Tag: Disability Awareness

  • The History and Future of Disability Pride

    The History and Future of Disability Pride

    As Americans, there are certain days we all recognize when we look at our calendars. Independence Day, Labor Day, Memorial Day, and Martin Luther King Day.  future generations of students will be taught about Barack Obama and Juneteenth. We have such a rich history to learn from and be proud of. However, there is a particular group of heroes that have been neglected. The time has come to acknowledge what they have done and call a new generation of advocates into action.

    Rosa Parks and Jackie Robinson are names every person in this country knows. Unless you have a disability, names like Judy Heumann, Brad Lomax, and Katie Cole are foreign to you. These proud patriots are some of the leaders of the protest that has come to be known as the 504 Sit-in.  Starting April 5, 1977, approximately 150 individuals with various disabilities occupied the Office of the U.S. Department of Health, Education, and Welfare in San Francisco for 28 days.  To require enforcement of The Rehabilitation Act that was signed into law a few years earlier. For nearly a month these brave people risked their lives. Going without medication and personal care. You would think after such an effort You would see change begin to happen, but it took 13 years to see any tangible evidence of equality.

    Blessed are the peacemakers, for they will be called children of God.
    Matthew 5:9 NIV

    Let’s talk about July 26, 1990. Without using Google most of the population are unaware that this is the day the Americans with Disabilities Act (ADA) was passed. This legislation means much more than handlebars in the bathrooms and curb cuts on sidewalks. It guaranteed civil rights for individuals with disabilities. There is a misconception that because of this law All the problems of the disability community are solved. Earlier this week the Department of Justice filed a lawsuit against the Chicago Cubs and Wrigley Field for significant violations after a multi-year renovation project. How long must we remain an afterthought?

     In the mid-1980s journalist, Geraldo Rivera did a series of stories exposing the horrific treatment of individuals in Developmental Centers.  Earlier this year a nursing home in Sussex County New Jersey made national headlines for having our most vulnerable citizens in inhumane conditions leading to death and malnourishment. Over 200 humans were locked away without committing any crime and deprived of due process. I love this country and I am a proud American but advocates like myself Can no longer stand by while we sponsor second-class citizenship. That is not in the Constitution I studied.

    Did you know that there is a disability pride flag? The colors are a separate concept from the rainbow flag identified with the LGBTQ community. The five colors represent the different needs and experiences of the individual. Mental Illness, Intellectual and Developmental Disabilities, Invisible and Undiagnosed Disabilities, Physical Disabilities, and Sensory Disabilities. The month of July is known as disability pride month, but what exactly is disability pride? I was asked this question a few days ago, and this was my answer. “Disability pride is loving and accepting yourself, even though the world will not.” 

    Ken Capone leads the charge to end sub-minimum wage in segregated workshops. In the year 2022, they are still legal.  Emily Voorde is a female with a disability. She is the Associate Director for Disability Community Engagement in the White House. Their tireless efforts are never seen.  New Jersey has its own coalition of heroes.  Keith Jones is a disability activist, award-winning author, and former presidential candidate. Project Freedom helps individuals obtain accessible housing. Their founder Norman Smith has a disability.

    The inscription on the Statue of Liberty reads “”Give me your tired, your poor, Your huddled masses yearning to breathe free, The wretched refuse of your teeming shore.””  This was written in 1883 139 years later and people like myself Can’t read it, because of all those steps. 

    The next generation of disability advocates must not rest. We need to rise up and continue the work that has been laid before us. In January of 2022, Governor Murphy signed a law updating New Jersey’s WorkAbility program, as of July of the same year the legislation is still not implemented. With these updates, Disabled New Jersey residents would be able to earn a competitive wage, pay taxes, and keep their health benefits. By entering the workforce people who can work can support those with more complex medical needs. If we invest in more medical group homes we can avoid tragedies like the one mentioned above. This would create more jobs for caregivers and relieve stress on the overwhelmed disability care system. On the national level, We must end the marriage penalty and raise the $2,000 asset limit set in 1983. America cannot become the land of opportunity until all Americans have a chance to thrive.

