#Autism parent support

[noisycowboyglitter]

"Autism Advocate Apparel: 'Autism Dad - His Fight Is My Fight' Design"

Dads on Duty: Standing Strong in the Fight for Autism

For dads of autistic children, the phrase "His fight is my fight" takes on a powerful meaning. It's a declaration of unwavering love, support, and fierce advocacy for their sons.

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These dads are the:

Strong and Silent Pillars: They provide a rock-solid foundation of love and stability, a safe space where their children can thrive.

Tireless Champions: They advocate for their children's needs, navigating therapies, educational systems, and social challenges.

Playful Partners in Crime: From building epic Lego creations to backyard superhero battles, they create lasting memories and foster joy.

This fight isn't just about overcoming challenges; it's about celebrating victories. It's the pride in seeing their child master a new skill, the joy of shared laughter, and the unwavering belief in their child's potential.

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Dads with autistic children are more than just fathers; they're heroes, advocates, and champions. They stand shoulder-to-shoulder with their sons, walking the path of autism together, one step at a time.

This description can be used for various purposes:

Product Description: Highlight products designed for dads supporting autistic children (e.g., sensory fidget toys, autism awareness t-shirts).

Social Media Caption: Share your story or the story of an amazing dad you know.

Blog Post Introduction: Discuss the unique role dads play in the lives of autistic children.

The puzzle piece: A symbol of autism sparking mixed emotions.

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Diversity Represented: Like a puzzle with many pieces, it reflects the vast spectrum of autism experiences, with each individual possessing unique strengths and challenges.

Complexity Acknowledged: It highlights the intricate nature of autism, a complex condition with varying presentations.

However, some within the autistic community view the puzzle piece as suggesting they are incomplete or need to be "solved." This has led to a growing preference for alternative symbols, like the infinity rainbow, which celebrates neurodiversity.

Regardless of the symbol used, promoting understanding and inclusivity for autistic individuals is the most important goal.

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Words of Strength: Inspiring Quotes by Autism Parents

Raising a child with autism comes with unique challenges and immense rewards. Here are some powerful quotes that capture the spirit of autism parents:

"The world needs all kinds of minds." - Unknown

"We may not have it all together, but together we have it all." - Anonymous

"Autism doesn't define our family, it refines it." - Unknown

These quotes showcase the resilience, unwavering love, and acceptance that define autism parents. They inspire others and celebrate the beautiful journey of raising an autistic child.

[my-autism-adhd-blog]

Why does everything I see about autism for parents or children? There’s this facebook page I like called Mrs Speechie P (who you’ve probably seen before), and she has great information. But it’s all for kids. I messaged her about this and she explained that she worked with children. But helping people who are adults that have been diagnosed (or self diagnosed) is just as important as helping kids. We need support too.

Say it with me everyone:

AUTISM. 👏AFFECTS. 👏ADULTS. 👏TOO.

[zebulontheplanet]

Thought I’d talk about my care today since a lot of people don’t talk about care they get from families and outside sources.

I am completely cared by my family. They 100% care for me in every way.

My siblings and parents take care of everything for me. From making meals, to making sure I’m safe, making sure I’m bathed, to making sure I’m handling everything correctly and just generally comfortable.

My family is not my caregivers though, and they make that very clear. They do not want the title of being my caregiver. Does that mean they do things that a caregiver would do? Yes. However, I will not force that title upon them if they do not want it. And I will not force them to act as my caregivers either.

My mother is especially the one to thank. She goes to every doctor appointment, every big outing, everything. She takes care of me in every way and I am extremely grateful for that. I get care that I like to call “support needs care” that means that they do what I can’t, and I do what I can. And that’s how it works.

Will I need a part time caregiver from the state in the future? Probably. And if I wasn’t leaving for a college program in April then I would be in the process of getting one. But I’m not at the moment.

