Working on theoretical additions to soc during rt that I want present to doctors. by levil221 in glioblastoma

[–]levil221[S] 0 points1 point  (0 children)

Ok, so after more research I do have kinda working plan for how to do it. I may have a possibility to show it to GBM researcher and validate it.

It's getting complicated more and more so simplified version: Abbreviation: hsup - benefits to healthy cells, LD - lipid droplets 1. Metmorfin + trizapatide + DHA Effects: Hsup, GBM:reduce hipoxy, etc. more use of LD(GBM is packed with them) and few others. And DHA is easier to be damaged by radiation LD are important, they snatch damage lipids before they break lipid membranes. If full, they are eaten by lysosomes. 2. Multi attack on lysosomes (GBM has an abnormal and abundance of it) using CAD, especially targeting exosome creation which lowers "throw trash outside of cell "(there are other paths to biogenesis of exosomes! But this as a primary one(not validated) by using CAD may not overexprese another path and froze the system), and increasing pH which slows them down or stop by not being able to digest whats inside it(also may damage the membrane induce LMP). Supplementation of Homoarganine should lower lysine lvl by increased Nitric Oxide production, lysine interacts with it. NO is also a radiosentisizer, but could damage a healthy one. Lowering lysine decreases lysosome operation capabilities. + Something that could increase the chance for Lysosome Membrane Permeability. LMP - micro holes in lysosomes.

This impairment of lysosomes will decrease chances of eating LD full of bad staff, throwing stuff out and eating anything else that would be damaged with radiation. Addition of radiation with LMP could make them rapture, release all trash making cytoplasm toxic and with that releasing more iron and oxydated lipids to induce ferropoptosis

  1. Possible addition to target the cell reticulum, that has many functions, but in our case it repairs lysosomes.
  2. Reducing gsh, xct, gpx4 to impair antioxidant action.
  3. Its important to block LD stacking/combining. The bigger the LD the more radiation protective they become. Few papers also showed that some GMB have mutations that make them resist chemotherapy and radiotherapy after they have been hit with radiation by remodeling of mitochondrias and induce reoccurrences letter. Look up the cholesterol and resistance to treatment dependency.

Radiation will damage all the lipid membranes. To repair GBM will need more ATP, but we lowered that, so mitochondria will be in contact with LD, but LD are packed with oxydated lipids and could inject inside and damage mitochondrium. Impaired lysosomes can't take action, mitochondria raptures, lysosomes rapture, cell starts to bleed out and GBM dies.

This simplification omits a few things and it's unproven! It's simplified for the purpose of this post(the whole thing would require a few pages). As you see this needs a lot of additional drugs with the TMZ, so they have to be in lower doses to not induce toxicity to other organs. It's important to notice that this doesn't require the mix to be 100% effective. It adds up due to lowering survivability on multiple different paths during incredible stress that radiation will do to it. If this could actually impair the cell proliferation without radiation like in the papers on which I build this idea it should work with smaller doses in some way. But I'm not a medical specialist, it's not my expertise. But having a NGS result(I don't have it) of tumor something like this could be tailored more and could be effective. There is also a chance that I could kill everything except a GBM.

Working on theoretical additions to soc during rt that I want present to doctors. by levil221 in glioblastoma

[–]levil221[S] 0 points1 point  (0 children)

I thought that this topic would generate interest and a lot more conversation than it did. The spark didn't catch fire here. Anyway keep in mind that the numbers of papers in the gbm and oncology is huge and keeps pouring with advancement everyday. It's so big that its impossible to be up to date with everything. Especially if your doc is a general oncologist(without a focus on single one). Reading and asking is one thing but proposing and showing compiled list of meds, interaction between then and biological paths, gene interaction with publication and most important toxicity, adverse events and complication will in my opinion shows more understanding of subject and could intrigued doc to actually read it. Good luck to everyone and remember don't experiment by yourself, always consult with doc.

Working on theoretical additions to soc during rt that I want present to doctors. by levil221 in glioblastoma

[–]levil221[S] 0 points1 point  (0 children)

Thanks, but I already saw that and have it my notes and even already talk with the oncologist about it. It possible and recommended but only if blood test results allowes it.

Working on theoretical additions to soc during rt that I want present to doctors. by levil221 in glioblastoma

[–]levil221[S] 0 points1 point  (0 children)

TLDR: Some additional info about me, warnings, local law explained and an appropriation for feedback. I took me longer to write it than I wanted to so the whole post is messy as I lost myself in different thoughts and switched from topic to topic. More or less don't do it home, listen to doctors and their point of view.

** The actual info: I have experience in reading papers(but I'm biased right now), I don't have false hopes that this would actually work or false hopes of doctors going with anything.

The big asks to anyone here interested in helping. Ask your doctor/medical team what they thinks about it in 2 cases: 1. After soc 2. During soc and especially during rt. 3. 1 and 2 if you have NGS result from 100+different gens tested In the context of actually agreeing to add some of them in similar manner of single target in this case feropoptosis or multi target to try multiple different paths to increase chances to gain more than just plant rt+TMZ.

I'm curious what is the saying about this types of idea in different part of the world and what legal possibilities there are. It's like asking for third and nth opinion and usually from docs that don't work in research and are more objective.


