[Lost]

I've been away from the message boards for a while and just saw your post. My heart truly goes out to you and I hope you can get some answers soon.  Please let us know how things are going.  Don't forget to take care of yourself too.....that's also very important.  ((hugs))

[Where to start]

Hello Karen!  I have heard about Opdivo having excellent results!  Please let us know how it does for you ((hugs))

[Hi]

Hello Rain!  Please let us know what you find out and if you have questions or just want to vent.....we are here!  ((hugs))

[Hoping for more time]

Reach out to us anytime dear one!  

[Hoping for more time]

My heart breaks for you Jan!  Please look into the lifeline partner program.  I wish it had been available for me when I was taking care of my husband.  If you ever need to talk or ask questions we are here for you also ((hugs))

[3aSherie Update: 1 year later!]

WOW.......just WOW   I am so very happy for you and hope the next scans are just as good for you!

[My Friend has Stage IV NSCLC]

I agree that it is most likely a combination of shock and denial.  Give your friend some time and when he's ready to share his feelings just be there for support.  Please keep us updated ((hugs))

[Medical Marijuana question]

I myself have not experienced it but I do hear many good things about medical marijuana being very helpful in dealing with the side effects related to cancer.  If you visit one of the dispensories in your area they can show you options for edible types you might be about to use such as brownies etc.  Please let us know if you decide to try something and how it works for you.

[Not sure if I have cancer but...]

The "unknown" and having to wait for answers in awful I'm sure.  I agree to stay away from Google.  There is too much conflicting information out there. I would suggest you make a list of questions and be prepared to ask away when you see your doctor.  Please let us know what happens.  ((hugs))

 

[Medicare plans....Help!]

I've heard the supplement "Part G" is the best.  I don't know if they cover the drugs you need but it's work looking into.  I have a neighbor who is receiving chemo (not sure which combo) and it's being paid for.  Her annual deductible is only $149.  That's excellent! 

[New member]

Hello Baker!  I myself have no experience with  Vinovallbin , however, I'm sure someone will follow me who does.  Welcome to our site and please keep us updated on your progress ((hugs)

 

[My loved one has lung cancer]

Hello Randii.....I am sorry to hear about your friend.  You said he doesn't have money for treatment.  Has he checked into some type of Medicaide perhaps?  There must be some type of resources that can help.  No treatment at all is not good.  Please keep us updated!

[How do you do it?]

I'm so sorry you are dealing with so much right now.  I was a full time caretaker for my husband with no help from anyone until I was forced to call hospice.  My advice to you dear one is that you can't take care of everyone else without taking care of yourself as well!  Please keep us updated and I wish the best for you.  ((hugs))

[Newbie!! Goes easy on me!!]

I certainly understand your concern and your questions.  I would suggest writing down "all" of your questions before seeing your doctor.  You're dealing with a lot right now and you need some answers.  Please keep us updated ((hugs))

[Stage 4 lung cancer]

Tarceva is a pill form of chemotherapy.  Your doctor should tell you when and how it's taken as well as any side effects. My husband had a rash from it which is common but can be treated.  Never hesitate to ask your doctor LOT"S of questions.  That is indeed their job.  

 

I'm sure others will follow with more information for you.  Please keep us updated.  ((hugs))

[Stage 4 NSCLC]

I'm so sorry to read your post but I am glad you are here.  I myself don't know anything about Optivo or side effects but I'm sure someone will follow me who can help.  Please keep us updated ((hugs))

[Stage 4 adenocarcinoma]

Hello and welcome to our site.  Can you tell us a bit more about what you've been through?  Have you started any treatments and what are they?  I'm sure others will follow that can help you so keep us updated.

[Stage 2B adnocarcinoma - lobectomy and facing chemo next week]

Hello Karen and welcome to Lungevity.  I'm sorry about your diagnosis but glad you are here.  I myself don't have any experience with the chemo combo you will be taking but I'm sure someone will follow me who can help.  Please keep us updated and let us know how you're doing!  ((hugs))

[Newly diagnosed questions to ask]

Just thought this might help prepare some of you when you're newly diagnosed. 

[My journal]

During my husbands illness with lc I kept a journal of daily events.  When he went to heaven in Oct 2009 a made a few entries afterward and put it away.  Since then I sold our home and moved away.  I hadn't seen that journal in almost 7 years and came across it today.  It brought back an avalanche of emotions and it feels like his passing just happened yesterday.  Today is a bad day for me

[Newly Diagnosed- rough time]

Hello Judy!  I'm so sorry to hear about what you're dealing with.  Please keep us updated and if you have any questions.....ask away!  ((hugs))

[Hi]

If you have questions or just want to vent......please do so.  Keep us updated ((hugs))

[INTRODUCE YOURSELF]

I would always recommend second opinions!  Please keep us updated ((hugs))

[radiation to brain]

I am so very sorry all this is happening to you!  I myself have no experience with brain radiation, however, I am sure someone will be here soon to help answer any questions you have.  My thoughts are with you and I hope to see some good news coming soon!  ((hugs))

[Stage 3a]

Hi Debi!  Many people have no symptoms but thankfully you had that x-ray taken.  Hope your treatment goes smoothly and glad your husband will be going with you. Please keep us updated!  ((hugs))