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Mic West
Platinum/Grammy Nominated Jhene Aiko Childish Gambino Logic The Game Method Man Dizzy Wright Boogie Marsha Ambrosius Royce da 5'9 Elzhi & more
Profit & Loss: First Quarter EP
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Mixed & Mastered by @micwest
Recorded at breaking bad studios
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
In November, we got the news that our sweet Zoe has Rett syndrome. Rett syndrome is a rare, genetic neurological disorder caused by a mutation on the X chromosome, specifically the MECP2 gene, which is why it primarily affects girls. It impacts brain development and how the body communicates with the brain, often affecting things like movement, motor skills, muscle tone, breathing, and communication over time. It’s a lifelong diagnosis, one she won’t outgrow, but we are learning to navigate with support, therapies, and a whole lot of love.
Trying to put into words how this feels as a parent… it’s hard. Some days we’re hopeful and focused, and other days we’re overwhelmed, scared, grieving or trying to process what this means for her future. There’s been a lot of learning, a lot of unknowns, and a lot of emotions that hit when we least expect them. But even with all of that, Zoe continues to show such strength, resilience, and light, she inspires us more than she’ll ever know.
I’m endlessly grateful for the support around us: our family, our friends, and Zoe’s amazing team at the Children’s hospital, who have shown us so much care, patience, and guidance. Her neurologist, from our very first hospital visit, advocated in ways I’ll forever be grateful for 🙏🏽 And to the International RETT Syndrome Foundation, thank you for the constant resources, stories, and connections we’ve made and continue to make. Knowing we’re not alone in this has meant everything.
Zoe is brave. She is loved beyond words. And we’re walking this journey with her. Learning, advocating, and showing up for her every step of the way. We love you our Zoe Bowey 💜✨
#rettsyndrome #rettsyndromeawareness #geneticdisorder
Grateful to have a song made about me by the talented Mic West 🙏🏽 blessed for the love and recognition.#MicWest #SongAboutMe #GratefulVibes #HumbleHustle #ViralMusic #MusicCollab #UpAndComing #StreetMusic #MusicLovers #SupportCreatives #NewMusicAlert #ColochoVibes
Me and my dawg @jag had a song placed on the show Bel Air. Feeling blessed ! More to come !
What’s your Why? - Episode 2
Honored to work with clients that share the same passion and vision. We believe music is a divine source of love and gives inspiration to people all over the world. Hopefully, this video shows the work behind the process and gives you that same inspiration.
Reach out to @micwest for all your recording, studio, music, and production needs!
Reach out to @consult_mga for any interest in promotional videos for your business!
Love & Light 💜
Director: @matt_arce
Cinematography/Editing: @agoodspot
Audio/Producer: @micwest
The Grand Finale produced by mic west @pagekennedy @royceda59 @kxngcrooked @3dnatee @losangelesconfidential @mysonne @dalocksmith @grafh @therealransom
My dawg @pagekennedy dropped a video with @elzhi & @methodmanofficial prod by me. Link in his bio . Check that out
View Instagram Stories in Secret
The Instagram Story Viewer is an easy tool that lets you secretly watch and save Instagram stories, videos, photos, or IGTV. With this service, you can download content and enjoy it offline whenever you like. If you find something interesting on Instagram that you’d like to check out later or want to view stories while staying anonymous, our Viewer is perfect for you. Anonstories offers an excellent solution for keeping your identity hidden. Instagram first launched the Stories feature in August 2023, which was quickly adopted by other platforms due to its engaging, time-sensitive format. Stories let users share quick updates, whether photos, videos, or selfies, enhanced with text, emojis, or filters, and are visible for only 24 hours. This limited time frame creates high engagement compared to regular posts. In today’s world, Stories are one of the most popular ways to connect and communicate on social media. However, when you view a Story, the creator can see your name in their viewer list, which may be a privacy concern. What if you wish to browse Stories without being noticed? Here’s where Anonstories becomes useful. It allows you to watch public Instagram content without revealing your identity. Simply enter the username of the profile you’re curious about, and the tool will display their latest Stories. Features of Anonstories Viewer: - Anonymous Browsing: Watch Stories without showing up on the viewer list. - No Account Needed: View public content without signing up for an Instagram account. - Content Download: Save any Stories content directly to your device for offline use. - View Highlights: Access Instagram Highlights, even beyond the 24-hour window. - Repost Monitoring: Track the reposts or engagement levels on Stories for personal profiles. Limitations: - This tool works only with public accounts; private accounts remain inaccessible. Benefits: - Privacy-Friendly: Watch any Instagram content without being noticed. - Simple and Easy: No app installation or registration required. - Exclusive Tools: Download and manage content in ways Instagram doesn’t offer.
Advantages of Anonstories
Explore IG Stories Privately
Keep track of Instagram updates discreetly while protecting your privacy and staying anonymous.
Private Instagram Viewer
View profiles and photos anonymously with ease using the Private Profile Viewer.
Story Viewer for Free
This free tool allows you to view Instagram Stories anonymously, ensuring your activity remains hidden from the story uploader.
Frequently asked questions
Anonymity
Anonstories lets users view Instagram stories without alerting the creator.
Device Compatibility
Works seamlessly on iOS, Android, Windows, macOS, and modern browsers like Chrome and Safari.
Safety and Privacy
Prioritizes secure, anonymous browsing without requiring login credentials.
No Registration
Users can view public stories by simply entering a username—no account needed.
Supported Formats
Downloads photos (JPEG) and videos (MP4) with ease.
Cost
The service is free to use.
Private Accounts
Content from private accounts can only be accessed by followers.
File Usage
Files are for personal or educational use only and must comply with copyright rules.
How It Works
Enter a public username to view or download stories. The service generates direct links for saving content locally.