Pick Your Walker
$ 2535  100%  $ 2000
  
  • GravatarKat and Poppy said (About 117 days ago)
    We love you Caden and we are so proud of you!! See you Tomorrow!!!
  • GravatarAmy Pardo said (About 118 days ago)
    Good luck tomorrow! We promise to walk with you next year!
  • GravatarDad said (About 118 days ago)
    Caden, Mom and Dad love you sooo much and we are very proud of buddy!!!
  • GravatarPhyllis Collins said (About 128 days ago)
    Caden. Now that you know I'm "fun to play with", wish I could come walk with you. We could take Ansley and MeeMaw to Chic Filet again!!
  • Gravatar Suann Southwick said (About 128 days ago)
    Nice pics cutie pie. See you soon.
  • GravatarErin Dee said (About 129 days ago)
    Good luck, Team Caden Roe! We love you.
  • GravatarJanet Glendening said (About 129 days ago)
    Looking forward to the walk. It will be fun just like last year. I'm so proud of you, Caden!
  • GravatarBenny said (About 184 days ago)
    This is a test of the leave a message on your team page for the spring walk
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Thank you for all your support!

Our son Caden is a very active 5 year old who lives with moderate hemophilia A.  Hemophilia A is a bleeding disorder where the blood clotting factor VIII is decreased or missing.  This causes bleeding for longer periods of time.  He was diagnosed at birth due to a family history.  Caden lives a fairly normal life with the exception of always being aware of his body more than others.  He is now able to tell us when he has a bleed before he loses range of motion.  This means it is also before he has permanent damage to a joint from hemoarthrosis (when bleeding in the joint occurs). 


 We are blessed to have had no major medical problems in the past year. Currently, Caden needs to be treated on average 4 times per month with Factor VIII.  Factor VIII is an intravenous medication that is made up from blood donations of more than 60,000 different people.  The Factor VIII Caden uses is synthetically made.  Caden has become more involved with his treatments.  He calls them "poke pokes" and likes to dictate where he is going to be stuck.  He then helps with the infusion process while keeping a smile on his face.  He is an amazing boy! 
   
 
Thank you,
The Alexander Family