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         Helping Allana's posts and comments across Aidpage (15)

        Comment on: Helping Allana

        Posted in Helping Allana on Jul 14, 2008

        I wanted to provide an update.

        My daughter Allana is doing great.

        She is in a wonderful new brace.

        Her ribs look great, and so does her posture.

        She no longer is required to go into surgery for casts and moldings.

        She is now seen closer to 4-6 months

        Her back is currently at the best it's been so far 23 degrees, on its own.

        She is walking well, riding scooters and living just like other 3 year olds.

        She is now in school and therapy and doing very well

        Allana is now receiving disability for developmental delays and speech problems stemmed from all her treatment but is in state programs for special schooling and is making big advancements.

        Thank you all for your kind thoughts and i will update again soon!

        Comment on: Helping Allana

        Posted in Helping Allana on Jul 14, 2008... modified on Jul 14, 2008

        Me, my sissy, and my mommy!

        Comment on: Helping Allana

        Posted in Helping Allana on Jul 14, 2008

        On my way to Shriners hospital, look in blog for more pictures of me~

        Comment on: Comment: ...

        Posted in Helping Allana on Jul 14, 2008

        I'm now a big girl and fly to Portland, but the Plane ride is long.....how sweet!!

        Comment on: Helping Allana

        Posted in Helping Allana on Apr 8, 2007... modified on Apr 9, 2007

        I am now working for this great website. If I get 50 people to download and use at least 20 times this toolbar by April 20th I get a bonus. It's for Chacha, the people powered search engine. We guides search for you and with my toolbar you will have this service right at your fingertips. Please help. My daughters next Dr.s appointment is the 19th and we will be broke afterwards, this bonus money could help!!!!!! Thanks
        Chacha Toolbar

        Comment on: Helping Allana

        Posted in Helping Allana on Apr 9, 2007

        I am now working for this great website. If I get 50 people to download and use at least 20 times this toolbar by April 20th I get a bonus. It's for Chacha, the people powered search engine. We guides search for you and with my toolbar you will have this service right at your fingertips. Please help. My daughters next Dr.s appointment is the 19th and we will be broke afterwards, this bonus money could help!!!!!!
        http://try.chacha.com/?rid=775 84

        Comment on: Helping Allana

        Posted in Helping Allana on Dec 30, 2006

        I wanted to post an update on Allana, though we are far from done with her treatment, Allana has officially gone into her last cast December 20 with a degree curve of 12 DEGREES..yaya so she is no longer considered severe, as a matter of fact she is 2 degrees from not having scoliosis at all, though she will more then likely need rib replacement surgery, she is doing much better. Feb. 21 she will have her last cast removed and be placed back in a brace for an undetermined amount of time if Dr. d'Mato decides not to recast her for stabilazation reasons. I wanted to thank everyone for there prayers and kind thoughts. Thank you

        Comment: ...

        Posted in Helping Allana on Nov 27, 2006

        Note: This aidpage was started as a comment on "Home page of Helping Allana"

        Comment on: Helping Allana

        Posted in Helping Allana on Nov 20, 2006... modified on Nov 20, 2006

        Comment on: Helping Allana

        Posted in Helping Allana on Nov 20, 2006... modified on Nov 20, 2006

        Helping Allana

        Posted in Helping Allana on Nov 20, 2006

        This page has been created to help aid in my daughter Allanas treatment and recovery. Accepting donations thru paypal, check or in any other form....Contact me anytime.

        In December of 2005 my daughter was diagnosed with a rare condition called Severe Idiopathic Infantile Scoliosis. Now Scoliosis can be somewhat common in adolescent children but is very rare in children under 3. As a fact of matter less then 1-2% of children under the age of 3 in the world will ever get this and less then 10% of those children will ever need treatment, my daughters condition is considered so rare because her spine developed below her left shoulderblade and has deformed her ribcage due to the bend in her back, possibly causing problems with things like her breathing and putting pressure on her heart. Even if we get her spine straightnened, she very well will still need rib replacement surgery.

        This condition is treatable and she will go on to hopefully lead a somewhat normal life, but currently requires surgery every 6 weeks and she will need therapy and bracing probably until she is 14 and has stopped developing and will probably need some sort of treatment for the rest of her life.

        Shriners however has been a godsend, paying for transportation and all of the medical treatment, she however is also developmentally delayed and between all the things she requires, we are strapped.

        We are here for any kind of assistance or help, and it would be greatly appreciated, and smiled upon by our daughter. I love everyone for there help,in any form, if even just reading this has brought a little attention to other people with this condition.

        Please contact me with any info, questions or donations or even just to see more pictures of my little Allana!!

         


         

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