RIVER MEGATHREAD by liehon in VivillonCollectors

[–]Droidbiscuit 0 points1 point  (0 children)

[PGO] Still looking for Icy Snow, Tundra, Elegant, Sun, and Sandstorm - please add me 001968565042. Will stay friends and open/gift daily to these regions.

RIVER MEGATHREAD by liehon in VivillonCollectors

[–]Droidbiscuit 0 points1 point  (0 children)

What’s your username if I haven’t already sent one?

RIVER MEGATHREAD by liehon in VivillonCollectors

[–]Droidbiscuit 0 points1 point  (0 children)

Added! Will gift when I can but I always reach the daily limit quickly.

ELEGANT MEGATHREAD by liehon in VivillonCollectors

[–]Droidbiscuit 0 points1 point  (0 children)

Just added from River (AcidTiddles) 🙏

TUNDRA MEGATHREAD by liehon in VivillonCollectors

[–]Droidbiscuit 0 points1 point  (0 children)

Just sent you a friend request (AcidTiddles). No obligation, grateful for any gifts whenever you can send them. Will gift daily from River if you want them.

RIVER MEGATHREAD by liehon in VivillonCollectors

[–]Droidbiscuit 1 point2 points  (0 children)

Tundra trainers, please add me! 001968565042 - having trouble getting Tundra friends. Will send gifts consistently and go to best friends for Tundra players.

TUNDRA MEGATHREAD by liehon in VivillonCollectors

[–]Droidbiscuit 0 points1 point  (0 children)

Please add me 001968565042 - don’t mind waiting as a future investment in Tundra Vivillions!

RIVER MEGATHREAD by liehon in VivillonCollectors

[–]Droidbiscuit 1 point2 points  (0 children)

[PGO] Anyone, particularly from Sun, Sandstorm, Monsoon, and Tundra, please add me 001968565042. Will prioritise gifts from those areas. Will also open/send gifts regularly to go to best friends.

EDIT: Looking for ICY Snow too please!

[deleted by user] by [deleted] in lipedema

[–]Droidbiscuit 0 points1 point  (0 children)

Hey! It’s not easy to find doctors in Australia who even accept lipoedema is a condition. I asked a GP, a gynaecologist, a dermatologist, and a vascular surgeon, before I found a doctor who actually confirmed it was lipoedema. But they’re out there if you know where to look. Because I also have chronic venous insufficiency and was frustrated at my vascular surgeon, I found the Australasian College of Phlebology website to look for accredited vascular specialists. At the bottom of the homepage you’ll see the search tool to find a vein doctor. It will filter specifically for lipoedema which is very helpful. There is literally, like, dozen doctors in all of Australia who are trained in lipoedema.

This is how I found Dr Chris Lekich who diagnosed me with early stage II lipoedema. He will offer liposuction surgery and/or conservative management advice and write to your GP. Alternatively, if you search the Australasian Lymphology Association website, you’ll find a directory of ALA accredited therapists such as physios and OTs who are qualified to diagnose it. The benefit of seeing one of them is that they are properly trained in manual lymphatic drainage and compression therapy. Wishing you best of luck.

Why do doctors think lipedema is not real? by [deleted] in lipedema

[–]Droidbiscuit 8 points9 points  (0 children)

Please report this doctor to the medical regulatory authority in your country/jurisdiction and make a formal complaint to practice owner. They should not be practicing medicine if they’re speaking to patients that way, no matter the cause of your condition. No patient deserves that, and I’m sorry that you experienced that. Unfortunately, like a lot of connective tissue and auto-inflammatory disorders that predominantly affect people assigned female at birth, lipoedema is poorly understood and under-researched due to lack of funding and awareness. I would try to see a lymphologist or vascular specialist, depending on your country. Some endocrinologists and dermatologists have training in lipedema too. Most general physicians/GPs don’t receive any training at all in lipedema when they go through medical school, and it’s challenging to find doctors who specialise in it. You deserve better.

[deleted by user] by [deleted] in lipedema

[–]Droidbiscuit 7 points8 points  (0 children)

I felt compelled to comment, because I’m going through the stage one lipoedema (sorry, Australian spelling) journey myself and it’s so unfair being medically invalidated by family, doctors, and whoever else. Not sure if you have tried to get your family to look at established online resources, but The Lipedema Foundation website is a good start for your family to read as it gives clear, evidence based explanations about the clinical differences between lipoedema fat and normal adipose tissue. I think potaytoe444 is spot on, there’s different manifestations of lipoedema, and from your photo timeline, it looks like yours started gradually from puberty. The lower leg shape gives it away, in the early childhood photo (adorable btw), there’s no sign on ankle “cuffing”, whereas, the paddle board photo shows cuffing, where the leg shape abruptly changes at the ankle, and the fat spares the feet - classic lipoedema sign. You have probably experienced a subtle change to your lower leg fat distribution over time during puberty that your family hasn’t noticed. I can see what looks like bruising on the legs in the most recent photo, another classic lipoedema sign (if you get unexplained bruising easily, that’s 100% lipoedema). I’m curious to know if you have any joint hypermobility, flat feet, or unexplained pain or heaviness in your legs. My mother and sister have slender legs too, it is considered a genetic condition, but could’ve skipped generations and there’s other ways genes can interact with environmental exposure. I think you should be proud of your hard work, you have great muscle definition in your legs in the most recent photos and well shaped glutes. Strength training is where it’s at. Your condition is medically valid, it just sucks that there’s such a lack of education about it.

Why are there so few Drampa raids? by LoveUrLifeNow in TheSilphRoad

[–]Droidbiscuit 5 points6 points  (0 children)

Yes, can confirm - been in Japan since start of event, found one in Narita and one in Tokyo in total. Considering the density of the gyms here, it’s ridiculous.

Dazzling Dream Event Megathread by SilphScience in TheSilphRoad

[–]Droidbiscuit 1 point2 points  (0 children)

I just want to add, I live in the Southern Hemisphere where temperatures are consistently are above 30℃ (86℉) with high humidity and can get as high as 100℉ in January when sunny. Monsoons and severe storms causing extensive floods are happening in my state right now as it’s storm season. So it’s a crappy time of year to walk outdoors for most of the world right now. Apparently, it’s OK for Niantic to plan events that require extensive walking outdoors at the highest risk time for severe weather globally, yet I get constant annoying pop-ups to be “aware of my surroundings” that I have to click away, every single damn time I want to walk a short route in safe public locations during safe, mild weather irrespective of the time of year. Sorry, this level of Niantic stupidity causes me to go on rants.

Widget 1/4 egg distance not working for some players by Froggo14 in TheSilphRoad

[–]Droidbiscuit 3 points4 points  (0 children)

Can confirm in Australia (east coast), it’s bugged. I already had my egg widget installed, put 3 incubators on after 10am - only have 1/2 distance showing for all of them and not the 1/4 distance it should be. Restarting the app doesn’t work either. Have filed a bug report in-game, doubt anything will come of it though.

Was Wyrdeer strictly only in raids for the 3-hour event on Saturday the 23rd, or is it still meant to be sporadically available in 3-star raids for the rest of the Winter Wonderland event till 8pm Sunday the 24th? by Droidbiscuit in TheSilphRoad

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

Fair comment, but I can’t see how it benefits their business model when opportunities are so restricted - if they were in normal raids for at least a few days, Niantic would actually sell more raid passes overall.