群衆のデザインプロセスを全面的に見直しているため、現在、新しいコメントは非公開になっていますが、引き続き確認し、検討しています。
今後のぬいぐるみに関するご提案をここに投稿してください。また、お気軽に投票してください。
他の提案も同様です!
投稿する前に、以下の点に留意してください。
1. 提案による参加は、参加者が支払いまたはその他の形の補償を受ける資格を与えるものではありません。
2. シンプルで過度に説明的ではないテキストのアイデアを共有します。
3. ファンデザイン画像は提案として受け付けておりません。そのための写真やリンクの提出はご遠慮ください。
4. コメントは公衆の閲覧に適切な内容でなければなりません。つまり、罵倒語、脅迫、成人向けコンテンツへの言及は禁止されています。
5. Plushie Dreadfuls のデザイナーを含め、ここに参加する人々に対して礼儀正しく敬意を持って接してください。
6. 同じ提案を何度も投稿しないでください。コメント欄で既に同じ提案を見つけた場合は、代わりに賛成票を投じてください。
7. 不正な手段でデザインを歪めたり誇張したりしようとすると、そのデザインは削除されます。
8. このスペースは管理されるため、不適切な行動があった場合はコメントが削除され、ユーザーが禁止される場合があります。
9. すべての提案が検討されるという約束はいたしません。
10. 楽しんでください!
1769件のコメント
Please one with Alexithymia and/or emotional surpression. I think its very common to surpress ones emotions.
Due to my autism i have a really hard time identifying my emotions causing me to feel really bad and empty all the time but i don't really understand in what way and why. I feel like a robot. it is super frustrating and it has caused me really bad trust issues in other people, and i cannot trust my own thoughts anymore.
I feel so alienated from myself. i wish i had a plushie who understood.
I would think a plushie that is expressionless, for the emotional distance. It would have muted colors for muted emotions. But make the colors on the inside of the ears like a galaxy, signifying a huge mysterious landscape that is not easily accessible. but make the stars little questionmarks. add a tiny shimmer if possible to the ears, indicating that emotional depth is hidden. like in videogames, the shiny things are often where treasures are hidden. Add some thin subtle lines on the face, signifying 'cracks' from the emotional pressure, while also indicating there is a barrier on our emotions. Then make the cracks in the color of the galaxy, because the galaxy of emotions is what we are hiding (from ourselves and others).
Make the heart in a dim colour. make it so that it is made out of puzzle pieces, but leave some pieces out on purpose.
On the paws, make clouds, for 'clouded vision'.
An ME/CFS bunny (I did not appreciate the idea that we take 'cat naps', I would have spoke up, but didn't know this proccess).
- Blues for ME/CFS awareness
- Sleepy looking eyes and large bags under them to show the fatigue, pale skin, I'm too exhausted for make-up
- Sleep mask – we can be sensitive to light and need a mask to sleep (yes, many of us with chronic fatigue also suffer from insomnia!)
- Messy, long ear fur, I don't have the energy to bathe often, and brushing my hair takes a toll on me
- Low battery patch on stomach to indicate low energy
- Zs on the inside of the ears
- Tail is a little flame to represent the spinal cord inflammation
- Wrist and ankle shackles connected to a weight that say ME, I feel weighed down and weak and like I need to pull my body along
could u do one on Dermatillomania?
I second PKD but I see that a Kidney Disease bun is in the works. PKD has impact more than half my family for as far back in generations as we have documented. New children born into our family have their first scan at 3 years old then every 3 years until adulthood. After that it’s every 5 years. I have 4 children ages 25 – 4 and 2 have been affected. There are 4 children from my parents and 3 of us have been affected. My oldest sibling is already on dialysis. One has passed. Only my sister is unaffected. My oldest child just gave birth to my first grandchild and he had developmental issues with his kidneys in the womb. Fortunately they resolved prior to his birth and were unrelated to PKD but we definitely held our breath. I love that you are in the process of giving representation to Kidney Disease. ❤️
panic syndrome
Charcot-Marie-Tooth disease – it's considered "the most common unknown disease" because it affects 1 in 2,500 worldwide, and yet most doctors have only ever heard the name once in med school but never interacted with a CMTer. It's a degenerative neuromuscular disease, primarily peripheral but can also affect the central nervous system in more severe cases like mine. There is no cure and no treatment outside of things like physical therapy, assistive devices, etc. Only type 1A is usually ever included in research, but there are dozens of other types that get no attention or research funding. It's almost always inherited, but mine is de novo, meaning that the genetic defect occurred while I was in the womb, so neither my parents nor my brothers are carriers.
Wheelchair user/walker user/cane user/etc. plushies
Cult/high control group survivor plushies
Absolutely agree!! I was diagnosed with IH in 2016 but a couple years ago they changed it to N2. They’re starting to think it’s basically the same thing though lol anyway, yes! One of the big differences with IH and N is that with IH you never feel rested, even after sleeping/napping
While the entire line is built to support, educate, and represent. A quintessential self-care rabbit would be super adorable, spa headband and all.
Id like to suggest a toxic shame bunny. Because of being shamed by my own family for every, from my weight to my interests and hobbies, I have a damaged self-esteem and a toxic relationship with shame.
Suggestion for plushies: I was born with a heart defect/disease so having a plushie with that health condition would be really awesome. There are so many types as well so it’s not just one plushie it many.
Ps I was born with aortic stenosis. There is also high blood pressure and mechanical valve plushie ideas.