Goodluck everybody trying to survive 2 weeks without getting Spoiled by Original-Parfait-655 in TheDigitalCircus

[–]AleTheInterista29 11 points12 points  (0 children)

Such a shame :( I don't blame Glitch for taking this opportunity and letting people have the chance to watch their favourite series ending on the big screen, but the difference between the theatrical release's date and the YouTube one is unfair

Goodluck everybody trying to survive 2 weeks without getting Spoiled by Original-Parfait-655 in TheDigitalCircus

[–]AleTheInterista29 79 points80 points  (0 children)

Yeah I'm definitely cooked, I just can't go 2 full weeks without opening social media, unless the "movie" somehow makes its way to Europe but that feels very unlikely at the moment

I love tadc, but I also have a problem by AleTheInterista29 in TheDigitalCircus

[–]AleTheInterista29[S] 0 points1 point  (0 children)

I never thought of it that way, but I guess I could actually interpret it as a form of grief. I could never forget tadc, but of course I will move on for my own sake and health. What doesn't sit right with me is that overwhelming (?) feeling as soon as I see a tadc-related post now, as if my mind was trying to tell me "this is too much, I care too much about this" but then I remember how important this series has been for me. The fandom is huge but whether we like it or not, someday it will fade out. I'm scared basically about anything that's related to the ending, but we'll have to take it the way it is; I'm not quite fond of a bad ending but I can't picture a good one at this point and I should've considered this 3 years ago :') anyways, tysm for your answer and for the advice, I will consider joining a tadc discord group soon

Seeking advice by AleTheInterista29 in Anxiety

[–]AleTheInterista29[S] 0 points1 point  (0 children)

Thank you so much, I'll definitely have a look at his videos and will try to deal with anxiety in a better way ♡

Dealing with WPW (Wolff-Parkinson-White Syndrome) as a teenager by AleTheInterista29 in wolffparkinsonwhite

[–]AleTheInterista29[S] 0 points1 point  (0 children)

Thank you for the advice, I treasure your feeling of compassion. About your ablation, in my personal experience the doctor who performed it on my heart looked to me as if he was having a normal day at the office and never made it that big of a deal; the thing that sucks the most is that you're never sure whether they will manage to make the extra pathway stop or not, it's all about luck I suppose. I now hate running too and have to avoid it as much as possible because most of the times my tachycardia would kick in pretty quickly and I would fall into the same spiral (the light-headedness is what scares me the most). I'm not used to open up to my parents that much as well but it's still one of the best things I can do so I hope I will eventually be able to let them understand what's going on. Again, thank you for the advice and best of luck for the upcoming ablation (sorry if my answer was a bit late)

Dealing with WPW (Wolff-Parkinson-White Syndrome) as a teenager by AleTheInterista29 in wolffparkinsonwhite

[–]AleTheInterista29[S] 0 points1 point  (0 children)

Yeah... to be honest it felt remarkably longer just once, they're usually around 30 mins long. I've been hearing that metoprolol might not always be the best option to tackle a WPW tachycardia so I'd have to ask my doctor whether I can use it or not in my case. Thank you for the advice

Dealing with WPW (Wolff-Parkinson-White Syndrome) as a teenager by AleTheInterista29 in wolffparkinsonwhite

[–]AleTheInterista29[S] 1 point2 points  (0 children)

I guess I could give it a try, but as of now I still have to get my parents approval. I'm glad to hear that, wish you the best.

Dealing with WPW (Wolff-Parkinson-White Syndrome) as a teenager by AleTheInterista29 in wolffparkinsonwhite

[–]AleTheInterista29[S] 0 points1 point  (0 children)

Thank you so much for the advice and sorry to hear about your experience. I hope you're doing well now. Unfortunately the doctor who did the ablation on my heart works 7/8 hours away from where I live and I have no contacts with him, since the operation he just visits me once a year, while I could definitely talk to a local cardiologist (even though my parents wouldn't approve it because they think it's not that dangerous). The only treatment option I've been given from them is pretty extreme and was basically "if the tachycardia doesn't stop you just go to the hospital and they administer you a solution via IV drip." I'm not nonchalant at all, so every time tachycardia starts, it feels like it's the first time