    Note: every advocate mentioned Is very well known. It is very easy to learn more about them if you just take the time

  • Disability Burnout Solutions

    Disability Burnout Solutions

    Have you ever felt burnt out? That’s what I want to talk to my readers about today. This is one of those posts that I’m going to love to write but someone is either going to say I’m mentally unstable or completely naive. I’m writing this because I know I’m not the only one. I’m not depressed, I’m actually in a very good mood right now.  Life is complicated. We all know that it’s how we compartmentalize those complications that matter. ask any mom if they have all locked themselves in a bathroom for 15 to 20 minutes just to get a break from their kids that they love more than anything. Any father has been known to blast the nastiest music when the kids step out of the car just because they’re tired of listening to Baby Shark. There is a day of the week that we’re supposed to rest and not do any work. Whether we take advantage of it or not is a whole different story but the day is there regardless. I can’t rest. I have disability burnout!

    “aren’t you sitting down in your wheelchair, so how can you be tired?” Let me be clear I absolutely and unequivocally love my life. I don’t want to change it. I love answering kids’ questions in public, even though their parents can sometimes be jerks. My father, who is my primary caregiver, can be one of the funniest people in the world. That doesn’t mean I don’t feel like a burden sometimes when I can see he is exhausted after taking me back and forth to doctor’s appointments.  I thank God every time I get a chance to write a policy for those who cannot speak for themselves.  My eyes still get tired at 11:30 at night when I’m still looking through my emails.  Being broke is not fun but I’ve never gone hungry or gone without a roof over my head. I don’t need to get married tomorrow but it would be nice to be truly missed by someone special when they had a bad day. getting that look that says “ I want you right now!”

    The hardest part about having a disability it’s not all the physical things I can’t do myself. is the fact that there will never be any days off. I don’t get to walk on Sundays. It’s not like losing 10 lbs by going on a diet. all the physical therapy in the world can only do so much, and I love my physical therapy sessions. Some parts of my body hurt every day. except for some breakthrough in science I am most likely going to die with this Cerebral Palsy I was born with. thinking about all this is and can be exhausting. There is a very difficult but simple way to handle this paradox.

    “We who are strong ought to bear with the failings of the weak and not to please ourselves. Each of us should please our neighbors for their good, to build them up.” Romans 15:1‭-‬2 NIV

     All you have to do is not deny it at all but refuse to dwell in it. Instead, you look at all the light that is around you and all that you can do for yourself. it could be as easy as reading these words or having them read to you.  giving up is easy finding great ways to continue that’s the challenge. That begins every day, isn’t that worth living for? I love you all, have a great day friends.

  • July is Disability Pride Month

    July is Disability Pride Month

    By Jesse Schwartzman

    The following statement and subsequent article are written and produced by Jesse Schwartzman He is a tremendous disability advocate who formerly worked on Governor Philip Murphy’s reelection campaign in New Jersey I hope you all enjoy his fresh perspective.

    Progress has been made but it is not enough. We are at least 15 percent of the population but do you see people with disabilities integrated into society?
    It is time to uplift voices and bring our own seats to the table.
    Look to your left and your right disability can be hidden and happen anytime.
    The intersectionality is insane.
    Be kind to everyone, especially yourself.
    Do your best and improve at least 1 percent each and every day.

  • 35th Trip Around the Sun

    35th Trip Around the Sun

    Salutations my beautiful readers I hope these words can make your heart smile for a few minutes. This message goes out to anyone that has a disability. This world will not understand you, this world will betray you. However, God will not because he does not make mistakes. By the time you read this, I would have just celebrated my 35th birthday. I’ve officially reached the age where you don’t want to count anymore! This year more than ever, I found myself contemplating the meaning of life as an adult with Cerebral Palsy. My heart and mind battled for several weeks leading up to the big day. This world and the society we built have placed a set of expectations on a person by this state in their life. How do you think I measure up?


    I have no traditional source of income. I’m still looking for a life partner. I have no children or anyone to pass down my legacy. I depend on others to live my life. Some would say I have no value in our society. This physical world has no expectations of me. Even if people never said it out loud, The look on their faces says “He can’t do anything for himself.” If I’m being honest with myself these assumptions are correct. So why don’t I give up? Every once in the blue moon I might get an Amazon gift card from my advocacy activities. Every time someone buys my book I wonder, I hope they read it and understand the message. What if it’s just sitting on the counter? Every woman I know is so busy they can’t return a text. At this age any woman I consider having a relationship with it’s probably going to have a child of her own, I’m not the usual stepdad girls look for. If I have nothing and will most likely never have anything of value, what is left to fight for?

