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    <title>topic Re: Chemo New bad Symptoms as end is near in Treatments and side effects</title>
    <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Chemo-New-bad-Symptoms-as-end-is-near/m-p/32278#M3701</link>
    <description>&lt;P&gt;Hi Sch&lt;/P&gt;&lt;P&gt;Sorry about your loss of feeling 12 months down the track. I have permanent numbness in hands and feet, but can still feel. I wear globes most of the time and wear thick socks which helps a bit. Around my 9th treatment I spoke to my oncologist about the permanent numbness and he reduced the dosage slightly, but now I think its back to normal, so will have to follow that up. &amp;nbsp;How did you go with chemo taste and any of the other side &amp;nbsp;effects? &amp;nbsp;&lt;/P&gt;</description>
    <pubDate>Sat, 30 Nov 2019 07:20:51 GMT</pubDate>
    <dc:creator>Albundy21</dc:creator>
    <dc:date>2019-11-30T07:20:51Z</dc:date>
    <item>
      <title>Chemo New bad Symptoms as end is near</title>
      <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Chemo-New-bad-Symptoms-as-end-is-near/m-p/32273#M3697</link>
      <description>&lt;P&gt;I’m slowly getting to the end of treatment with two cycles &amp;nbsp;left, one next week &amp;nbsp;and then last one two weeks latter. I didn’t know what side effects I would get so it was learning experience. &amp;nbsp;It was my 3rd cycle when the cold sensitivity started in my hands and feet. I was also unable to have any cold drinks and understand &amp;nbsp;now all the people who commented it was like swallowing SHades of Glass. Chemo taste now means a lot of foods taste bland. Strange but the cold sensitive issue is now worse in my feet and hands basically numb all the time, but I can now have cold drinks. &amp;nbsp;Constipation is now a major issue initially early on in treatment just having extra prune juice was the fix, but it just got worse and needed more over the counter medication. I'm on a high fiber diet drink plenty of water but the constipation is now worse and painfull when I poo it stings. I googled this and found other people with same issue describing going to the loo as passing shades of glass! For me having the operation was a walk in the park compared to the 12 recommended cycles of Chemo .&lt;/P&gt;</description>
      <pubDate>Fri, 29 Nov 2019 13:58:44 GMT</pubDate>
      <guid>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Chemo-New-bad-Symptoms-as-end-is-near/m-p/32273#M3697</guid>
      <dc:creator>Albundy21</dc:creator>
      <dc:date>2019-11-29T13:58:44Z</dc:date>
    </item>
    <item>
      <title>Re: Chemo New bad Symptoms as end is near</title>
      <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Chemo-New-bad-Symptoms-as-end-is-near/m-p/32274#M3698</link>
      <description>&lt;P&gt;Hi Albundy21,&lt;/P&gt;&lt;P&gt;I did 12 cycles of folfox. The last few sessions were definitely the worst.&lt;/P&gt;&lt;P&gt;The loss of feeling actually got worse 2 weeks following completing all of my chemo.&lt;/P&gt;&lt;P&gt;&amp;nbsp;&lt;/P&gt;&lt;P&gt;&amp;nbsp;When I first started chemo, the side effects would only last a couple of days.&amp;nbsp; But over time,&amp;nbsp; especially the last few cycles,&amp;nbsp; there was no relief.&lt;/P&gt;&lt;P&gt;&amp;nbsp;&lt;/P&gt;&lt;P&gt;Twelve months on and I still have feeling loss in my hands and feet.&amp;nbsp;&lt;/P&gt;&lt;P&gt;&amp;nbsp;&lt;/P&gt;&lt;P&gt;-Sch&lt;/P&gt;</description>
      <pubDate>Fri, 29 Nov 2019 14:39:54 GMT</pubDate>
