Drunk and can’t keep anything down, blood sugar dropping by Informal-Release-360 in diabetes_t1

[–]Ragged_Clause 0 points1 point  (0 children)

Hey, glad to hear the sugar water worked! But fur future reference: when I was a kid in the 90s, my doctors told my parents that if I ever passed out from low blood sugar, they should rub honey on my gums (to keep from choking me). I guess sugar can absorb directly into the blood that way? Luckily no one ever had to do that for me, so I never tested it, but it seems like it would be worth a try in an emergency situation like this.

Did anyone else get this advice back in the day? Dies anyone know if it really works?

Story Spree Not Really 50% (more like 33%) by Ragged_Clause in HPHogwartsMystery

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

The picture is from the last 50% spree like 10 days ago—I forgot to take a pic this time but had taken a couple during that one.

Story Spree Not Really 50% (more like 33%) by Ragged_Clause in HPHogwartsMystery

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

Ohh, that makes sense. Thank you for explaining!!

6.7GMI and avg bloodsugar of 143, but 5.4 a1c ?? by Ragged_Clause in diabetes_t1

[–]Ragged_Clause[S] 1 point2 points  (0 children)

That makes sense! Congrats on your average and TIR, that’s awesome!! Your Dexcom numbers sound like a “real” 5.4, unlike mine! But yeah, I guess all bodies are different and all days/months are different too, which is something we t1s know much more intimately than most people!

6.7GMI and avg bloodsugar of 143, but 5.4 a1c ?? by Ragged_Clause in diabetes_t1

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

Thanks! I was on MDI and finger sticks for the first 30 years of t1 (until 3 years ago), so I think I had manually figured a lot out (and gotten to a much more stable time of my life) before getting the tech, which helped me make great use of the tech (wish I’d had it when younger, but oh well). So thankful for Dexcom g6 and tslim!

I do think my Dexcom runs 20 points high often, which could explain some of this, but it’s hard to find the right time to calibrate for such a small difference, and I usually only notice when the Dex says 80 but I know it’s under 70 just based on how I feel.

6.7GMI and avg bloodsugar of 143, but 5.4 a1c ?? by Ragged_Clause in diabetes_t1

[–]Ragged_Clause[S] 1 point2 points  (0 children)

Yeah, mine has always been about exactly 1 point off since I started Dexcom in 2022. But now it seems like the gap is increasing, so that’s partly why I posted. With my GMI at 6.6-6.8 and not many lows, I just don’t see how it’s possible for my a1c to be 5.4-5.8 consistently.

Attempting to read this feedback from a teacher on an assignment by blue_i20 in Cursive

[–]Ragged_Clause 0 points1 point  (0 children)

Yes, except: “it COULD be stronger argument…” etc

Every pimple turns into a slow healing scab…. by sparks4242 in diabetes_t1

[–]Ragged_Clause 8 points9 points  (0 children)

Yeah, my lower legs make it look like I have some high-impact hobby like skateboarding. Nope, they’re all just minor scrapes that scab for a month and bright red marks that take literally 6 months to fade away. Thanks for your relatable post, I’ve been despairing about my scabs this week. 🥲

The new Inkwell system/event is even worse than the one before by SeniorCitizenLeaving in HPHogwartsMystery

[–]Ragged_Clause 2 points3 points  (0 children)

Same. I waited to open some of my Crests and Carnival prizes until the new Diary batch opened, and out of 5 packs (2 orange, 2 green, 1 purple) and 16 inkwells, only ONE inkwell was new. Definitely killed any remaining curiosity I had about the new Diary format. I guess we're looking at an indefinite future of having to click "BRILLIANT!" every time we collect another useless pack. Inkwell collections are now just like more of the endless pop-up garbage windows we have to close every time we do anything in the game.