    "And without faith it is impossible to please God, because anyone who comes to him must believe that he exists and that he rewards those who earnestly seek him." Hebrews 11:6 NIV


    I found my answer in Jesus and his grace! I fight for his love and his grace that I don’t deserve and cannot earn. Yes, I will admit a few weeks ago I was angry, frustrated, and hurt with the outcome of my life. I’m a sinner, a hypocrite and many people are much more deserving than I am. Especially amongst my disability community. So many people have no voice and died in the last few years with this global situation. I don’t like this world but it is so seductive.

    "Consider it pure joy, my brothers and sisters, whenever you face trials of many kinds, because you know that the testing of your faith produces perseverance." James 1:2‭-‬3 NIV   

    I don’t always understand why I was put on this planet that doesn’t understand me and will not accept me. All I know is that I have faith in God’s perfect plan. He uses weakness for his own good and his own Glory. In the long run, I will reap the benefits with my savior Jesus Christ. A general does not use his best warriors for easy battles. They’re saved for the important ones. Wherever you go though it is only temporary God’s kingdom is forever Thank you for these few minutes together friends see you next time.

  • Toes in the Sand

    Toes in the Sand

    I want to wish all my readers a wonderful Wednesday. for this week’s post, I decided to share an excerpt from my first publication Confessions From Disability  Limbo  Available exclusively on Amazon Please enjoy see you next Wednesday. I welcome all comments Good and bad.

    There is a question that every person with a disability gets asked a few times in their life. “What would you do if you had an entire day without your disability?” The first thing I would do is get up as early as possible because I know I would need every minute. I would stand up and use the bathroom all by myself. It always felt a little emasculating to pee sitting down to be perfectly honest. Then I would get dressed and find a baseball glove and throw some pitches on the mound. I have no interest in batting. Just let me throw the ball, to get rid of all of my frustrations. Next, I would get in the car and listen to whatever music I wanted, because no one could change stations but me. I would drive to as many friends as I could just to give them hugs. Something that no one realizes is because I’m sitting down, I’ve never actually hugged someone. I always have to wait till they give me one. Make a quick stop at the beach next, just to feel the sand on my toes. 

    The last thing I would do is get all dressed up and go dancing. This is what I want most of all. I would find the prettiest girl on the dance floor and dip her just like they do in old movies. I know what you’re thinking. “You could go dancing now.” I have taken my wheelchair out on the dance floor many times. But I want to go to a club and dance all night. Even though I have tons of wonderful staff and Friends I have nobody to go to stay out all night with and just dance. I would dance until the last minute until I fell because the 24 hours had expired. Then I would get back to my chair with a gigantic smile on my face.

  • Stand and Hug

    Stand and Hug

    “Can you stand up?” That’s something I get asked all the time. So let me answer the question once and for all. The answer is yes and no at the same time. I can bear my weight which creates the illusion that I’m standing but in reality, I can tip over at any moment once someone places me in that standing position. The only way I can stand semi-independently is if I’m holding on to a grab bar or something of that nature. Eventually, my arms will give out and I will be down on the floor until someone comes and picks me up. Let me be clear, when I say I am bearing my own weight in this case it means that I’m doing the work my muscles are sustaining my body mass in this position. Someone still needs to help stabilize me. They should not have to exert any effort at all. The ironic thing is so many people in my life have never seen me do this activity. I only do it when I am about to transfer or in some therapeutic setting. You don’t need to be a physical therapist or a caregiver to get me into this position. It just takes a lot of practice, not skill. The practice is just confidence-building for the other person to realize you are not going to drop me and we really can’t hurt each other. The cool thing about this activity is that it is in the perfect position for me to hug others.

    Finally, brothers and sisters, whatever is true, whatever is noble, whatever is right, whatever is pure, whatever is lovely, whatever is admirable—if anything is excellent or praiseworthy—think about such things. Philippians 4:8 NIV

    Something people don’t realize is because I’m always sitting down I can never give the people I love a gentle embrace. I always have to wait for them to give me one. People know me in one of two ways: a loudmouth obnoxious joker or a constant professional looking for the next opportunity to advocate for others. People are so used to seeing me in a seated position they don’t even think twice about seeing me stand up. The look of shock and horror I receive when I ask people “Can you send me up so I can give you a hug” never gets old. Sometimes I don’t ask because I know they would feel uncomfortable. That’s one of the reasons why I choose to publish this. We live in a world where showing affection is often wrong and frowned upon. So many people require simple human contact. These are the people I’ve always wanted to hug but never have.

