E900030 Posted July 27, 2007 Share Posted July 27, 2007 Hi My name is Deb my husband John was diagnosed with NSCLC on March 4,2007. On March 6, he was admitted to hospital with pneumonia He was ther 25 days. He has just reently started radiation and chemo 15 rads down and 3 chemo. I have recently started a new job Hubby pushed me TO GO FPR IT!!! I am having difficulty concentrating on learning it,but I have to do it since we have not received short term disability money for since May. I hope I can cope with all this confusion It feels like we are on a rollercoaster with more downs than ups. Thank you for listening to me vent Quote Link to comment Share on other sites More sharing options...
recce101 Posted July 27, 2007 Share Posted July 27, 2007 Hi, Deb, welcome to the LCSC! I'm sorry to hear about your husband, but glad you found us. Of course you're super-busy right now with a new job on top of everything else, but please, as soon you get a chance, give us more details on your husband's condition -- what cell type of NSCLC, stage, symptoms, specific chemo agents he's getting, etc. That will help us give you solid, useful information whenever you have questions along the way. The best to you both, and Aloha, Ned Quote Link to comment Share on other sites More sharing options...
beatlemike Posted July 27, 2007 Share Posted July 27, 2007 Hi Deb and welcome,Im so sorry about your husband.I hope you find help and support here.Prayer being said for the both of you. Mike Quote Link to comment Share on other sites More sharing options...
ernrol Posted July 27, 2007 Share Posted July 27, 2007 Deb, Welcome to the site. Please keep us poted. Stay positive, Ernie Quote Link to comment Share on other sites More sharing options...
MsC1210 Posted July 27, 2007 Share Posted July 27, 2007 Hello Deb and welcome I am sorry you had a reason to find a site like this, but am glad you have joined us. Please feel free to vent any time you need or want to. We are here for you and will be glad to listen as well as offer you advice and support. When you can, filling in the profile will give us an idea of what treatments your husband has had and is currently going through. Just click on my profile at the top of the page and it is pretty simple from there. Let us know how we can help... Christine Quote Link to comment Share on other sites More sharing options...
Ry Posted July 27, 2007 Share Posted July 27, 2007 Welcome to the wives club no one wants to join. I am glad your husband has recovered from pneumonia and is in treatment. I am sure it is hard to deal with the new job and being a caregiver. Keep us posted on how he does. Rochelle Quote Link to comment Share on other sites More sharing options...
fillise Posted July 27, 2007 Share Posted July 27, 2007 Deb, Welcome to our little corner of the Internet! Feel free to ask lots of questions. Someone on the board has likely experienced whatever you want to know about. The support here is tremebdous. Susan Quote Link to comment Share on other sites More sharing options...
hawkeye Posted July 28, 2007 Share Posted July 28, 2007 Sorry you had to find us but glad you did. There is alot of information and help on this site. I know this from personal expierence. Remember that you are not alone at anytime cause we are always here.Prayers for you and your husband. Quote Link to comment Share on other sites More sharing options...
jeiland Posted August 8, 2007 Share Posted August 8, 2007 welcome to the site and hang in there. I vent sometimes too. Take care and keep us posted Quote Link to comment Share on other sites More sharing options...
Kaffie Posted August 8, 2007 Share Posted August 8, 2007 Deb, Welcome...It sounds like you are very busy right now, and confused I hope you come and read up on some of the profiles, you will see that there are so many survivors here doing great, many for years and years. Quote Link to comment Share on other sites More sharing options...
Maryanne Posted August 11, 2007 Share Posted August 11, 2007 Hi Deb, Welcome here. So sorry about the news about you hubby. So many here have walked in your shoes including myself. I know who scared you must be. This site has been a G-d sent for me. I know we can help you through this as we understand about rollercoaster rides. You just want it to stop so you can get off, but it just keeps going and going. It is a newending ride, but it will slow down and become more tolerable as you get use to the "new norm". It will never be the way it was but it will get better. Sometimes work is really good as it helps take you mind off your problems for awhile. I also know at the same time how hard it is to concentrate when your mind wonders back to the situation. Also being a new job it must really be hard for you But do this for him as well as yourself for he is the one who pushed you to "Go for it". Please place a profile that will appear at the bottom of your post, so we can understand what kind of LC he has what his staging is and what treatments he is getting. Just click on my profile at the top of this page. Then go to signature at the bottom of the profile page and add in his history. We are always here for you. Please know the LC is not a death sentence. There are so many new treatments out there. Keep us posted on his progress. Good luck with your new job. Maryanne Quote Link to comment Share on other sites More sharing options...
IAAM Posted August 13, 2007 Share Posted August 13, 2007 Welcome to the site. You will find a lot of support here, I have. Sorry to hear about your husband, please keep us posted. I vent all the time, thankfully many will listen! Good luck with your new job. I can imagine how hard it is to concentrate. I've experienced this many times, but not with a new job! So I wish you and your husband the best. -E Quote Link to comment Share on other sites More sharing options...
barbara5452 Posted August 18, 2007 Share Posted August 18, 2007 Hi Deb, welcome and hope you and your hubby are having a good day today. I know how it is feeling pulled two different ways with work and health issues. Just go with your heart and do the best you can. Quote Link to comment Share on other sites More sharing options...
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