Williams Syndrome Association
Williams Syndrome Association
The WSA is the most comprehensive resource for people and families living with Williams syndrome as well as doctors, researchers and educators. The WSA provides resources, support and the latest medical information to help your child today and throughout his/her life.
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it was awsome meeting everyone
Gigi love the intellectual developmental differences. Great way to describe a person. ❤
I'm so glad to see yall out of your boxes. 😂 I'll be ready to see this movie forsure.🏀 Bring on the love ❤ Emmy is literally a great name for a talented young woman who will surely be Emmy award winning in the future. 🏆 Brendan is definitely a wonderful addition to any movie, podcast, concert, play, and definitely podcast. He is one of the best 💙❤️💚 Keep spreading awareness.
Thank you so much Pim :)
Prayers for everyone not feeling well 🙏🏽 Happy birthday Stella 🎂 🥳 🎉 A back to school podcast will be great. It's so tough in some kids to go back and get back into the schedule of things. Prayers for the family and teachers and students having to venture that this up coming school year. We DEFINITELY needed the footage of yall in your tomfoolery 😅 Thank yall for all the updates and spreading the awareness 💙❤️💚
Jamboree is the place to be 😊
Can't wait to hear and see the convention. 💙❤️💚
Thank yall for the podlet 😅 love the video and word 😂😂
I love you guys
Donate to the Williams syndrome association
I love y'all, my people and greetings from New Zealand💙❤💚
DONATE FOR AWARENESS OF WILLIAMS SYNDROME 💙❤️💚
Hey👋
@@perrytito Hey Perry 👋🏽
Great podcast. Beautiful rendition of the Star Spangled Banner, Stella!🇺🇲
Brendan I keep learning stuff about you all the time. You were on a show on MTV. 😮 that is awesome. You are truly a man with many wonderful qualities and difficult experiences you can share. 😊
Great podcast. Great cause Weekend for Williams ❤
What a gut wrenching, wonderful episode. It reinforces the need to cherish everyday with our precious ones. It also encouraged me to do all I can for WS awareness. ❤
Let me just start by saying I almost didn't watch this episode. (Wasn't sure my emotions could handle it) I couldn't imagine losing a child. Obviously most of the viewers are here because of a person with WS so you automatically think of your WS blessing and it can hit hard. I just thought...... just start the video and see what happens, if it's too much you can stop and come back later or not. Thankful I thought that because while there were tears it was still very informative and gave a positive message and a message of hope. Thank you to both the mothers for sharing their experiences with us. ❤ keep raising awareness 💙❤️💚
One of my favorite things is watching week after week and learning something new and interesting about Brendan...... i mean how have i not learned he is a sailboat enthusiasts ⛵️😁
Growing up as a kid my family was big into sailing so I spent quite a bit of time on a variety of different kind of boats. Definitely miss being on the water for sure, but hope to get back out there at some point :)
Micah was such a great guest with such wonderful and honest expierences. Love to hear the job life for adults with disabilities. I think it is very important for their lives to get experiences and learn task that give them independence and confidence. Not to mention the company is getting a wonderful employee😊
What a wonderful way to raise funds and awareness for Williams Syndrome by having a dance performance. Love that idea. Prayers for Avery and her precious ❤️ heart. 🙏🏽 i agree the wsa organization is really such a blessing to many. 💙❤️💚
Thank you so much Sofia for sharing your heart. I love that my little granddaughter with WS has women like you to be her role model. I would love to, someday, see you on the WSA board. God bless you! Wonderful episode!❤
Cheers from Paraguay.
Hello!
❤️❤️❤️❤️
I love this podcast so much ❤
The KZread transcript is incorrect! My name is actually spelled with an F, not a PH!
Hi from Italy. Is there a way to communicate with you, Sofia?
Thanks for having me!!
Our pleasure!
I feel like I say this every episode but yall really get the best guest. Sophia was a pure delight and a MUST have on again. She is very informative and sweet and funny and HERSELF which is extraordinary!!!!!
Happy Williams Syndrome Awareness Month 💙 ❤️ 💚
I agree with Jen. Meeting others with Williams syndrome is such a amazing thing. You get all these stats, info, test, and search the web for more. I found watching videos of others with WS was very helpful. Of course everyone is different but it does give you a chance to better understand. 😊
Love hearing the yearbook messages ❤
Love that Mike and his parents found out his diagnosis from 60 minutes. Speading awareness is truly life changing. CP can definitely go hand and hand with WS along with Autism. Many dual diagnoses. What a wonderful story. Mike and Jen seem like such kind people. The stars definitely aligned for them ✨️ 💙❤️💚
What a wonderful episode. So much wonderful information and experience sharing. ❤️ As hard as it is to hear and share some tough stories it does get information out there on how others dealt with difficult situations. It hurts my heart to hear Brendan was bullied because he is such a awesome young man but it does show how you can overcome difficult times and still be awesome. Keep sharing and educating others. 💙❤️💚
Can't believe it has been a year. 🎉 Sooooooooooo happy to see Steph and sending many prayers 🙏🏽 and good vibes her way with her health and wellness journey. Wonderful episode and loved the questions being directed towards yall this time. Can't wait to see what all yall will have the next year to come 😊💚❤️💙
Love the new intro ❤ as always very entertaining and informative 💙❤️💚
Great information and discussion. Thank you!
I'd love to see some of Alexandra bracelets making skills. ❤ or videos of their dance classes
My daughter has Williams syndrome. I take her to dance classes. She takes ballet, tap, lyrical, acro, hip hop, stretch, and jazz.
Hello a,m Dave from the 🇳🇱 a,m have willams beuren syndrome to a,m happy to a talk programma comming
There is another reason we need to determine this and I need somebody to advise me on the first step to take is because I would love for my sister to be able to make friends with others who have Williams so she can finally find her own group in this lifetime .
Thanks for reaching out. Due to the holidays, we have not seen your comments until today. Our website is always the best place to look first for resources. There are tests that doctors can order that are take-home swab tests, so your sister may not have to go downtown to get tested. I would ask your sister's doctors about that - specifically if she sees a cardiologist. I agree that it would be nice if she had a firm diagnosis so she could find a community and be eligible for some of the services and resources the WSA provides, but it is her choice if she would like to be tested. If you have any other questions, please contact me at [email protected]. Joel Liestman Director of Family Support
Merry Christmas and thank you for sharing your holiday with us! As a William's Syndrome grandma, I have learned so much listening to your podcast. ❤
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Great discussion addressing some difficult issues. Thank you for your vulnerability and genuineness.
Hi everyone ❤️
What a great episode with the WS committee talking about the upcoming convention. Great energy and very informative and helpful information to process the excitement and stress of the convention. 💙❤️💚😊
Brendan is such a great story teller. I knew he was interesting and love hearing his experiences and adventures before but this scary haunted experience was a literal edge of my seat kinda story 😳
Thank you so much, talking about those experiences brought back so many memories but i'm glad i was able to tell that part of my life in that way :)
Love the Halloween effects 🎃 Love the back to the future costume. Love the miss bubble. Lol welcome alien 👽
Hi everyone ❤️🩹