If you're dealing with an issue related to life with cancer, this thread is a place to vent your thoughts or feelings. It can be personal, related to treatment, or the cancer itself.
No judgement. No politics. Replies should be supportive.
If you're dealing with an issue related to life with cancer, this thread is a place to vent your thoughts or feelings. It can be personal, related to treatment, or the cancer itself.
No judgement. No politics. Replies should be supportive.
So I will start. I'm in active treatment so I try to avoid exposure and remind my family that my reactions to some things might come off like I've been possessed. My family all knows this and does a good job accommodating the mood swings.
My biggest trigger is the dexamethasone. By day three every muscle, every molecule in my body feels like it's vibrating at warp speed and I want to crawl out of my body. I absolutely h8 myself in this phase. Anyone else?
You are amazing Denise! I hate steroids but unfortunately they are a necessity in treatment. I do better with Dex vs Prednisone / the hardest thing for me was the insomnia and feeling hungry.
I hope I won’t need it anytime soon, but know sometimes we need it.
Did you have to take two dexamethasone a day? If so, when did you take your second d one at the latest. I'm trying to find a time that lets me sleep better.
I took morning and dinnertime but still had insomnia - I can’t remember exactly what my dose was now, but it started pretty high (6 mg possibly) because I originally had a brain tumor and a lot of brain edema - I needed to have a high dose eventually, I tape her down and then mine went off, but it was a very slow taper. Once I switched to IO it was no longer needed. Not my favorite thing, but it did help.
another small vent today.
Cancer may have weakened me a bit but I ask for help when I need it. So when I go to do something I am fully capable of doing, like carrying in a light bag, my water bottle, emptying the dishwasher, the dryer, or the vacuum, don't stop me or order me not to do it.
If I don't do it now I'll lose the ability faster. They are coming from a place of love and I appreciate that. I love them too.
I am 82, ULL lobectomy 2019 staged 2B. Fall of 2024 SBRT to right lung.
Resulting inflammation from the SBRT has left me with sob and fatigue beyond what I have ever experienced. Late Feb flu made it worse. This is an exasperating new normal for me.
I am learning to take a break between activities. I attend a senior citizen center, enjoy meeting others and attend exercise classes including aerobic, strength, Tai Chi and Qi Gong 5 days a week. Exercise seems to reduce inflammation. I do not eat foods that cause or worsen my inflammation. Gratitude is important. I try not to compare myself to others. I recently learned laughing at myself helps. I look forward for swimming early summer.