New cancer blog

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Oneeyeddog
Posts: 101
Joined: Sat Apr 06, 2013 11:06 am

New cancer blog

Postby Oneeyeddog » Fri May 17, 2013 6:46 am

I have started a blog about my treatment and feelings blah blah blah.

http://theoneeyeddog.tumblr.com

Perhaps of interest for other newbies going through something similar. For the veterans, perhaps not much to see here. :) Hope some will find it interesting.

Cheers,

OED
Colon cancer Stage 3c (dx April 2013) at age 36
Resection and temp ileostomy (4/17)
12 rounds of FOLFOX (May-Oct 2013)
NED (August 2014)
http://www.theoneeyeddog.com

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raym
Posts: 1263
Joined: Sat Apr 16, 2011 11:08 am
Location: South Central PA

Re: New cancer blog

Postby raym » Fri May 17, 2013 9:41 am

I didn't see any place to comment on your blog but I wanted to note something. You had mentioned that they can use the port or CT contrast. My experience is that does not happen as the tech doing the injection is not trained on the use of a port (and there are several different kinds). Thanks for sharing the blog!
3/11 IIIC +/FOLFOX
4/12 HIPEC
6/12 Chmo/Rad
9/12 XELIRI+Avast/Zltra
9/13 Plvic Absc,stpd chemo
11/13 Tumr rmvd frm Lap Port incis
12/13 Xeloda
1/14 Cardiac Issue no Xeloda/5FU
3/14 Irinotecan
6/14 Stopped chemo
8/14 Clin Trial
9/14 Infectn - Stpd Trial

Oneeyeddog
Posts: 101
Joined: Sat Apr 06, 2013 11:06 am

Re: New cancer blog

Postby Oneeyeddog » Fri May 17, 2013 10:01 am

Hi Raym, thanks for your note. That's what they told me -- that they could use it for CTs, but perhaps you're right that in the end they'll just do it the normal way. No biggie.
Colon cancer Stage 3c (dx April 2013) at age 36
Resection and temp ileostomy (4/17)
12 rounds of FOLFOX (May-Oct 2013)
NED (August 2014)
http://www.theoneeyeddog.com

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Guinevere
Posts: 3358
Joined: Tue Oct 11, 2011 4:19 pm
Location: NE TX

Re: New cancer blog

Postby Guinevere » Fri May 17, 2013 10:52 am

Good job on the blog! I'm looking forward to reading the your next entries.

My understanding is a trained nurse can access the port for contrast CT if what you have implanted is a power port. Alas, we found out mine isn't. But blood draws as well as chemo through the port is a heaven sent thing to me. I can't imagine doing it any other way!

God bless ~
Guinevere
Hrt atk - Feb 11
CRC4 DX - Apr 11
APR liver rsct, procto - Jul 11
Folfox/Avastin - Sep 11
Xeliri - Nov 11
Iritux - Jun 12
Break - Jan - Mar 13
Iritux - Mar 13
Stivarga - Aug 13
Folfiri - Oct 13
Exhausted treatment options - May 14

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lohidoc
Posts: 454
Joined: Tue Aug 09, 2011 6:37 pm

Re: New cancer blog

Postby lohidoc » Fri May 17, 2013 12:04 pm

Good thoughtful writing. Don't shy away from exploring the darker sides of this disease. I know we are all meant to be brave, battling, positive and so on, but it is not like that - how could it. Face this disease in all its aspects - sunlight and shadow.

I tried to follow you on Tumblr - had to sign up, computer now deluged with celebrity pictures, fashion whatever and ground to a halt.

Good luck.
"Half of what I know is wrong. I don't know which half."

Age 56
Dx 19/7/11
R. hemicolectomy 25/7/11
IIIc, 7 / 23 nodes,
no mets
Folfox 21/8/11
CT Scan 6/3/12 NED
CT Scan 21/6/12 30+ lung mets, 2 retroperitoneal tumours
marcdu4.wordpress.com

ams5796
Posts: 2298
Joined: Fri Feb 06, 2009 10:07 am

Re: New cancer blog

Postby ams5796 » Fri May 17, 2013 12:59 pm

I really like your blog. Great writing and you hit on some really interesting points.

I really could relate to the feeling of being so out of the loop of life when I first got diagnosed. I can remember walking around the mall and being so sad? envious? something? when I saw all the folks just living their lives. The moms pushing the baby strollers, people laughing, shopping , eating...it all got to me. I felt like I lost the innocence of my life. I knew things would never be the same. I guess that's why we cancer folks are always talking about "the new normal."

I look forward to reading more.


