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BostonButt49
Posts: 4
Joined: Sat Sep 03, 2011 10:39 am

new member

Postby BostonButt49 » Sat Sep 03, 2011 10:50 am

I have just joined as a member. I have had colon cancer surgery already. Dealt with multiple mets in liver, brain and lungs. Having liver resection next week. Looking for support and someone to talk to. Heard about the forum from my best friend who has a family member going through this.

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tdsamal
Posts: 619
Joined: Tue Dec 29, 2009 12:49 am
Facebook Username: malby.tammy
Location: Salem Oregon

Re: new member

Postby tdsamal » Sat Sep 03, 2011 12:44 pm

Welcome,
Glad you found us. You will find this forum very informative and knowledgeable. We have many people that can share their experiences with you. I like it because everyone on here knows what you are going through and can understand how you feel. It is my place to go when I have questions and want answers. It sounds like you have alot going on and I'm sure like all of us you feel very overwhelmed. Tell us a little about yourself. Sounds like you might be from Boston?
Tammy
Dx st IV CC & colon resection 11/09
Way to much to list
Last recurrence December 2017

Seriously, WTF?
Posts: 602
Joined: Wed Nov 17, 2010 10:48 pm

Re: new member

Postby Seriously, WTF? » Sat Sep 03, 2011 12:50 pm

Welcome, feel free to come here any time day or night.Someone is always around to help you. hang in there!
ALWAYS IN MY HEART!
5/7/2013

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

Re: new member

Postby CRguy » Sat Sep 03, 2011 4:03 pm

Welcome to the best forum nobody wants to have to join !
Feel free to contribute or engage, to whatever degree you feel comfortable, lots of good folks here.
Sending positive vibes and best wishes your way.

Oh, and if you are from Boston.....we want the Stanley Cup back ! :mrgreen:

In Harmony
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

BostonButt49
Posts: 4
Joined: Sat Sep 03, 2011 10:39 am

Re: new member

Postby BostonButt49 » Sat Sep 03, 2011 5:09 pm

Hello to everyone. I live near Boston and I was DX in April 2011. Had Colon resection in late May and radiation ablation in lungs and gamma knife radiation on brain in June. Developed pneumonia and was in a bad way for a few weeks but doing better now. I am having a liver resect done next week. Believing it will take care of the remaining mess. Could not have made it through without friends and family. I have had to be out of work since May and it is a challenge.

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CheeseHead
Posts: 1171
Joined: Sat Jul 31, 2010 2:36 pm
Location: Netherlands

Re: new member

Postby CheeseHead » Sat Sep 03, 2011 5:42 pm

Hi Butt,

Welcome to the forum. It's a great place to vent, get information, or just talk.

Good luck with your liver resection next week. I found out my first was scarier in advance than it really turned out to be. The second was... easy... relatively speaking of course.

Hang in there,
Cheese
    2008
    10 Stg 4 colon srgry
    12 Xelox/Avast
    2009
    05 Liver srgry
    -12 Xelox
    2010
    05 Xelox
    08 Iri/Vect
    11 Liver srgry
    2011
    01-05 Iri,Vect,Xeloda
    09 CyberKnife
    2012
    03-07 Ph I trial
    08-11 Regorafenib
    2013-
    Xeloda
    Vecti
    Iri
    Xelox

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Phuong
Posts: 1508
Joined: Mon Jun 14, 2010 10:43 pm
Facebook Username: Phuong Ly Gallagher

Re: new member

Postby Phuong » Sat Sep 03, 2011 5:48 pm

Welcome! I had 2 liver resections - one partal and the second one took the left lobe of my liver. While not as easy as the VATs resection for the lung, it was not to bad to recover from. I did lots of walking and you'll find exercise threads (not to mention the adventures of cycling and hiking) here that encourage us all to stay as active as we can. It certainly helped me with the healing process.