Talking about care that autistic people get is so important, and talking about what they do is so important. They are here for me. They advocate for me when I cannot. They help me with so much, and they deserve recognition for that. Caregivers and parents are a vital part of the autism community. Do they overstep sometimes? Yes. But that doesn’t mean that they shouldn’t be talked about. Not talking about them leaves out a big part of the community, and leaves out a big part of higher support needs people. Our caregivers and parents are vital parts to us. They are vital parts to our lives.

Caregivers and parents do things that people couldn’t even imagine. And everyday it’s a battle for them. This is not a “boo hoo, poor caregivers and parents” post. This is a post bringing awareness to something that is vital to a lot of peoples lives.

Recognize caregivers and parents. Recognize what they do. Listen to them. Listen to the people they are caring for.

[snakeautistic]

Having undiagnosed autistic parents is a double edged sword, because on one hand they understand your experience intimately even if they can’t explain it, set up your life in a structured way with lots of margins, and assure you that you are not broken or defective for who you are because they’re the same way, but at the same time they also expect you to just ‘suck it up’ and push forward in a hostile neurotypical world because they had to do it too, and dismiss your concerns with ‘that’s just how our family is.’

[gods-favorite-autistic]

Honestly as somebody who has friends who are going through so much more than me esp in their home lives I extremely get Fabian because it’s like yeah it isn’t perfect but it’s a million times better than what they have to deal with so like you just kinda have to be grateful for what you have and try not to complain yknow

[tara-fantastico]

It's interesting that in the whole process of starting university, moving cities and beginning to live on my own with all that entails the ONLY thing that has required my parents' contact information specifically is the disability accommodation application. Almost as if they don't consider disabled people to be adults or something.

Don't get me wrong, it's great that the OPTION exists, cause I'm sure there are disabled people that need/prefer to have their parents involved in the process but it was not possible to exclude them from it, which at least i feel is kinda ableist?

[kimjunnoodle]

WE GOT THE KEYS TO THE BEACH HOUSE BABY

[sukibenders]

Looking back at Girl Meets World, it will forever irritate me especially for how they handled/treated Angela. Oh this show really hated black women because how do you not only 1.) describe her, one of (correct me if I'm wrong) only few black and MAIN characters of the og show, as a "concept" 2.) have characters show obvious disgust at the small mention of her name 3.) depict her as a homewrecker for a new relationship that, really, shouldn't have ever happened 4.) have her old friends treat her like dirt and her old lover like she is the root of his problems, when there was nothing but positive love there 5.) reuse all the concepts from said previous love story just to elevate the new ship with a yte woman and 6.) compare her to Hurricane Katrina, one of the deadliest hurricanes that caused significant numbers of death, harm, misplacement, and trauma to people, largely of whom were black? Mind you, all these points I mentioned were toward the only main black character of the OG show before the spinoff, and the only, from what I can remember, black female character of the spinoff who didn't even stay long. Not even getting into the racist drama with some of the members on set, but you cannot look me in the eye and tell me that the way the show handled Angela, her story, and her relationship with the other characters + Shawn wasn't fucking disrespectful, you can't because I won't believe you.

[autismcultureis]

autism culture is being level 1 autie and not taken seriously.

.

[oncominggstorm]

My aunt decided a good way to wish me a happy birthday would be to text me a picture of me & my dead dad from my 22nd birthday.

Like yay thanks, I totally wanted to be sad and missing my dad on my birthday. I definitely wasn't trying to do the "out of sight out of mind don't think about sad things" thing to get through it without crying or anything 👍 Definitely wasn't already struggling missing not getting a happy birthday text from him 👍👍

[aacalienz]

My support needs are not being met living with my parents. I’m not homeless anymore and they took me back. But they still treat me as non disabled for the most part, which just sets me up to fail. They expect me to be fully speaking and I just can’t measure up.

[noisycowboyglitter]

"His Voice for Autism: Personalized Notebook for Tracking Goals and Progress"

"His Voice Autism Awareness" likely refers to an initiative or organization dedicated to raising awareness about autism from a male perspective. This focus is significant because autism spectrum disorder (ASD) is often diagnosed more frequently in boys than in girls, though research suggests this may be due to differences in how autism presents across genders.

