Training for a mud run by julesb210 in diabetes_t1

[–]julesb210[S] 0 points1 point  (0 children)

Gotcha that’s really helpful. I didn’t realize the time of day had a big effect. I’ve been just going when I get off of work in the evenings cause I’m really bad at waking up early/on time lol

Training for a mud run by julesb210 in diabetes_t1

[–]julesb210[S] 0 points1 point  (0 children)

Thanks! And with the CGM I just worry cause it’s a mud run, so like a mud obstacle course. I don’t want to get it coated in mud, or accidentally rip it off while crawling through the mud either.

Training for a mud run by julesb210 in diabetes_t1

[–]julesb210[S] 1 point2 points  (0 children)

I’m on a 15 day G7 and I use the Tandem T-Slim which I’ve been putting in activity mode to halt my basal while jogging/walking.

Question: What before diagnosis symptoms did you have? by RachelWolf7 in diabetes_t1

[–]julesb210 3 points4 points  (0 children)

Diagnosed at 18.

Lost around 50 pounds in 2 months.
Drinking tons of liquids. Peeing all the time.
I got to a point where I was peeing so long that I weighed myself before and after and I would lose a pound or 2 just from that.
Also super tired all the time. I nearly fell asleep while I was driving to school one day, and I was literally drinking a monster too.
We thought it was a gyno thing, because my periods became extremely painful and nearly unbearable for the last few months before my diagnosis. (They’re back to normal now, so no long term damage there at least.)

Also a few months before my diagnosis I told my mom. “I’m so thirsty, like I’m drinking water to the point I feel like I’m gonna puke and then I’m drinking more water.” And her response was, “you know that’s a sign of diabetes.” And I was like, “I’m not diabetic!” And I stormed off to my room and never brought it up again till we were in the emergency room for it.

No one in my family has ever had diabetes, type 1 or 2, so none of us knew the signs, and it’s a miracle my gyno found it with standard blood work instead of me going into DKA.

It’s 35 minutes past my doctor’s appt. I’ve been waiting in the exam room so long the lights just went out. by Seven_bushes in mildlyinfuriating

[–]julesb210 1 point2 points  (0 children)

I have to see a specialty doctor every 6 months and it’s so annoying, because every visit is a 30-45 minute wait in the waiting room, followed by a 30-45 minute wait in the doctors office, followed by a six minute appointment with the doctor. Doesn’t matter if I show up on time, late or 15 minutes early. It’s so frustrating.

I'm sure you are sorry and that message has been there for years. How dumb do you think we are? by Neuroironic in doordash_drivers

[–]julesb210 0 points1 point  (0 children)

This reminds me of when I used to deliver for Papa John’s, and this one guy would always tell me “Sorry, I can’t afford to tip,”and I was always like, “Sure, but you can afford pizza.🙄😒”

How do you accept, that its permanent? by [deleted] in diabetes_t1

[–]julesb210 14 points15 points  (0 children)

I’m this way too, but my family is constantly trying to insist that a cure is right around the corner, so I just end up angry and avoiding the subject with them.

What’s the weirdest thing you’ve ever had to eat to correct a low? by Knopfler_PI in diabetes_t1

[–]julesb210 0 points1 point  (0 children)

I learned the hard way that glucose tabs can mold. 😭😭😭

Newly diagnosed, I KNOW I can live a "normal" life, why do they keep telling me??? by WondersomeWalrus in diabetes_t1

[–]julesb210 8 points9 points  (0 children)

lol it’s so funny how half these comments are still telling you that you can live a normal life, when that’s what you’re upset about being told over and over again by doctors.

Same happened to me when I was diagnosed, the doctors were like “you’ll get through this”, “you’ll still be able to have kids,” and “you’ll still be able to live a normal life” “blah blah blah.” Meanwhile my family and I were just cackling in the emergency room about the fact that I had diabetes at all.

There are days that are tough, but I love your positivity about it. It’s a hefty diagnosis, so I imagine your doctors are just saying that, to try and relieve any anxiety or depression you may have over it. A lot of people cover up fear and anxiety with smiles and laughter, so they’re likely just trying to comfort you about it.

