Our Salted Miracle story.
The Cystic Fibrosis community is near and dear to our hearts as we had all 3 girls diagnosed within 3 years(2021,2022,2023). December 2023 we saw the worst of how fast CF can impact and reality sunk in (but so did our faith) with a significant drop in lung function. By the grace of Jesus and an answer to our prayer, her lung function was restored to full function 3 weeks later (Isaiah 40:31) (Not by might, not by power, but by the Spirit of the living God Zechariah 4:6). We have seen his wonder working miracle power(Matthew 19:26.) Even though our girls continue to defy odds, with every diagnosis by the hand of Jesus and his constant guidance. We are forever grateful for his healing hand over them and all the Glory belongs to him and him alone.
CF still has no cure and so many are still losing their lives to this awful disease daily. We won't stop until CF stands for Cure Found. Your donations go to a non profit organization called Cystic Fibrosis Foundation to help research and fight for a cure for all CF fighters. Though there has been a lot of progress with modulators that are helping people it also is affecting others with severe side effects. Not all qualify for this medication or others and not all are benefitting from it. Praying we see the day that CF stands for Cure Found. We are blessed our girls have atypical CF, we pray and believe it stops with them. We know God holds the future in his hands. So we keep fighting in prayer. We continue to cling to his word and promises, and We keep raising awareness for a cure.
The best way you can support us is by praying for a cure daily.
The next way is to join our team and come walk with us in May we would love to have friends and family along side us. I know the girls would love to have y'all as well. You can click in the link and hit join team (under the donate button). You can also donate as little as a $1 and even set your goal to that amount.
If you are a friend or family member out of state you can join virtually and I promise it too means the world to us and our girls.
The last thing is donate if you can financially even if it's a dollar I promise it doesn't go unnoticed. We appreciate every single penny and prayer.
We wouldn't be where we are today if it wasn't for God's grace, favor, guidance and your continual prayers. He is a faithful God and he has done miracle after miracle. Thank you Jesus and to him be the glory.
Cystic Fibrosis picked the wrong family to mess with
2 Corinthians 5:7
1 Samuel 1:27, Isaiah 40:31, Jeremiah 33:3
Psalm 103-5, Matthew 8:17, Mark 5:34
Thank you beyond measures!
#saltedmiracles #Cystersquad #fightinginprayer #conqueringcysticfibrosis #cysters #Harkcomstrong #nooneinthisfamilyfightsalone
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.