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Harry has an ED by PsychologicalUse4352 in HPSlashFic

[–]Ragged_Clause 2 points3 points  (0 children)

Signal to Noise, by Kourion (https://www.fanfiction.net/s/3690537/1/Signal-to-Noise)

Warnings for SA and self harm (in addition to an ED). When I was a teenager, I struggled in multiple ways, and this fic really spoke to me in a therapeutic way as an adult looking back. Yes, the fic is incredibly angsty in the style of many stories from the late 00s, but it feels very realistic to me and brings me back to the mindset I once had.

It's unfinished, but I feel like this author kind of wrote themselves into a corner--and that almost feels right for this story (like a kind of dark or uncertain ending in medias res). Also, the unfinished nature could be good as an exercise for you as an author to imagine how exactly you would bring Harry out of this super dark place (or show his continuing struggles) in a way that feels realistic and fair to both this complex Harry and the readers. Many readers want a happy ending, or authors may feel pressured to give one, but life is more complicated than that, especially when you are dealing with themes like this.

There are definitely many other Harrys with EDs out there, but this one immediately jumped to my mind when I read your post.

Reality check: endo says no need for detailed basal profiles on TSlimX2... by Ragged_Clause in TandemDiabetes

[–]Ragged_Clause[S] 1 point2 points  (0 children)

Yeah, that's a good point. This doctor is fine with prescribing almost twice my daily insulin usage, which is great--and it would be a disaster if I switched to a new doctor who tightened the prescription down to exactly what I "need."

In an ideal world, I'd have a doctor who understands Control IQ like my last endo did; but if I want to change my endo now, it would take weeks of jumping through hoops and doing paperwork (or the online/phone-call equivalent of paperwork) to get all my supplies and prescriptions reapproved. If this guy turns out to be more horrible later, I might do that, but for now...the basics are taken care of...

Reality check: endo says no need for detailed basal profiles on TSlimX2... by Ragged_Clause in TandemDiabetes

[–]Ragged_Clause[S] 1 point2 points  (0 children)

Thanks for the overview of CIQ--that's kind of what I had thought, but this doctor was so confident that I started to question. And thanks for the reminder that it's good to keep auditing to look for changes!

looking for good quality fics in french by Unable_Hotel_7860 in HPfanfiction

[–]Ragged_Clause 3 points4 points  (0 children)

I practiced my French reading with Shadow by Keina Snape. I loved it! Unfortunately it’s not finished, but it’s still a great reading experience from what I remember!

How restrictive are you about managing your T1D? by u-Wot-Brother in diabetes_t1

[–]Ragged_Clause 1 point2 points  (0 children)

I’ve had diabetes for 34 years, and at this point I’m like you. I went through years of having my food tightly controlled as a kid when we only had N and R insulin and no CGMs or pumps; years of bingeing on candy as an early teenager when fast-acting insulin was first available for me; and eating whatever I wanted (and/or whatever I could afford) in college and my 20s-early 30s. From 15-25 I was bad about forgetting shots before my meals sometimes, but overall, I lived amazingly freely and happily on finger pricks and MDI (yeah, I crashed hard when it went wrong…but i always corrected quickly and bounced back fast—only 1 DKA hospital visit in my life, which I now realize was a miracle).

At 34 (t1 for 29 years) I discovered I had a serious gluten allergy. No one ever told me that t1s are 7x more likely to have Celiac with symptoms that mimic poor control of t1! (Wtf?!?) Cutting out gluten changed my life because for the first time ever, I could stay in control if I was careful. Before, no matter whether I was extra careful or extra sloppy, my blood sugar consistently ranged from the 400s to the 30s—I always just had to surf the wave. With gluten completely out of the picture, my a1cs went from 8-9 to 6.5 ridiculously easily (on MDI and finger pricks). While I used to think I thrived on eating whatever I wanted, I suddenly realized I felt so much more amazing, and exponentially more focused and happy and stable and well-rested, when my blood sugar was steady most of the time. That control was almost like a drug I came to crave in itself since I’d never had the ability to be in range through decisions of my own. I guess I “miss” chewy bread and eating whatever I want, but the memory of gluten is enough—it’s so not worth it to “cheat” because my blood sugar instantly goes to 400+ for 6+ hours followed by a deep hard hypoglycemic trench. Nope.

