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Posts posted by michellep
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Please let us know what happens on your next appt! ((hugs))
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Great news! Keep up the good work and let us know how you're doing!
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Linda,
I am so sorry you are having to deal with so much. I don't have any advice on a good place for treatment but I'm sure there are members here who can help.
Please keep us updated on how you're doing ((hugs))
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I hope you can find out why this is happening to you! Please keep us updated ((hugs))
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I was so sorry to see this update. My thoughts and prayers are with you ((hugs))
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I too am sorry to hear this! There is no doubt you are a fighter snowflake! Please keep us updated ((hugs))
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I too am hoping you get some good news ((hugs))
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Hello Debbie! I am so sorry about your diagnosis but am glad you found all of us here. I am not familiar with small cell lung cancer. My husband had non-small cell. However I am very familiar with the insurance companies and the work it takes to get them to help pay for needed tests and medications. I too had Blue Cross of California and every time I turned around they were denying us. My husband was prescribed Tarceva and we had to pay for it ourselves. It was over $3,000 a month. It's just not right!
It seems you are a very strong young woman and I am happy you have your husband and daughter near you.
Please keep us updated and also read our other forums. There are many survivors out there! If you have questions......please ask away ((hugs))
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I too am hoping it's just scar tissue. Please keep us updated ((hugs))
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Thanks for the update! Yes, the brain scan is great news! Please let us know when you hear about the biopsy ((hugs))
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I am so glad Donna was able to post for you! There are many survivors here. Please browse our other forums for a wealth of information and support. Also, if you have questions or concerns please ask!
I say....Celebrate her Birthday
Keep us posted ((hugs))
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I too am very glad that you found us but sorry for the circumstances. I myself am not familiar with the type of cancer your partner has been diagnosed with but I'm sure others will follow me who are. Please browse through our other forums and I'm sure you'll learn a great deal. ((hugs))
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I agree with Randy. I was also a caretaker and I felt like there wasn't enough time to worry about myself. I didn't have any help and survived on approx 3 hrs of sleep a day. It WILL take it's toll on you. I hope you can reach out and get some help somewhere. Love is a powerful tool when we are caring for a loved one and we tend to push ourselves to the limit, but eventually it will catch up with you.
Please let us know how things are going for both of you ((hugs))
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I too am glad you're able to start with a clinical trial! Please let us know how things go for you ((hugs))
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Wonderful news!
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I too hope the doctor can explain this. Please let us know ((hugs))
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My husband had the same diagnosis as your neighbor and he also took the came chemo combination. The chemo combo was too harsh on his system so they changed him to Tarceva. Please let us know how your neighbor is doing.
I'm sure others will follow with more information for you. ((hugs))
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I am so sorry that you're dealing with so much all at once. I'm glad you found all of us here though. Please browse through our forums and you will find a wealth of information and if you have any questions, please ask. Keep us updated please ((hugs))
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Hello Ryan and welcome. Your story is really inspiring and you sound like a great guy! Please keep up the good work and keep us updated! ((hugs))
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Hope both you and your sister are doing well! ((hugs))
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The news of reduction is great! Keep us updated ((hugs))
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I agree! Please ask again and if you aren't happy with this doctor find a second opinion. My husband's doctors were horrible at communication. Please let us know what you find out! ((hugs))
Newbie - hope this is where I introduce myself. confused.
in INTRODUCE YOURSELF!
Posted
I too agree with Randy about the notebook. I'm happy that you're doing well and hope you continue to do so. Please keep us updated ((hugs))