Help The Abernathys To Overcome Chronic Illness

Goal:

 USD $175,000

Raised:

 USD $1,875

Campaign created by Joanna Dowlearn

Campaign funds will be received by James Abernathy

Help The Abernathys To Overcome Chronic Illness

Heal me, O יהוה, so that I am healed. Save me, so that I am saved, for You are my praise. Jeremiah 17:14

So… friends, our friend Kaleigh Abernathy is suffering from significant health issues. I'll share the short story first, then I’ll tell the longer version in an “Update” post.

First, it should be explained, while the amount we are trying to raise may seem very high (more on those specifics later), this fundraiser is a 6-in-1 as Kaleigh and all 5 of her children are dealing with Lyme Disease. This chronic infection causes symptoms and suffering that many specialists compare to cancer. Since 6 family members are all experiencing significant health complications from the same illness, and due to the persistent and severe nature of the condition, a sizable financial fund is needed for ongoing testing and treatment, which can only be achieved with substantial community support.

That said, Kaleigh herself has been predominantly bedridden for over a decade with this debilitating disease, and she’s been sick even longer; suffering with this infirmity for over 3 decades. The infection triggered or exacerbated many conditions, including severe Postural Orthostatic Tachycardia Syndrome (a.k.a. POTS), Mast Cell Activation Syndrome (a.k.a. MCAS), causing Kaleigh sensitivities or allergies to most foods, spices and herbs), Mold Allergy, Multiple Chemical Sensitivities (causing Kaleigh to be severely reactive to innumerable chemicals and almost anything with a distinct smell), Ranaud's Syndrome, major hormone imbalances, chronic fatigue, chronic pain, arthritis, muscular and skeletal issues (multiple practitioners have said that if she doesn't get multiple massages a week, which she hasn’t been able to afford, she'll end up needing surgery), as well as significant neurological, thyroid, sinus, and gastrointestinal issues. The children are also experiencing many of the same issues listed above, as well as others listed below.

Having so many different diagnoses can seem rather unbelievable, but these many conditions are often interrelated; and while any one of them can be extremely challenging, the combination of these multi-system infections and disorders/conditions can be devastating, and our cherished friend is suffering tremendously because of the havoc these combined issues are wreaking on her body.

If you have ever been touched by Kaleigh, through her immense faith, tremendous kindness, beautiful heart, extensive knowledge and wisdom, wonderful creativity or quirky sense of humor, or through the online children's Bible ministry she runs, all despite her own suffering, or by any of her precious children, then I urge you to please, sincerely consider contributing to their care.

All 5 children are also experiencing symptoms of Lyme. The CDC has recognized that a mother can pass Lyme disease to a baby in utero. It seems that all of Kaleigh's precious little ones had acquired Lyme during pregnancy and had been sick for their whole lives. The children have also been bitten by many ticks individually, so they could have gotten new infections, compounding their issues, just like Kaleigh did (more about that in the detailed story).

So not only has Kaleigh been suffering for a very long time, but so too have all 5 of her children. Every day is a challenge for each of them individually and all of them collectively. They all suffer with a vast range of symptoms from hypermobility, chronic pain, chronic fatigue, vision complications (including color blindness from the swelling of the optic nerve from the damage of Lyme Disease), seizures, brain fog, breathing difficulties, MCAS, alpha gal syndrome, POTS; Kaleigh’s oldest son has such severe nervous system involvement that he had been struggling to stand or walk for over a month at the beginning of this year (2025), and though now he is improving some, the physical and mental fatigue continues to interferes with all aspects of life. Even basic chores can be so taxing on their bodies that the children often must lie down for extended intervals to rest; this may even mean lying on the floor right where they were working because the stress and exhaustion are so intense. Sometimes, the children are too weak and too sick to play or do school work.

And, of course, there is the stress and strain that Michael endures, having to witness all that is occurring, while assuming the heavy responsibility of a father and husband trying to take care of his entire family as they suffer. One man can only do so much; he has carried a heavy load in attempting to provide for the needs of his family. The strain of not being able to provide for all of the many and specific needs of his wife and children, to ensure they are healthy and whole, is a lot for him to carry on his shoulders.

That weight has quite literally caused Michael physical pain in addition to the mental and emotional pain of seeing your loved ones suffer. His job is very physical, and it has contributed to major fatigue, caused a herniated disc, as well as musculoskeletal damage. Michael lives and works in pain daily, trying his hardest to protect and provide for his family. But, despite his hard work for and devotion to his family, the expense of this disease (multiplied by 6), along with special dietary needs and all that is involved to try to help the family live healthier lives, it just isn't possible for Michael to provide all that is needed all by himself.

The family has already spent an enormous amount of money on Kaleigh's health throughout the years, over $250,000; and though she has had some improvements, she still continues to be predominately bedridden, struggling daily with a plethora of symptoms, while the children are getting worse as time goes on.

