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    <title>topic Re: Esophagus cancer in Treatments and side effects</title>
    <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12905#M2654</link>
    <description>Yes, we're still here.  I was diagnosed with tumour &amp;amp; mets to lymph nodes, stage iv, in July 2013.  Had Radiation, then 6/12 chemo.  CT scans show tumour much reduced.  Lucky with chemo, mainly just fatigue, no nausea.  Will now remain on chemo via PIC line, to be monitored every 3/12.  This site is quite helpful, there are others, ex UK &amp;amp; USA - some better than others, so search around. It is definitely scarey, what stage are you?  Sorry you're chemo is making you feel bad - don't hesitate to discuss this with yr oncologist - if you've had radiation, that cld be the cause.
Do use this site to vent feelings/thoughts you're not yet ready to share in person.  We've all been there, and plsd to help you cope with this catastrophe. Wishing you all the best.</description>
    <pubDate>Wed, 29 Jan 2014 05:49:36 GMT</pubDate>
    <dc:creator>zelfren</dc:creator>
    <dc:date>2014-01-29T05:49:36Z</dc:date>
    <item>
      <title>Esophagus cancer</title>
      <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12904#M2653</link>
      <description>Hi all
Was wondering if ther is anyone out there who may be going through the same thing as myself.
I am into my 4th week of chemo for esophagus cancer.</description>
      <pubDate>Wed, 29 Jan 2014 03:40:06 GMT</pubDate>
      <guid>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12904#M2653</guid>
      <dc:creator>Chutneyferrit</dc:creator>
      <dc:date>2014-01-29T03:40:06Z</dc:date>
    </item>
    <item>
      <title>Re: Esophagus cancer</title>
      <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12905#M2654</link>
      <description>Yes, we're still here.  I was diagnosed with tumour &amp;amp; mets to lymph nodes, stage iv, in July 2013.  Had Radiation, then 6/12 chemo.  CT scans show tumour much reduced.  Lucky with chemo, mainly just fatigue, no nausea.  Will now remain on chemo via PIC line, to be monitored every 3/12.  This site is quite helpful, there are others, ex UK &amp;amp; USA - some better than others, so search around. It is definitely scarey, what stage are you?  Sorry you're chemo is making you feel bad - don't hesitate to discuss this with yr oncologist - if you've had radiation, that cld be the cause.
Do use this site to vent feelings/thoughts you're not yet ready to share in person.  We've all been there, and plsd to help you cope with this catastrophe. Wishing you all the best.</description>
      <pubDate>Wed, 29 Jan 2014 05:49:36 GMT</pubDate>
      <guid>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12905#M2654</guid>
      <dc:creator>zelfren</dc:creator>
      <dc:date>2014-01-29T05:49:36Z</dc:date>
    </item>
    <item>
      <title>Re: Esophagus cancer</title>
      <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12906#M2655</link>
      <description>Hi I had stage IV esophagus cancer. I had chemo which enabled me to start eating again and killed the tumour completely and the biopsy's after the surgery all came back clear so I decided not to have further chemo after my surgery and I am now just over 2 years clear. 
The chemo was not as bad as I expected in regards to nausea but then I was constantly sick prior to the chemo but the tiredness floored me after the big doses for a few days.
Good luck and hope all goes well and feel free to ask any questions and  will help as best as I can.

Kas</description>
      <pubDate>Wed, 29 Jan 2014 09:58:28 GMT</pubDate>
      <guid>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12906#M2655</guid>
      <dc:creator>kasianne</dc:creator>
      <dc:date>2014-01-29T09:58:28Z</dc:date>
    </item>
    <item>
      <title>Re: Esophagus cancer</title>
      <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12907#M2656</link>
      <description>Hi I had stage IV esophagus cancer. I had chemo which enabled me to start eating again and killed the tumour completely and the biopsy's after the surgery all came back clear so I decided not to have further chemo after my surgery and I am now just over 2 years clear. 
The chemo was not as bad as I expected in regards to nausea but then I was constantly sick prior to the chemo but the tiredness floored me after the big doses for a few days.
Good luck and hope all goes well and feel free to ask any questions and  will help as best as I can.

