← Return to Mass on lung and lymph nodes
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Replies to "Hi Angela - my name is Maureen. I live south of Detroit and about a half..."
You are so fortunate that the doctor is going to have the pathologist there and everything! That is great. I have to wait while this doctor is on vacation, then when he gets back meet with him again, THEN set up the brochoscopy. Come on! I don't know if I'll be able to stand any procrastination! You are NOT a baby!! You are scared, terrified, but maybe the news will be a little bit better than you think it will be?! Just because of the mass, that doesn't mean it's all cancer either. Mine is large also, and it's odd I haven't really had any symptoms and still don't, but my blood work is off the charts! I can also feel that mass or something is in there now if I take a real deep breath sometimes...I think it's because it got irritated when it bled and I spit up blood. Today I found out that I need to have iron IV infusions because my levels are at 12 and they should be between 50-170, I just can't bear the thought of horrible news either!!! I usually crack up during the day at least a couple times, but I know that's normal. We are both terrified and we are human so I think we are both doing the best we can right now in a terrible situation!!!
Also in Milwaukee here I am with the Vince Lombardi Cancer Clinic and I am hoping they have clinicals and stuff but I dont' really see that there are any Research Hospitals near me. My sister is a nurse and she told me to get some Ivermectin and start taking that 1 time a week. There is some research that it can help cancer patients or stop the cells from dividing. I've tried to read up on it, but I would eat a centipede if they said it could help!
I know there there’s been some improvements in treatment in the last few years and that’s why I’ve chosen a research hospital to have access to clinical trials if needed.