Kaleigh and her family have tremendous needs, but the harsh reality is that those who fall beneath the poverty line, as well as most working and middle-class people, can rarely afford proper testing and efficacious Lyme treatment. In the present economic climate, medical care of any type can be extremely costly, but Lyme treatment takes immense resources in addition to what it costs for standard care.

But why? Because Lyme Disease itself is a debilitating and complicated disease that can create multi-system dysfunction. Sadly, treating Lyme Disease is very expensive for a single person, let alone a family. According to lymestats.org, patients spend on average $53,000 for out-of-pocket expenses for treatment, doctor visits, testing, and supplements per year. Keep that in mind as we consider that 6 of the 7 Abernathys are very sick with Lyme disease.

The overwhelming majority of those who achieve remission (because there is no known cure at present) and regain even a modicum of their health are not merely fortunate, but they tend to be rather wealthy. They already had existing funds and resources to afford the best doctors and to pay for the most effective treatment for the years it takes to get better; most folks simply do not have this amount of money at their disposal. For most, once you have found the treatment that is effective for you, it still takes at least 1-3 years of that treatment to see improvement.

As a community, we can help alleviate the burdens of a precious family and of a vital member of our ranks… a wife, mother, daughter, sister, and friend, who gives of herself even out of her own lack and in the midst of her own suffering. We need to raise enough money for Kaleigh and the children to obtain appropriate testing and to try several treatment options over a few years' span until they can reach remission. The goal amount may seem high, but the sad truth is that the typical cost for treating Lyme amounts to many multiple tens of thousands of dollars on average, per individual per year. Your contribution can help to greatly improve, if not save, the life of our friend and her children.

And while I know that so many of us are burdened in this present economy, and suffering in a system that was not built for us, I ask you to prayerfully consider contributing to assist Kaleigh and her family, knowing that no gift is too small; every single dollar counts and is so greatly appreciated. Your generosity will be felt beyond words.

If you cannot contribute personally, please share Kaleigh's story as far and wide as possible so that others may hear and be moved to help support our friend and her children in their time of significant need.

I want to say thank you in advance to any and all who find it in their hearts to donate to this fund; may your gift be returned to you many times over. May our heavenly Father bless you a thousand times over.