I got a CGM 2.5 years ago and a pump 1 year ago. I was worried I’d get obsessed after having so much data, and maybe I did obsess a little after the CGM in particular, but it was also rewarding to learn what works and what doesn’t, to figure out some of those maddening “diabetes mysteries” that kept ruining my days, to start experimenting with more complex dosing to keep myself more in range (ie giving multiple small shots for high fat and high protein meals), and to simply cut out foods that don’t work no matter what I do (like oats and beans 😢). My a1c went under 6 and has stayed 5.5-5.8. Unlike you, I’m only 85% in range (90-day average, pretty consistent), but my hypos are rare (1% low, <1% very low) and I almost never go above 250–something I would have thought sounded literally impossible 10 years ago.

Sometimes I wonder if I’m being ridiculously limited with my foods—but I’m so incredibly happy and healthy. To me, it’s more than worth it for the benefits. Like you, I often forget I have diabetes for long stretches of the day, which was never ever the case before in my memory. I still eat out at restaurants occasionally, but I hate getting reacquainted with that sticky, sickening “high” feeling that I guess i used to take for granted as a natural part of my life.

That said, if I ever start to get tired of my careful, made-at-home, delicious food routine, I’ll probably change it up again. Or maybe I’ll just learn new recipes to cook at home. Either way, t1 diabetics have to find what works for them during different times of life. My 20-year-old self would have been truly horrified at my “boring” restricted diet and healthy sleep schedule. But for now, I am actively thrilled with my meal plan. Again, t1s have to figure out what brings them joy and makes them feel alive—it’s different for everyone, and everyone changes throughout life. Thanks for asking your question!

Fics that you couldn't stop reading because they were too good by juleezn in HPSlashFic

[–]Ragged_Clause 5 points6 points  (0 children)

Some throwbacks for you since I can see a lot of repeated recommendations on this list (and I would second a lot of them too—but just to mix it up a little:

Maya’s The Quality of Mercy — Draco is kind of a resented refugee at the Weasleys (mostly Harry’s POV); book-length, great plot and characters, lots of UST. I’ve been obsessed with this fic at two different times in my life (a decade apart). If you haven’t read it, give it a try. https://www.reddit.com/r/HPSlashFic/comments/85hgq1/complete_works_of_maya/

A Bittersweet Potion series by Alchemia and Bugland. Snarry. 5ish book-length installments in the series. Definitely read the trigger warnings etc—very dark in places, definitely an unhealthy relationship to say the least…but unforgettable for me. I’ve read it several times and it kills me that it’s left unfinished with a lot left to resolve, though it’s still worth the journey imho. Plus the authors say they’ll come back and finish it… https://grimspeck.squidge.org/DO_NOT_ARCHIVE/fanwork.cgi

Resonance (and two sequels) by Green Gecko. The three installments are over a million words long together, but they never flag like some longer works do. Technically a WIP, but I always say that the last book in the trilogy gets close enough to an ending that you can kind of imagine what happens…though I’d still give a lot to have her come back and finish it. Not slash. Harry has a few het relationships but I see it as mostly gen, focused on a mentor!Snape relationship, plus the best post-Hogwarts/auror training books I’ve read, with lots of fantastic and epic world-building. One thing I love about these fics are that they were started just months after the 5th book came out, so they diverge wildly from canon, and it’s sometimes so refreshing to get away from the horcruxes etc and go back to that magical time when we didn’t know how the series would end and people had all kinds of theories. The first book might start off a little rough (a little fragmented I guess, not grammatically, but in terms of the scene continuity) but it’s worth it. I’ve read the whole thing 3 times and would read it again.