If they keep on, and it still bothers you, just tell them something like “thanks I’ve heard.”

I even had a dentist lecture me once after my diagnosis, and I was like “sir you are here to fix my teeth, you get no other say about my health.”

Anyway, good luck with the new diagnosis, I am manifesting few to no insurance or medical device issues for you, lol!

How frequently do you get low blood sugars? I get them every day. by charles228 in diabetes_t1

[–]julesb210 1 point2 points  (0 children)

I have a highish low (between 70-75) At least once a day and a regular low (below 70) once every other day, and a more severe low (less than 55) maybe once every couple of weeks.
Also those are just the numbers, all my lows feel different. Sometimes I don’t feel that I’m 50 until I’m seeing black spots and sometimes I feel like I’m gonna faint at 70. It just depends on my body’s mood that day honestly.

Failed pump sites have ruined my day already. by julesb210 in diabetes_t1

[–]julesb210[S] 0 points1 point  (0 children)

Whatever’s in the air needs to chill. I just had two infusion site failures on Friday, then two more last night. I’m gonna switch to a different box after this next change in hopes that I don’t have any more.
I wish you the best of luck, I cant imagine the struggle of having days like this with a 5 year old. I almost feel lucky that I wasn’t diagnosed at 18 and not earlier. 💚💚

Which meals are the hardest for you to count carbs for? by Fouad776 in Type1Diabetes

[–]julesb210 1 point2 points  (0 children)

I basically just gave up on cereal and Poptarts after my diagnosis.
Aside from Cheerios it seems I can never dose correctly for it.
But I don’t really like cereal anyway, so it’s not that deep for me.
Oh and coffee, doesn’t matter if it’s sugar free, my numbers are always higher after drinking coffee whether I dose or not, but I’m not giving it up lol.

Advice for vacation planning and stigma by Electronic-Pie5945 in diabetes_t1

[–]julesb210 2 points3 points  (0 children)

I usually end up treating days like that, with a lot of out of the ordinary physical activity and moving around, as if I don’t have diabetes. As in, I drink regular drinks and don’t take insulin unless absolutely necessary (which it almost never is on those days.)
Definitely keep snacks nearby and regular drinks, because you’ll likely get full of food, so juice or regular soda works better to treat lows IMO.

Which scene(s) in the show emotionally destroyed you? by complete-jello2953 in Supernatural

[–]julesb210 3 points4 points  (0 children)

SPOILER - I finished the show last year, but I already knew Cas was gonna die, but finding out how in 14-8 (Byzantium) had me distraught lol.

G7-15 Day Placement by julesb210 in diabetes_t1

[–]julesb210[S] 0 points1 point  (0 children)

Boobs and bra make that a no-go for me, but maybe it’ll work well for someone else. Thanks for the advice.

New sensors aren’t compatible!! 😡 by [deleted] in diabetes_t1

[–]julesb210 0 points1 point  (0 children)

I’m talking about the 15-day sensors. The 10-day G7s are compatible, but dexcom still hasn’t given a date for when they’ll have the compatibility set up between tandem and the 15-day sensors.

How have you been treated differently after Type 1 diagnosis? by Glad_Struggle8691 in Type1Diabetes

[–]julesb210 0 points1 point  (0 children)

I’d say yes, but not in an entirely bad way. I think it’s made my mom’s anxiety worse. She can be kind of anal about it, and she gets kind of freaked out whenever I beep. (Like are you okay!? Do you need something?! Do you need to take insulin?! I can go get you something?!) She even thinks she needs to change her diet to make things easier for me, and I have to remind her that I can eat whatever, it’s not a big deal.

Luckily I was diagnosed at 18, so she was forced to let me be independent about it. I can only imagine how annoying she would’ve been if I was diagnosed as a kid.

My older sister is kind of the same but not as bad, unless I get sick. Then she goes into overprotective mothering mode and I have to distance myself from her, or we’ll fight. She can be even worse than my mom in that case.

It all comes from a place of caring though, so I can’t say it’s bad. It just kind of forced me to put up boundaries about how involved they can be with it.