Kim Maddux
  • Female
  • United States
Share on Facebook
Share on Facebook MySpace

Kim Maddux's Friends

  • Linda Rang
  • Leeandra Arhdeacon
  • Cynthia Lammi
  • Moein
  • Nicholas Dobes
  • jessica santini
  • Cori
  • Jamie
  • Ana Vaish
  • Traci Griffin
  • amy
  • Kulwant Pannu
  • Michele Perry
  • Joel Rhodes
  • Beth Kilgore

Maddux Family

Profile Information

About me:
I am a stay at home mom with 3 kids. My husband and I have been married for 13 years and we live in Alamo, CA, near Oakland/San Francisco area. I love to read and scrapbook in my free time. I grew up on Southeast Texas and moved to Northern CA in December 1996.
About my family:
Alex is 11 and in 5th grade. He is a good reader, gifted writer, loves Legos and playing with his baby brother and sister. He is doing really well. He still gets around really well. He has a motorized scooter for trips that require alot of walking (MDA payed for) and we got him a Razor kid-size ATV. He loves it and rides all over the neighborhood with it. We also have twins, Ellie and Austin who are 4 years old. Alex is an awesome big brother and they adore him.
Name(s) of child(ren)/individual(s) with Duchenne:
Age(s) of child(ren)/individual(s) with Duchenne:

My Family Blog

Kim Maddux's Photos

  • Add Photos
  • View All

Kim Maddux's Blog

MDA Camp - Bay Area / Occidental, CA

Posted on February 17, 2009 at 5:16pm 1 Comment

Just wanted to let you all know that my son, Alex will be attending camp this summer. I am excited and nervous all at the same time. I just spoke to the camp director to get our application. If any other families have a child attending, let me know.



Good visit with Dr. Wong and Staff for my son, Alex

Posted on July 31, 2008 at 7:05pm 1 Comment

Hi all -

I am happy and thankful today and wanted to share. My husband and almost 9 year old son, Alex are in route back to California from a 2 day visit with Dr. Wong and staff. We are pleased that he is doing very well and on some tests a little better than last year. I have been on this rollercoaster for 4 years and it is nice when we have good today.

I can't wait to hug my son tonight when he gets home!

Thanks for listening..


Comment Wall (36 comments)

You need to be a member of PPMD Community to add comments!

Join PPMD Community

At 2:28am on September 2, 2010, Leeandra Arhdeacon said…
Hi kim,i was wondering if you will be attending the stride and ride at the oakland zoo? we are curious on what goes on and were considering on going. Any imput would be great.
At 8:13pm on August 23, 2010, Lesley Wilson said…
Hi Kim,

I never touched base with you to see how the get together went! I'm hoping we can make the next one.

Hope all is weel with you and your family!

At 1:02am on April 13, 2010, Lesley Wilson said…
Hi Kim,
Thank you so much for the note!! I wish we could come on Saturday, but it is Jordan's 4th Birthday, so we will be celebrating with a little party! ;o)

I'm trully hoping I can attend the next function, I would love to get to meet you all.Hope all is well... take care!

At 1:42am on November 3, 2009, mariela pedroza said…
thank you for your comment, we need some help, we are trying to decide to go to UC Irvine or Dr. Wong, ? so many different opinions from different parents? If you have a chance to talk I will greatly appreciate it, thank you
At 6:41pm on August 26, 2009, Kimberly Hannan said…
Oh, since I am out of that loop I hadn't heard. But it is better to be safe than sorry. John would have cried all week. He LOVED it. But since it does attack the lungs that definitely would not be good. I will have to remember to ask next year. I hope all is well with you and the family. Take care!
At 8:31am on August 26, 2009, Kimberly Hannan said…
Hello---we chatted about camp several months ago. I was wondering how it went? Did he have fun? How did you do? I hope it was awesome and you had a nice break. IF you get a minute, let me know. I would love to hear all the details. Have a great day! Kim
At 11:00pm on August 25, 2009, Keith Van Houten said…
Kim - I got part of my private message through to you, but part 2 keeps getting a timeout error and won't go through. Send me a message with your regular email and we can continue the conversation. Thanks, Keith
At 11:47am on March 20, 2009, Kimberly Hannan said…
I added Johnner's picture. It ended up there twice....not sure why. This was taken during his last year of school 05-06. He graduated June 6, 2006. I will add more. I have zillions. Enjoy.
At 8:36am on March 19, 2009, Kimberly Hannan said…
Thank you. Johnner's progression was fairly swift comparing him to some of the other boys we met. At seven he was very contracted and had cord releases and tendon transfers and went into long leg braces and a manual chair part-time. He walked in the long leg braces for the next four years. He did well in the house or inside but outside it was really difficult. He would get tired but we went his speed so he could enjoy his life and live it just like he wanted to :) We say we got to smell the roses thanks to him..... At 11 he "sat down for good." That still breaks my heart. But shortly after this he got his power chair and it was FABULOUS. He had independence and we had to run to keep up with him. The next few years were really good. He was getting around, living life, and having fun. Then he started to have lung function issues and the lumbar lordosis started. He had spinal fusion, rods, at about 14. That was really hard for him and if I had to do it again....I am not so sure it would be done. My own opinion. He did bounce back and was pretty good but the lungs kept failing and then his heart was getting weak and cardiomyopathy started to set in. So lots more pulmonology and cardiology appointments. Johnner had decided early on no feeding tube/ventilation. At 18 he had all of his medical power of attorney and DNR paperwork done. We always said he was the man "driving the car" and we were riding was hard for him to make the choice....he was getting tired. In the spring of 07 he got REALLY sick and his lungs clogged with mucous. He did not want to go to the hospital. At this time we had lots of nursing hours at the house.....we took care of him and got through this. He lost 30 pounds in three weeks. It was so hard. But he pulled through and the last 15 months were rough. He was so tired, weak, couldn't do what he wanted....but we had a great time doing what he could and loving every extra minute we had with him. We brought hospice in and it was a really good thing. He had a stroke, July 2--his dad's birthday-- at the end and that is how he went, the next day. I miss him so much. But I am blessed to have been given Johnner and he was hear to teach us lessons. I hope we were wise enough to learn them. Ask me any questions you want to and I will be happy to answer, etc. I know it is rough....but as I was told a zillion times you are given only what you can handle....I wondered why God thought I could handle is because he knows DMD boys need extra special must be awesome, too. Take care.
At 2:45pm on March 10, 2009, Rodney Foster - Sam's Dad said…
Hi Kim, What type of Scooter does your son use? Our OT has recomended the gogo elite and the lynx. The one we choose will be modified to better suit a child.These are light and transportable due t o the modular design. Sam is only six but we don't want him to tire himself out walking long distances. Sam is still steroid free but that probably won't last alot longer.

Need help using this community site? Visit Ning's Help Page.



© 2023   Created by PPMD.   Powered by

Badges  |  Report an Issue  |  Privacy Policy  |  Terms of Service