Cheryl and Nathan's big day
Sorry for the short remarks but cheryl will be out of recovery any minute, and Nathan within an an hour.
But the bottom line.......(and all of your with this disease will understand)...........NATHAN HAS produced Pee Pee.
Wow, so simply but elegant words, right? So thats the bottom line in all of this, right?
I will issue something more "Director like" shortly, but for now, time to savor this as a parent.
bill
UPDATE:; a few numbers:
Creatinine: 2 hours after the transplant 4.6..........6 hours after transplant 1.6.....2 days after transplant..... ,7
BUN: One day ago 60....... 6 hours after translant 9.1 !!!.......2 days after transplant........21...a surprise
Views: 96
Comment
-
Comment by lisa ann peterson on September 9, 2011 at 11:28pm -
sooooooooo awsome i am so glad to hear your great news.. god bless your family
-
Comment by Gene Billingsley on September 6, 2011 at 10:57am -
Bill what great and awesome news!!! We are soooo happy for you all and especially little Nathan!
I would joke that donating a kidney is like giving birth, but I think Cheryl's already got an idea about that! lol.
Take care and we'll keep up the prayers for you all.
Gene...
-
Comment by Joy Lewis O'Brien on September 3, 2011 at 8:07pm -
Fantastic! Many congratulations and hope for a quick and easy recovery for both!
-
Comment by Kathy Yates on September 3, 2011 at 4:54pm -
Congratulations, Congratulations!! Am so happy to hear that everything went well. Nathan's numbers are so awesome...What a wonderful change your lives are going to encounter.
-
Comment by Dana M Simone on September 3, 2011 at 10:44am -
Tears of joy for Nathan - and the rest of the family....SO HAPPY!
-
Comment by Linda Burke on September 2, 2011 at 10:28pm -
Looking forward to an update when you have time - hope all is well.
-
Comment by Kerri Grey on September 2, 2011 at 6:12pm -
Such exciting amazing news!!!! Praying all stays well for you all xox
-
Comment by Jodi Kayler on September 1, 2011 at 11:56am -
All I can say is "WOW!".
-
Comment by Jessica Olivia Frysz on September 1, 2011 at 10:59am
-
Very good to hear that Nathan and Cheryl are now into their recovery phase. Hope that everything stays where it is and stays positive!
-
Comment by Danna Vaughn on September 1, 2011 at 10:48am -
Special prayers for you and your family! What a big, big day!
WELCOME - Friends, Family Members, Patients, and Researchers - JOIN US!
The Foundation for Children with Atypical HUS encourages patients and investigators to share information and explore options/resources as we work together to gain insight into this rare complement disorder. By increasing contact opportunities with researchers and medical personnel interested in helping the aHUS community, our stories foster a better understanding of atypical hemolytic uremic syndrome.
Sharing information, inspiration and support for one another, we seek to gather together people and knowledge as we strive to improve the lives of patients and families dealing with a diagnosis of aHUS.
NEW DIAGNOSIS OF aHUS?
Be proactive! Get the medical basics of aHUS, what lab values to monitor, and areas of concern...check out the "aHUS Bootcamp" and "About aHUS" tabs at the top of this page!
If your doctor has never treated a case of aHUS, please print out our 'Doc to Doc Registry' and ask him/her to contact a physician versed in the complexities of aHUS and new options for 2011 genetic testing and treatment.
************************
NOTE: Our 'Send a Message" function on each Member's page allows for private discussion of personal content. As with any social network, be cautious about giving personal contact information (home email info, phone number) until you have an established relationship with another person, organization, or associated website.
Did you know...
• • • • • • • • • • • •
It is estimated that there are about 300 cases of aHUS in the U.S., and it is most common with young children. The condition is life threatening and either can be chronic or can recur at intervals.
more factoids...
Help us fight the battle
Your tax-deductible purchase of one or more bracelets will directly fund research to help end the tragedy and heartbreak that aHUS families live with every day. Each bracelet has an appraised value of $825, but your purchase price is only $295.
Or you can donate a specific dollar amount-every dollar will help the Foundation for Children with atypical HUS atypicalHUS.50megs.com
Donations may be made via credit card or Paypal. If you prefer, checks made payable to The Foundation for Children with Atypical HUS may be mailed to:
Atypical aHUS Foundation
19 Olde Colony Lane
Cape Elizabeth, ME 04107
For pearl bracelet orders, please allow extra time for processing checks.
Badge
© 2012 Created by ALPHA MARKETING.
Powered by
You need to be a member of The Foundation for Children with Atypical HUS to add comments!
Join The Foundation for Children with Atypical HUS