@whatilovetodo: The hate comments will never be louder than the reason I share. I share my children and our journey because someone out there needs to know they aren’t alone. I share to advocate, spread awareness, show the reality of disability, and push for the funding, services, accessibility, and support our families desperately need. Our world was built largely for typical people. It’s time we build a world where people with disabilities don’t have to fight so hard to belong. If our story helps even one family feel less alone or helps someone see disability differently, it’s worth it. ❤️ #DisabilityAwareness #DisabilityAdvocacy #InclusionMatters #SpecialNeedsParenting #AngelmanSyndrome

sears.rat :

The only concern I have is with ai and creepy people online

Valerie Coffey685 :

People who don't live this life do not understand! They just don't. Even if they have good intentions, they just can't understand.

Abbielouisexox :

Your an inspiration and your family are amazing 💖

bre3534 :

I am so with you! You have my support.

Lily Calavan :

Your a great advocate for the disability community

. :

I respect what you do - you are using a platform to advocate for your children

RiverBear :

I found that my child did not have ODD but autism with PDA because of this app. I brought the information I learned to her provider who also did more research and agreed. We changes her therapy and have seen dramatic improvements

Mari lewis :

I believe you help the parents that have accessibilities

Leanne Morse :

You are absolutely right, and I know people who work in special education have confirmed that the government cutting off funding really is happening and it is a problem. This is not about special treatment. This is about giving services to people with disabilities that they need in order for them to thrive and these services can be speech, behavioural therapy, music therapy, and accommodation such as having a one on one. Services are there in place to help provide solutions to challenges. My questions are when it comes to money where is it going? What is it going to be used for? Why do services cost the way they do? What I detest is when people without disabilities generally take their own abilities for granted and use their abilities to shame disabled individuals and the people just don’t listen to the full situation. This has to be addressed and thank you for pointing that out.

Jen :

I appreciate your videos, I also have special needs child and it helps to see I'm not alone.

Hollydolly :

Girl I don’t understand why do people give hate your a wonderful mum and I am going to cheer you on and I am soo shocker how you manage to pull it off you strong and you keep on going girl love u 💖💖💖💖💖💖

AdvocatingLikeAMom :

Say it louder for the people in the back

fabhuntress33 :

No your job, your alliance should be with your kids. I understand Griffin will not be able to contest this footage later in life but Sawyer absolutely could and that's a line I think you need to draw.

Sydney Morales :

your videos are so good

XoGwe_🇿🇦 :

It's not built for disabilities period!!! I'm so sorry you have to go through this. I pray your purpose gets more solidified through Jesus Christ and you become the voice for the voiceless 🙏🏽.

Steeler nation :

I stand with everything you said in this video and I couldn’t agree more

Lois Sullivan :

what you share is very important for parents with special needs children. Thank you for sharing.

hannahb__123 :

love your page, I have 2 beautiful pickles with Fragile X and agree fully, sharing our lives changes lives! ignore the hate x

New age Mary Poppins :

I feel you on this. We're from Colorado. My son has a speech pathologist. Colorado has none, and ours is digitally in Tennessee. How is that helping my son's speech.

kendra-not scott :

Zahratalyemenx :

💯

luanaandreeastefu :

user67890976543 :

👏

Georgia Morrison :

understand you