<?xml version="1.0" encoding="UTF-8"?>
<rss xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:taxo="http://purl.org/rss/1.0/modules/taxonomy/" version="2.0">
  <channel>
    <title>topic Advice on treatment options for neuro endocrine lung cancer in Treatments and side effects</title>
    <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Advice-on-treatment-options-for-neuro-endocrine-lung-cancer/m-p/15395#M1842</link>
    <description>My mum was diagnosed 3 weeks ago with neuro endocrine lung cancer stage IV. The find was incidental after taking mum to emergency with a broken collar bone from a fall, standard CT scans discovered the cancer. It has been a busy 3 weeks with mum undergoing brain surgery 2 weeks ago to remove one of the biggest tumors. We've now moved onto radio and are meeting with chemo doctors in a week. I'm searching for a second opinion and Peter Mac has been suggested to me. I'm after advice around the best doctor/hospital to ask for a second opinion as I don't feel I'm currently getting enough information on the diagnosis, treatment and option for clinical trials. Any advice/experience is greatly appreciated.</description>
    <pubDate>Thu, 26 May 2016 04:18:04 GMT</pubDate>
    <dc:creator>Emily_B</dc:creator>
    <dc:date>2016-05-26T04:18:04Z</dc:date>
    <item>
      <title>Advice on treatment options for neuro endocrine lung cancer</title>
      <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Advice-on-treatment-options-for-neuro-endocrine-lung-cancer/m-p/15395#M1842</link>
      <description>My mum was diagnosed 3 weeks ago with neuro endocrine lung cancer stage IV. The find was incidental after taking mum to emergency with a broken collar bone from a fall, standard CT scans discovered the cancer. It has been a busy 3 weeks with mum undergoing brain surgery 2 weeks ago to remove one of the biggest tumors. We've now moved onto radio and are meeting with chemo doctors in a week. I'm searching for a second opinion and Peter Mac has been suggested to me. I'm after advice around the best doctor/hospital to ask for a second opinion as I don't feel I'm currently getting enough information on the diagnosis, treatment and option for clinical trials. Any advice/experience is greatly appreciated.</description>
      <pubDate>Thu, 26 May 2016 04:18:04 GMT</pubDate>
      <guid>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Advice-on-treatment-options-for-neuro-endocrine-lung-cancer/m-p/15395#M1842</guid>
      <dc:creator>Emily_B</dc:creator>
      <dc:date>2016-05-26T04:18:04Z</dc:date>
    </item>
  </channel>
</rss>

