<?xml version="1.0"?><rss version="2.0"><channel><title>pickles's Discussion RSS Feed</title><link>http://www.nationalbreastcancer.org/mynbcf/members/pickles/discussions/rss</link><description>pickles's Discussion RSS Feed</description><item><title><![CDATA[taxoil]]></title><link>http://www.nationalbreastcancer.org/mynbcf/members/pickles/discussions/8956</link><guid>http://www.nationalbreastcancer.org/mynbcf/members/pickles/discussions/8956</guid><description><![CDATA[Does anyone have any ways to help with the pain from the chemo taxiol? I just received my first dose three days ago and I have took pain pills, aleve and took hot bath nothing is helping. Any suggestion?]]></description></item><item><title><![CDATA[SOOOOOOOO TIRED]]></title><link>http://www.nationalbreastcancer.org/mynbcf/members/pickles/discussions/8608</link><guid>http://www.nationalbreastcancer.org/mynbcf/members/pickles/discussions/8608</guid><description><![CDATA[Well next week I start on my third round of chemo and I am soooooooo tired. The first time I did chemo I got headache really bad so they decreased my steriods and that has helped. But this time it has really wiped me out. But one good thing about it is I haven't really been nausautated(not spelled right). But I have slept for days. I have to be woke up to drink water. It took me 4 hrs. to eat a pudding cup. I go for chemo every two weeks instead of every three weeks. My chemo is called AC. Which is doxorubicin and cyclophorous. ]]></description></item><item><title><![CDATA[BLESSED]]></title><link>http://www.nationalbreastcancer.org/mynbcf/members/pickles/discussions/8539</link><guid>http://www.nationalbreastcancer.org/mynbcf/members/pickles/discussions/8539</guid><description><![CDATA[This is just my observation. I was thinking today really how lucky I am. Sure I have BC, I have to have chemo and raditation. But at least I haven't been told there is no hope for me. So I am really blessed. I am the first person to admit that I have complained about it all but I have decided today that I am blessed.]]></description></item><item><title><![CDATA[help]]></title><link>http://www.nationalbreastcancer.org/mynbcf/members/pickles/discussions/8522</link><guid>http://www.nationalbreastcancer.org/mynbcf/members/pickles/discussions/8522</guid><description><![CDATA[Has anyone that every taken chemo had problems with headache.]]></description></item><item><title><![CDATA[HELP]]></title><link>http://www.nationalbreastcancer.org/mynbcf/members/pickles/discussions/8425</link><guid>http://www.nationalbreastcancer.org/mynbcf/members/pickles/discussions/8425</guid><description><![CDATA[I had breast surgery in Feb. I am fixing to start chemo. I was told by my radigolist and also the chemotheraphist that they are worried about my breast. That when I get through with chemo that I might have to have surgery on my breast again. I was also told that most people in my age group that the aggressive of the cancer is in the 5 to 10%% that mine was 80%%. That they were also going to give me more doses of chemo then they usually give. Has anyone had that experience.]]></description></item></channel></rss>