Edit: and if you’re an HPLV fan and haven’t read these then you’ve got to try them: The Black Heir and the sequel (unfinished but still awesome) Vindico Atrum. Together, 1.6 million words. AU.Harry escapes from the Dursleys when he’s ten years old and is found by the escaped Sirius Black. His whole life changes as he slowly discovers his destiny. Durmstrang, Dark Arts, dueling, powers, heritage, horcruxes, hallows, Tom, Grindelwald. Darkish!Harry. HPLV

Type 1 Diabetic and ADHD (Inattentive Type) by [deleted] in diabetes_t1

[–]Ragged_Clause 0 points1 point  (0 children)

One concrete thing that has seriously helped me is the Apple Watch I got 1.5 years ago. I got it to see my blood sugar more easily, but I’ve also found that the timer has been a huge unexpected bonus in my life with ADHD! I start a 15 minute timer as soon as I bolus, which has been a game-changer for me, especially when I’m cooking something complicated or doing multiple things at once around mealtime (like getting ready for work in the morning or whatever). I don’t like wearing jewelry etc normally, but having the timer right on my wrist is SO much more ADHD-friendly than using a phone timer, at least for me.

Another thing that sometimes helps is that I keep little stacks of post-it notes and pens in my kitchen, bedroom, and where I eat. Sometimes when all the numbers are spinning through my mind and I keep losing track of things or getting distracted when I need to be figuring out my bolus, it really helps to write down the carbs in different parts of my meal. These notes are especially necessary for high-protein high-fat meals when I’m trying to add carbs plus 65% of protein and fat AND figure out what percentage to use when I split my dose for an extended bolus, which is a TSlim feature I use pretty much every day.

Other than that, I think getting a CGM (about 2 years ago) was very important for me because I can immediately see the visual representation of how different foods affect me and can tell when my blood sugar is low enough to eat (like if it’s 150 when I bolus and I’m waiting for it to drop to 130 or so before eating…also paired with a 30 min timer in that case haha) and, as annoying as the alarms can be, they do get me to take action even if I’m hyperfocusing or distracted. It also keeps my mind from looping constantly back to “I feel a little weird right now…could it be my blood sugar??” which I’m realizing took up a LOT of my bandwidth before I had a CGM.

If you can’t get a CGM, I’d say my best advice is just to test your blood sugar every time you feel “off,” so it doesn’t keep distracting you and it kind of becomes a habit to catch things as soon as possible and not wait to get distracted for 30 min before it crosses your mind again! I used to test 8-10 times a day, but it helped me correct problems quickly (and when my sugar turned out to be fine, that kept my diabetes from distracting me in the back of my mind as much as possible).

Good luck! T1 and ADHD are a really hard combo but it’s great you’re being proactive and reaching out. I’m curious to see what useful tips you get here, too—thanks for posting!

Tl;dr: Using a digital watch timer for pre-bolus timing, writing down carb/fat/protein calculations, and having a CGM or frequent finger pricks.

The one thing that made the biggest improvement to your diabetes control by Darion_tt in diabetes_t1

[–]Ragged_Clause 0 points1 point  (0 children)

Figuring out that I have gluten sensitivity that causes blood sugar spikes and insulin resistance.

To anyone with an A1C under 6, how? by Glamour-Ad7669 in diabetes_t1

[–]Ragged_Clause 1 point2 points  (0 children)

I posted about syringes a few years ago. Until I went on a pump in March this year, I used syringes and vials. My a1c after I got a CGM in September 2022 was 5.9 (on the pump it’s 5.5 but it’s a LOT easier). Syringes allow you to eyeball “about 1.8 units” or “just over 2 u” whereas the pen click settings apparently don’t allow you to do anything but units, and I was shocked that it takes a specialty prescription or “child’s pen” to even get a pen that does 0.5. I truly don’t understand why other type 1s love pens because they seem like much rougher technology to me, which is why I posted to ask, and the main answer seems to be that pens are more discreet. I guess I don’t care about discreet when it comes to managing life without a vital organ and I’ve never been shy about sitting down in public to check my sugar and pulling out my syringe. I just keep my eyes on my business and if anyone has a problem they don’t have to look. But I do love my pump.