      <guid>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Chemo-New-bad-Symptoms-as-end-is-near/m-p/32274#M3698</guid>
      <dc:creator>sch</dc:creator>
      <dc:date>2019-11-29T14:39:54Z</dc:date>
    </item>
    <item>
      <title>Re: Chemo New bad Symptoms as end is near</title>
      <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Chemo-New-bad-Symptoms-as-end-is-near/m-p/32276#M3700</link>
      <description>Hi Albundy21,&lt;BR /&gt;I would rather have diarrhoea than constipation. When I get constipation, I take Coloxyl with Senna &amp;amp; a sachet of Movicol. They help alot.&lt;BR /&gt;&lt;BR /&gt;Budgie</description>
      <pubDate>Sat, 30 Nov 2019 00:04:32 GMT</pubDate>
      <guid>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Chemo-New-bad-Symptoms-as-end-is-near/m-p/32276#M3700</guid>
      <dc:creator>Budgie</dc:creator>
      <dc:date>2019-11-30T00:04:32Z</dc:date>
    </item>
    <item>
      <title>Re: Chemo New bad Symptoms as end is near</title>
      <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Chemo-New-bad-Symptoms-as-end-is-near/m-p/32278#M3701</link>
      <description>&lt;P&gt;Hi Sch&lt;/P&gt;&lt;P&gt;Sorry about your loss of feeling 12 months down the track. I have permanent numbness in hands and feet, but can still feel. I wear globes most of the time and wear thick socks which helps a bit. Around my 9th treatment I spoke to my oncologist about the permanent numbness and he reduced the dosage slightly, but now I think its back to normal, so will have to follow that up. &amp;nbsp;How did you go with chemo taste and any of the other side &amp;nbsp;effects? &amp;nbsp;&lt;/P&gt;</description>
      <pubDate>Sat, 30 Nov 2019 07:20:51 GMT</pubDate>
      <guid>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Chemo-New-bad-Symptoms-as-end-is-near/m-p/32278#M3701</guid>
      <dc:creator>Albundy21</dc:creator>
      <dc:date>2019-11-30T07:20:51Z</dc:date>
    </item>
    <item>
      <title>Re: Chemo New bad Symptoms as end is near</title>
      <link>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Chemo-New-bad-Symptoms-as-end-is-near/m-p/32279#M3702</link>
      <description>&lt;P&gt;Hi Albundy21,&lt;/P&gt;&lt;P&gt;&amp;nbsp;&lt;/P&gt;&lt;P&gt;Effect on my taste was minimal. It was there, but minor effect.&amp;nbsp; So taste is mostly back to normal.&lt;/P&gt;&lt;P&gt;It was painful if I touched, drank of ate anything cold, but that has resolved.&lt;/P&gt;&lt;P&gt;To this day I don't like drinking cold drinks (I prefer room temperature), but that is more because of remembering how unpleasant it was during chemo. No big loss there.&lt;/P&gt;&lt;P&gt;So just loss of feeling/numbness in my feet. Feels like I am walking around with big thick socks on, even if I'm outside in the cold.&lt;/P&gt;&lt;P&gt;&amp;nbsp;&lt;/P&gt;&lt;P&gt;So no real complaints. Most of the side effects for myself are related to my surgery. I've had a few major surgeries, so this is to be expected I guess.&lt;/P&gt;&lt;P&gt;I still have my family, I can still run and walk, I can still work.&lt;/P&gt;&lt;P&gt;&amp;nbsp;&lt;/P&gt;&lt;P&gt;-sch&lt;/P&gt;&lt;P&gt;&amp;nbsp;&lt;/P&gt;&lt;P&gt;&amp;nbsp;&lt;/P&gt;</description>
      <pubDate>Sat, 30 Nov 2019 07:53:47 GMT</pubDate>
      <guid>https://onlinecommunity.cancercouncil.com.au/t5/Treatments-and-side-effects/Chemo-New-bad-Symptoms-as-end-is-near/m-p/32279#M3702</guid>
      <dc:creator>sch</dc:creator>
      <dc:date>2019-11-30T07:53:47Z</dc:date>
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