hello hope everyone has a good bank holiday,bye.&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=223146&amp;AppID=18342&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="Ovarian cancer" scheme="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/archive/tags/Ovarian%2bcancer" /></entry><entry><title>here for a talk anytime</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/here-for-a-talk-anytime" /><id>https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/here-for-a-talk-anytime</id><published>2009-04-24T21:23:59Z</published><updated>2009-04-24T21:23:59Z</updated><content type="html">never feel alone i know how that feels myself at times so join in here there is someone always to just listen if you just need that..&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=223145&amp;AppID=18342&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>update about platelets</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/update-about-platelets" /><id>https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/update-about-platelets</id><published>2009-04-24T12:00:28Z</published><updated>2009-04-24T12:00:28Z</updated><content type="html">hi there everyone,just to say platelets were ok so had my last chemo yesterday,saw doctor on wednesday,she said the cancer markers were great as were all the other tests so for now its 1ct scanto end the trial i was on then just blood tests,and a check at outpatiens in 6weeks,so for now thats it just a couple of weeks on feeling horrid from my last chemo nothing to worry about hope some of you have good news.&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=223144&amp;AppID=18342&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="Platelets" scheme="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/archive/tags/Platelets" /><category term="blood tests" scheme="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/archive/tags/blood%2btests" /><category term="chemotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/archive/tags/chemotherapy" /></entry><entry><title>low platelet count</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/low-platelet-count" /><id>https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/low-platelet-count</id><published>2009-04-21T15:55:35Z</published><updated>2009-04-21T15:55:35Z</updated><content type="html">here i am again having a moan went yesterday for my blood test was told today you need another blood test so off down to the hospital asked them why did i need one oh your platelets are low ,so i am due my last chemo no 6 on thursday now who knows tomorrow off down the hospital for my review with the doctor i suppose i will be told then if i can still have it you know i feel as if i live at the hospital you keep trying to put yourself togeather somehow but this week i feel really low with it all anyway i feel a little better now sorry about the moan.&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=223140&amp;AppID=18342&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="Platelets" scheme="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/archive/tags/Platelets" /><category term="Hospital" scheme="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/archive/tags/Hospital" /><category term="chemotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/archive/tags/chemotherapy" /></entry><entry><title>water infection ok</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/water-infection-ok" /><id>https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/water-infection-ok</id><published>2009-04-03T12:46:55Z</published><updated>2009-04-03T12:46:55Z</updated><content type="html">just thought would let you know water infection ok now just cleared up in a few days so worries over for now end on month may last chemo sessions no 6 so i will keep my fingers crossed with everything else i will be ok well as much as you can be with this illness.take care everyone.&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=223138&amp;AppID=18342&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/marie_millie/archive/tags/chemotherapy" /><category term="infection" scheme="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/archive/tags/infection" /></entry><entry><title>water infection</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/water-infection" /><id>https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/water-infection</id><published>2009-03-27T10:48:27Z</published><updated>2009-03-27T10:48:27Z</updated><content type="html">hi there can anyone help me i was told the other day my water was positive and needed another test the doctor told me this does happen at times when having chemo,ok,she said would sort out antibotics when the results came back so at the moment i am drinking loads of water and cranberry juice,my next chemo is next thursday so i suppose they will sort me then just surprised they leave you so long in discomfort any other ideas i can try thanks.&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=223137&amp;AppID=18342&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/marie_millie/archive/tags/chemotherapy" /><category term="infection" scheme="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/archive/tags/infection" /></entry><entry><title>hols abroad.</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/hols-abroad" /><id>https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/hols-abroad</id><published>2009-03-21T09:19:42Z</published><updated>2009-03-21T09:19:42Z</updated><content type="html">hi there everyone can anyone answer this question can you still get hol insurance easy when you have cancer,i would like to know for the future.&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=223131&amp;AppID=18342&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="abroad" scheme="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/archive/tags/abroad" /><category term="insurance" scheme="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/archive/tags/insurance" /></entry><entry><title>ovarian cancer</title><link rel="alternate" type="text/html" href="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/ovarian-cancer" /><id>https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/posts/ovarian-cancer</id><published>2009-03-12T21:11:20Z</published><updated>2009-03-12T21:11:20Z</updated><content type="html">       this blog is about ovarian cancer,i wish there were more people on this site that could give more information i.e. tips on basic foods you can eat when chemo takes your taste away,how to try and cope when you become constipated,what you can try to help yourself,the list goes on and on i suppose an a to z what more can i say as for myself not having any close family i look forward to the help many thanks&lt;div style="clear:both;"&gt;&lt;/div&gt;&lt;img src="https://community.macmillan.org.uk/aggbug?PostID=223124&amp;AppID=18342&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="Ovarian cancer" scheme="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/archive/tags/Ovarian%2bcancer" /><category term="chemotherapy" scheme="https://community.macmillan.org.uk/cancer-blogs/b/marie_millie/archive/tags/chemotherapy" /></entry></feed>