Finn Greyson’s Journey : Our 1% Miracle

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Finn Greyson’s Journey : Our 1% Miracle

Following Finn Greyson, our 1% Miracle Baby. Join us as we navigate his clubfoot journey and raise vital funds for his medical care this May/June.

Thank you for being part of his village!

26/06/2026

Big milestone for our little warrior! 🥹💙

This morning we had our appointment with Dr Fraser, and Finn officially wore his LAST cast! We have now moved on to the next phase of his clubfoot journey, boots and bar!

Finn has been fitted with Mitchell Ponseti boots, and our new routine will be 23 hours a day in them, with one hour off for bath time and his leg and foot exercises. It's a big adjustment, but we are ready!

I'd be lying if I said I wasn't a little nervous about what strangers might think when they see him in his boots. But the moment they were on, something shifted in me, and I thought, I know his story. I know every appointment, every cast, every milestone. That's exactly why I chose to share this journey, so that people can learn and so that other parents walking this same road know they are not alone.

Finn, you continue to blow me away. The resilience and contentment in you is something I will never stop being in awe of. You have no idea how proud you make me, my boy.

Our next checkup with Dr Fraser is in 6 weeks, and we will keep you all posted as always. Thank you for every kind word, every check-in, and every bit of love you've sent our way. It truly means everything. 💙💙💙💙

12/06/2026

Finn's Foot Update 🥺💙

Since birth, our little guy has officially received 4 casts as part of his clubfoot treatment, and what a journey it has been!💙

It's been a real learning curve from the start. Clothes simply don't fit over the cast, and bath time became a back-breaking 60+ minute ordeal trying to soften the cast over the tub. That was, until we discovered that vinegar cuts that time down by about 45 minutes, an absolute game changer!🙏💙

The second-to-last cast was by far the hardest. During that session, Finn's tendon was stretched properly for the first time, and watching him in that pain was something we will never forget. I couldn't hold back my tears. It's one of those moments that tests every ounce of you as a parent.😪💙

But today, today was a big day.

We visited our orthopedic surgeon, Dr. Robert Fraser, and he delivered the news we have been working so hard towards,

We are on our LAST cast.🙏😭💙

Dr. Fraser is confident that Finn will not need tenotomy surgery, which is beyond relieving to hear. This cast stays on for two weeks, and after that, Finn moves into his boots and bar (surf shoes), the next phase of his treatment.

The progress over these past few weeks has been nothing short of incredible.This boy is so strong, and we are so proud of him. 💙💙💙

03/06/2026

Happy International Clubfoot Day! 💛

At our 21-week anatomy scan, we were completely shocked to learn our little boy Finn had clubfoot. Like so many parents, we worried about how it would affect him and hoped it wouldn’t cause him any harm.

But from the moment he entered the world, his care team moved quickly, he received his very first cast just 2 hours after birth. Today we’re on his second cast, and we’re already seeing such amazing progress. His little foot is getting stronger with every step of this journey.

This day is all about spreading hope and awareness: clubfoot is treatable, and early intervention makes all the difference! We’re so grateful for the Ponseti method and the incredible doctors and nurses walking beside us.

Every step truly is a victory. To all the clubfoot warriors and their families, you are not alone, and brighter days are ahead!
💛💛💛

30/05/2026

30|05|2026

We have some good news to share, Finn's jaundice levels have come down enough that we were able to stop the double phototherapy. That felt like such a relief after everything.💙

However, the past few days have brought new challenges. Finn's sodium levels were very high, which led our incredible paediatrician to order a cranial ultrasound of his brain. We held our breath waiting for those results, and thankfully, it came back with no abnormalities. We are so, so grateful.🙏🏼💙

But his hydration levels remained low and answers were slow to come, so a kidney and abdomen ultrasound was ordered next.

The following day, Finn was diagnosed with Hydronephrosis of the left kidney.

On Monday he will be having a specialised X-ray called a VCUG to determine the severity. We did attempt it already, but they were unable to place the catheter beforehand, so we are waiting for Monday. Based on the ultrasound alone, the team suspects a Grade 4 or Grade 5 case. Once we have those results, we will sit down with his medical team and put a treatment plan in place. For now, his right kidney is fully functional and keeping our little boy healthy and strong. 💙💙

Monday is also the day Finn sees the orthopaedic surgeon to have his first cast removed and his next one put on, so it is going to be a big, full day for our brave boy.

It has been a hard few days. I am homesick. I miss my husband. I miss our animals and the comfort of home. But we are still here, still fighting alongside Finn, and Monday cannot come soon enough.

Stay strong, little big guy. We are right beside you and love you so much.
💙💙💙💙

27/05/2026

26|05|2026
Update: Yesterday afternoon we were admitted to the NICU as Finn's jaundice levels have continued to rise. He is currently receiving double phototherapy light and we are praying his levels have come down enough for us to finally go home. We miss daddy so much, and nothing quite prepares you for sitting next to your baby, watching him under those lights, and not being able to just pick him up and hold him. It is one of the hardest things. We are staying strong for our boy and hoping for good news soon.
💙💙💙💙

26/05/2026

Introducing Finn 💙
22|05|2026 @ 13:47
4.09kg, 51cm

On Wednesday the 20th of May, I was admitted to hospital after a preeclampsia diagnosis. Just two days later, on the 22nd, our boy made his entrance into the world via c-section. We were nervous, overwhelmed, and already mentally running through every checklist imaginable: medical aid, newborn checks, and most importantly, getting Finn's clubfoot treatment started as soon as possible.

