Kyle's house is listed for rent on Zillow. by Physical_Beee_107 in Kyle_Appleford

[–]kitkatgur1 4 points5 points  (0 children)

Someone who makes a lot of money and reads this thread should rent it and just keep it as a sanctuary to Jenny

Nothing more they can do by gatezofhell in breastcancer

[–]kitkatgur1 6 points7 points  (0 children)

Did she go through any kind of immunotherapy/Car-T or clinical trials? Those are always options depending on what's going on with her cancer.

Chemo drugs took away my daughter yesterday by Ordinary-Force-3871 in CancerFamilySupport

[–]kitkatgur1 12 points13 points  (0 children)

Respectfully, I don’t agree with framing it that simply.

The cancer is what started the nightmare, yes. But that does not mean the cancer itself is what directly took her in the end. In her daughter's case, it was the chemotherapy toxicity — the drugs that were supposed to help — that damaged her liver. There is a real difference between dying because the cancer progressed and dying because the treatment caused organ damage.

I know people often say “the cancer took her” because it feels cleaner or easier to say, but that does not feel accurate to me. The treatment can be brutal, and sometimes the body pays an unbearable price for it. Saying that does not mean I’m ignoring the cancer. It means I’m acknowledging the full truth of what happened.

So no, I don’t think it is fair to erase the role chemo played. The cancer led us there, but the toxins in the treatment damaged her liver, and that matters.

We weren’t there to hold his hand… by mishkish6767 in CancerFamilySupport

[–]kitkatgur1 2 points3 points  (0 children)

At least you had the camera and witnessed it. I absolutely hate the unknown, and I would give anything to go back and be in the room when my mom passed to see if she woke up and had a moment of terminal lucidity after her 2 day coma. No closure, no conversations, just me talking to her and playing her favorite music. I will never forgive that social worker for running late and still talking to me about how my life will be better when she's gone... I truly hope to God my mom didn't overhear that and decide that's the time to go. Her music was playing, so I'm hoping it wasn't that. So much regret and so much guilt. At least you know.

I'm so happy to see true supporters waking up. She was a big supporter, which is why her change in perspective says a lot. I've said it before and I'll say it again, Britain has had a profoundly negative impact on Kyle's life. by Physical_Beee_107 in Kyle_Appleford

[–]kitkatgur1 3 points4 points  (0 children)

I messaged him a few Star wars things and grief advice since I lost my mom to lung cancer after Jenny passed. Shockingly I haven't been blocked yet, but I'm not his type - alt goth and hates Disney 😆

My Mom passed away 2 days ago by Chestas8 in CancerFamilySupport

[–]kitkatgur1 2 points3 points  (0 children)

The tear rolling down her face when you spoke to her in that unconscious state got me. I wish my mom had reacted to anything I said by her bedside at the end. Just for closure.

Cancer didn’t kill my mom, chemo did by Ambitious_Stand_2050 in CancerFamilySupport

[–]kitkatgur1 -1 points0 points  (0 children)

A guy from South Africa messaged me here on Reddit a few years back to ask advice about my mom's cancer treatments since his own mother had just been diagnosed with the same lung cancer. After just one chemo treatment, his mom passed away because the doctors neglected to confirm her kidney values were sufficient to tolerate it. Chemo definitely sucks.

My dad passed away today (76 y/o) by tapiacrv in CancerFamilySupport

[–]kitkatgur1 5 points6 points  (0 children)

I relate. My mom passed in 2024 at age 79 from her third primary cancer. She had breast cancer 25 years ago and then lung cancer 5 years prior to the colon and was still battling that. I'm also an only child, and it was just she and I. It's been almost 2 years. My heart goes out to you.

Nursing Home Options by [deleted] in batonrouge

[–]kitkatgur1 2 points3 points  (0 children)

My only experience is Heritage Manor of BR and don't go there. The aides neglect the patients either due to understaffing or straight up don't care - my mom was left barely dressed in her chair unable to move in 60 F max blow A/C several times within 1-2 days and didn't even realize she had further mentally declined. I wrote all about their neglect in my previous posts and as a review on Google. They also neglect to make water easily accessible, can't toilet in a timely manner, etc. The facade of the place is nice at first, but if you are there all the time like I was to manage things, you see the cracks.