    My parents, step-parents, and grandparents have all felt my embrace since they have all transferred me at one point or another. So even though I love you all very much this list is not for you. Thank you for your strong and kind hugs throughout the years. Please remember like always the order doesn’t matter because I love them all in one way or another.

    First, I owe so many hugs to my little cousins. I usually only went to Puerto Rico on vacation and I was so much older than most of them. A lot of them have never seen me without my wheelchair. 

    Next would be without a doubt my colleagues at the New Jersey Council on Developmental Disabilities becoming an advocate changed my life. Some of my colleagues watched me grow up in front of their eyes. I would give every one of them a hug. I know standing up in the middle of a board room it’s probably not the most professional thing but I think if I ever really did this they would make an exception. 

    Both of my siblings are next, I have a twin brother with a similar disability because we’re both sitting down most of the time. I’ve never hugged my brother. I am a notoriously non-crier but  I’m pretty sure this one would make me a little Misty to say the very least. Picture it living with someone for over 30 years and never hugging them.  My little sister who is no longer little has now gone off to college and even though she is “normal” she never actually stood me up. I have no doubt she can do it since she has seen it done a thousand times. It’s just one of those things we never got around to. She has never come into the house or left the house without giving me one. I just think I owe her one now.

    Finally, there’s one person I can’t wait to hug: my future girlfriend. It will be such a wonderful experience holding her and letting her feel safe and warm just before kissing her. As with all my blogs, I hope this changes your perspective on the human experience. I dare all of you to go out this week and give more hugs. Somebody will need it even if they don’t say it. Thank you for reading and see you next Wednesday.

  • Silent Warriors

    Silent Warriors

    Support The Work

    Podcast Platforms

    How do you use your voice? Our voices are one gift we usually take for granted. I know I do. As an advocate I always try to remember That I don’t speak for myself, I speak for others as well if not more. We all speak too much and say things we shouldn’t. Could you imagine not being able to say anything at all? We need to stop complaining about every little thing and appreciate what we already have. I have been fortunate enough in my travels to meet some wonderful individuals who are non-verbal. They are some of the best people in this world, only we never take the time to notice. I hope this post will shine a light on those we have forgotten. This past year has been difficult for all of us. Imagine being scared and not being able to express it or fully understand it.

     This will not be the longest post I have ever written or even the most eloquent, but I pray it makes the biggest difference in changing our collective perspective. Below are 10 simple sentences that we’ve all said, but if we could never have said them at all, our lives would have been greatly affected. 

    The Lord said to him, “Who gave human beings their mouths? Who makes them deaf or mute? Who gives them sight or makes them blind? Is it not I, the Lord?” Exodus 4:11 NIV

    To my dear friends who have never spoken a word, thank you for your patience and understanding from lack of mindfulness. Please take your time reading each statement and let it flow through you.

    1. “I don’t like the feeling of this shirt.”
    2. “Why do my shoes not feel right?”
    3. “How long is this car ride? I have to go to the bathroom. “
    4. “What happened to that gracious lady who always remembered to put mayonnaise on my sandwiches? “
    5. “I don’t want to eat this sandwich, it’s so dry.”
    6. “Your hands are icy.”
    7. “My ear hurts. I really think I need to go to the doctor.” 
    8. “I don’t want to watch this TV show. Why do they always put it on?”
    9. “That person really hurt me! Don’t put me with them!”
    10. “I wish the girl knew how pretty she really was.”

    Disability Limbo Newsletter

    I started Letters from the Limbo as a way to connect with you on a deeper level. Twice a month, I send out an email filled with personal anecdotes, professional updates (like my recent reelection as Vice Chair of the NJCDD), and the policy insights I don’t share anywhere else. This isn’t just another email—it’s an unfiltered look at the life of a disability advocate. Join my community and get an exclusive, honest look at the work that matters

    ← Back

    Thank you for your response. ✨

    Warning
    Warning
    Warning
    Warning.

  • Answering The Call

    Answering The Call

    Support The Work

    Podcast Platforms

    Happy Wednesday my wonderful friends. As always I hope this message finds you well. I want to issue a small warning to my readers I’m going to talk about my spiritual growth as a disability advocate in this post, If it is not the content you are interested in please come back next week.   saying that, I might lose some followers but I’m confident whoever this message is meant to reach the Holy Spirit will lead them to it.

