Chest pain

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mstults
Posts: 1327
Joined: Fri Nov 30, 2012 11:23 am

Chest pain

Postby mstults » Tue Feb 12, 2013 9:22 pm

Anyone else have chest pain in the right chest area while taking folfox + avastin? It starts the day my port is unhooked and last 4-5 days. I thought the catheter had migrated as it has before but X-rays say not. The dr suggested acid reflux but I'm already on pantaprazole. It gets to about a 7 or 8.
Male Age 53. Dx CC with numerous liver mets 6/23/12. Colon res 6/24/12. Started folfox 7/24/12. Added avastin 8/27/12. CT 12/27/12 still showing shrink. Took 17 rounds of FOLFOX. Then 5-FU + Avastin. Switched to Irinotecan for 1 yr. CEA rose to >400. Switched to Vectibix 2/18/15. CEA decreasing. Scans show some growth in liver mets. Lung Mets stable to shrinking.

https://www.facebook.com/michael.stults2/about?ref=home_edit_profile&section=work

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KarMel
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Joined: Wed Oct 14, 2009 7:48 pm
Facebook Username: Karin Gray
Location: Indiana

Re: Chest pain

Postby KarMel » Tue Feb 12, 2013 9:34 pm

Do your anti nausea drugs cause constipation or bad gas. I have serious pain from that. Also, does it start after eating? Worse with fatty foods? Maybe gall bladder?
Stage IV, April 2009.
Treatments...multiple .
Currently none
"It is well, with my soul"

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CRguy
Posts: 10476
Joined: Sun Feb 10, 2008 6:00 pm

Re: Chest pain

Postby CRguy » Tue Feb 12, 2013 9:37 pm

My quick take advice is : get the docs to take IT and you seriously, figure out what is going on and maybe get a pain management specialist on board if all the "other usual suspects" are ruled out.

Could be port related, could be cardiovascular.....could be a WHOLE number of things. I've had a lotta FOLFOX but no Avastin, so I may not be the one to give advice...except to say if it is truly 7-8 on a 10 pain scale.............. you need to get somebody's attention and figure it out.

Sometimes pain is inevitable on this Journey....suffering from it, is NOT.

Let us know how it works out,
sending you mega Cheers
CRguy
Caregiver x 4
Stage IV A rectal cancer/lung met
17 Year survivor
my life is an ongoing totally randomized UNcontrolled experiment with N=1 !
Review of my Journey so far

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mstults
Posts: 1327
Joined: Fri Nov 30, 2012 11:23 am

Re: Chest pain

Postby mstults » Wed Feb 13, 2013 2:25 am

Thanks cr. I'm taking a treatment now. Going to see what happens. Will probably go to ermif it starts again. And karmel boot ideas but I don't have a gallbladder. It doesn't seem to be affected by food or drink. It's continuous butt worsens when I take a deep breath or lay where pressure is on the chest. That's why I thought it was the port. Funny it doesn't hurt while the infusion is running. Imreallymfeel like its the chemo irritating veins. If so the only alternative is to reduce doseages. And I do have high tolerance for pain.
Male Age 53. Dx CC with numerous liver mets 6/23/12. Colon res 6/24/12. Started folfox 7/24/12. Added avastin 8/27/12. CT 12/27/12 still showing shrink. Took 17 rounds of FOLFOX. Then 5-FU + Avastin. Switched to Irinotecan for 1 yr. CEA rose to >400. Switched to Vectibix 2/18/15. CEA decreasing. Scans show some growth in liver mets. Lung Mets stable to shrinking.

https://www.facebook.com/michael.stults2/about?ref=home_edit_profile&section=work


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