We thought this would be a fun way to post updates on Olivia and Madi's ever-changing world for family & friends to see!
About Me
- Kristy and Brian
- Brian & I met online in 2000 and married in June 2003. Olivia was born April 14th, 2006, a week before due date! She has blessed us in so many ways. She had an AVM bleed in her brain at 5 mo. and had emergency surgery to remove it. She's been through 4 surgeries total, all by age 5. Oct. 6, 2006 was the date of the AVM bleed and she endured PT, OT, and Speech Therapy through Early Intervention Services until age 3. Now, only OT once/wk and an IEP through school w/sped ed, OT and Speech. Madison was born 6.29.09 and is growing up too fast, talking up a storm, potty training and enjoying time with her family and friends at daycare and church. Her cute little personality blossoms more every day. :) The girls are best friends and get along really well about 99% of the time.
Liv and Madi
sweet girls :)
Showing posts with label Doctor. Show all posts
Showing posts with label Doctor. Show all posts
Sunday, June 24, 2012
Madi 3 yr checkup
Madi's 3 yr checkup went great! No crying-she was such a big girl. Had to get one shot-Hep A, and she didn't even flench. In 50th percentile for height and about 70th percentile for weight, coming in at 32lb 9.6oz.
I took her to Red Robin for a shake and burger for a treat afterwards! And we went to Toys R Us to buy bicycle helmets for her and Liv.
Tuesday, February 16, 2010
appointments




Since the new year, Olivia and Maddie have both been their share of sick. Olivia had a few bad days with vomiting/fever/no appetite, due to sinus drainage and a viral infection. Maddie had more of the head congestion, now is coughing some, too. Other than that, Olivia had an appt. with Dr Apfel today after 4 months previous and gaps in her head are same size as before. She thinks the bone that's there is not defective, but just doesn't have something to attach to to grow and so we'll have to fill in the gaps again whether we do the same surgery as last time or we use a synthetic piece that would be patient specific, made just for Olivia. We're talking within a year or two, so no hurry. She is going to get more info from the supplier of the synthetic piece about options with children. So, we'll see her again in June, then October and be thinking about our options until then. We met with City of Salem schools last week and they want to do a full evaluation on Olivia to see what she may qualify for as far as therapies, etc. through the school system. She's doing well in her new Two Steps Up class, but we feel she's a little behind in speech and attention span. Daycare is going to try her again in the Connect Three's class March 1st. She went to the Curious George Live show last week and we've taken her to see Seasame Street Live and gone to an indoor carnival at the mall this winter. She's doing good in therapy, progressing--just slowly. Mrs. Robin has been having Olivia wear the sewed shirt during activity time daily for constraint therapy and Ms Jenny (OT) does the same for about 10 minutes a session. Olivia is more willing to use her right hand now, however it's still difficult for her to use it for many things. Assists well. Please pray for us and for olivia's head, God's will be done! His grace carries us through turmoil. We are blessed!
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