To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍
To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍
To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍
To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍
To the whole team, @netflix @netflixmena @timashomali , @shirin_kamal , @isshomali , @issam.husseini , the crew, the cast, and last but definitely not least, the fans; thank you🤍 Layan’s death resonated with a lot of people; and while she’s a fictional character in a fictional story, it cannot be closer to reality. In this day and age, honor killings still exist in many societies and cultures, the same ones you and I live and thrive in. Not only do laws need to be changed, but people’s mentalities. Countless lives were lost and ruined in the name of honor. Whether they were women who made a “mistake”, women who were accused of a “mistake”, or simply women trying to exist in societies that target them yet claim to protect them. If you aren’t familiar with the atrocities committed against women and girls at a rate thats far from believable in the name of a backwards concept; I urge you to educate yourselves and fight for a change. We owe it to the lives lost, and to the lives that are at risk. To Layan, I’ll always cherish you. Goodbye. 🤍
whole lotta lovinnnn’ 🫶🏼
whole lotta lovinnnn’ 🫶🏼
whole lotta lovinnnn’ 🫶🏼
whole lotta lovinnnn’ 🫶🏼
whole lotta lovinnnn’ 🫶🏼
whole lotta lovinnnn’ 🫶🏼
call me Ted Mosby 👢
call me Ted Mosby 👢
call me Ted Mosby 👢
call me Ted Mosby 👢
call me Ted Mosby 👢
me by @zaidallozi (again)
me by @zaidallozi (again)
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6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!
6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!
6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!
6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!
6 months seizure free!!!! 💜 To be completely honest, a part of me never thought I’d go a month without having a seizure, let alone six! My epilepsy diagnosis in 2022 completely changed me and the way I look at life. Apart from the physical side effects my diagnosis and the prescribed medicine had on my body, my mental health was in shambles. To say I was depressed was an understatement. I felt scared, hopeless, and alone. At the time I believed my life was over. I lost opportunities, people, and more. To be even more honest with you, there were multiple times where I wholeheartedly believed I couldn’t do it anymore, not only did I feel like a burden to myself, but to others. I wanted it to stop more than anything. I was ashamed of my epilepsy. I was ashamed of the fact that I can’t do the same things my friends do without worrying about having a seizure and burdening the people around me. It even got to a point where if I felt a seizure coming at an outing, I’d hide in the bathroom so no one would know. (0/10 don’t recommend I hit my head on the toilet and that shit humbled me). After a WHILE, I came to realize that epilepsy is just a part of me, and just like anything else thats a part of me, it doesn’t define me. I can’t confidently say I’ve completely come to terms with the fact that I have a neurological condition, but I’m definitely more at peace with it. To anyone that has been diagnosed with epilepsy, please know that you are not alone. You got this. Patience and consistency is key! To everyone that doesn’t have epilepsy (lucky asses), I urge you to educate yourselves on what epilepsy is, the effects it can have on a person, and what you can do to help someone struggling with epilepsy and/or seizures. I’m grateful for the endless support and love I receive from my friends and family, from you guys too! (some of u) (some of u sent me gifs of flashing lights) (I laughed but pls don’t do that). I plan to continue raising awareness about epilepsy, and if I’m lucky enough, I would be a reason for someone to have hope if they need it. 💜 you!