     Everyone has a little voice inside their head that tells them what to do, I believe that voice for me was the Holy Spirit. “It said three things, “advocate, encourage, and read. “ It’s no secret that I do not like to read. I have not read a full book since high school and I’m not ashamed to admit that.  I kept on ignoring the voice but it wouldn’t shut up! So, on a Saturday night, I downloaded a few Bible apps not expecting anything of it.

    For me, no burning bush or demons was making my head spin.  just a few words when I was alone in quiet time. little by little I found myself spending more time with the Holy Father God taking baby steps into a much larger world. This past week I took a giant step! For those of you who don’t know I was appointed to the New Jersey Council on Developmental Disabilities (NJCDD) in September of 2016. I thought this would be the greatest achievement of my life, a chance to finally be recognized. People could finally acknowledge me as a person and not another “Boy in a wheelchair” Equal to every major organization for the last two years we’ve done all of our work virtually.  We were finally able to hold our first public meeting In a hybrid format. That’s when everything changed for me.

    But by the grace of God I am what I am, and his grace to me was not without effect. No, I worked harder than all of them—yet not I, but the grace of God that was with me.” 1 Corinthians 15:10 NIV

    Over the last 2 years, I have been on countless Zoom calls being the voice for people who don’t have access to technology. The truth is in a zoom box meetings become less formal. It’s easy to be more confident in your socks while sitting in a big comfortable chair next to your bed. I believe this shutdown happened for a reason it made us all sit back and reflect. The work I do does not benefit others, It is for others. I did not earn a spot at the table with my colleagues I don’t deserve to be at the table with them. I was chosen to be there with them. I may never have a big fancy house. Girls may never let me out of the friend zone. Thanks Some days, but I know it’s for a greater purpose. Thank you,  Lord Jesus, for making me the way I am. Thank you to anyone who took the time to read this I will see you next week.

    Disability Limbo Newsletter

    I started Letters from the Limbo as a way to connect with you on a deeper level. Twice a month, I send out an email filled with personal anecdotes, professional updates (like my recent reelection as Vice Chair of the NJCDD), and the policy insights I don’t share anywhere else. This isn’t just another email—it’s an unfiltered look at the life of a disability advocate. Join my community and get an exclusive, honest look at the work that matters

    ← Back

    Thank you for your response. ✨

    Warning
    Warning
    Warning
    Warning.

  • When One Door Closes Another One Opens

    When One Door Closes Another One Opens

    Support The Work

    Podcast Platforms

    By: Nicholas Taubenslag

    NOTE: I am very excited to welcome my very first official contributor Mr.Nick Taubenslag. You can find out more about him by clicking on the writing team. tab. Kevin G. Nuñez

    We all have issues to change and work on.  It’s the paradox of two different mindsets that we can choose to have in our lives. The two different mindsets are “The Victim” and The Champion.” It all depends on how we individually look at ourselves and our present reality.

    When in the victim one can feel several emotions from anger, depression, and sadness due to past negative experiences. The reason behind this mindset is a lack of self-confidence and limited self-worth.  Some  questions in this mindset that we  might ask ourselves are: “What’s in it for me?”  “Why have these past situations affected me so deeply?”, “Oh poor me if only I could go back in time and do it all over again.” This mindset only leads to a lot of ruminating thoughts, seeking professional help, and being stuck in a mental quicksand which could be exhausting to pull ourselves out of. The victim focuses on a selfish mindset. It’s more focused on the immediate gratification of our own individual needs.  For example, worrying about how much money one is going to make in order to survive. Over time a person in this mindset gets burnt out and loses the much-needed courage to change this mindset into a more uplifting one.

    The champion mindset is centered around treating others with kindness, love, and respect. Their internal outlook is one of self-confidence, unconditional self-love, compassion, and inner strength. Some questions that a person with this mindset might ask themselves: “How may I serve you?” “What is my life purpose?” and  “What are my goals in life?” Having this mindset tells the universe that we want to make a difference in people’s lives.

