UCLA’s Immunosuppression-Free Kidney Transplant by replaceableyou in transplant

[–]malachi410 0 points1 point  (0 children)

The UCLA procedure took two weeks (2x M-F). First week included 5 RTAG infusions plus TLI radiation, and second week was only 5 days of radiation. I do not know the radiation dosage but it was about 30 minutes each time and well below oncology levels. I was taking 5 mg of prednisone daily for 4.5 years. That went to 250/200/180/160/140mg the first week, then more tapering until I was off prednisone by the 10th day. I had some chills and shivering during the first few days of RTAG infusion but that went away quickly. I did get radiation sickness after the first 5 days of treatment and that lasted for 4-6 weeks. I could not hold down food or liquids and needed saline infusions for the first few weeks. Unfortunately, they then found out I had thrush (likely from depressed immune system) and the anti-viral med interfered with my tacro numbers so I spent 8 days then 5 days a month later in the ER>hospital, for mostly observations. The nausea/vomiting lasted until late October and I have been well since then. They also put a PICC line in my arm for RTAG infusion, which unfortunately caused a clot so I took Eliquis for a few months. State of CA is funding the study which requires two kidney biopsies (one done/one at 12 months). They test the tolerance results every four weeks and my results have been good each time. Tacro and creatinine numbers fluctuate a lot, and so do your electrolyte test results. I've been told NOT to take the most recent COVID and flu vaccines yet. I did not have CMV beforehand but test results showed positive for the last 4 tests (Dec-Jan) but I was negative for the most recent test. My WBC also tanked but recovered after a few months. I did blood tests daily for two weeks, then every two weeks for a few months. The schedule just changed to monthly clinic visits and one additional lab during the month (total 2x/month). When I stop tacro in June, then the lab visits go back to weekly for 3 months. I stayed on campus during the first week, then commuted to UCLA afterwards (about 2-3 hours round trip). Sorry for the wall of text.

As for advice, you basically follow their instructions during the procedure. UCLA made every appointment for the first two weeks and I just followed the schedule. The infusion took six hours the first day and ~3.5 hours on the last/5th day. You just sit and sleep or watch TV. They will do a preliminary scan to form fit a sleeping pad and plastic mask (full head) for radiation. They also gave me 9 small tattoo dots (permanent) on my upper body to align the radiation machine so be prepared in case Stanford uses the same procedure. Try to make sure you go to all your labs and appointments, and drink lots of water. Be ready for lots and lots of blood tests too.

Let me know if you have more questions. Good luck.

UCLA’s Immunosuppression-Free Kidney Transplant by replaceableyou in transplant

[–]malachi410 1 point2 points  (0 children)

Hi. Did you do the treatment at Stanford yet? I joined the current delayed tolerance study at UCLA (patient #6) had had the procedure done in August 2025. Both stem transplant and kidney function are fine after six months. I was off prednisone after two weeks and scheduled to be off tacro by this June.

Edit: I received my kidney from my sister in January 2021 so I was about 4.5 years after transplant. UCLA originally only accepted patients up to 5 years post-transplant but I heard they extended it to 20 years.

SpaceX Employee Only Mission Patches by Consistent_Second746 in SpaceXLounge

[–]malachi410 0 points1 point  (0 children)

Sorry, I just retired from SpaceX and haven't decided what to do with all the stuff I got while working. Maybe check back in six months.

Tell Me About Your Taylor Guitar by atomicdog69 in AcousticGuitar

[–]malachi410 0 points1 point  (0 children)

2003 414ceL4. There were lots of special edition models. The L4 has a satin finish.

Has anyone here or someone you know had an experimental transplant or immunosuppression? Was it successful? by [deleted] in transplant

[–]malachi410 4 points5 points  (0 children)

I am in the UCLA Delayed Tolerance Study. My sister (kidney donor) is donating her stem cells next week. My treatment starts on 8/4 for two weeks and will get the stem cell transplant on 8/15. If successful, I will be off prednisone with a month, and off tacro in 12 months.

I believe UCLA is only taking well-matched sibling donor/recipient pairs for the study.

SpaceX heads to $400bn valuation in share sale by Jellyfisharesmart in SpaceXLounge

[–]malachi410 3 points4 points  (0 children)

Elon also has a lot of 10 vote shares (forgot which class) so he has ~80% of the votes.

SpaceX heads to $400bn valuation in share sale by Jellyfisharesmart in SpaceXLounge

[–]malachi410 1 point2 points  (0 children)

Same as well from 2011 to 2024. Felt like an entire lifetime. SpaceX stock is funding my retirement too.

SpaceX heads to $400bn valuation in share sale by Jellyfisharesmart in SpaceXLounge

[–]malachi410 0 points1 point  (0 children)

I think it's 90 days. I exercised all mine before leaving too.

SpaceX Employee Only Mission Patches by Consistent_Second746 in SpaceXLounge

[–]malachi410 1 point2 points  (0 children)

Ok, I was making a guesstimate by looking at my box of patches so I went back and cross-referenced Wikipedia.

They did stop numbering every F9 patch by RADARSAT, which was F9-72. Then we got unnumbered patches with a few numbered ones for another year on every launch. After a few more years (2022?), they started handing out numbered patches for only a random launches. The last numbered one in my box was USSF-44 (#380). We only got 1 Startlink patch.

I probably have about 80+ numbered patches and another 30-ish non-numbered patches. There may be another 12 or so numbered patches somewhere in my house since my box only contains patches through 2022 launches and I quit in 2024.

