@user2140669952980: Double cross earrings will be sold out soon#earrings #silverearrings #jewelry #fyp #earringslovers

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greenaway.vargas
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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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