Hello from Lee in London - Stage IV-b
LeeinLondon
Member Posts: 103
Hello everyone;
My name is Lee and I have EC with mets to the liver and lymph nodes. My wife is Daisylin in these forums, and BTW it's London Canada, not England
I've been lurking for a few months and want to thank you all for contributing to a very valuable resource, and how empowering to find a focused forum populated by such courage. I also think it's important for patients to learn of the experiences of others; I know that before diagnosis the guy in the wheelchair was a "them"... the man with the medical appliance on the subway was a "them". At the moment of diagnosis we are all very clearly reminded that there is just "us", and we're all in this together.
I think that forums like this help patients and caregivers to act more as a team, I know that Chantal would go stir crazy if she wasn't actively involved in my care. Having a curiosity and a determination to sift through all the information overload out there really helps.
So helloto all, and I look forward to contributing to the EC forum.
- Lee
PS: My story can be found at:
www.yurbo.com/leescancer
My name is Lee and I have EC with mets to the liver and lymph nodes. My wife is Daisylin in these forums, and BTW it's London Canada, not England
I've been lurking for a few months and want to thank you all for contributing to a very valuable resource, and how empowering to find a focused forum populated by such courage. I also think it's important for patients to learn of the experiences of others; I know that before diagnosis the guy in the wheelchair was a "them"... the man with the medical appliance on the subway was a "them". At the moment of diagnosis we are all very clearly reminded that there is just "us", and we're all in this together.
I think that forums like this help patients and caregivers to act more as a team, I know that Chantal would go stir crazy if she wasn't actively involved in my care. Having a curiosity and a determination to sift through all the information overload out there really helps.
So helloto all, and I look forward to contributing to the EC forum.
- Lee
PS: My story can be found at:
www.yurbo.com/leescancer
0
Comments
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Welcome Lee,
Chantal
Welcome Lee,
Chantal displays a great deal of compassion and insight in her post. It’s a pleasure to have you both on the network.0 -
WELCOMEbirdiequeen said:Welcome Lee,
Chantal
Welcome Lee,
Chantal displays a great deal of compassion and insight in her post. It’s a pleasure to have you both on the network.
Welcome to our "club" Lee. I've read many of Daisylin's posts and am always encouraged by her inputs. Glad you finally got on board. Lots of good people here with a LOT of advice, suggestions and experiences. I was blessed to find this site after my diagnosis.0 -
Welcome to our little EC family
Lee,
It is great to see your post. I know you and Chantal have had your share of challenges over the last few months. Many of us who have had this disease know well the ups and downs of chemotherapy, waiting for the results of tests, and getting up each morning wondering how today is going to go.
I guess we are members of the "one day at a time club".
I will be praying that things go well for the placement of your feeding tube and it brings relief.
Best Regards,
Paul Adams
McCormick, South Carolina
DX 10/22/2009 T2N1M0 Stage IIB
12/03/2009 Ivor Lewis
2/8 through 6/14/2010 Adjuvant Chemo Cisplatin, Epirubicin, 5 FU
6/21/2010 CT Scan NED
3/14/2011 CT Scan NED
Life may not be the party we hoped for, but while we are here we might as well dance!0
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