@tavasperu: ¡Estilo, confort y energía para los más peques! 💜👟 Las nuevas Adidas Runfalcon 5 Kids (modelo JQ8139) combinan diseño, ligereza y sostenibilidad 🌱 ¿Tu peque ya tiene las suyas? ✨ Cloudfoam para máxima comodidad 🌱 Hechas con materiales reciclados 💨 Ligeras, resistentes y llenas de color 📍Disponible ya — ¡Corre a por ellas! #AdidasKids #Runfalcon5 #JQ8139 #ZapatillasInfantiles #NiñosActivos #ModaSostenible #BackToSchool #SneakerLovers #AdidasOriginals

Tavasperu
Tavasperu
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Saturday 12 July 2025 02:10:35 GMT
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xiimenacurii
Xiimena Curii :
en negro tendrá ?
2026-06-26 11:31:43
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dafn862
dafn :
😁
2025-10-17 09:47:13
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This is not something I regularly post about and I do not share my children’s faces on social media bc I’m very protective of them, but I do feel this post is very important to me and I’m ok with sharing one video of my sweet girl when she just a few months old.  . Oh what I would do to go back in time to hug myself and tell her that you’re going to be so amazed by your daughters resilience and everything will be ok.  . You know as a first time, mom as well as a first-time being introduced to a child with a limb difference it’s something you can’t even express into words. My first reaction was guilt that I wasn’t educated on limb loss/differences. My second reaction was what do I do now? So if you’re a parents or guardian who just found out their child, has a limb difference, there are some things I want tell you.  . First and foremost, the limb loss/ difference community is absolutely wonderful and it’s going to be a permanent home of support for you. Do all the research you can, read all of the books and I promise it’s going to be ok.  The hardest thing is watching your child struggle, but in that struggle is where they learn. I think that was the biggest obstacle I had to overcome. Knowing that I had to let my child struggle in order for her to adapt and learn her own body. Of course I’m right there to help her whenever she needs, but if I were to do everything for her, she wouldn’t have learned how to adapt so well. This of course  just my experience and opinion and everyone’s experiences are different!  . I also want to give some advice about prosthetics. Now, of course our DR.’s team is just there to help and support us because they know what they are doing. We were offered prosthetics many times over the years and each time I declined. Here are the reasons why. If I were to give my child a prosthetic from the beginning, she wouldn’t have adapted so well to her own body by learning how to use it without a prosthetic.  (Again, this is our story and my own opinions that does not reflect anyone else’s). I have spoken to several adults with limb differences and they told me that my choice was a good and they completely agreed. This doesn’t apply to everybody, but I’m very proud of myself for making that decision. Now, at the age of almost 4 years old, my daughter is interested in prosthetics. She’s more aware about her body and can make decisions for herself which I fully support in whatever she wants to do. We will be taking her to Shriners for when she’s ready. I highly recommend Shriners hospital by the way! There there are also so many resources that I can provide each one  for you with if you’re interested. There are a lot of nonprofit organizations that help those who have children just like ours.  . Lastly, I wanted to tell you that everything is going to be ok and you’re going to be blown away by just how amazing your child is. This is really emotional for me to open up about and I really hope that this post reaches all the parents or guardians who are about to have a child with a limb difference or has one. @Shrine@Shriners Children’sf@luckyfinprojectm@No Limbitations Texasare just a few off of the top of my head who I know have a TikTok! They also have Instagram and websites you can follow.  . #limbdif#limbdifferencei#luckyfin
This is not something I regularly post about and I do not share my children’s faces on social media bc I’m very protective of them, but I do feel this post is very important to me and I’m ok with sharing one video of my sweet girl when she just a few months old. . Oh what I would do to go back in time to hug myself and tell her that you’re going to be so amazed by your daughters resilience and everything will be ok. . You know as a first time, mom as well as a first-time being introduced to a child with a limb difference it’s something you can’t even express into words. My first reaction was guilt that I wasn’t educated on limb loss/differences. My second reaction was what do I do now? So if you’re a parents or guardian who just found out their child, has a limb difference, there are some things I want tell you. . First and foremost, the limb loss/ difference community is absolutely wonderful and it’s going to be a permanent home of support for you. Do all the research you can, read all of the books and I promise it’s going to be ok. The hardest thing is watching your child struggle, but in that struggle is where they learn. I think that was the biggest obstacle I had to overcome. Knowing that I had to let my child struggle in order for her to adapt and learn her own body. Of course I’m right there to help her whenever she needs, but if I were to do everything for her, she wouldn’t have learned how to adapt so well. This of course just my experience and opinion and everyone’s experiences are different! . I also want to give some advice about prosthetics. Now, of course our DR.’s team is just there to help and support us because they know what they are doing. We were offered prosthetics many times over the years and each time I declined. Here are the reasons why. If I were to give my child a prosthetic from the beginning, she wouldn’t have adapted so well to her own body by learning how to use it without a prosthetic. (Again, this is our story and my own opinions that does not reflect anyone else’s). I have spoken to several adults with limb differences and they told me that my choice was a good and they completely agreed. This doesn’t apply to everybody, but I’m very proud of myself for making that decision. Now, at the age of almost 4 years old, my daughter is interested in prosthetics. She’s more aware about her body and can make decisions for herself which I fully support in whatever she wants to do. We will be taking her to Shriners for when she’s ready. I highly recommend Shriners hospital by the way! There there are also so many resources that I can provide each one for you with if you’re interested. There are a lot of nonprofit organizations that help those who have children just like ours. . Lastly, I wanted to tell you that everything is going to be ok and you’re going to be blown away by just how amazing your child is. This is really emotional for me to open up about and I really hope that this post reaches all the parents or guardians who are about to have a child with a limb difference or has one. @Shrine@Shriners Children’sf@luckyfinprojectm@No Limbitations Texasare just a few off of the top of my head who I know have a TikTok! They also have Instagram and websites you can follow. . #limbdif#limbdifferencei#luckyfin

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