    In 2021, I had some very scary events. I was on many different meds. While I was on these meds I sunk into a deep depression. As a result, I had to move back to my parents house.  I didn’t know how I was going to pull myself out. Luckily, I had my parents, men’s group therapy,  my counselor, and a famous hypnotist to help pull me out. I tried working out among other things to try and pull myself out.  I was stuck in the victim mindset at first but trusted my intuition to heal and become a champion. 

    The lessons of 2021 were courage, help from others, and resilience. My family motto illustrates this section perfectly. It’s all about never giving up and always trying. If you try your best you can accomplish anything.

    Ever since going to New Jersey Partners In Policy Making back in 2019 I have been living my life purpose of self-advocacy specializing in expanding transportation options for people with disabilities. I also have been accepted into Jespy House, an independent living community with a social outlet already built with numerous clubs built-in. As well as mental health built-in. It’s like I am on the verge of becoming a champion in my own right. 

    What this past year has taught me is to have relentless courage, determination, and a positive outlook on life. A very wise former Admiral Navy Seal William H. McRaven Author of “Make Your Bed Little things that you can do to change your life and maybe the world.” illustrated this point perfectly when he wrote in his book “never ever ring that bell.” which is a sign of quitting. 

    In conclusion, A very wise man once asked, Are we here for a season or a reason? If we are here for a season we are like a leaf on a tree when its time is finished it just blows away in the wind, in other words, forgotten. However, if we are here for a reason we will have lived a life with genuine kindness, compassion, and action. By having this question in the forefront of our minds we can all become champions in our own lives. When one door closes in our lives,  I strongly feel it’s a huge opportunity to train ourselves to go the distance and come out the other side to open that door to a better future.

    Disability Limbo Newsletter

    I started Letters from the Limbo as a way to connect with you on a deeper level. Twice a month, I send out an email filled with personal anecdotes, professional updates (like my recent reelection as Vice Chair of the NJCDD), and the policy insights I don’t share anywhere else. This isn’t just another email—it’s an unfiltered look at the life of a disability advocate. Join my community and get an exclusive, honest look at the work that matters

    ← Back

    Thank you for your response. ✨

    Warning
    Warning
    Warning
    Warning.

  • Get to Know Each Other

    Get to Know Each Other

    Support The Work

    Podcast Platforms

    Hello everyone, let’s spend a few minutes together and escape from life. I wanted to have some fun today. I designed this website and blog to be an ongoing conversation to bridge the gaps between the disability community and the general public conversation but I can only give you one perspective. I need you guys to get involved as well, Therefore I came up with this list of questions for anyone who takes the time to read it. Feel free to answer all questions or as many as you feel comfortable.

    "My flesh and my heart may fail, but God is the strength of my heart and my portion forever.
    Psalms 73:26 NIV"
    1. This should be obvious, can someone give me an accurate description of what it’s like to run?
    2. It always takes me about an hour and a half to get ready for the day with the help of others. How long does it usually take you to get ready for the day?
    3. What is the first thing you think of when you see someone in a wheelchair or some other visible disability?
    4. Do you put your socks on before or after you put your pants on? I never really have a choice, so I never really thought about it.
    5. I know I need help in the bathroom; I have to inform people. Why do people always announce it when they leave the room?
    6. Every parent wants a “healthy” child, what exactly is that to you?
    7. What exactly is so “inspirational” about people with disabilities?
    8. We live in a world where physical appearance is idolized, what is so hard about looking at the person?
    9. Why do people want to spend so much time alone on the toilet? Balancing is tricky for me. I want to get off of that thing as soon as possible. Why do you want your leg to go numb?
    10. How long can you stand up before you feel tired?
    11.  How long can you sit down before you feel tired? 
    12. What’s one physical activity that you’ve always wanted to do? My list is a little long.
    13. What’s one fear when you socialize or date someone with a disability?
    14. f you had my disability what would be the one thing that scares you?

    I hope this made you laugh, or at the very least give you something to think about. Do you have any questions for me? That you want me to answer in a blog? See you next time.  Have a great day.

    Disability Limbo Newsletter

    I started Letters from the Limbo as a way to connect with you on a deeper level. Twice a month, I send out an email filled with personal anecdotes, professional updates (like my recent reelection as Vice Chair of the NJCDD), and the policy insights I don’t share anywhere else. This isn’t just another email—it’s an unfiltered look at the life of a disability advocate. Join my community and get an exclusive, honest look at the work that matters

    ← Back

    Thank you for your response. ✨

    Warning
    Warning
    Warning
    Warning.