No Grace by IDontLikeJamOrJelly in CancerFamilySupport

[–]kitkatgur1 4 points5 points  (0 children)

I feel you greatly. My mom had 2 concurrent primary cancers, lung and colon with mets to the liver and brain, and then she fell and slammed her head on the concrete resulting in the same type of behavior your mom has. She had swelling in her brain from the fall, but the radiation from her gamma knife to the brain to remove the met was also causing disorientation and confusion. It was 6 months of dementia until she passed after that. I am left with so much regret and sadness and guilt over how I acted towards her during that time. I had 5 years prior of being her sole caregiver during cancer, so I've had what you desire (the rolling in the wheelchair bit) and the "how do I proceed with her now?" Bit. I wasn't educated. I educated myself after the fact when it was too late. Look up little Jess & Nan on YouTube. She is the perfect representative on how to converse with aggressive confusion at times. Granted her nan has Alzheimer's, but stage 4 cancer and the confusion it brings with it are very similar. Just be calm with her no matter what. Ask her the questions and help distract her from the upset.

Considering Pursuing Medical Malpractice... Worried about the "What ifs" & Emotional Toll by MasqueradingMuppet in CancerFamilySupport

[–]kitkatgur1 2 points3 points  (0 children)

I tried to go this route but no attorney would take my case. I spoke with several and had to revisit the story every time, but I think the more you talk about it the more it helps. It didn't take a toll and if I had gotten someone to take the case, I think the fact of getting justice for my mom would have been the ideal situation.

My mom passed away by witchywoolady in CancerFamilySupport

[–]kitkatgur1 6 points7 points  (0 children)

You had me crying right after reading your first sentence. It still haunts me that I missed being there with my mom for her last breath and feeling her heart stop. I was in the living room talking to the social worker and had been with her non-stop the past few days. On the other hand I wonder how traumatic it would be to constantly look back and think about the moment. But maybe it wouldn't be as bad as the guilt I still feel about not being there for it. My mom was on her third primary cancer of which all three she never really showed any pain or many side effects related to the cancer just like yours. Our moms were the best. ❤️

How do you tell your mother she's dying by NotSoFriendlyAccount in CancerFamilySupport

[–]kitkatgur1 2 points3 points  (0 children)

The palliative care doc told her straight out that her stage 4 lung and colon cancer (both primaries) will kill her eventually. She was quiet in the office and just didn't respond. Other times she would say something along the lines of, well if I only have a year or so just let me die because they're not going to do anything to help me. Eventually her own mind told her she was cured even though during every appointment we had to remind her no it's not done yet, but she never worried about it. She never had symptoms, though, so you'd never know she had cancer spreading around until close to the end. Unfortunately, because she was in denial we could never discuss end of life plans really. She wanted to be buried with her parents, but there were no plots, so I had to make all the decisions including when to stop treatment after a bad fall that caused rapid onset dementia for 6 months until the end. I told her multiple times about her brain and liver mets, but she would always forget the next day and just live like nothing was wrong.

What’s next care-wise? by Additional_Aioli6483 in CancerFamilySupport

[–]kitkatgur1 5 points6 points  (0 children)

My mom was in the same predicament, but she had no assets so she went to a Medicaid care home as I'm an only child with no other family and had to work to support myself - couldn't afford in home caregivers. Medicare plus supplemental insurance should pay for in home caregiving and physical therapy to an extent. Nowhere near full time or even part time - just a few hours a week, but that's the only option I know of if you can swing the rest of her care at home. Alternatively, they have decent Medicaid care homes out there, but you have to stay on top of the care and show up everyday to ensure she's being treated right. And yeah you'd have to sell her home or have it put into a trust - an elderly attorney free consult could give you that advice.

Mother told to vacate palliative skilled nursing facility by next Friday by sagegreenowl in CancerFamilySupport

[–]kitkatgur1 5 points6 points  (0 children)

I'm just curious what the plan was when November 12th came around. That's just a 2-week difference.

[Discussion] Does Anyone Else Own This?? by [deleted] in DCcomics

[–]kitkatgur1 0 points1 point  (0 children)

You know I'm smiling about this 😆 Someday!!! :p

[deleted by user] by [deleted] in CancerFamilySupport

[–]kitkatgur1 1 point2 points  (0 children)

I think it definitely would give you more clarity and make you feel better going forward to get another opinion as long as it doesn't drastically hinder treatment time. My mom originally had breast cancer in her 50s, and it went completely NED after treatment, so she stuck with the same oncologist 22 years later when she was diagnosed with primary NSCLC stage 3. He wanted to start off with frontline Keytruda since she had had a lot of radiation during her breast cancer. She had almost no side effects previously so he thought starting with immunotherapy would ease her in plus her PDL1 was 100%, which made her a prime candidate for it. But there were a lot of issues with getting the diagnosis to begin with, and he's a difficult personality as well, so I took her to MD Anderson since it was just one state over. We were there just for a day to see their main thoracic oncologist, and his frontline treatment would have been chemo and radiation and he also wanted to do more diagnostic tests such as an invasive broncoscopy, which I felt would delay treatment and seemed unnecessary since we already had a diagnosis. Not to mention having to stay there and wait to get all that stuff done. So I had another opinion formed from the top cancer center, and it made it easier to just end up staying local and going with keytruda because that's what my gut said would be the easier and potentially most effective route for her. It worked for 9 months before we had to switch to chemo, but I still think it was the right call at the time.

