Persistent fatigue and brain fog, 5 months post chemo

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Kbelo
Posts: 20
Joined: Tue Aug 07, 2018 8:19 am

Persistent fatigue and brain fog, 5 months post chemo

Postby Kbelo » Mon Jun 03, 2019 3:23 pm

I finished 6 months of chemo (FOLFIRINOX - FOLFOX plus Irinotecan) in January. My neuropathy is improving to the point where I don't mind it as much, but I really struggle still with fatigue and brain fog. I'm working out many days a week to boost energy levels and stamina, and doing brain games to exercise my brain, but most days I'm still finding myself napping, and feeling mentally dull. I'm curious if anyone has experience reducing fatigue or improving brain fog? Also, how long did these symptoms stay with you? Did it improve when you returned to work (which I will be doing in the next few weeks or months). Thanks!
Stage 3B CC - diagnosed at 40
Bowel resection May 2018
28 nodes removed 1 with cancer traces
FOLFIRINOX started July 2018 for 6 months, finished Jan 2019.
1/19 - CT Scan shows NED
2/19 - CT Scan shows NED
5/19 - CT Scan shows NED
8/19 - CT scan + MRI show NED
2/20 - CT Scan shows NED
8/20 - CT Scan shows NED

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juliej
Posts: 3114
Joined: Thu Aug 05, 2010 12:59 pm

Re: Persistent fatigue and brain fog, 5 months post chemo

Postby juliej » Mon Jun 03, 2019 8:11 pm

For most people, chemo brain improves within 9-12 months after finishing chemo. For a small group of patients, it can take years to get better, but there's no reason to think you're in that group yet.

However, since you're only about 5 months out, you might have a while to go. But chemo brain doesn't just disappear all at once. It gradually gets better so you should see a steady improvement starting around now.

It's good you're working out regularly and doing brain games! :D You might also take some vitamin D and B12 and see if that helps.

Just so you know -- if you continue to have cognitive issues when you return to work, you have the right to ask for "reasonable accommodations". ADA protections include trouble concentrating, thinking, and/or communicating - all of which relate to the side effects of chemo brain.

That could mean anything from being given a note taker who goes along with you to meetings, or your employer buying you a tape recorder so you can record meetings to help you remember what was agreed upon there, or a whole host of other accommodations. I don't think you'll need it, but I just wanted you to know the possibility exists.

Hope this helps!
Juliej
Stage IVb, liver/lung mets 8/4/2010
Xelox+Avastin 8/18/10 to 10/21/2011
LAR, liver resec, HAI pump 11/2011
Adjuvant Irinotecan + FUDR
Double lung surgery + ileo reversal 2/2012
Adjuvant FUDR + Xeloda
VATS rt. lung 12/2012 - benign granuloma!
VATS left lung 11/2013
NED 11/22/13 to 12/18/2019, CEA<1

Gravelyguy
Posts: 382
Joined: Thu Jul 05, 2018 6:03 pm

Re: Persistent fatigue and brain fog, 5 months post chemo

Postby Gravelyguy » Mon Jun 03, 2019 9:14 pm

Juliej, that was very informative. I will just add, it took me about 10 months before I felt more like myself. I am a teacher and didn’t realize how much I was suffering from chemo brain until I was back in the classroom with a 100 questions and decisions coming at me.

At about 1 year I felt as sharp as I was before chemo.

Hope this helps,

Dave
6/17 dx mRC t3n1m1 very low rectal tumor 2 liver Mets 1.3 cm and .9 cm

6/17 begin 4 rounds Folfox w/Vectibix
9/17 short course radiation
10/17 rectal and liver resection LAR with coloanal anastomosis (no rectum left)
11/17-3/18 8 rounds Folfox
6/18 still NED!! Takedown
8/28/18 still NED! CEA .8 new low for me
10/18/18 colonoscopy clear
12/12/18 CEA .9 still NED!
6/11/19 CEA 1.0
12/19/19 CEA 1.0 still NED!
6/17/20 CEA 1.1 still NED!
12/15/20 CEA 1.1still NED!
12/16/21 CEA 1.2 still NED!


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