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Mass on lung and lymph nodes

Lung Cancer | Last Active: Mar 5 9:06am | Replies (149)

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@detroitmom23

Hi Angela - my name is Maureen. I live south of Detroit and about a half hour away from Ann Arbor University of Michigan Hospital where I’m being seen. There’s only a few people who know what I’m going through and my husband is glass half full and I’m glass half empty - he tries to keep things positive. I’m glad in a way but sometimes I feel like he doesn’t know what it’s like to feel like I’ve been handed a death sentence. Sometimes I get so uptight , especially in the evening that I jump in the car and just ride around. We are not abnormal to be so upset. When I got my MRI last week I was in a women’s changing room getting into gown met two other women. One appeared to be about 50 and said she’s been dealing with breast cancer for several years. She was crying because of claustrophobia and being inside of MRI. The other lady was probably in her 70’s and also crying. She lost her husband last year and had cancer in her sinuses. I felt so bad for them! As for my symptoms- ever since the beginning of this past summer I’ve had sharp pains off and on in one ear. The pain also caused my jaw to feel sore. I thought maybe it could be a dental problem so saw dentist and no issues. Then went to ENT dr and no issues with ear. Went to primary dr and he thought I might have a pinched nerve so ordered a car scan of my neck. At the last minute he said by the way let’s get a lung screen too since I’m a smoker. So I did both the same day. Mass on lung 😞. I’m usually an information junkie and want to read about what I’m dealing with - but this is too much. The stats are not good at all. So I try to avoid the internet. And I still haven’t read my brain MRI results. I’m so scared that I’ve asked my dr to tell my husband the diagnosis after all my tests are done - I can’t bear to hear it. They told me they will know the results of biopsy right when they are done doing it. The pathologist will be in the surgery room. I don’t want to know that day either. I don’t handle general anesthesia well and don’t want to wake up to dreadful news. I’m such a baby!

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Replies to "Hi Angela - my name is Maureen. I live south of Detroit and about a half..."

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.

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!