Skip to main content

31 for 21: Down syndrome footprint

I came across this recently, and thought it was interesting… DownSyndromeFootprint.org

Check it out and share your thoughts. I’m curious.

Comments

  1. not my favorite.

    Not all people with DS have the toe gap. Too much focus on one little feature.

    I get where they're coming from, though. A for effort, C- for execution.

    ReplyDelete
  2. As much as I'm not a fan of the yellow and blue Ds colors, while this is cuter, I still don't think someone who didn't know DS would get it.

    I really think they need to totally rebrand Down syndrome. The name is bad, the colors are bad, the Awareness month is bad (come on October competeing with Breast Cancer awareness? Right, good idea.)

    I'm all for starting with a clean slate on the name and everything that goes along with it, lol. But I'm a big thinker!

    ReplyDelete
  3. I like it. But I have that foot. And why not focus on one little thing? Especially a cute thing?

    ReplyDelete
  4. I think they are so cute, but one of those "insider" designs that only a member of the club would get. And maybe not even then! I have a T-shirt that says "Angels are made with 47 pieces" and wore it to our Down syndrome picnic and about a dozen people asked me what that meant!!

    ReplyDelete
  5. Well, coming from someone who has an e-store and happens to have a similar design, I think they need to go bigger and not focus ALL on one thing. Kennedy doesn't have the toe gap either. Can't wait to see if Kellsey does! Anyway, the Down syndrome clothing market is huge these days... to each their own... I hope they find their market and wish them great success :).

    ReplyDelete
  6. Speaking of shirts, we've been on a big "Cat in the Hat" kick at my house with my middle baby. My oldest thinks we should get 3 shirts.

    A "Thing 1" shirt for her
    A "Thing 2" shirt for middle girly
    and "A Thing 3-21" shirt for the baby...

    But I think only a small group would find it as amusing as we all would...

    ReplyDelete
  7. Thank you all so much for sharing your feedback! I really appreciate open and honest communication about what we are doing with downsyndromefootprint.org. I would love to share with you where we were coming from with this idea. After 3 years of having a blue and yellow awareness ribbon on our vehicle and not one question we decided to create the Down syndrome footprint and place it on our vehicle with our daughters name because it was personal to us and had meaning. To our surprise and delight we started receiving so many questions and comments, “Cute foot with your daughter’s name, but why the large space between the big toe and the little toes?” After answering this question over and over again we were thrilled to talk about our daughter and raise awareness without forcing it on people. Yes, we do realize that not all children with Down syndrome have this and Annaliese actually has only a small gap between her toes, but it is a recognized medical marker of Down syndrome and it is cute and fun loving like a lot of our children. I think that one of the comments made on your blog really hit home when she mentioned we need to bring an attractive twist to Down syndrome. Since Annaliese was born 8 yrs. ago I have searched and searched for appealing and cute things that represented our daughter. Since we struggled to find them, we created the Down Syndrome Footprint Symbol and wanted to share it with others.

    I am excited to say that we are now becoming a non-profit with 100% of our proceeds going directly back to individuals with Down syndrome and families of individuals with Down syndrome. Our mission is this, 1) Raise Down Syndrome Awareness and 2) Provide education, training, and employment to individuals with Down syndrome. We are currently starting a product line made by individuals with Down syndrome and also their family members. It is so important to us that when Down syndrome awareness items are sold they truly benefit the Down syndrome community.

    Thanks to the great responses and demand that we have received I am excited to say that over the next 3-6 months our product line is expanding significantly and our website will be changing to meet the quality of the products we offer!


    Katia
    downsyndromefootprint@yahoo.com
    downsyndromefootprint.org

    ReplyDelete

Post a Comment

Thanks for commenting!! I only ask that we all keep it positive, respectful, and clean. Comment moderation is on for now. (As this is my blog, I reserve the right to delete any comment I deem inappropriate for any reason.) If you use the anonymous option, be sure to sign your name. Thanks!!

Make it a great day!!

Popular posts from this blog

31 for 21: What to say

I have encountered plenty of people who ask "How old is she?" when Braska and I are out together here and there. They always guess her age about 5 months younger than she is, but that's ok, since that's what size she is. I have said several times that I can imagine it will bother me a bit more, although still not a huge deal, when she turns one next month and I see their reaction to that, as she still is in her car seat/carrier when we're in a restaurant or in a store since she doesn't sit up. Today, I met some friends for brunch. The waitress was a nice enough, very young girl, and she started cooing at Braska right away. That's nice. I don't mind, Braska likes the attention, and I'm proud of my cutie. The waitress asked her age, and I told her 11 months. She then said, "But she's not walking yet?" as she noticed that she was up to the table in her car seat/carrier. I just agreed and said, "Not yet." She said she h...

Can I get a do-over?

If you are in need of a laugh at another's expense, I invite you to read on... really, it's totally ok. I can take it. This might end up long, but I wanna remember this special day. Oh so special... Today is my first day to have both girls and be on my own. Yeah, it's been two weeks, but I'm apparently slow at learning how to deal with this kind of thing. I knew it would be a challenge, but I thought with starting way early, we could make it. The quick ending is that we did make it...but that's not really the whole story. Kinlee's been sleeping til about 9 am or so after getting up twice in the night. That's ok, I'm dealing with it. But since Braska is supposed to be at school at 10 am on Mondays, I thought I better not sleep in like I prefer, and instead, I should get up and get things moving earlier to be sure we're on time. Not a problem, since Braska decided to be up twice last night in addition to Kinlee's two times. One time overlapped...so...

Little call, big letters

This will make more sense to you DS moms and families out there... I apologize for the cryptic nature, but you'll have to trust my reasoning. Braska had a lab draw on Tuesday last week. The GI called me Wednesday and said there were some significantly elevated levels in the results. Ok fine. Not like we've never had an abnormal lab. But then he used *those* words...the C word and the L word. Said he'd be talking to hem/onc. We needed to go redraw on Friday morning. We didn't freak or anything, but when I hung up the phone, I thought, "Wow, so that's what it's like the first time they mention it." We took her for her draw again on Friday morning, and we figured everything was fine since we got no call over the weekend. Yesterday I checked in with them. Dr. R confirmed that everything was clear, almost in a "weird way," but they checked with the lab to make sure it was a viable result. All is well. Follow up in 6 months as usual unle...