• Our Mission

    Our Mission

    Our mission at PCD Smiles is to bring smiles to hospitalized primary ciliary dyskinesia, no mater their age; through the gift of a cheer package. Currently serving only The United States and Canada.
  • Request Cheer Package

    Request Cheer Package

    Know of a hospitalized primary ciliary dyskinesia patient? Please visit our “Request a Cheer Package” link and fill out our secured form to submit them for a cheer package today!
  • Donations

    Donations

    Our cheer package program runs on donations. To see how you can help PCD Smiles, visit our donations section today!
  • The PCD Artist Project is a collaborative effort by artist to raise awareness for PCD & support the PCD Smiles cheer package program. Visit our exhibits today!
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  • Nothing is Sacred when you have PCD

    Nothing is Sacred when you have PCD

    There are a lots of things that I’ve had to get used to as I grew up doing life with PCD. One of those things was learning that unlike most others I had no privacy. I mean absolutely none...
  • Nasal Washes, Yay or Nay?

    Nasal Washes, Yay or Nay?

    Are you Team Yay or Team Nay when it comes to nasal washes for you or your loved one with primary ciliary dyskinesia (PCD)? Nasal washes are an integral component to PCD care, or rather they could...
  • Disordered Sleeping and Sleep Disturbances in PCD

    Disordered Sleeping and Sleep Disturbances in PCD

    Disordered sleeping and sleep disturbances are more common in PCD than once thought. It’s not surprising given that you need to be able to breathe properly in order to sleep properly. Sleep related...
  • Can I live a Holistic Lifestyle with PCD?

    Can I live a Holistic Lifestyle with PCD?

    There are no studies into holistic lifestyle alongside a primary ciliary dyskinesia (PCD) diagnosis. There are however a few antidotal reports from the PCD patient population where patients have...

Dear Smile E.

I have no support system. I mean absolutely nothing. How do I find one?

Signed,

Alone

Dear Alone,

I can totally relate to being all alone. This disorder is no picnic especially when you have no support system. If you’re connected with a PCD clinic or are being cared for at a cystic fibrosis clinic you can ask to talk to their clinic social worker. The social worker can help aid in connecting you to resources. Also you could look into joining a church community, social community, or something like that to connect with others who might be a support system of sorts. A support group is also a great place to start. I know most PCD support groups are online and it’s okay to reach out to them. Have you checked out the Adult PCD Patient ONLY group on Facebook yet? Feel free to send me a private message of Facebook and I can help you find it.

Yours Truly,

Smile E. Turtle

Do you have a question for Smile E.? 

Please EMAIL your questions to; This email address is being protected from spambots. You need JavaScript enabled to view it.

And tune in next Sunday to read the latest Ask Smile E.

Join our Facebook group Turtle Talk Café today, click here.

We have several ways that you can donate to PCD Smiles;

- Visit Smile E. Turtle's Amazon Wishlist

- For more information on how you can donate, please visit our "Donation" page to check out our "Do & Don't policies.

- Or sponsor a PCD Smiles cheer package today!

- To shop for your “Official” turtle care ribbon gear today, visit PCD Style or Smile E. Cove

Thank you for your consideration!

  • Hits: 43
What do I do if I have no support system?

What do I do if I have no support system?

Dear Smile E. I have no support system. I mean absolutely nothing. How do I find one? Signed,...
PCD Smiles’s 1st  Biennial Fundraiser Painting 4 Smiles

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Can you help us reach our goal? PCD Smiles’s 1st Biennial fundraiser Painting 4 Smiles runs the...
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“Regular clinical visits to monitor disease status are key. Aggressive treatment is recommended to...
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Cilia are thought to play an important role in organ placement during the embryonic stage of...