Friday, July 18, 2008
Eleyna's blessing
We blessed Eleyna on Sunday, July 6, 2008. It was such a special day. I got teary eyed watching all of the men I love walk to the front of the chapel to bless my little girl: my husband, my dad, my Grandpa George, Tyler and Grandpa Rassmussen. What a wonderful bunch! The blessing Bryson gave her was beautiful. I had the opportunity to bear my testimony during the meeting and express how lucky I feel to be the mother of two. I am amazed at the faith the Lord has in me to give me such precious children to care for. He must think I have real potential. :-) It is strange to me that the world might think I am exchanging the best years of my life for drudgery as a stay-at-home mom. I'm not saying that I don't have hard days-I DO! But it is worth it. One of my young women came up to me after the meeting and told me she really needed to hear what I said in my testimony. That meant so much to me! Grandpa George bore his testimony too and said a few things about Hunter. The thing he said that stuck out to me the most was that most people come to earth to learn, but a few people come to teach-like Hunter. So true! It was a very sacred, beautiful meeting. I love my ward more than I can say! After sacrament we headed back to our house for food and visiting with the fam. My mom, Janeen and Leigh all helped me with the food so I didn't have any stress on the big day. Thank you so much girls!


Tuesday, July 1, 2008
Flaming Gorge camping trip
Bryson took us camping this past weekend to Flaming Gorge. I was very hesitant about going with a four week old baby, but it actually turned out okay. We left Friday morning. After we arrived at our campsite, Mustang Ridge, we set up camp. Thankfully we brought our canopy so the kids had some shade to nap in while we unpacked. It was really hot that afternoon!
Wednesday, June 18, 2008
Check-up at PCMC
On Monday we ventured up to Primary Children's for Hunter's check-up with the neurologist. Hunter's seizures have been pretty unstable lately so we wanted to discuss other treatment options in case we decide to make a change. Lamictal, Depakote and the Ketogenic diet were the three alternatives the neurologist raised as possibilities. A couple of families with disabled children have been visitors on our blog recently and I thought I would see if anyone has experience with the above treatments. We are hesitant to dive into anything new because nothing is guaranteed to deliver better results than the meds we are on right now. Though, the possibility that a different treatment might improve Hunter's quality of life is highly motivating. Since summer is such a healthy time for Hunter, we will probably make a change sooner rather than later.
Hunter working out with Tiff (his PT)
Father's Day
Saturday, June 14, 2008
Subscribe to:
Posts (Atom)