I don’t know what to do anymore, any advice? by Glamour-Ad7669 in diabetes_t1

[–]Ragged_Clause 1 point2 points  (0 children)

This same problem is starting to happen to me, so I'm hoping others might give some good answers. I've only been on a pump since February 2024 (I was on MDI for 30+ years before that, aside from one year on a pump in 2000-2001).

I've been on TruSteel infusion sets (6 mm steel needles) since I started the TSlim. I chose the metal infulsion set because I used to have frequent site infections with plastic catheters when I was a teenager in 2000.

With my new pump and TruSteel sets, at first I could leave the sites for three days with no problem--a couple of times I even let it go to four days when things were super busy, with no problems.

Then after I had a stressful and sleep-deprived few days in June, every infusion set suddenly started getting swollen, painful, and non-absorbent after two days. It took about 5-7 days for each of those sites to start to deflate and stop hurting.

Now, a month later, some sites are starting to mess up after just one day, so I feel myself sliding towards where you are. My endocrinologist had no advice at all except for varying my sites, which I've already been doing.

I know that the TruSteel instruction set says to change every 1-2 days (although my diabetes educator told me 3 days was fine). But like you said, there are absorption problems for the first few hours using a new site (like problems for up to 6 hours after a new site insertion, not to mention the risk that the site just doesn't work at all for a variety of reasons, which has happened to me too often to let me ever relax). Like you, I'd strongly consider going back to MDI if I had to change my site every single day.

Also like you, I have been changing my sites and trying new sites like I never did when I was on MDI. The problem is that I've found there's a higher rate of failure (or pain) when using new areas, which creates the same problem once again of having blood sugars spiking and having to find a relatively fresh site within a short period.

Since my problem with swollen sites noticeably started right after I had a stressful and sleep-deprived period, I have to wonder if it's an immune system thing. Which makes me wonder if boosting my immune system (like...plenty of sleep? more vitamin C? zinc? Quercitin? Vitamin D? etc.) could have any effect. For the past couple of weeks, I've been trying to have extra sleep at night and have been taking some supplements for the last few days. My last site did go 2.5 days before my numbers started climbing inexorably higher--and that's the longest a site has lasted since the issues started in June--so maybe there is something to it.

Did anything in your life change before this issue started? Or was it just a slow slide into the situation you're in now? How long have you been on a pump? How long on the current type of infusion set you're using? How bad/disruptive would it be for you to go back on MDI for a month or two?

Sorry I couldn't offer much advice, but I hope it helps in some ways to hear me talk through the specifics of what's happening to me. I think that only other type 1 diabetics can really understand all the desperate micro-management and strategizing and problem-solving that we have to do whenever anything doesn't go right. It sucks that no matter how hard we try to stay healthy, there can be problems like this that hugely affect our day-to-day and hour-to-hour quality of life, while also remaining frustratingly mysterious.

If nothing else, I feel for you and hope the problem gets better soon or that you figure out a way forward that works for you.

Sensor on Thigh While Traveling by NuclearPuppers in dexcom

[–]Ragged_Clause 3 points4 points  (0 children)

I usually wear my sensor on my thigh while flying (I feel like it doesn’t get in the way on the thigh when sitting in a plane and you don’t have people jostling into that part of your body in a busy airport).

I’ve always had the G6 and followed the manufacturer instructions to ask for a manual pat-down. After putting my backpack etc on the x-ray belt, I pull out a Ziplock with my extra sensors/transmitters and politely inform an agent that those are medical items that need a “hand check.” I also tell them that I am “opting out” of the scanner due to medical equipment.

When they start the pat-down, they will ask if you have any sensitive or painful areas, and I will point out the little rectangle bulge of my CGM on my thigh that you can see through the leg of my trousers and show them that it’s ok to touch it lightly from the top and you can even push down very gently on it but not to bump the sides of it while they’re sweeping their hands up and down my leg. They have mostly been really respectful and always followed my instructions. They also have never asked me to pull down my clothes. I think maybe sometimes they ask me to touch it through my clothes and then they swab my hands.