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The phrase emphasizes the importance of hearing and understanding the experiences of individuals with autism, particularly males, in their own words. It suggests a platform where men and boys with autism can share their stories, challenges, and triumphs, providing insight into their unique perspectives and needs.

This initiative might involve various activities such as public speaking events, social media campaigns, educational programs, or support groups. The goal would be to increase understanding of autism, reduce stigma, and promote acceptance and inclusion.

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By highlighting "His Voice," the program likely aims to address specific issues that males with autism face, such as social expectations, communication challenges, and navigating relationships. It may also focus on providing role models and mentorship opportunities for younger boys on the spectrum.

This approach to autism awareness underscores the importance of first-hand accounts in shaping public perception and policy regarding neurodiversity.

An "Autism Mom Quote" typically refers to a short, powerful statement that encapsulates the experience, emotions, or perspective of a mother raising a child with autism spectrum disorder (ASD). These quotes often reflect the unique challenges, joys, and insights gained from parenting a child on the autism spectrum.

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Such quotes might express unconditional love, advocate for acceptance, or highlight the strength required in their role. They can be inspiring, educational, or simply honest reflections of daily life. Autism mom quotes often serve to raise awareness, provide support to other parents in similar situations, and challenge societal misconceptions about autism.

These quotes are frequently shared on social media, printed on t-shirts, or used in awareness campaigns to foster understanding and empathy.

Autism Parent Quotes are concise, impactful statements that capture the experiences, emotions, and insights of parents raising children with autism spectrum disorder (ASD). These quotes often reflect a range of sentiments, from the challenges and triumphs of daily life to profound realizations about love, patience, and neurodiversity.

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They serve multiple purposes: offering support and validation to other autism parents, educating the public about the realities of autism, and advocating for acceptance and understanding. These quotes frequently appear on social media, in support groups, on merchandise, and in awareness campaigns, helping to build community and foster empathy among both autism families and the broader public.

[neuroticboyfriend]

i'm autistic and i'm disabled by it. it took me half a lifetime to learn skills that i had been dependent to my parents for. the only reason i had to suffer through learning them is because my parents withdrew support. my mom did help sometimes, but my dad actively forced me into situations he knew would cause me meltdowns and panic attacks. i was severely agoraphobic because of it. i had to learn to survive, and the skills are still very surface level. if something unexpected happens, i don't know how to deal with it. which makes me anxious/confused at best, and throws me into hyperventilating panic at worst.

yes. the ableism and abuse disabled me. it made things harder. but in a world where i was just given the support i needed, i would still be disabled as an autistic person. because i still wouldn't have the skills. i would still have limits. i would just be healthier, happier, and safer. and i deserve that. all autistic people do, regardless of disability status.

[sophiestarpaw]

When I would draw furries at like age 7, my mom would be so proud of them that she’d show them off to her workmates

It’s nice to have parents that aren’t embarrassed of my interests. In fact, she always supplies my interest by buying me stuff and accessories. Her support was a big reason I was comfortable dressing scene when people made fun of it at the time.

[no-brain-just-good-omens]

I love making up and acting out my silly little scenarios in my head. I know nobody’s going to tell me on my birthday that as my present they’ll pay for my first appointment of gender-affirming healthcare, but I now know exactly how I’d react if they did!

[pumpkinspicedmochi]

Can't stop think about how I brought up using an aac device to my mom ( I started explaining using an aac app particularly not the device itself before she said this) and she straight said it would make me worse and then tried to say she knows for a fact because she is a medical professional (she is but still wtf) and said "if you have to use a notepad , anyway you are fine , you talk fine stop trying to add more stuff onto it" I'm not "adding" anything wtf and I don't talk fine , most times I struggle to speck and get overwhelmed from talking a lot ..she has a thing where she doesn't want me to "look disabled" but seriously why do you want me to not use what I need ..I even confided in her that I was nervous to use aac because I would be worried the device would be annoying to people and she laughed and said "yeah , it would be annoying" .. she 100% used to me just forcing myself through pain/ignoring my pain and ignoring my needs to make things easier for her (which obviously causes some serious issues)