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Olivers JourneyThis Blog is to share the journey of our Son Oliver living with Wiskott Aldrich Syndrome and his subsequent Treatment and Bone Marrow Transplant
http://oliverswas.blogspot.com/
This Blog is to share the journey of our Son Oliver living with Wiskott Aldrich Syndrome and his subsequent Treatment and Bone Marrow Transplant
http://oliverswas.blogspot.com/
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https://oliverswas.blogspot.com
This Blog is to share the journey of our Son Oliver living with Wiskott Aldrich Syndrome and his subsequent Treatment and Bone Marrow Transplant
oliverswas.blogspot.com
Olivers Journey: October 2009
http://oliverswas.blogspot.com/2009_10_01_archive.html
This Blog is to share the journey of our Son Oliver living with Wiskott Aldrich Syndrome and his subsequent Treatment and Bone Marrow Transplant. Sunday, 25 October 2009. The days are flying by and Oliver (by the grace of god) continues to do well. He is eating and drinking normally (apart from the usual behaviour issues with eating! And he is having his Hickman line removed on Wednesday! We are hoping that Oliver will be able to start nursery in January, it all depends on his counts though. He reall...
Olivers Journey: March 2009
http://oliverswas.blogspot.com/2009_03_01_archive.html
This Blog is to share the journey of our Son Oliver living with Wiskott Aldrich Syndrome and his subsequent Treatment and Bone Marrow Transplant. Tuesday, 31 March 2009. News and slight date change. Other news is that we are having another baby! I will keep you all posted. Paige, keep us updated on Ayden! Sunday, 8 March 2009. Well, its been a while since I last posted. Oliver is now 3 1/2 and running us ragged. He continues to bruise extremely easily and we continue to have our heart in our mouths b...
Olivers Journey: 2010!
http://oliverswas.blogspot.com/2010/01/2010.html
This Blog is to share the journey of our Son Oliver living with Wiskott Aldrich Syndrome and his subsequent Treatment and Bone Marrow Transplant. Sunday, 3 January 2010. Its mind blowing that he has been through more than most adults have in his four years and this never fails to astound me. During this arduous journey most people around us have been incredibly supportive. Apart from Daves employer. Do these people not understand that he wasn't going in for his tonsils out? Oliver at 5 months.
Olivers Journey: January 2010
http://oliverswas.blogspot.com/2010_01_01_archive.html
This Blog is to share the journey of our Son Oliver living with Wiskott Aldrich Syndrome and his subsequent Treatment and Bone Marrow Transplant. Sunday, 3 January 2010. Its mind blowing that he has been through more than most adults have in his four years and this never fails to astound me. During this arduous journey most people around us have been incredibly supportive. Apart from Daves employer. Do these people not understand that he wasn't going in for his tonsils out? Subscribe to: Posts (Atom).
Olivers Journey: April 2011
http://oliverswas.blogspot.com/2011_04_01_archive.html
This Blog is to share the journey of our Son Oliver living with Wiskott Aldrich Syndrome and his subsequent Treatment and Bone Marrow Transplant. Wednesday, 6 April 2011. Well its now April 2011 and its coming up to two years since Olivers transplant in May 2009. He is doing great and just had confirmation that he can go to annual appointments at GOSH and can have his MMR which is great news. Im going to make this an annual post on transplant anniversary. Subscribe to: Posts (Atom). Oliver at 5 months.
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Find a Family - The Wiskott-Aldrich Foundation
http://www.wiskott.org/patients-and-families/find-a-family
Application Process and Timeline. Find a Clinical Trial. Find a Support Group. Find a Clinical Trial. ASCGT NIH Gene Therapy Symposium. September 26-27, 2011. Bethesda, MD. Physicians in the U.S. Find a Clinical Trial. Clinical Trials and Studies. IL 2, Eltrombopag, IVIG. Find a Support Group. Please register and sign up for the Wiskott-Aldrich Syndrome group). This is an active forum where many families have come together to provide support and share information with each other. If you have a mo...Happy...
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Oliver Smith-Wellnitz: Circus Artist
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Olivers Journey
This Blog is to share the journey of our Son Oliver living with Wiskott Aldrich Syndrome and his subsequent Treatment and Bone Marrow Transplant. Wednesday, 6 April 2011. Well its now April 2011 and its coming up to two years since Olivers transplant in May 2009. He is doing great and just had confirmation that he can go to annual appointments at GOSH and can have his MMR which is great news. Im going to make this an annual post on transplant anniversary. Wednesday, 17 February 2010. Seems ages since I l...
oliversweate's blog - Oliver - Skyrock.com
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Hello My name is Oliver. This is my website I made with my dad (in about 2 seconds). Here are some of my favorite web games. Here are some of my favorite YouTube videos:. I Made a Poop. Check out my new movie page! Follow me on Instagram @Oliverwarp6.
