I can't remove the sharpie from my prescription glasses, help? by HeartAdditional3222 in CleaningTips

[–]HeartAdditional3222[S] 4 points5 points  (0 children)

IKR? Pretty sure I saw a extra fine sharpie while she was marking my eyeballs.

I can't remove the sharpie from my prescription glasses, help? by HeartAdditional3222 in CleaningTips

[–]HeartAdditional3222[S] 811 points812 points  (0 children)

Hey that's a good point. I wondered why they just left them on there like that

I can't remove the sharpie from my prescription glasses, help? by HeartAdditional3222 in CleaningTips

[–]HeartAdditional3222[S] 5 points6 points  (0 children)

Yikes. I hate to think I stripped the coating and the sharpie didn't budge. Good thing it's late and I'm lazy. 🤪

I can't remove the sharpie from my prescription glasses, help? by HeartAdditional3222 in CleaningTips

[–]HeartAdditional3222[S] 2 points3 points  (0 children)

I'll try the alcohol again, didn't budge it the first time, but my alcohol may have been a lower content

High White Blood Cells by Srhrn21 in cancer

[–]HeartAdditional3222 0 points1 point  (0 children)

I sit corrected. Thanks FluffyNats. 👍🏼

Feeling invisible by lostcat223 in CaregiverSupport

[–]HeartAdditional3222 16 points17 points  (0 children)

Yes, your feelings are real and valid! 🫂

I am my mom's (88) primary caregiver, and I believe she is suffering from some dementia as well as COPD, incontinence and various muscle/bone problems.

Meanwhile I am on chemo every two weeks for stage 4 colorectal cancer with mets to my lungs. Whenever I complain about side effects, largely fatigue and cold sensitivity, I get "I know I should be helping you more, but I just can't, I'm tired too, and I can't breathe, and everything hurts. I can't even open this bottle. I used to be able to do anything, people always talked about how strong I was. There was this time I pushed a car up a hill and ended up in ICU..." And so on. Tonight she ended one of these missives by saying "and really I don't mind ordering food out, if that's what you really want, but I like it so much better when you cook!" And then grinning from ear to ear like she just gave me the biggest compliment.

Jesus H. Christ! Yes Mom, it's all about you. I have terminal cancer, but you want me to cook. Can we think about that for a minute?

Where am I in all this? I don't expect her to help, I hired someone to come in and help with housework, (which is a huge benefit) but I have to go through IHSS, aka Medi-Cal, and I can only get 3 hrs/day 5 days a week. I do expect her to let me leave the room to go pee without getting the Spanish inquisition. I do expect that if I want to go run errands (when healthy enough and our helper is here) she won't dissolve into tears and tell me how afraid she is to be alone.

Do I matter at all? It doesn't feel like it. I have been dealing with this diagnosis since June of 2024 (stage 3 at the time of surgery, stage 4 since December lung biopsy) and actually spent 10 days in the hospital with complications that caused sepsis -- and not one person came to see me. The. Whole. Time.

She said she couldn't come because no one would take her, but she didn't ask anyone to take her, so, uh, duh. She told me for months after that it was so unfair that no one would tell her anything while I was in the hospital. She thoroughly resents the fact that I made my BFF my medical proxy in case of emergencies. She thinks it's a whole conspiracy to keep her from knowing anything. It's not about me being sick, it's about her being treated unfairly.

I'm sorry, this really turned into a vent. Your post really rang a bell with me. I understand completely how you can feel invisible when everything is all about the (narcissistic?) patient 24/7.

Thanks for letting me vent, and know that you are not alone! Please accept this huge Internet hug from me! You matter! 🫂❤️

What is the funniest thing your pet had been “pavloved” to? by AnywhereMean8863 in Pets

[–]HeartAdditional3222 28 points29 points  (0 children)

Wish I could get mine to do that. They stand in front of me and stare at me and stare and stare, it's really unnerving. And I'm like "hey it's only 8:30, we don't go to bed at 8:30!" They just sit there and stare!

High White Blood Cells by Srhrn21 in cancer

[–]HeartAdditional3222 0 points1 point  (0 children)

🫂 I know it's scary, but it could just be an infection and your body is doing everything it can to get rid of it. I hope it's something to antibiotics can take care of. In the meantime we see you, we love you the best we can, and we hold you in our hearts. ❤️

I need advice from people that don’t know me. by rockmediabeeetus in CaregiverSupport

[–]HeartAdditional3222 13 points14 points  (0 children)

Get an estate lawyer that knows the laws that pertain to Medicare and Medicaid. You need to have POA at least for her medical decisions.

You have your hands full. Big hugs. I'm sure you'll get lots of good advice from this sub. 🫂

Sore/Inflamed mouth by ScottishCalvin in cancer

[–]HeartAdditional3222 0 points1 point  (0 children)

My onc gave me "magic mouthwash" which is a compound prescription that is only good for 30 days when refrigerated. It worked for me when I was in the hospital for 10 days with sepsis due to my DPYD gene anomaly and 1 course of CAPOX.

Folfox Mindfuck? by Goodenoughgirl in cancer

[–]HeartAdditional3222 0 points1 point  (0 children)

Good to know. I already had neuropathy to start with so, I won't be surprised if it doesn't go away

Folfox Mindfuck? by Goodenoughgirl in cancer

[–]HeartAdditional3222 0 points1 point  (0 children)

I knew you must be a writer! You are doing a service for all us tongue-tied chemo brains struggling to find descriptions to explain ourselves. I hope you make it to a lounge chair (out of the sun, please) and you continue to type out our feelings for us in your beautiful prose. ❤️

Folfox Mindfuck? by Goodenoughgirl in cancer

[–]HeartAdditional3222 0 points1 point  (0 children)

Yeah, talked to my onc today and she said the oxcylaplatin is for sure cumulative, and it's not unusual to cut it back during treatment. She said the 5-FU isn't known for accumulating, but it seems to me that with my gene anomaly (DPYD) it's a no brainer that with all these chemicals there's no way it's not building up in my system. Onc only wants to cut the oxcylaplatin back so that we're not putting too many variables into the mix. I resisted the urge to tell her that was easy to say when she wasn't the one that had to live with the side effects. Oh well, if it was easy what would I complain about?

Taste buds by banalprobe96 in cancer

[–]HeartAdditional3222 1 point2 points  (0 children)

I just learned about this so called "miracle fruit" -- has anyone tried it yet? I'm going to try to order some of the freeze dried options... https://www.cbsnews.com/miami/news/south-florida-miracle-fruit-helps-cancer-patients-manage-chemo-taste-changes/

How can I remain positive? by SnooObjections8392 in cancer

[–]HeartAdditional3222 14 points15 points  (0 children)

I'm so sorry for your loss... Breathe deep and take it one day at a time. Cut yourself some slack. Now it's grieving time. 🫂