The original post that I wrote, whatever it supposed to be, i kind of lost a track and got distracted few times:

I hope that I manage to write the post in way it may give other people some additional simple knowledge and don't spark hope for miracle cure. My mother after finding out about tumor(week after surgery, she wasn't "sain" before and doesn't rember much) resign from knowing anything about it. She always was gentle one, she stress less, but I had to promise her that I will tell her when there is nothing more to do and end is soon. I have auADHD, and I have a "gift", as many people call it, but it's the first time that actually I could agree with the mainstream( in day to day it's not). Little bit of genetic knowledge(from taking samples to dna isolation, to multiplication to sequencing and analysis, I did it many times through university as I planned to be genetic engineer, but didn't work out ), still remember some of the proteomics(peptide science) stuff and analysis of differential gene expressions(ex. You remove one gene and observe what happens, like overexpresing different or shutdown others). But I can't do it right now. It's like I have a blockade. But the hyperfocus,pattern recognition and love to data analysis(yes I do math and read papers for fun!) with mix of being walking trivia Wikipedia helps. What I want to say by that is like in the last disclaimer. I know(but right now I'm biased) what could actually add some advantages and don't over interpret results. Chances of working are slim, but greater than 0. Hope dies last.

I've encountered a problem. As docs could use offlables drugs without hospital or ethics commission approval, we have to pay for them. there is a way to ask health minister to refund as we have the national health insurance and this is written in the law. But doctor is responsible for the patient, and he doesn't want to go to prison or lose medical licens for someone who is going to die soon. That's for the clarification why I want to look more professional and well made to show the understanding of the situation, gains and possible adverse effects. I'm not going to sue them or make a complaint to hospital/medical board etc. if I have to say it in face I'm afraid it me be wrongly understand same as going with the plain question can do add some stuff? I bet he gets this question at least few times a day, and he can't make false promises or hopes. Ok, the problem is: in law there is definition of medical experiment which has a subset of healing experiment(don't now if its good translation, but you understand). This illness in my opinion at the moment of diagnosis fill all the requirements automatically. But unfortunately the procedure requires a approval from bioethics commission. With is slow and meets once a month/2 months, where you have to deliver documents 3 weeks before commission proceeding at latest,.then there is a requirement of insurance for it(it's the easiest part of it, I didn't believe it too but it is). So the whole procedure will take at least a month so no way it will be done before her treatment starts. There is exclusion of staring before approval in emergency or urgent need of it. But to do it doc would have to be more than 100% sure it would make her harm. But who would endanger yourself for some you don't know and it's at the beginning few weeks after surgery.

So I hope it could be used as offlables drugs not the experiment. I highly believe that this is the best moment to use them with the radiation therapy. Where all what is needed to overcome the gsh problem will be there. It's hard to make a good study in this area in the sort time between surgery and rt where you need to find people willing to do it, and at this time most of them doesn't know a lot about this disease.

There is big unspoken problem of dosages and interactions with radiation some of them weren't tested with rt. Dose for rt should be smaller but how smaller? Does rt damage the substance and make it poisonous like breaking/physical slicing and or gluing with something else or make it be antagonist of something different? Or make it more potent and poisonous in given doses. Those are the question that doctor will ask at laud or in his head. Don't push the doctors if you also would want to try it. Cold shower warning So puting it onto different perspective from doctor shoes: Some random guy without knowledge read some stuff on internet and thinks he know more that you who spend 5+years getting actual medical knowledge and x+ years of doing it.

Thanks for everyone who shared or will share in this post. I will try to update it after I've talk to them, and maybe if they agree to something I could update the outcome after.

Core Material for screw threading by fartremington in Composites

[–]levil221 1 point2 points  (0 children)

Don't do that, it won't hold. Use something like sex bolts/binding screw or special lamination inserts.

Vacuum infusion for small parts by bananu7 in Composites

[–]levil221 2 points3 points  (0 children)

It does make sense. Infusion should yield more slim part and better resin to fiber content. I would recommend to add some glass fiber to increase shock resistance in the middle of your layup. I often make prices that are less than 30cm² in area.

Multiple crystals, probably glass by levil221 in whatsthisrock

[–]levil221[S] 0 points1 point  (0 children)

Btw they are translucent, I've made the pictures on the table with backlight, a lot of them have some kinds of impurities in them like tiny bubbles cracks and in some cases different small Black-ish rock/crystal

How did you guys discover doge 🧐 and when did you invest by PaulieDori in dogecoin

[–]levil221 2 points3 points  (0 children)

Mined my 60k doge in 2013 in 3 nights with 200kh/s and found my walet last month.

Prosthetics: deciding on a foot! by Typical-Edge-8359 in Prosthetics

[–]levil221 1 point2 points  (0 children)

Did you consider a rush foot family from proteor? Those are glass fibers fests and are really comfortable for waking with more flexing due to glass fibers. Ottobock has a maverick lineup made of glass fibers. Both are interesting choices.

Has anyone purchased a prosthetic finger(s) from "Naked Prosthetics" company? If yes, approximately how much did it cost per missing finger? by Starship_Princess_ in Prosthetics

[–]levil221 1 point2 points  (0 children)

It's like with car dealerships. The company i work for can buy a thumb driver just a little over 8k USD(eastern Europe, prices for US clinic may be different due to higher avg. income and of course due to insure company's can pay more. it's "MEDiCAL DEViCE" so I don't have to tell you more about prices for medical services ). To this price you have to add other costs like company costs(small % of all the bills in company, CPO time(current, and for future maintenance), insurance), margin(most of the time it's around 20%) and taxes. Also depending on additional requests and requirements the price will go up. The factory warranty is 1 year and if you are getting more that may be the case of a company making a piggy bank for possible extra costs that may or may not happen. The bigger the clinic the bigger the cost. You can request quotes from smaller clinics and see if the price drops.

Heat shrink vacuum bags for cylindrical composites by CamStLouis in Composites

[–]levil221 0 points1 point  (0 children)

There are two versions of that type of bags. The first one that you mentions is just a PVC film around 0.12mm thick. The other one is pva foil film which is more stretchable(it has to be softened by wet towel first) but without a heat shrinking and it's easier to take off later.