jenandiggy blogspot.com

Team Magnus

Our son Magnus was born November 19, 2009 with a serious congenital heart defect, HLHS. I set up this blog to keep our family and friends updated on his condition, and to connect with other families dealing with HLHS.

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Just Joshua

Wednesday, July 26, 2017. In addition to being followed by a new team, they added a breathing treatment upped a few meds, and decided they want another cath. As we understand, this disease is another symptom of heart failure. And quite serious at that. The first few weeks after learning about his PB were pretty rough for me emotionally.

Because I Said So

Friday, April 19, 2013. And finally the third question that I totally flubbed. the one everyone asks and the one everyone wants the answer too, how do I do it all? Thursday, March 28, 2013. C of course was a champ. The good news from the cath is that with her fenestration closed, C sats at 92. Holy wow! Other than that not so great news, C was fine with the rest of the cath. This time we had a practitioner with Healing Touch come in and do healing touch with C af.

neck on wood

Then we zipped right out of there, into a gorgeous fall day, sun shining, fall leaves blazing and beautiful blue skies.

My Life. Its a little messy, its a little crafty, but its all good.

Wednesday, January 25, 2012. PLEASE PICK GRACE FOR THE SF GIANTS COMMERCIAL! Who thinks GRACE would make an AWESOME addition to a SF GIANTS commercial? Dear Giants Commercial Selection Committee,. I think my daughter Grace belongs in a Giants commercial. She just turned 5 years old earlier this month. As a matter of fact her birthday party was Giants Theme. I have to say she rocked her Giants T-Shirt with a black tutu.

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Team Magnus

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Our son Magnus was born November 19, 2009 with a serious congenital heart defect, HLHS. I set up this blog to keep our family and friends updated on his condition, and to connect with other families dealing with HLHS.

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This web page jenandiggy.blogspot.com states the following, "Our son Magnus was born November 19, 2009 with a serious congenital heart defect, HLHS." We saw that the webpage said " I set up this blog to keep our family and friends updated on his condition, and to connect with other families dealing with HLHS." It also said " Thursday, May 21, 2015. So, not as good as wed hoped, but not as bad as it could have been. I dropped Magnus off in the cath lab around 1230 pm I stayed there until he had fallen asleep. After that, Iggy and I proceeded immediately to the cafeteria, as wed been NPO all morning."

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