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HIJAB TOBRUTT
HIJAB TOBRUTT
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Thursday 19 March 2026 08:38:13 GMT
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Learn your rights and advocate for yourself!  https://form.jotform.com/SCILF/sci-pressure-sore-survey?utm_id=97758_v0_s00_e231_tv2_tp1_a1den1nla9sq4w&fbclid=IwY2xjawSEUhRleHRuA2FlbQIxMABicmlkETFFbVhVeWNXZjFwa0hTZ1dic3J0YwZhcHBfaWQQMjIyMDM5MTc4ODIwMDg5MgABHqpKpeJT8poCV956F1LHuuaj4TfjHMu0FyN_QPiJQp-ODbr0wIjdRl2YTzEb_aem_6_OJDA2-IFRVkvc_PVHEQw  If something feels wrong and you’re not sure what it is, write it down and if it’s really bothering you, show it to a DHS officer, therapist or a social worker and see what they have to say about it. If you’re getting the subpar treatment at the doctors office or for any procedure, automatically report it to the hospital and keep records of everything you report in case they don’t do anything about it. If they don’t after you show them all the evidence, then you have enough for information to file a lawsuit. Honestly, more lawsuits should be filed by people with disabilities far more often than they currently are, but the reason most people don’t file is because it’s expensive to retain a lawyer and most of us don’t have enough money. Especially if you’re only income or money is your social security disability check. Secondly, we’re so used to just taking whatever we can get when it comes to any kind of system so people give up and assume there’s nothing they can do. It’s really scary that it gets to the point where people give up and just accept treatment or care that they know they deserve better of!      It took me so long to learn this and I’m still not doing a great job at it. I think I do a really good job with it during doctors visits, procedures, and things like surgery, even though  my boyfriend is always with me, like 24/7 and people have tried to talk to him instead of me, but he’s so used to letting me take the “stage“ when it comes to talking to people when we go out, as I am much more extroverted than he is. He likes to watch me interact and talk to other people. He says I’m like a “firework“ going off when I’m around other people. He says I light up the place. So incredibly sweet. But anyway, he sits back and lets me go up first and speak loudly and clearly to them so they know I’m the one to talk to, not him.  #knowyourrights  #disabilityadvocate  #wheelchairlife  #neurologicalcondition  #bedsores
Learn your rights and advocate for yourself! https://form.jotform.com/SCILF/sci-pressure-sore-survey?utm_id=97758_v0_s00_e231_tv2_tp1_a1den1nla9sq4w&fbclid=IwY2xjawSEUhRleHRuA2FlbQIxMABicmlkETFFbVhVeWNXZjFwa0hTZ1dic3J0YwZhcHBfaWQQMjIyMDM5MTc4ODIwMDg5MgABHqpKpeJT8poCV956F1LHuuaj4TfjHMu0FyN_QPiJQp-ODbr0wIjdRl2YTzEb_aem_6_OJDA2-IFRVkvc_PVHEQw If something feels wrong and you’re not sure what it is, write it down and if it’s really bothering you, show it to a DHS officer, therapist or a social worker and see what they have to say about it. If you’re getting the subpar treatment at the doctors office or for any procedure, automatically report it to the hospital and keep records of everything you report in case they don’t do anything about it. If they don’t after you show them all the evidence, then you have enough for information to file a lawsuit. Honestly, more lawsuits should be filed by people with disabilities far more often than they currently are, but the reason most people don’t file is because it’s expensive to retain a lawyer and most of us don’t have enough money. Especially if you’re only income or money is your social security disability check. Secondly, we’re so used to just taking whatever we can get when it comes to any kind of system so people give up and assume there’s nothing they can do. It’s really scary that it gets to the point where people give up and just accept treatment or care that they know they deserve better of! It took me so long to learn this and I’m still not doing a great job at it. I think I do a really good job with it during doctors visits, procedures, and things like surgery, even though my boyfriend is always with me, like 24/7 and people have tried to talk to him instead of me, but he’s so used to letting me take the “stage“ when it comes to talking to people when we go out, as I am much more extroverted than he is. He likes to watch me interact and talk to other people. He says I’m like a “firework“ going off when I’m around other people. He says I light up the place. So incredibly sweet. But anyway, he sits back and lets me go up first and speak loudly and clearly to them so they know I’m the one to talk to, not him. #knowyourrights #disabilityadvocate #wheelchairlife #neurologicalcondition #bedsores

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