@meheecansavage: Azure Vs Two time Lms #forsaken #edit #azuretime #cool #lastmanstanding

Meheecansavage💛
Meheecansavage💛
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Region: US
Saturday 22 August 2026 17:32:24 GMT
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sp4wn1stg0r3_1yip
⋆𐙚˚~𝐢𝐭𝐫𝐚𝐩𝐩𝐞𝐝~⋆𐙚˚ :
azure having the same hatred I have for math😭
2026-08-23 10:42:10
250
mantis.shrimp
CAIN :
more hateful than the embodiment of hatred himself 😭🙏
2026-08-23 17:01:25
16
voidenoxalt
Azure :
Wait didn’t azure never wanted to hurt two time he was forced to?
2026-08-23 02:29:22
66
officialgarythecat
Gary :
ITS NOT THAT DEEP CALM DOWN.
2026-08-23 16:14:53
12
dust7876
photato :
Bro he sounds like Gabriel
2026-08-23 19:06:26
1
arongerman
Silver :
antes a nadie le gustaba y ahora ya les gusta
2026-08-23 07:25:59
15
lowkoipu
ччч ⚛️ :
For some reason Azure's crash out similar to Tuco's crash outs
2026-08-23 09:21:18
15
.angelzure
AZURE #1 FAN & YUME‼️ :
azure mentioned
2026-08-23 09:11:11
23
hayden_ac0
Hayden-ac :
Put ts of Spotify
2026-08-23 03:33:44
8
azzoz.alnashi
عٌزٍوٌزٍ♕ :
Aberrant jhone doe
2026-08-23 17:29:30
0
meheecansavage
Meheecansavage💛 :
Yo this is blowing up my phone call tf down😭
2026-08-23 03:58:10
10
ilovecorndogs561
Schlip Schlop :
Yo that fumble was actually crazy 😞
2026-08-23 00:52:35
15
able1531
Something :
how did you survive with that horrible pathing
2026-08-23 12:51:18
0
To see more videos from user @meheecansavage, please go to the Tikwm homepage.

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My recovery does not look like everyone else’s, and that’s okay. 🩵 Traditional ED treatment has not worked for me. That doesn’t mean traditional treatment is “bad” or that it can’t be incredibly helpful for someone else. It means I am not someone else. I’m neurodivergent, and the way I experience food, sensory input, routines, rigidity, anxiety, and ED behaviors has to be taken into consideration when my treatment is designed. That’s why my ED specialized registered dietitian and care team have had to individualize my approach. For me, putting all of the emphasis on calories and numbers can become counterproductive. My treatment focuses on the actual foods I’m able to eat, expanding variety, challenging food rules and fears, working with sensory needs, increasing flexibility, and making nourishment more manageable. And I want to address something I know can be confusing when you see my videos: Some people may look at a meal I’m eating and assume I’m eating “low calorie” or still purposely restricting. I understand why it might look that way from the outside, but you are seeing one moment, one meal, or one food. You are not seeing my entire nutritional plan or the work happening with my care team, you especially don’t see my high risk of RFS or the times I have gone into the early  stages of RFS bc I did, in fact, want to eat more. I am not choosing foods based on a desire to restrict or trying to show people how to eat as little as possible. My recovery is much more complicated than what can be determined from a photo or a 30-second video. I share a lot, but I still don’t share every single detail of my treatment publicly, because my recovery is not content for other people to dissect. It is inporrsnt for me to speak on, advocate for and to educate. And I will continue to do that.  That does not mean nutrition isn’t being taken seriously. It doesn’t mean calories don’t matter physiologically. And it doesn’t mean I’m simply “eating whatever I want.” It means my care team is looking at the whole person and the barriers keeping me from being nourished, rather than assuming one treatment model will work for everyone. Some people may disagree with this approach, and that’s okay. You don’t have to recover the way I do. This is my recovery, my body, my brain, and my care team. 🩷 I will always advocate for individualized ED care, because sometimes the treatment that works isn’t the most traditional one. Sometimes it’s the treatment that finally meets the person where they actually are. 🫶🏼  #neurodivergent #neurospicy #recovery #recoveringoutloud #recoveryjourney
My recovery does not look like everyone else’s, and that’s okay. 🩵 Traditional ED treatment has not worked for me. That doesn’t mean traditional treatment is “bad” or that it can’t be incredibly helpful for someone else. It means I am not someone else. I’m neurodivergent, and the way I experience food, sensory input, routines, rigidity, anxiety, and ED behaviors has to be taken into consideration when my treatment is designed. That’s why my ED specialized registered dietitian and care team have had to individualize my approach. For me, putting all of the emphasis on calories and numbers can become counterproductive. My treatment focuses on the actual foods I’m able to eat, expanding variety, challenging food rules and fears, working with sensory needs, increasing flexibility, and making nourishment more manageable. And I want to address something I know can be confusing when you see my videos: Some people may look at a meal I’m eating and assume I’m eating “low calorie” or still purposely restricting. I understand why it might look that way from the outside, but you are seeing one moment, one meal, or one food. You are not seeing my entire nutritional plan or the work happening with my care team, you especially don’t see my high risk of RFS or the times I have gone into the early stages of RFS bc I did, in fact, want to eat more. I am not choosing foods based on a desire to restrict or trying to show people how to eat as little as possible. My recovery is much more complicated than what can be determined from a photo or a 30-second video. I share a lot, but I still don’t share every single detail of my treatment publicly, because my recovery is not content for other people to dissect. It is inporrsnt for me to speak on, advocate for and to educate. And I will continue to do that. That does not mean nutrition isn’t being taken seriously. It doesn’t mean calories don’t matter physiologically. And it doesn’t mean I’m simply “eating whatever I want.” It means my care team is looking at the whole person and the barriers keeping me from being nourished, rather than assuming one treatment model will work for everyone. Some people may disagree with this approach, and that’s okay. You don’t have to recover the way I do. This is my recovery, my body, my brain, and my care team. 🩷 I will always advocate for individualized ED care, because sometimes the treatment that works isn’t the most traditional one. Sometimes it’s the treatment that finally meets the person where they actually are. 🫶🏼 #neurodivergent #neurospicy #recovery #recoveringoutloud #recoveryjourney

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