This update is a little overdue… but here we go! Leah is doing much better since she was discharged from the hospital early November. However, the question remains: What is the cause of the high fevers she was having??? Currently, Leah is still on daily steroids to keep the fever at bay. When we tried to wean her off the steroids after the hospital, the fever came back. She has gone through a series of appointments and testing to get to the root cause.
A Positive Note: New CF Drug becomes available - TRIKAFTA!On December 8, 2019, Leah started Trikafta. Some of you may be aware of the waves this most recent CF medication has made in the news. This has been the most promising drug released so far. Trikafta is a CFTR modulator, which means it works by helping to correct the gene defect that causes CF. This is the third modulator medication Leah has been on, and by far, the one that we have noticed the most response for Leah. Leah’s PFT went up 10% since she started on the medicine and is the highest it has been since last August! We want to thank you, our community, who has supported us over the years to help fund the research and development of these medications that are making a difference in the CF community! THANK YOU!!!! Leah's Front Line is registered for the 2020 Great Strides walk! You can register today and join us! Denver Consultation with NTM expertsBack to figuring out the fevers… with the decline Leah had in her health as she was fighting these fevers, it became clear that it was time to address the possibility of Leah’s NTM being the main culprit of these fevers. So, doctor referred Leah to do a consultation with leading NTM experts in Denver, CO. This past week, we headed out to Colorado. The appointments went really well. We believe having both Dr. Martiniano and Dr. Daley involved in Leah's care will be of tremendous benefit as we move forward in monitoring and treating Leah's NTM. Their level of expertise and experience in treating patients with NTM is reassuring that we will be good hands. It was really good to hear from them some of the medications and treatments that are in the pipeline and being investigated. It gives us hope for more effective treatment when the time comes to start treating again. They both said the fevers could possibly be from the NTM. Talking with both of them, we have identified symptoms that would indicate the need to restart NTM treatment as well as discussed in general what that treatment would look like. Plan Moving Forward
Follow the Yellow Brick RoadOn a personal note, we have musicals in the air at our house. Leah is a munchkin in the Wizard of OZ musical at her school. Hannah is a big kid and a salsa judge in the Matilda musical at her school. Both girls are super excited to be part of these productions. If you are looking for some fun, quality family entertainment or a date night with your special someone, the Wizard of OZ will run March 5-8 and Matilda will run March 13-15. Love to see you there!
7 Comments
Michelle Buell
1/18/2020 06:59:05 pm
I am praying for you continually Leah! You are such a young warrior! I'm so excited to hear that you are able to start the new CF drug! I was in The Wizard of OZ as one of the witch's soldiers when I was in eighth grade haha! I will try to come see those productions! Hannah is in Matillda, too! This is quite the musical family! Much love, and I hope to see you soon! =)
Reply
Chris Balkema
1/18/2020 10:20:34 pm
Thank you for sharing. We are so encouraged about the possibilities with the new drug. We are praying for you Leah and your whole family.
Reply
Mina
1/18/2020 11:04:54 pm
SO glad to have this update!! I think of u guys SO much!!!! Praying for these specific issues for Leah!
Reply
Dan Stayskal
1/19/2020 06:45:57 am
Praying for Leah and for her to continue to see improvement. The new medication sounds so encouraging! Praying also for continued strength and peace for the entire family as together you guys battle CF. We love you!
Reply
Karri Combs
1/19/2020 09:05:04 am
It’s been so exciting over the years to see all they are doing to help CF patients. Continuing to pray for you all in this journey.
Reply
Katie Baier
1/21/2020 07:00:07 am
The blessing of a new drug that is working is everything! We’re praying Specifically for the above mentioned for Leah and for your family. xo
Reply
Karen J.
1/21/2020 09:30:32 pm
So nice to see Leah’s bright smile through it all. Prayers for improvements in Leah’s health so she can carry on as the little munchkin:-)
Reply
Leave a Reply. |
About us
We are truly blessed. We want this to be a place we can share updates on how Leah is doing with her CF. As well as a place to share our hopes, dreams, and prayer requests. Thank you for loving and supporting Leah as she fights everyday to add more tomorrows. SubscribeArchives
April 2022
Categories
All
|