CSN Login
Members Online: 1

You are here

Great news!

CSN is getting an upgrade. All of your posts will still be here, but the website will have a new look, new features and be mobile-friendly. To prepare for the changes, the site will be down briefly at the end November. We’ll continue to provide updates as we get closer.    

I’m new

Clyoung300's picture
Clyoung300
Posts: 1
Joined: Dec 2020

Was diagnosed 4 months ago. Do not understand or know how to handle this or where to get support. This is the craziest worst ride ever.

Bay Area Guy's picture
Bay Area Guy
Posts: 521
Joined: Jun 2016

Welcome to the group, although none of us ever wanted to join.  It would be helpful to know a little bit more about your diagnosis, like how it was diagnosed, approximate size and location, and what your doctor(s) have said about it.  You're in the right place for support.  The folks here are all very caring and very giving.  The main piece of advice I'll give you is to NOT search the internet for information.  Much of what's out there is dated and, frankly a lot is just plain wrong.  You can drive yourself crazy (and I know that from first-hand experience) trying to navigate the internet regarding this condition.  Just know that absolutely amazing progress has been made in treatments, both surgical and non-surgical.

icemantoo's picture
icemantoo
Posts: 3359
Joined: Jan 2010

Folloe up in the Bay Area Guy's questuitions so we can give tou a hand.

 

 

 

 

 

icenabtoo

stub1969's picture
stub1969
Posts: 931
Joined: Jul 2016

Four months....that's a long time with the feelings that come with being newly diagnosed.  I hope you have a support system around you to help ease the anxiety and worry.  For now, Bay Area Guy provided some of the basic questions that we need answers to in order to provide advice and support.  We've all been through the diagnosis and follow up procedures that come with RCC.   I'm hopeful our experience can be helpful to you.

Take care--

Stub 

Deanie0916
Posts: 439
Joined: Nov 2016

You will find good information and support here. You're not alone.

Scottie22's picture
Scottie22
Posts: 86
Joined: Apr 2013

There is a wealth of information and support on this site. All of us have had the diagnosis experience and have got help here. There are many different experiences and no one size fits all. It was a massive shock to me also but members immediately spoke up with help and advice. I did not feel alone or lost as I had done. My left kidney was removed almost 8 years ago and I now have a yearly follow up the last one in August of this year and to date all is still well. Thinking of you, we've all been there.

Subscribe to Comments for "I’m new "