Christopher's STARband Journey

Hello Friends. I received some emails yesterday that the link to Christopher's Blog was not working. I have checked it and checked it again. It seems to be okay now. You can click the link to get there. http://www.alexandrasphate.org/christophers_journey.html

Thanks!

Meet Christopher! Our newest STARband Kid!

Hello. Meet Christopher. He is our newest STARband kid. Our foundation was able to donate a helmet to Christopher's family with the help of Orthomerica. We are so glad that we could provide assistance. For more information on Christopher and his journey visit his blog, on our website, here .

www.alexandrasphate.org

ONly 4 days left to submit your pictures for April

Hey everyone. There are only four days left to submit your photos for our kid of the month club for April 2010. Send your photos to gary@alexandrasphate.org or go to www.alexandrasphate.org to submit them there.

Thanks.

Christopher gets his new STARband today.

Check our website at www.alexandrasphate.org for updates on Christopher's Journey with his new STARband. He received it this morning and we hope to keep you informed regarding how the progress is going.

Thanks!

Only one week to send your pictures for our kid of the month club!

Hey folks. Only one week left to send your pictures of your little on in his /her CRO for our April photo contest. Check it out and we will post the winner on 5/3. Good luck. Send your pictures to photos@alexandrasphate.org if you'd like. Thanks

Christopher's STARband Journey

Good Day! As you may already know, AlexandrasPHATE, recently donated a STARband CRO to a local family. It looks as though Monday 4/26 is the day for the initial visit and the first time that Christopher will wear his STARband. His family is going to allow you to follow their journey by blogging on our website, www.AlexandrasPHATE.org. There you can get updates on progress, correction, and just plane ole' feelings that are happening as the remolding process is going on. If you have any questions or need any more information, feel free to contact the family by clicking here.

We look forward to any feedback you may have regarding this real-time journey with the Christopher and his STARband Cranial Remolding Orthosis. You can reach AlexandrasPHATE at contactus@alexandrasphate.org.

Alexandra has GRADUATED from her STARband!!

Well, for those of you that have been following Alexandra's Story, she has officially GRADUATED from her STARband today. We met with the Orthotist and we mutually agreed that it did its job on Alexandras Plagiio correction. Thanks to everyone that has been supportive during this time. We will continue to do our best to assist families affected by Torticollis Plagiocephaly and CROs through our foundation www.alexandrasphate.org. Many Thanks again!!

Misshapen heads worry mothers of infants - CharlotteObserver.com

Misshapen heads worry mothers of infants - CharlotteObserver.com

Hey Friends,

Check out this great story about loving mothers being worried about their childs head shapes. It is true to life and if you don't know, you wont know.

We are going to the Orthomerica Summit. How exciting.

We have been invited to the Orthomerica Summit and are excited to attend. Hopefully we will be able to spread the word about www.alexandrasphate.org and STARband. Togther we can assist families affected by Torticollis, Plagiocephaly and Cranial Remolding Orthoses.

Alexandras PHATE donates helmet to Pittsburgh Family

Well friends! We've done it. Alexandras PHATE has officially donated a Cranial Remolding Orthosis to a family in the Pittsburgh Area. No better feeling than when you can help someone close to home. Thanks to Orthomerica and Union O and P for your kindness and caring. We couldn't have done it without your support. Our new family will have a daily blog on our website so that you can follow Christophers Journey with his CRO. Check us out at www.alexandrasphate.org for more information. =)

What a great Day!!

Here is our new flyer for the foundation. This is a rough draft, but you get the idea. We will be taking these to local orthotists, peditricians, neurosurgeons and giving them to families.

If you need anymore information, please visit our website at www.alexandrasphate.org

Thanks!

Are infants with Flat-Heads on the rise?

Check out a great article from March 2010 on Plagiocephaly by clicking here. It is unbelievable how common this condition is becoming. Lets get the word out to our peditricians and doctors.

Our Cranial Remolding Orthosis is almost behind us!

Dear Friends,

It appears that we are almost to the end of our CRO program. Our orthotist said that we are week to week now and it won't be much longer. It started way back on Halloween 2009, and seems like forever since we could hold our baby close. Soon (within a couple of weeks), we will be able to store our helmet away forever. Then it will be our job to continue to assist families who need help regarding Plagiocephaly, Torticollis and CRO. Visit www.AlexandrasPHATE.org for more information.

Alexandra's PHATE kids of the month March 2010

Well everybody. We were unable to pick just one PHATEs kid of the month for March. It was too close a race so for 3/2010 we have co-winners. Congratulations to Angelo and Lucy. Thanks for all of the pictures! Submit your pictures beginning today for April's contest. photos@alexandrasphate.org