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I just adore my Baby Girl's smile!


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My daughter's life has continued with the decision of 2 selflish families making the decision to donate their child's organs. Thank You...

Welcome to my daughter Savannah’s web site. Savannah was born with a rare metabolic disorder called citrullinemia. It is unknowingly passed on from generation to generation. She was missing 1 of 6 enzymes that is located on chromosome 7 that helps breakdown and remove nitrogen from your body. This process is known as the Urea Cycle. The result of missing this enzyme causes excessive accumulation of nitrogen, in the form of ammonia, in your blood stream. Excessive amounts of ammonia can cause anorexia, lethargy, projectile vomiting, rapid breathing, irritability, brain damage, coma and death (if treatment is not quick or effective). When left untreated, brain damage, coma, and death will occur. That is what happened with Savannah’s twin brother’s Zack & Luke. We knew they were sick but metabolic testing at birth wasn’t state required at the time. When we finally did find out what was wrong it was to late to save them. With the next pregnancy we had pre-natal testing, CVS & Amnio Synthesis, to confirm Savannah’s diagnosis. Within 5 minutes of her birth she was whisked away to the NICU to begin her life saving treatment. In April of 2004 we decided it was time for a liver transplant. Savannah was having more and more hyperammonemia episodes, coming out of each one leaving us wondering if brain damage had been done and will surface later in her life. It was taking her longer to respond to the life saving medicines. We knew she was becoming more at risk with each episode. December 9, 2004 Savannah received her gift of life from a wonderful family who lost their Baby Girl but wanted to give life to others through her. We are forever grateful to them. Amazingly, January 24th 2006, Savannah recieved her second gift of life. What a miracle's we have witness. Thank you to all donors and their families.
Savannah’s road has not been an easy one. She has had many many complications since her transplant but continues to fight and her family continue to believe that God is in control.
January 2005 Savannah received her 2nd gift of life!
Thanks for stopping by and don’t forget to sign her guest book!

Use this "make a donation" link to make a donation via Paypal with a credit card or transfer funds from your bank account securely.


To make an automatic tax deductible donation you can go through Eblen Charities. You must indicate that it is for the Savannah Loftis Fund. Otherwise it will go into the organization and not benefit Savannah. You can mail or drop off these deductions at:

Eblen Charities
12 Regeant Park Blvd.
Asheville, NC 28806


You will receive a letter from Eblen for tax purposes.Thank You!

To view our 1st transplant photo journal click on this link:
Savannah's Liver Transplant Photo Journal It is easiest viewed by clicking on slide show & you then can adjust the speed.
Thank you to all families who make the choice to be a donor or to donate. Thank you for the gift of life!

Journal

IT'S ABOUT TIME!

Yes, it has been a very long time since my last update. I still have a few paople who say they still check this website. To you I say Thank You for your continued concern and love and this is update for you.


We just celebrated 4 years since Savannah's 1st transplant and in a few days will be her 3rd year post second transplant. In reflection all I can say is what a ride. The hard times definately outweighed the good times for almost 2 years but this past year has been so very close to normal and I expect this year to actually be normal. Last year we dealt with the narowing where the graft was made in her main artery to narrow so much that she had to have 2 veinograms. That is where they would put the baloon into the artery and stretch it with hopes of it stay open. It was successful both times. Although this is a temporary fix her ultra sound last week should so much improvement we are hoping not to repeat an ultrasound until January 2010 at her yearly check up. Totally amazing! Enough medical...


Savannah is in the 75th percentile for height & weight. Yes, I will be the short one. EJ shot up last year and is now 6 fett or maybe 6'1" by now. Savannah is continuing with tap, jazz, ballet & this year hip-hop lessons. She is getting ready to start soccer after I was told I needed to cut the strings (by her PA) and let her do ANYTHING she wants to. I was always concerned about her enlarged spleen but that is no longer an issue. It continues to shrink! Thank you God.


She is growing into a fine young girl. She has definate opinions, strong willed and cautious. She has been making huge progress at school and is now only requiring special help with her writing! Reading to her is a joy and her speech is totally fine. In December she was a maid and a toy flute in the 2nd grade performance of the Nut Cracker.


As for the rest of us I have been working full time for 1 year & 1/2 now. Dad is still working and EJ is now 18... Goodness me where does time go?? My mom, sister & mother-in-law have all firgured out how to live normally again now that we are not living at the hospital.


So, as you can see, life for Savannah & her family has been so blessed this past year. Again, thank you to those of you who still visit here and we continue to ask for prayers for our family.

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E-mail Author: reneeloftis@verizon.net;

 
 

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