Ann
Stage 3C (or 4?) Rectal Cancer 01/07
2/10 lung mets
3/11 VATS
6/11 VATS
7/13 lung met
2/14 SBRT
NED 8/14
5/17 scan and MRI found treated spine met

Busymamaof3
Posts: 193
Joined: Fri Sep 07, 2012 1:37 pm

Re: New cancer blog

Postby Busymamaof3 » Fri May 17, 2013 3:04 pm

Yes, I too find myself looking at the world around me sometimes and feeling like I am a distant observer. Other times I will be out and think to myself that no one would pick me as a cancer patient. Just a woman in her 40s going about her business.
Dx Stage IV CRC 8/12, 40yrs old
3 kids under 10
10/5/12 1 met to liver
folfox w/avastin 4 rds
Folfox alone 4 rds
HIPEC/CRS 2/13/13
PT3N1cM1
Back on Folfox 3/12 - 4/23/13
It is back 8/23/13
FOLFORI 9/13-1/14 cea up
Folfox 1/13
Hipec w crs #2 2/27/14

Grace14
Posts: 418
Joined: Mon Oct 24, 2011 7:42 pm

Re: New cancer blog

Postby Grace14 » Fri May 17, 2013 3:22 pm

I can so relate! I would look around and see people enjoying their lives and would be so envious! I was so jealous of old people I wanted to get old like them! It's so funny how we all feel the same way!

I remember for my SIL's Bday a bunch of us went out to eat, and I felt like I didn't belong there! I had to leave I was so sad! Nobody will ever know unless in our shoes how it feels to be diagnosed!

Great blog!
Diag Stage 2a R/C April 2010 at 38
Rad/chemo 6 weeks
Apr surgery July 2010
Folfox 4 months
Jan appendix removed
Feb diag papillary thyroid cancer no treatments stage1
Ned so far!!!
Mother of 4 boys 21 18 11 8

manders
Posts: 53
Joined: Sat Jul 13, 2013 7:32 pm
Location: Pacific Northwest

Re: New cancer blog

Postby manders » Fri Aug 16, 2013 1:12 am

Thank you for sharing your thoughts and experiences in your blog. I am just at the beginning of this journey and did find it interesting. Your post about diet cracked me and my husband up since we have been in the process of improving our own diets.
Mom to 2 (2008 and 2018)
Diagnosed at 34, 7/9/2013
Sigmoid colon resection 7/24/2013; Stage 3b; T3 N2a; 4/14 lymph nodes
Folfox 8/28/2013 - 2/7/2014

NWgirl
Posts: 6659
Joined: Sat Feb 02, 2008 3:24 am
Facebook Username: Belle Piazza
Location: Battle Ground, Washington

Re: New cancer blog

Postby NWgirl » Sat Aug 17, 2013 4:24 pm

I couldn't access the site - not sure why I was blocked (?). Blogging, what little I do, is very therapeutic for me - I hope it helps you in your journey as well. And as for the port, they use mine for contrast all the time. I have a power port. I do have to make arrangements in advance so that there is someone there to access it properly - sometimes the nurse in the imaging dept. isn't trained on how to access the port. I'm so tired of getting poked multiple times by nurses trying to find a vein I now INSIST that they use my port. I have to raise a fuss sometimes, but it's worth it to use the port vs. my arm - or worse yet, my hands. Ouchy.
Belle - "Don't Retreat - Reload"DX 10/07 Stage III Rectal
Surgery 11/07; 27 of 38 nodes
Perm Colostomy 8/11
12/10 recurrence lungs & LN's
VATS Jan 2011
Radiation Oct 2013
Chemo for Life
2012 Colondar Model

Val*pal
Posts: 860
Joined: Sun Feb 10, 2013 1:24 pm
Facebook Username: Valerie Barkus Kantner
Location: Metro Detroit, Michigan

Re: New cancer blog

Postby Val*pal » Sun Aug 18, 2013 3:32 pm

I just read some of your blogs today, and I am hooked! You're a fantastic writer who is willing to share some of the darker sides to struggling with cancer. Thank you so much. Though I kind of get what my husband is going through, I know I don't truly know, so your blog gives me more insight. My husband is a bit of the strong, silent type who doesn't always share his fears and worries. This helps. I'm looking forward to more of your blogs. I also bought your Kindle single. :D
DH dx'ed May '11, age 62
Jul '11: resection Stage IV
10/11: 6 mo Folfox
8/12:thyr canc, surg/tx
2/13: peri mets
2/13: Firi/Avas
6/13: Ok
8/13: break
10/13: Lung, peri, mets
10/13: Firi/Erb
1/14: Erb Fail; spread
5/14: Tx stopped
6/20/14: At rest


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