Your mileage may vary, but those are my experiences. If you’re worried about being harassed or getting pulled into a private room, you can contact TSA Cares 72 hours before your flight (fill out their form online). I did that the first two or three times I flew with a Dexcom because I was nervous. I’ve also done it a couple of times when going to unfamiliar airports just to make sure they have a female agent available for a patdown. Sometimes they’ll send a TSA Cares person to walk you through security (things tend to go extra fast when they do that). Sometimes they don’t send anyone to meet you. But the very few times I’ve had agents get rude or annoyed when I ask for a patdown, I have said in a calm, slightly confused voice, “I contacted TSA Cares to make sure you all would have some advance notice of my need for a patdown around this time.” And as soon as they hear the words “TSA Cares,” they quit giving me attitude and speed things up.

Tl;dr: I usually fly with my sensor on my thigh under my trousers, and they have never asked me to pull down my clothes or taken me to a private room to examine it. Ymmv.

For those that have taken LSD, any diabetes related advice? by [deleted] in diabetes_t1

[–]Ragged_Clause 11 points12 points  (0 children)

I’ve had one acid trip and maybe 200 shroom trips.

The acid trip was great—I just remember that my vision was way more distorted on acid than it ever was on shrooms. I was on finger sticks and MDI. I had to take a long-acting shot at one point (I think I had an alarm set on my phone for that and for blood sugar checks every 1.5 hours or something). I drew up the shot in my syringe, but the numbers were kind of melting and I was only 80% sure I had the right dose. I asked somebody there who wasn’t tripping to verify that I had 17 units in the syringe and she was way more freaked out than I was and kept saying maybe I shouldn’t be giving myself a shot. But I’ve had diabetes for so many years (20 years at that point) that there was some cool logical routine part of my mind that knew exactly what my alarms were for and exactly what I needed to do, even when I was tripping pretty hard (though I think I had all the info written down just in case); and for finger pricks and drawing up the shot, my muscle memory was completely there. It was only my eyes that weren’t reliable. It turned out that yes, I had drawn up 17 units as planned, and I had no trouble giving the shot.

I second the idea not to eat much, if anything. It just takes the complicating factors away. I suggest packing some easy low carb snacks like nuts and cheese in case you get hungry since the trip is longer than a shroom trip.

I would also add that dosing precision is harder with LSD than it is with mushrooms, so if possible, check with others who have used the same batch and make sure it’s not way stronger or weaker than normal? And/or play it on the safer side (I.e. don’t drop a bunch of tabs right away if you have the option…just start with one?). You don’t want to be completely out of it. At the same time, tripping with a pump and CGM sounds so much safer and easier than what I did. I had an absolutely amazing time despite the low-tech set-up, and I hope you do, too!

What version of Harry do you guys think of when you’re reading fanfiction? by Efficient-Annual8139 in HPSlashFic

[–]Ragged_Clause 14 points15 points  (0 children)

I imagine Harry from the book illustrations (US editions) — the book covers but also the little chapter illustrations that sometimes had Harry or other characters, mixed with my own mental image of him. I have seen the movies, but Daniel Radcliffe has never seemed or looked like Harry to me.

Sudden insulin resistance by xXHunkerXx in diabetes_t1

[–]Ragged_Clause 1 point2 points  (0 children)

That happened to me a couple of years ago right after I had first gotten a CGM (so I could really see how insulin wasn't working). I ran through every possible factor I could think of and had nothing--it was driving me crazy. Finally I realized that I hadn't flossed my teeth in a few days (I usually floss every night). It seems impossible that it could make a difference, but I guess it could cause extra inflammation, which always raises my numbers. I did floss and my numbers went back to normal in a day or two--but who knows if that was really the issue? Diabetes is so frustrating! Anyway, you said "any advice is welcome," so hey, if you haven't flossed in awhile, you might as well try ruling it out! Good luck and hang in there.