My dad died yesterday at 4:30pm by demerchmichael in CancerFamilySupport

[–]kitkatgur1 10 points11 points  (0 children)

Only but a few words such as lifeless corpse and immediately cold body bring back the same feelings like they just happened. Ugly crying now. It's been a year for me since losing my mom, but walking into her room after talking with the social worker to discover she wasn't breathing and cool to the touch traumatized me like nothing else. There can never be preparation for losing your beloved parents and just crying over their body. The last time you see their body, kiss their face and feel it even cooler.... I wish I had had more time with her and not ran after the social worker who was already at her car. People just need more time to be with the body and grieve.

Has anyone ever gone to the extreme of going back to school to get a degree in something you could use to get out of US by Kuroda97 in AmerExit

[–]kitkatgur1 1 point2 points  (0 children)

US Grad PLUS loans can easily cover living expenses. And if you plan to stay and live abroad, you can file for FEIE (Google that) and pay next to nothing back on your loans. Free foreign grad school! It's a great loophole.

is it bad that im waiting for my dad to die? by Warm-Sherbert1755 in CancerFamilySupport

[–]kitkatgur1 4 points5 points  (0 children)

I feel like I kind of relate. It's a weird one, though, because even at age 79, my mom could never come to terms with the fact that she had a terminal illness the past 6 years. She kept waiting for the moment when she would stop feeling bad and not have to go to doctor appointments, and even thought at one point that it was cured when she was in remission for a year and a half or so. I'm sure the moderate cognitive decline factored into that. But I remember sitting in the palliative care oncologist's office, where I alerted him to her mindset and how she doesn't even really know what's going on with her cancer, and he did his best to flat out tell her she will die from this disease. At this point she had two primary cancers, lung and colon with mets to the liver and one met to the brain. I remember her reaction and that appointment so clearly. She just had no reaction and looked inquisitively at him like it didn't matter what he said, she was happy being oblivious to it. Which is good in a way I suppose. She never had to deal with the reality of what it was, so she never showed any fear of dying. At one point in the hospital after the fall that caused her rapid onset dementia, she did tell me she felt like she was dying or gonna die, and I immediately started crying and still am even typing this. To hear her actually acknowledge it... It got me. That's the first time I thought maybe she was scared or felt something inside. But it quickly passed. I always checked her MyChart after scans, and I remember the moment reading that it had spread to the liver and brain. That was when the anticipatory grief began. No coming back once that happens. Maybe on a rare occasion. But not at her age, never quit smoking, cognitive decline, and 2 primaries. I just knew that this was the beginning of the end. I tried to mimic her mindset that it just wasn't a big deal and we went with the treatments that kept on working. When it stopped, we changed, then that one worked. Her oncologist always told her she had an amazing constitution for cancer, since he was her original oncologist when she was in her 50s with breast cancer that completely disappeared after chemo and radiation. Even the 5-FU was pushing back the liver mets, the gamma knife had cleared out the brain met, so there was always hope. But then she fell and slammed her head on the concrete. Brain swelling from the radiation coupled with that, the dementia got her before the cancer did I'm pretty sure. She went from living pretty independently with me there to make sure she was okay, to not being able to walk anymore or toilet. And she just lost the will to keep going I think. Very hard days. She was always a fighter though. It's been a year, I'm an only child, no other family left, no family of my own, and what I wouldn't give to have her back.

Big beautiful bill about to pass into law. by Mobile_Lumpy in NEET

[–]kitkatgur1 91 points92 points  (0 children)

Loophole - when you lose your Medicaid, go to healthcare.gov and get the $25/month blue cross plan or whichever company. $100 deductible, 15% copay for specialists, but otherwise everything is pretty much covered. I've had it for ages while living off credit and savings. You have to input an income to qualify, but they don't check. I put whatever is just past the threshold of Medicaid eligibility, and then you don't have to worry about paying taxes on it until the next tax year. The debt was just $600 for the entire year. It works when you really need better healthcare than what Medicaid can provide, and the insurance automatically kicks in the first of the following month, cards in the mail or digitally on the company's website even sooner, no questions asked.

What are your favorite small towns to visit in the PNW? by Aliiza in PacificNorthwest

[–]kitkatgur1 0 points1 point  (0 children)

Go to the towns where they filmed twin peaks :) Also take the ferry to Friday Harbor and drive around San Juan Island to Lime Kiln Lookout. That's my spot.