#kimpossibooty

[spellkasper]

Little late for Valentine's Day but I just HAD to draw Kimpossible.

My socials: Discord Server Instagram Twitter Bluesky Tiktok Commissions

[0idontgetsleep0]

Floyd: Christmas morning you can find me slapping a novelty sized bow on the hood of my car and parking in front of random houses until I hear excited screaming then speeding off around the corner to find my next mark.

Floyd: this will be most of my holiday.

[idendrawx]

SHEGO from kim possible another commission completed! shego from kimpossible, if you want to order a commission I have a price menu I also have patreon, take a look around my patreon and see what I offer, there are succulent waifus and I have a monthly magazine format where you will have access to different parts of the magazine by level menu commissions prices https://www.tumblr.com/idendrawx/711758183922876416/commission-menu-peach-daisy-rosalina-pauline-and?source=share

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[clonerightsagenda]

kimpossibooty said: I’m sure you’re doing your due diligence and all, but I’m in the same place. I talked with my old GP about hEDS, they checked the main joints they usually check for EDS, but my wrists and fingers etc aren’t super mobile, so they brushed it off. But a pain specialist and two PTs now all agree I have hEDS based on everything else I have going on so 🤷🏻‍♂️

kimpossibooty said: Basically if you think it’s a possibility, don’t just take their no as a definite fact. EDS is a super weird family of stuff, and the checklists are always weird with how many requirements are needed and how many options there are etc. Like I’m not saying you have EDS and shouldn’t listen to anything else, but also it’s just a super weird thing in general, so it’s hard to tell, but it still could be a thing. I just know I’m desperate to have a diagnosis that actually fits, so if you think it may be that, then you’re told by one doctor it’s not based on just some of your joints but no other diagnosis makes sense, don’t lose all hope, it doesn’t mean it can’t still be that 

kimpossibooty said: Sorry for the super long reply!!! I just relate a lot and am going through the whole impossible process myself so I have a lot of thoughts

Nah it’s cool, I finally put the pieces together about all my stray symptoms and asked for an ANA test because of seeing other people talking about their problems, so it’s helpful.

Like I said, I do intend to ask about it, although I don’t have any of the skin issues associated with EDS. That being said, most of my research has led me to suspect lupus is what’s waiting for me at the end of the road... I am simply Not Dying Enough for my rheumatologist at this stage.

[elanorsparkles]

last night I dreamt I met @ trainthief and @ kimpossibooty, except they were exactly one (1) person. they were doing stand up comedy and magic tricks in my brand new, large, non-existent irl house. (I wrote them a letter first) they left, and then there was a tornado. Except it wasn't a tornado. A gust of wind had just caught all the pamphlets from a nearby baptist church

[arthnerdianlegends]

My Wonder Woman Ace Pride shirt arrived today! It’s perfect and I love it! It’s also the first ace pride thing I’ve bought!

kimpossibooty designed it!

[marymrstn]

so this is a thing apparently

[audiophiliacfan]

Oh Hagrid.