This is a community supported site that provides a place for family, friends, and patients with Chronic Granulomatous Disease to share information, stories, and ideas.

Welcome

Welcome to the new and improved CGD Café! The old forums are still available to read and search but is not accepting new posts. Also, you will need to create a new account here (your login from the old site won't work).  We plan to add/tweak things as we go along but right now we have these features turned on:

  1. Community forums
  2. User blogs so you can keep everyone up-to-date on your story
  3. Front page news stories
  4. Ability to create static information resources (pages)
  5. Guidebooks (book pages)

Please note: This is a community site and needs your help to stay alive and vibrant! Please help out by submitting content (book pages, blogs, forums, stories) whenever you can.

Submitted by Tracy on Sun, 2006-11-12 22:31. read more | login or register to post comments

Please Pray for Sean Van Ness~attached is an email from Sue

Okay people~ Let's get our praying and positive thoughts going for SEan Van Ness. Today I received this email from Sue.

Please contact her with your thoughts and love@ purpleloversue@yahoo.com

 Hi everyone.

I did go home last evening with the girls and attended one of the benefits in Spencer at the Grange.  Lordy, Lordy!  Theresa, Kathy, Lauren & Sondra...you guys did an awesome job pulling this together in such a short time period especially!   I am so impressed and so thankful!  To all of you who helped in whatever way, thank you so much.  It was great to see everyone also--very bittersweet!  
So to give you an update...I got back with the girls early this afternoon and immediately noticed that Sean's heartrate had dropped significantly.  So after a meeting with the doctors, Sean's condition has worsened and unless there is an act of God (aka MIRACLE), he is not expected to live.  The time frame is not known...he still has a fight but it is diminishing.  Sean is still responding heartwise...his heartrate goes up when we talk.  No drastic measures will be used at this point, but he will be kept comfortable at all times.
I can't think of anything more to say except keep praying and thank you for everything.  I will be in touch.
Love,
Sue

 

Submitted by LaDonnaKaye on Sat, 2008-04-05 15:36. LaDonnaKaye's blog | 4 comments

Domenic

Hello, I don't write in very often but i do visit the site atleast once a week.Connie it is great to read how Ben is doing. My son Domenic is turning 6 this month and also started kindergarden this year. He has been doing so good a few sores around his bum has been the only issues and a little more predisone has helped that. He has scheduled appointment  coming up this month at the  NIH his third trip check up only.I can say he is definately a very active boy as i write he is brawling with his 4 year old sister who is allready taller than him and out weighs him.We still have no luck trying to get the town to remove mulch in our local playground and his elementry school won't budge on their playground in the school yard either.He brings his own toys to school and plays in a seperate paved area and all his friends join him.  Zach and Jaxsen you guys are allways on my mind and i pray that you have a speedy smooth recovery.I'll write again soon.

Submitted by mcenci on Fri, 2008-03-07 17:56. mcenci's blog | 7 comments

An Update on Ben

Hello to my CGD family,

I thought I'd update everyone on my Ben as it's been a while.  Ben's health has been remarkably well over the last year.  He started kindergarten in a public school in the fall and I was pretty terrified at what was in store with that.  Thank God, we've been infection free so far. Laughing

Ben has also been playing soccer in the local recreational league.  We just began the spring season of it and he's so happy out there on the field.  Watching the beauty of him with the other children, laughing, running, falling, getting up... it always fills my heart to the brim.

Submitted by Bensmom on Tue, 2008-03-04 21:46. read more | Bensmom's blog | 2 comments

Fluid around Mason's heart

I have a son with CGD and it has been awile since I have made a post but we are in the hospital and we came in because he was not acting like himself and come to find out he had fluid around his heart.....Yet to be detemined what the fluid is but we do know that it is not a bacterial infection?!!  He also has several lymph nodes throughout his body that are very inflamed just curious if anyone else has had these same issues with the fluid around the heart that can maybe give the docs a better idea on what to look for?  Also we are located in chicago at the University of Illinois if anyone is

Submitted by masonsmom on Mon, 2007-09-17 12:05. read more | masonsmom's blog | 4 comments

having a baby w/o cgd

has anyone wanting to have a baby investigated this institute ? please respond... 

http://www.genesisgenetics.org/pages/services.html

 The scientists and doctors at Genesis Genetics, headed by Mark Hughes, MD, PhD, performed the world's first Preimplantation Genetics Diagnosis (PGD). Since that time we have been helping couples for problems with more genes, causing more inherited illness than anyone else in the world.

Submitted by tessie on Thu, 2007-09-13 09:54. read more | tessie's blog | 5 comments

bone marrow transplant

I have CGD and so does my 11 year old son Jordan. We went to have HLA typing done for a bone marrow transplant 1 1/2 weeks ago. Jordan does not have any full siblings so hopefully there will be a match in the bone marrow bank. We were told at the hospital where he will have the BMT that there were eight boys that have had a bone marrow transplant 4 with unrelated donors all but one survived and are all healthy and living without cdg(praise GOD). The one that died was very sick with cgd related infictions before they even started the BMT, his chances for survival were not good to begin with.

Submitted by tessie on Wed, 2007-09-12 19:52. read more | tessie's blog | 2 comments

Having Kids

I was just wondering if anyone knows the chances of me having a child with CGD. I know they are probably pretty high since I have CGD and my mom is a carrier. Me and my fiance would like to have kids some day but I really don't wanna have to put a kid through the things I've been through if I can help it. If anyone has asked a doctor about this and knows the odds please let me know. Thanks

Submitted by mattjkemm on Sat, 2007-09-08 22:21. mattjkemm's blog | 4 comments

New Member

My name is Matt Kemmerer. I am 24 yrs old and live in Fairfax, IA. I was diagnosed with X linked at 6 months old. I have recieved all of my treatment at the University of Iowa . It's been great there. I have gone through quite a bit over the years so if anyone has questions about procedures or infections I've prolly had it done so ask me anything. I have had 3 lung surgeries including a resection of my upper and middle lobes of my right lung.I have had your typical CGD infections through the years (pnuemonia's, aspergilious,solmenella) but have also had Nocardia twice. This was nasty and it resulted in surgery both times including my resection. Also a big important thing I do recieve Social Security Disability. It took me years and years of fighting through paperwork and legal junk but I went to court in June 06 and won. It's nice because I cant work full time because I would be way to tired and it helps pay bills but the big plus is medical coverage. We all know how expensive drugs are and this helps a ton. Thanks for reading and feel free to ask anything.

Submitted by mattjkemm on Mon, 2007-09-03 16:10. read more | mattjkemm's blog | 11 comments

IDF Conference

The conference in St. Louis is getting close.  Anyone else out there going?  This will be my first time.  I hope to meet some of you when I am there.

 

Vickie

Submitted by Vickie on Thu, 2007-06-07 12:44. Vickie's blog | 1 comment