Go Sox!!!
Phuong
Phuong
http://sonofamotherlessgoat.net/
dx'd Stage III Rectal (T3 N1 M0)
Now Stage IV mCRC

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Bill5107
Posts: 1376
Joined: Sun Jul 11, 2010 5:50 pm

Re: new member

Postby Bill5107 » Sat Sep 03, 2011 9:55 pm

Welcome aboard neighbor! (I'm 2 hours from Boston) Sucks that you need to be here of course.

I've found this to be a great online home through my cancer journey. Great resources here and folks always willing to help where they can.
2010-07-02 Dx rectal cancer (Stage 3)
'-07-21 Chemoradiation
'-10-13 APR surgery, 10/18 nodes still active
'-11-22 12x2wk rnds FOLFOX
2011-12-07 Mets X-P
Don't retreat, reload!

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mum
Posts: 37
Joined: Sun Aug 14, 2011 12:04 am
Location: Christchurch New Zealand

Re: new member

Postby mum » Sun Sep 04, 2011 4:58 am

Kiora from New Zealand which is our welcome.You will get so much support from this forum and we all have a connection to our world wide friends.
My daughter is going through her experience with this colon cancer issue and we both enjoy sharing the friendship through this site.
Lots of earthquakes happening in Christchurch at the moment and has been going on for a year now.We live 30 kms south of the city.
Rachael said that for a cancer person everyday is an earthquake.She is so right.
Do hope you doing o k at the moment and we send you a big hug from KIWI land Cheers Rachael and her mum

BostonButt49
Posts: 4
Joined: Sat Sep 03, 2011 10:39 am

Re: new member

Postby BostonButt49 » Mon Sep 05, 2011 4:57 pm

Thank you everyone. It is good to know there is somewhere to go for information and conversation.
I have my liver resection in the morning at 7am. Pretty anxious. :(

Novamomof2
Posts: 51
Joined: Mon Jul 04, 2011 8:37 pm
Facebook Username: michelleantoniomartin
Location: Fairfax, VA

Re: new member

Postby Novamomof2 » Mon Sep 05, 2011 5:56 pm

Welcome!
I just started posting on this forum too! Have any questions you need answers to, this is the place!
'10: Xel & Rx for 31 cyc/lung wed/resct, Tmp ileo.2010, trial fr 11/10-10/11, 10/2011 LN chest area, new node left clavicle,Thor surg, 12/11; 8 or 9 nodes, cancer , Xel & Avs 1/12 to 9/12, Cyber for neck nodes 2013,MEDI-565 trial

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Anji
Posts: 506
Joined: Mon Jun 14, 2010 12:07 pm
Facebook Username: pray for larry edge
Location: Kentucky

Re: new member

Postby Anji » Mon Sep 05, 2011 6:14 pm

Welcome! You will find a wealth of information and support here. Know that I am praying for your liver resection in the morning. And please, when you are able, be sure to update us and let us know how you are doing!

Anji
Anji
Wife to Larry, Stage IV Colon Cancer, with mets to liver
Diagnosed 1/10 at age 44
Folfiri + Avastin 2/10 to 7/10
Liver resection and ablation 9/10
Numerous mets to lung and liver 1/11
Folfox + Avastin 2/11 to 6/11
Folfiri + Vectibix 6/11 to ???

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Kathryn in MN
Posts: 2970
Joined: Mon Sep 14, 2009 12:25 am
Facebook Username: Kathryn Finn-Blume
Location: Minnesota & Mexico
Contact:

Re: new member

Postby Kathryn in MN » Mon Sep 05, 2011 6:46 pm

Welcome! Sorry you need to be here, but glad you found us since you do. Best wishes for tomorrow's surgery and your recovery. You've been through a lot already - you sound like you are very tough and will get through this final round of surgery/treatment well. Please check back and update us on how you are doing once you feel well enough.
CRC AUG09 Age 47
Sig Res T4a N2a Mx, KRAS mut codon13
Mets bones & nodes
FOLFOX, FOLFIRI, Avastin, Radiation
Irinotecan, Zaltrap & STAR RFA
APR13 pleurisy & ascites - more chemo & draining
http://www.caringbridge.org/visit/kathrynblume


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