Thursday, September 20, 2012

Miss Jennah is 5 years old!

First, I’d like to thank all of my readers for your friendship and continued support. We have several new friends who have started following our blog and many have requested an update on our little Miss Jennah. I haven’t blogged in nearly 5 months, which is kind of a good thing, because it means I haven’t been totally depressed or had much to complain about! But I do apologize to those of you who have long awaited an update.

A lot has happened since spring! Jennah finally returned to preschooWP_000346l after her brief sabbatical, just in time for graduation. Of course, she had a meltdown during the ceremony and we had to leave early … pretty much sums up her entire school year! Nonetheless, we will greatly miss her teachers, assistants, and therapist at Phantom Lake Elementary. They were all extremely supportive and put up with Jennah’s bad attitude on a daily basis. Our preschool experience was invaluable and I feel so blessed that we were able to come back to the U.S. and provide Jennah with these opportunities.

We started the summer off with the Northwest Run/Walk for Epilepsy. With the DSCN4026support of some really great friends and Snoqualmie Springs School, we were 2nd highest non-hospital team in Seattle raising over $2200 for Epilepsy Foundation Northwest!

We spent the summer at home as all anticipated travel plans were cancelled after our hospital stay in March. We wanted to allow Jennah to stabilize while WP_000308we made medication adjustments and introduced a new medication, Baclofen, for spasticity management. Spasticity is basically her super-tight muscle tone, especially in the lower extremities. We want to treat this to avoid the severity of the impending scoliosis that is already occurring, and also to avoid deforming her bionic hips that were reconstructed only last year. It was a busy, but very fun summer, as we entertained friends and family from Dubai, Thailand, Texas and California! Jennah did have an increase in seizures with the summer heat, but overall, we were very successful in getting a good balance in her meds and have seen some noticeable improvements in her muscle tone.

Jennah celebrated her 5th birthday on August 1! I am so proud of our Little Miss Jennah … she has endured so much in 5 years: a complicated birth followed by 18 days in the NICU; 2 CT scans; 3 MRIs; at least 20 x-rays; approximately 10 EEGs, 6 of which were 24-hr monitored stays in the hospital; a VEP confirming her CVI; 2 swallow studies; a g-tube placement (3 days inpatient); two emergency room visits, both resulting in hospital stays; a 3-day ICU stay complete with intubation and central line placement following a grand mal/status epilepticus episode; a 14-day stay including a PICC line placement; a bilateral hip reconstruction (3 days inpatient) with 6 weeks in a full-body spica cast and 6 months recovery; and countless other pokes, tests, assessments and clinic/doctor visits. With all this, I count our blessings that this is all that we have had to endure. There are many others who have to go through so much more, those who have to use that CAP badge at Seattle Children’s much more than we do.

I am happy. Truly happy and feeling so truly blessed for how well Jennah is doing and for all that we have. As always, I am so thankful for my friends, family, and all those who support us and pray for us. Now it is my turn to return the support and prayers to a dear friend who is in surgery as I type. Also, to the moms of other children with special needs who I know are not doing as well right now … God bless you and give you all strength. Have faith. xo


  1. It's about time! I'm glad to hear that things are going so well for Jennah and the family. Love you!!

  2. No worries and lots of love to you!!!

  3. Just happened across your blog and so glad I did. Jennah is such a beautiful child. It's great to read that she's doing well. I was mom to a daughter with severe spastic quad cp for 27 years before God called her home this past May. She too was on Baclofen but we did the baclofen pump. It was the only therapy that had a positive impact on her spasticity and quality of life. I'll be hoping and praying you realize similar success with it for Jennah. If you ever want to connect with a large network of CP families, please consider visiting us @ Cerebral Palsy Family Network. I would love for our families to meet your beautiful family. You would be an inspiration to so many. Good thoughts, best wishes and lots of prayers.

    1. Thank you so much for your comment! I apologize that I have just barely seen this comment from you. :( I am so very sorry to hear about the loss of your daughter. Thank you for your kind words of support. I will check out the CP Family Network as you suggest! I hope that you will continue to follow my blog (and I hope I can post more frequently!) and lend out any thoughts you may have. Best wishes to you ...

    2. I can't wait for the day when I can hug all three of your angels. Because of Jenna, your family has such an amazing opportunity for holiness. What a gift. Much much much love to you all.

    3. Renee, it was you whom I was thinking of the day I wrote this entry. I write when my heart is heavy and my mind full. I remember thinking of very little aside from your surgery and had to write an entry to calm my mind. Thank you for sharing your journey and reminding us the power of prayer, love, and support. xo