One hour and thirty minutes after he was born, Dr Fraser, our incredible orthopedic surgeon, was already at his side assessing him. His findings: idiopathic right clubfoot, and a left foot deformity that requires no treatment and will resolve on its own. Without skipping a beat, Dr Fraser took Finn straight to the nursery and applied his very first cast, all the way up to his hip, just two hours after he was born.

For the next four weeks we'll be making weekly trips to Hillcrest to have his cast removed and reapplied. After that, he'll be assessed for a possible Tenotomy, followed by Mitchell boots and bars, and then our 23-hours-a-day wear journey begins.

I honestly expected him to be in pain or distress with the cast, but this little boy is an absolute warrior. It's like it's barely there. Clothing is a bit of an adventure, zips and fitted pants are not our friends right now, and bath time looks a little different. Sponge baths only until this Friday, when we get to remove the cast ourselves and he finally gets his first real bath!

I'm going to keep sharing Finn's journey here, because if another mama or papa ever finds themselves facing a clubfoot diagnosis, I want them to know you are not alone. It is not a terrible diagnosis. You find your new normal, and you keep going.

Welcome to the world, Finn. You are already the bravest person we know.
💙💙💙💙💙

29/04/2026

And just like that our journey is completed, we can bring Finny safely into this world😭💜 I have fought so hard for this the past three months and what felt like it would never happen....I was shocked by everyone's support, love and selfless donations ,we have a village a huge one for that!! I don't have words how I'm feeling right now, my emotions are all over the place! Gratitude is a major feeling, peace and happiness is overflowing. I can rest now for the next three weeks 😭😭😭💜💜 Thank you to everyone who has been apart of our journey, this is not goodbye but merely a beginning of our story! 💜💜💜💜

21/04/2026

🚨 URGENT: THE 4-WEEK FINAL SPRINT IS ON! 🚨
The finish line is officially in sight, but the clock is ticking faster than ever. We have exactly 28 days left to secure the medical fees for Baby Finn’s birth and his vital clubfoot treatment.

We are so incredibly close to making this happen, but we need one final, massive push from our amazing community to bridge the gap!

💙THE STATS:
✨ Raised so far: R 36,851 (75% of the way there!)

✨ Remaining Goal: R 12,149

✨ Time Left: 4 Weeks

💙 WHY THE URGENCY?
To ensure Finn gets the best start in life, our specialist OBGYN and Orthopedic team must be locked in at Westville Hospital. This ensures his Ponseti treatment begins the very moment he is born. We’ve fought for 7 years for this 1% miracle—we aren't stopping now!

💙 HOW WE HIT THE GOAL:
The Power of 60: If just 60 people donate R200 today, we cross the finish line immediately! 🏁

Share this post: Your one share could reach the person who helps us close this final gap.

💙 HOW TO DONATE:
🔗 Back-a-Buddy (Quick & Easy): https://www.backabuddy.co.za/campaign/help-our-1-miracle-baby-with-vital-medical-care

🏦 Direct EFT (No Fees):

Reference: FINN DONATION

Bank: Capitec

Account Holder: MISS MICHELLE GREYLING

Account Number: 1643768032

Branch Code: 470010

SWIFT/BIC: CABLZAJJ (For International)

📖 Read our full story in the South Coast Sun:
https://www.citizen.co.za/south-coast-sun/news-headlines/local-news/2026/03/12/miracle-baby-on-the-way-for-amanzimtoti-couple/

Thank you for being the village that brings Finn home safely. Let's do this! 👣💙

16/04/2026

THE MOMENTUM IS REAL: OUR MIRACLE FINISH LINE IS WITHIN REACH!

We are absolutely speechless. Just days into our final countdown, the most incredible thing happened. We received a massive R5,000 donation that has completely shifted the landscape of this journey!

To the generous soul who sent that gift, and to everyone who has stepped up since our last post: Thank you. You haven't just given us money; you’ve given us the peace of mind to focus entirely on Finn’s arrival.

💙 The Updated Scoreboard:
We are moving closer to the finish line every single hour.

✨ New Total Raised: R36,851 (We’ve hit 75%!)

✨ The Final Gap: Only R12,149 to go!

✨ The Clock: 4 Weeks remaining to secure Finn’s medical care at Westville Hospital.

💙 Why This Matters Now
With the remaining R12,149, we will officially lock in the specialist team and the hospital space Finn needs the moment he is born. We are so close to ensuring that his clubfoot treatment starts without a single day’s delay.

💙 Let’s Finish This Together
We’ve spent seven years waiting for this miracle. Now, we are just one final push away from crossing the finish line.

How to help us bridge the last R12,149:

✨ The "Power of 60": If 60 people donate just R200, we are DONE!

✨ Donate: Every bit,no matter how small,gets us closer to the goal.

✨ Share: This journey has reached so many because of YOU. One more share could be the one that closes the gap.

🔗 Donate via BackaBuddy: https://www.backabuddy.co.za/campaign/help-our-1-miracle-baby-with-vital-medical-care

🔗 Donate via EFT (Reference: FINN DONATION):

Bank: Capitec

Account Holder: MISS MICHELLE GREYLING

Account Number: 1643768032

Branch Code: 470010

🔗Read our story in the news: https://www.citizen.co.za/south-coast-sun/news-headlines/local-news/2026/03/12/miracle-baby-on-the-way-for-amanzimtoti-couple/

Thank you for being part of Finn’s village. We can almost feel him here. 👣💙

Address

Amanzimtoti
4125

Telephone

+27646691511

Website

https://www.backabuddy.co.za/campaign/help-our-1-miracle-baby-with-vital-medical-care

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