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Cover lost wages while Brandon stays home
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Support hospital and treatment expenses
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Bring some relief during an incredibly stressful and painful time







β¨ Update on Jessi β¨
We’re so happy to share that as of yesterday, Jessi is officially in remission from nephrotic syndrome! π This means her kidneys are working normally again and the protein in her urine has cleared. It’s a huge milestone and we’re incredibly grateful.
At the same time, her doctor reminded us that with nephrotic syndrome, relapse is expected and fairly common. Most children will relapse — sometimes multiple times — especially within the first year after their initial diagnosis. Infections like colds or even small illnesses can trigger these relapses. Pneumonia being the most serious.
The encouraging part is that relapses are treatable and most children will respond well again to medication if they did the first time. Over time, most kids grow out of the condition completely, though the timeline is different for each child.
We’ll continue monitoring Jessi closely, keeping an eye on her urine protein, and following her care plan to catch any relapses early. For now, we’re celebrating this important step and feeling hopeful about the road ahead. π Thank you for all the love, support, and prayers for our girl — they mean the world. π

—She said the thing she is the most excited about is that she can eat french fries again sometimes and that she doesn’t have to take yucky medicine every morning.
Because of fluid retention she has had to completely cut salt down to the bare minimum which is so much harder than it seems. Especially for a kid.


We want to sincerely thank everyone who has reached out, prayed, sent love, or simply kept us in your thoughts. Your kindness and support have meant so much to us.
As many of you know, our sweet Jessi Rae has been facing a very tough battle with minimal change kidney disease and nephrotic syndrome. It’s been a frightening and emotional journey, but Jessi has shown extraordinary courage and strength throughout it all.
When she was first admitted, she was in tremendous pain, unable to walk, and had a very low heart rate. It took several days to receive a clear diagnosis. Due to severe swelling, she wasn’t even able to provide a urine sample at first. Doctors eventually placed a catheter, which was very painful for her — but from that, they confirmed she was losing a significant amount of protein in her urine, and her blood levels were severely low in protein.
She then underwent three days of albumin infusions, which helped her release 21 pounds of excess fluid. We were told this treatment had only a 50/50 chance of helping, so we feel incredibly fortunate that it worked so well for her. Jessi also received four IV steroid treatments each day for seven days, as her body wasn’t able to absorb oral medications due to her internal swelling.
Each morning began with blood draws and we would anxiously wait for lab results. While her numbers are still slow to improve, they’ve stopped declining and are now trending in the right direction — a step forward.
Despite everything she has been through, Jessi Rae has faced each day with remarkable bravery. We are beyond proud of her strength and resilience.
Looking ahead, we will continue working closely with the nephrologist at Seattle Children’s Hospital. Jessi will remain on steroid treatments as we carefully monitor her fluid retention and protein levels. We have been told to expect 8-10 weeks before she could be in full remission.
Thank you again for your love, encouragement, and continued prayers. Please keep Jessi Rae in your hearts as she continues on her path to healing.
Gram And Aunt Dee Dee
$1,000 β’ Recent donation
Cathleen Dullinger
$1,000 β’ Top donation
Rachelle & Josh Sanderson
$500 β’ First donation

Fallon Allen is the organizer of this fundraiser

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Fundraising for




β¨ Update on Jessi β¨
We’re so happy to share that as of yesterday, Jessi is officially in remission from nephrotic syndrome! π This means her kidneys are working normally again and the protein in her urine has cleared. It’s a huge milestone and we’re incredibly grateful.
At the same time, her doctor reminded us that with nephrotic syndrome, relapse is expected and fairly common. Most children will relapse — sometimes multiple times — especially within the first year after their initial diagnosis. Infections like colds or even small illnesses can trigger these relapses. Pneumonia being the most serious.
The encouraging part is that relapses are treatable and most children will respond well again to medication if they did the first time. Over time, most kids grow out of the condition completely, though the timeline is different for each child.
We’ll continue monitoring Jessi closely, keeping an eye on her urine protein, and following her care plan to catch any relapses early. For now, we’re celebrating this important step and feeling hopeful about the road ahead. π Thank you for all the love, support, and prayers for our girl — they mean the world. π

—She said the thing she is the most excited about is that she can eat french fries again sometimes and that she doesn’t have to take yucky medicine every morning.
Because of fluid retention she has had to completely cut salt down to the bare minimum which is so much harder than it seems. Especially for a kid.


We want to sincerely thank everyone who has reached out, prayed, sent love, or simply kept us in your thoughts. Your kindness and support have meant so much to us.
As many of you know, our sweet Jessi Rae has been facing a very tough battle with minimal change kidney disease and nephrotic syndrome. It’s been a frightening and emotional journey, but Jessi has shown extraordinary courage and strength throughout it all.
When she was first admitted, she was in tremendous pain, unable to walk, and had a very low heart rate. It took several days to receive a clear diagnosis. Due to severe swelling, she wasn’t even able to provide a urine sample at first. Doctors eventually placed a catheter, which was very painful for her — but from that, they confirmed she was losing a significant amount of protein in her urine, and her blood levels were severely low in protein.
She then underwent three days of albumin infusions, which helped her release 21 pounds of excess fluid. We were told this treatment had only a 50/50 chance of helping, so we feel incredibly fortunate that it worked so well for her. Jessi also received four IV steroid treatments each day for seven days, as her body wasn’t able to absorb oral medications due to her internal swelling.
Each morning began with blood draws and we would anxiously wait for lab results. While her numbers are still slow to improve, they’ve stopped declining and are now trending in the right direction — a step forward.
Despite everything she has been through, Jessi Rae has faced each day with remarkable bravery. We are beyond proud of her strength and resilience.
Looking ahead, we will continue working closely with the nephrologist at Seattle Children’s Hospital. Jessi will remain on steroid treatments as we carefully monitor her fluid retention and protein levels. We have been told to expect 8-10 weeks before she could be in full remission.
Thank you again for your love, encouragement, and continued prayers. Please keep Jessi Rae in your hearts as she continues on her path to healing.

Fallon Allen is the organizer of this fundraiser

Support Β Bn CulbrethΒ by donating to this fundraiser