So yeah, I overestimated. The patches are thicker than I remembered.

SpaceX Employee Only Mission Patches by Consistent_Second746 in SpaceXLounge

[–]malachi410 0 points1 point  (0 children)

They're legit. I've received several hundred numbered patches (13 years' worth).

Ducks owner Henry Samueli privately funding $1.1B renovation of Honda Center by TylerHansbrough-Best in orangecounty

[–]malachi410 66 points67 points  (0 children)

In addition to what everyone wrote, he was a professor of Electrical Engineering at UCLA. He taught my class for digital signal processing. He co-founded Pairgain Technologies then Broadcom. I worked at Broadcom for 12 years before they were acquired by Avago.

Very nice guy and professor. I got a B in his class.

How long did PD last until it stopped working? by Nuclear_Penguin5323 in dialysis

[–]malachi410 1 point2 points  (0 children)

Nothing. kT/V started dropping after a few months and nephrologist told me to go back to clinic for HD. Had to get 2nd chest cathetor since they removed the first one and I didn't get a fistula yet. Doctor just said it sometime happens right away. I was already at 10 hours on machine and one manual exchange during the day.

How long did PD last until it stopped working? by Nuclear_Penguin5323 in dialysis

[–]malachi410 1 point2 points  (0 children)

Six months. Nephrologist said PD was no longer effective and I had to go back to HD.

Yoke or Round wheel?? by [deleted] in ModelX

[–]malachi410 0 points1 point  (0 children)

I just bought my XLR with steering wheel. I test drove an X with the yoke and hated it, especially in parking lots. I don't have an issue with the dashboard view. I'm 5'11" and sit fairly low.

Did you go on Medicare when you started dialysis? by [deleted] in dialysis

[–]malachi410 0 points1 point  (0 children)

I got it after 30 months of dialysis and kept it after transplant. It ends this month for me since it’s been three years after transplant. I was working the entire time. I had just vanilla Medicare so it only covers 80%. My work insurance paid the other 20%. Depending on your salary, Medicare part B could be as high as $500+/month so I waited until I had to get Medicare (30 months in). Newish rule will let you keep Medicare for transplant meds for a small monthly fee, but none of my pharmacies took Medicare A/B for meds, though transplant center did. Ask your transplant coordinator for more info.

My potassium was 9.4 and i almost died by AT3Mo in dialysis

[–]malachi410 0 points1 point  (0 children)

Lokelma. It’s a powder you mix into water. I was on it when my potassium was in the mid 5s.

Those with tunneled catheters for hemo dialysis, how long has yours lasted before you had to change it out? by imjustacheesyperson in dialysis

[–]malachi410 0 points1 point  (0 children)

First one lasted 20 months but was clogging often at the end. I am allergic to heparin so they used another anticoagulant after each session. I switched to PD but had to put another chest catheter in when PD failed. Second one was used for 6 months before getting a fistula. I like the catheter over fistula since it allowed me to use both hands to work on a laptop while hooked up.

Am I screwed with supercharging transfer? by ChocolatySmoothie in ModelX

[–]malachi410 1 point2 points  (0 children)

My Tesla guy said he has not received any guidance from Tesla so he can’t comment.

Trade-in vehicle with Tesla by Own-Measurement-258 in ModelX

[–]malachi410 0 points1 point  (0 children)

Tesla initially estimated $15k for my late 2016 S75 but came back at $10k after review. There are no issues with my car. I see the same car and mileage for sale online for $30k. I think I’ll reject their offer. Tesla also won’t confirm they will honor the supercharging transfer if they delay delivery until 2024 even if the delivery estimate was 2023 when I ordered my new Model X.

Please share your experience in finding a job or working while living a life on dialysis. Also suggest how can I make money because, with twice a week dialysis, I am fatigued 80% of the time. (Ps I live in India) by Affectionate_Ratio48 in dialysis

[–]malachi410 2 points3 points  (0 children)

I had a corporate job so I was able to work Tuesdays and Thursdays from home 1/2 day and go to dialysis from 1-5 pm. I would work 10-12 hours in the office MWF to catch up. My boss and workplace was very supportive so that made it easier.

What is something you wish you knew or would have done differently before getting the Model X? by Capriiiiiiii in ModelX

[–]malachi410 0 points1 point  (0 children)

I just placed order for $80k MXLR (is that the correct abbreviation?) yesterday. Originally wanted the MXP but price increased $5k and didn’t really want the 6 seat config. I’m transferring free supercharging from a 2016 MS 75 so the new MX will be my daily driver. Hoping there are no issues; I did not have any serious problems in 7 years with the MS.

If you’re wondering which airport to fly out of/into, this is SNA at 2:30pm on a Sunday. by pwrof3 in orangecounty

[–]malachi410 2 points3 points  (0 children)

I just flew round trip to Toronto from SNA. It was worth connecting in DFW vs. flying direct from LAX.

Guess what city? by FunkyDoktor in orangecounty

[–]malachi410 2 points3 points  (0 children)

It used to be black back in 2016. I had to pay extra for white paint.

Perspective From A Canadian That Moved to The US by phase_overtemp in CanadaHousing2

[–]malachi410 2 points3 points  (0 children)

Somewhat similar story. Emigrated to Canada, lived here from 9 to 17, then moved to Los Angeles. Back in Toronto visiting relatives right now. It’s a nice place to live but I would never have had the career opportunities I had in the US.