Kas</description>
      <pubDate>Wed, 29 Jan 2014 09:58:29 GMT</pubDate>
      <guid>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12907#M2656</guid>
      <dc:creator>kasianne</dc:creator>
      <dc:date>2014-01-29T09:58:29Z</dc:date>
    </item>
    <item>
      <title>Re: Esophagus cancer</title>
      <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12908#M2657</link>
      <description>Zelfren thanks for you thoughts.
Yes I am having chemo  goes like this 1 full on 4 hour dose at the clinic and for the next 3weeks the annoying "baby bottle" 24/7. Through a PICC line
This is repeated 3 session times. I am now on the. 2nd  session. My age is 70 "young" &lt;span class="lia-unicode-emoji" title=":slightly_smiling_face:"&gt;🙂&lt;/span&gt; 
Biggest problem is nausea, the doc said today to take the nausea tablets 3 times a day, so that's what I will do now instead of when I feel nausea.. I have stage 3 esophageal  cancer and they are looking for surgery after the end of this chemo treatment.
Get headaches, told doc about that today and he put me straight down for a CT scan,  apprently  all is well in that area.
All fun and games..haha. I must admit that the doctors and nurses are absolutely  great. I not sure where you are my friend, but I am in Ballarat, Victoria , Australia.
Zelfren, my thoughts are with you mate, hang in there, and we will beat the dreaded beast.</description>
      <pubDate>Wed, 29 Jan 2014 10:09:18 GMT</pubDate>
      <guid>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12908#M2657</guid>
      <dc:creator>Chutneyferrit</dc:creator>
      <dc:date>2014-01-29T10:09:18Z</dc:date>
    </item>
    <item>
      <title>Re: Esophagus cancer</title>
      <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12909#M2658</link>
      <description>Kas

Yea the tired part creeps up on you. Can sleep in the chair at the drop of a hat.
I have the PICC in my right arm, and I am right handed, makes for great fun when having a shower.
Good luck also to you my friend.
Greg</description>
      <pubDate>Wed, 29 Jan 2014 10:16:07 GMT</pubDate>
      <guid>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12909#M2658</guid>
      <dc:creator>Chutneyferrit</dc:creator>
      <dc:date>2014-01-29T10:16:07Z</dc:date>
    </item>
    <item>
      <title>Re: Esophagus cancer</title>
      <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12910#M2659</link>
      <description>A tip for the PICC line and showering wrap eh top of your arm in cling wrap over the PICC make life a lot easier, although in the end I resorted to a bath as I also had  feeding tube in my stomach and it became easier to wash round the and my arm in an inch or tow in the bath.

Kas</description>
      <pubDate>Wed, 29 Jan 2014 10:19:24 GMT</pubDate>
      <guid>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12910#M2659</guid>
      <dc:creator>kasianne</dc:creator>
      <dc:date>2014-01-29T10:19:24Z</dc:date>
    </item>
    <item>
      <title>Re: Esophagus cancer</title>
      <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12911#M2660</link>
      <description>We tried a couple of things, found the best result so far was a plastic safeways bag with a small hole, then slipped it over and up the arm with the baby bottle, then taped around under the arm.
Times like this i wish we had a bath...haha

Greg</description>
      <pubDate>Wed, 29 Jan 2014 10:28:10 GMT</pubDate>
      <guid>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12911#M2660</guid>
      <dc:creator>Chutneyferrit</dc:creator>
      <dc:date>2014-01-29T10:28:10Z</dc:date>
    </item>
    <item>
      <title>Re: Esophagus cancer</title>
      <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12912#M2661</link>
      <description>I used to wear the baby bottle on my arm all the time with a piece of tubi-grip the nurses gave me when they changed it, I then stole my husbands shirts to wear when I left the house to hide it so it was quite funny as people did not know I was on continuous chemo unless i took the shirt off and one medical place I went to thought my baldness was fro taking part in the biggest shave. So wearing the bottle like this enabled me to wrap myself u with cling wrap.

Kas</description>
      <pubDate>Wed, 29 Jan 2014 10:33:44 GMT</pubDate>
      <guid>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12912#M2661</guid>
      <dc:creator>kasianne</dc:creator>
      <dc:date>2014-01-29T10:33:44Z</dc:date>
    </item>
    <item>
      <title>Re: Esophagus cancer</title>
      <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12913#M2662</link>
      <description>Hi i just found out I have esophageal cancer and I will start chemo and radiation therapy on Monday 23 June. I have read the other posts and I will have a Picc line with 4 days of continuous chemo as well as daily radiation therapy. I am soooo scared. I have had previous stomach surgery and so they told me that surgery is not an option.
I am a single mum with two young boys and I guess I just need some support.
Kim</description>
      <pubDate>Wed, 18 Jun 2014 15:05:07 GMT</pubDate>
      <guid>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Esophagus-cancer/m-p/12913#M2662</guid>
      <dc:creator>madmik</dc:creator>
      <dc:date>2014-06-18T15:05:07Z</dc:date>
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