Faith's Blended Diet and Other Things that Help with Her Digestion

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This page contains affiliate links and Faith's Mom may earn a commission if you use them. As an Amazon Associate, Faith's Mom earns from qualifying purchases.  Learn more.   Ever since Faith was born, she has struggled with her digestion. When she was in the NICU, she would spit up after eating even the tiniest amount of formula. Her dad and I were convinced her tummy was too small to handle large volumes of food. Sometimes when she ate, her heart rate would drop really low, which is why she needed to be in the NICU for longer. She just could not get the hang of eating and breathing at the same time!  Faith receiving food through an NG tube in the NICU.  Grandma giving Faith a bottle when she was 2 months old.  After finally bringing her home, eating continued to be an issue as she struggled with severe reflux and constipation. We tried various formulas, but she was never able to drink enough formula to gain a lot of weight. She also had trouble burping, and she...
2 comments

Adaptive Equipment for Children with Cerebral Palsy

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Adaptive Equipment for Children with Cerebral Palsy

Faith in her stander, a common piece of adaptive
equipment for kids with cp

Comments

  1. Danaus ClarusJanuary 23, 2011 at 1:08 PM

    I'm so sorry for the late reply. I've been completely wrapped up in a holiday pause. I just got out of the relaxation period. :)
    I hope that you and Faith and a wonderful Christmas.
    She's absolutely adorable!

    DanausClarus

    ReplyDelete
  2. Cari JeanJanuary 24, 2011 at 2:43 PM

    I've been wondering where you were! Always good to get in some relaxation time!

    ReplyDelete
  3. AnonymousMay 18, 2011 at 7:44 AM

    This looks great I have never seen anything like it before thanks for sharing.


    Pizza Equipment

    ReplyDelete
  4. shujaktkJanuary 14, 2012 at 11:43 AM

    my jasmine have cerebral problem, she is now 4 year but still can not walk, talk, i am so sad for her, because here doctor said, this type problem can not solve ...so i am so sad for jasmine, i wish one day she catch my finger and walk with me, i wish she can call me BABA, i wish to see smile on her face always....i wish only...

    ReplyDelete
  5. Cari JeanMarch 2, 2012 at 8:26 PM

    Shuja - is there not any therapy programs in your area for Jasmine? They can be extremely helpful - they may not be able to help your child walk or talk but she can still be strengthened in her mind and the abilities that she does have. Also, it is good to put hope in God and trust in Jesus - He is our healer!

    ReplyDelete

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