Barb1260
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Posts posted by Barb1260
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DFK-When I spoke to the PA about the 5mm mystery nodule, she said we will watch it for now. Because I usually see the Oncologist to go over scans, I moved up that appointment to Thursday before the infusion. The scan was 2 weeks early so the follow up wasn’t until October 3rd. Not that I don’t trust the PA, but this is my life, I now have a few questions that I need her to answer.
- Charles and Rower Michelle
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Hey Ron. Sorry you had a rough day. Fingers crossed till you share your results
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Hi Kate and welcome. I’m on the same treatment track as you it seems and will get # 11 on Thursday. The fatigue drives me nuts as it comes on suddenly and usually when I’m in the middle of doing something. Every one here is supportive. Heck, I could be a real whiner sometimes and someone will always respond with a positive thought. Give a shout whenever needed. We are all here for each other
- Kate7617 and Sillycat1957
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Hi Roseann. Welcome. Sorry to hear about all your side effects so soon after you started. Keep us posted. I get weird little aches and pains but nobody can say for sure if related. We are all trail blazers on this stuff.
- DFK and Sillycat1957
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Hey Charles. I know it’s easy to fall down that black depression hole. I tend to dwell on the bad parts of the results and not the good. I should be happy the right side tumor is stable and not one lymph node was mentioned. I also don’t understand why they do CTs then PETS if they find something. Makes more sense to me to get all the information the first time. But I’m not a doc and I’m sure it’s insurance related because I had to fight for the last PET.
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Thanks Charles. I’m rooting for you too. I sometimes feel like throwing in the towel, cash it all out, stop all the chemicals being put in me and just take to the road until I can go no more. But alas, I come back to reality, put the gloves back on and come out swinging once again. Somebody needs to do a better inventory of their Durva stock. That seems a little unprofessional. Have a good night!
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Got my CT 2 1/2 weeks early today because of chest and back pain since Friday night. PA almost certain the chest pain is due to the hiatal hernia discovered on my post radiation PET CT in April. Back pain in same spot as the post radiation pain. They are not sure why it’s there again but maybe it’s from the radiation? Let the waiting begin. At least I don’t have to worry about going for the next 2 weeks, it’s already done. Now I get to add a gastroenterologist to my repertoire. Joy
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Sorry to hear this Bob. After all that. I’m crossing my fingers that it’s not a recurrence.
- DFK and Robert Macaulay
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DKF-yay on #17. I had #10 today. No issues except blood work not done until after because my port wouldn’t give blood. They had to put something in it and let it sit for 45 minutes to unclog it. I’ll get the results next week. Nobody is concerned about the mouth issues I had. The PA said if it goes away in a couple days it’s probably not related. My thoughts are-who really knows? I asked how many patients got through the 26 infusions from her practice. Said 2 or 3 with very minor side effects so that’s a positive.
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Tomm/glad you’re getting less fatigue and you are taking the thyroid med. after last week’s infusion I got really tired on Saturday and that lasted until yesterday. So I guess my side effects are starting. I’m also experiencing mouth sensitivity and a burning sensation. Just like my eyelids did and eventually went away. Another thing to discuss next Thursday. Still not complaining as it’s nothing debilitating and I can deal with it. I can’t wait until we do #13-we ca celebrate the halfway point. Have a good weekend.
Durvalumab
in IMMUNOTHERAPY
Posted
Good news Ron. Sounds like a great plan. I personally love radiation and tried to keep going but alas the radiation oncologist said it would kill more than the tumor.
You got this!!