Jump to content

I'm happy to be here


Starkey

Recommended Posts

Hello All,

I'm glad to be a part of this group.  I heard about it on a FB post and thought it would be beneficial for me.  I was diagnosed in September with non small cell and they removed my left lung on October 19th.  I am now in treatment once a week for 4 months.  The chemo has been very challenging and have been in bed most of the time.  I live alone and grateful that I have friends that at times take care of me and feed me.  After my chemo, I have a month of rest, then 6 weeks of radiation.  That I my fear, because there is a possibility that I might be oxygen dependent.

My faith is strong and I am looking for possible groups and persons who would want to connect and share stories and recoveries.

Thank you.

Link to comment
Share on other sites

Hi Starkey,

Welcome to the Lung Cancer Support Community! I am glad you have some friends that come by and that your faith is strong. I wanted to let you know that Savor Health is a great resource that sends you healthy meals. http://www.savorhealth.com Also we can conenct you to a 1 on 1 personal LifeLine mentor that can talk to you. Here is the link to get started if you are interested http://www.LUNGevity.org/LifeLine

 

Cindy

Link to comment
Share on other sites

Starkey,

 

I once feared I'd be dependent on oxygen also.  I had a home 02 generator for a time after my lung was removed, then once again after my second line chemotherapy.  I used the rented machine for a short time and as I recovered, my 02 levels climbed and stayed constant above 92 percent.  So I went off oxygen.

 

I've found this pattern consistent with a number of lung cancer survivors.  But, some need it for extended periods, indeed for life.  Do I understand you are receiving both chemo and radiation after surgery?  Post surgical chemo is expected but conventional radiation is not.  Did they find additional metastatic disease during your surgery?

 

Stay connected with us.  You'll have many questions and we might provide useful advice and insight.

 

Stay the course.

 

Tom

Link to comment
Share on other sites

Starkey,

 

   I am oxygen dependent and I totally understand your fears of becoming oxygen dependent. It sucks...to put it nicely.We are so glad you found us. I am so sorry the treatments are so rough. I was diagnosed in September as well with Stage IV Non Small Cell. Keep your faith...that is what will help you get through this. The Life Line program, as Cindy mentioned, sounds like it would be a great fit for you!

Link to comment
Share on other sites

are you getting anything with your chemo to help energy levels and nausea??? sorry you have to be here but glad you are so we can help ya out!!!

Link to comment
Share on other sites

Join the conversation

You can post now and register later. If you have an account, sign in now to post with your account.

Guest
Reply to this topic...

×   Pasted as rich text.   Restore formatting

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

×
×
  • Create New...

Important Information

By using this site, you agree to our Terms of Use.