Deu 1:11 ‘יהוה Elohim of your fathers is going to add to you a thousand times more than you are, and bless you as He has spoken to you!

~~~~~~~~

For those interested in reading more of Kaleigh’s story, you can check the “Update” area for the more detailed story.

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Joel 2:25 “Then I shall repay you the years that the swarming locust has eaten… 26 “Then you shall eat – eat and be satisfied – and shall praise the Name of יהוה your Elohim, who has done with you so wondrously. And My people shall never be put to shame.

If you would like to hear from Kaleigh, here's an interview she did several years ago about her condition, where she shares more about Lyme. She got bit again, was reinfected, and got sicker after this interview was recorded.

https://youtube.com/playlist?list=PLDQlzvq3dbjvjV93atvR_y0LB1ADuBKKT&si=EAcC3zA624_X15u4

*For more information about Lyme Disease, its seriousness, severity, and its financial toll, you may wish to watch:

Under Our SkinThe Monster Inside Of MeThe Quiet EpidemicI'm Not Crazy, I'm Sick

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Anonymous Giver
$ 100.00 USD
28 minutes ago

Jean Boshears
$ 15.00 USD
17 hours ago

Occasionally, I hear of different natural approaches to Lyme disease. It truly is a challenge for folks with this situation. And I’m sure they’ve done some research over the years and speak with the specialists. Let us thankYahweh for what he’s about to do for them by His supernatural power.

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Matthias Timm
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Anonymous Giver
$ 1000.00 USD
14 days ago

You and your family are in my prayers. I hope that you will find relief and healing. May our Father bless you and take care of you always.

Anonymous Giver
$ 100.00 USD
14 days ago

Yahweh bless you and keep you! 🙏 prayers for your family

Meaghan Simons
$ 20.00 USD
16 days ago

Praying for you

Updates

Update Detail Story #2

April 6th, 2025

Continued... 

So not only has Kaleigh been suffering for a very long time, but so too have all 5 of her children. Every day is a challenge for each of them individually and all of them collectively. They all suffer with a vast range of symptoms from hypermobility, chronic pain, chronic fatigue, vision complications (including color blindness from the swelling of the optic nerve from the damage of Lyme Disease), seizures, brain fog, breathing difficulties, MCAS, alpha gal syndrome, POTS; Kaleigh’s oldest son has such severe nervous system involvement that he had been struggling to stand or walk for over a month, and though now he is improving some, the physical and mental fatigue continues to interferes with all aspects of life. Even basic chores can be so taxing on their bodies, sometimes the children must lie down for extended intervals to rest; this may mean lying on the floor right where they were working because the stress and exhaustion are so intense. Sometimes, the children are too weak and too sick to play or do school work.

In addition to all of this, Lyme takes a huge emotional toll as well. It has been extremely difficult for Kaleigh to have to fight for her life while not being able to express her motherly instinct and take care of her beloved children. It's also very hard, emotionally, for the family to lack sufficient funds to provide proper treatment or care for Kaleigh herself and for the children. The children also deal with their own emotional concerns, having watched their mom suffer, their father work so hard, all while struggling with their own health challenges.


And, of course, there is the stress and strain that Michael endures, having to witness all that is occurring, while assuming the heavy responsibility of a father and husband trying to take care of his entire family as they suffer. One man can only do so much; he has carried a heavy load in attempting to provide for the needs of his family. The strain of not being able to provide for all of the many and specific needs of his wife and children, to ensure they are healthy and whole, is a lot for him to carry on his shoulders.


That weight has quite literally caused Michael physical pain in addition to the mental and emotional pain of seeing your loved ones suffer. His job is very physical, and it has contributed to major fatigue, caused a herniated disc, as well as musculoskeletal damage. Michael lives and works in pain daily, trying his hardest to protect and provide for his family. But, despite his hard work for and devotion to his family, the expense of this disease (multiplied by 6), along with special dietary needs and all that is involved to try to help the family live healthier lives, it just isn't possible for Michael to provide all that is needed all by himself.


The family has already spent an enormous amount of money on Kaleigh's health throughout the years, over $250,000; and though she has had some improvements, she still continues to be predominately bedridden, struggling daily with a plethora of symptoms, while the children are getting worse as time goes on.


Kaleigh and her family have tremendous needs, but the harsh reality is that those who fall beneath the poverty line, as well as most working and middle-class people, can rarely afford proper testing and efficacious Lyme treatment. In the present economic climate, medical care of any type can be extremely costly, but Lyme treatment takes immense resources in addition to what it costs for standard care.


But why? Because Lyme Disease itself is a debilitating and complicated disease that can create multi-system dysfunction. Caused by bacteria in the Borrelia family. Lyme is most commonly transmitted by the bite of a Deer Tick.


Sadly, despite increasing information, Lyme is greatly downplayed by modern Western medicine. There's been no significant research done into Lyme Disease in 40 years; no effort to advance testing or to make it more sensitive and accurate; and no work on finding efficacious treatment, to say nothing of a cure.


Patients' symptoms are frequently ignored, their pain is overlooked, their debilitation is dismissed; they are often misdiagnosed, mistreated, medically neglected, and gaslighted, resulting in years' worth of agony and anguish. And because the allopathic medical establishment under-reports the number of cases and minimizes the severity of this disease, most of those who are afflicted must seek physicians who have endeavored to better understand and try to treat Lyme Disease, outside of the standard, ineffective protocols.


Further, because of its tentative status, Lyme Disease is not covered by most medical insurers; therefore, Lyme sufferers pay for doctors visits, testing, and treatment out of pocket, very often ending in financial hardship. Patients often see multiple doctors and must endure numerous treatments to try and find relief; and this, because there is no general consensus on how this disease is to be managed, even among the most renowned names in the field. The numerous consults, plethora of tests, and varied treatments all combine for an astronomical price tag.


Treating Lyme Disease is very expensive for a single person, let alone a family. According to lymestats.org, patients spend on average $53,000 for out-of-pocket expenses for treatment, doctor visits, testing, and supplements per year. Keep that in mind as we consider that 6 of the 7 Abernathy's family are very sick with Lyme disease.


Kaleigh and her family have tremendous needs, but the harsh reality is that those who fall beneath the poverty line, as well as most working and middle-class people, can rarely afford proper testing and efficacious Lyme treatment. In the present economic climate, medical care of any type can be extremely costly, but Lyme treatment takes immense resources in addition to what it costs compared to care for many other chronic conditions. The overwhelming majority of those who achieve remission (because there is no known cure at present) and regain even a modicum of their health are not merely fortunate, but they tend to be rather wealthy. They already had existing funds and resources to afford the best doctors and to pay for the most effective treatment for the years it takes to get better; most folks simply do not have this amount of money at their disposal.


As a community, we can help alleviate the burdens of a precious family and of a vital member of our ranks… a wife, mother, daughter, sister, and friend, who gives of herself even out of her own lack and in the midst of her own suffering. We need to raise enough money for Kaleigh and the children to obtain appropriate testing and to try several treatment options over a few years' span until they can reach remission. The goal amount may seem high, but the sad truth is that the typical cost for treating Lyme amounts to many multiple tens of thousands of dollars on average per individual per year. Your contribution can help to greatly improve, if not save, the life of our friend and her children.


If you cannot contribute, there are things you can do to help make a difference in the lives of this precious family. Prayers and sharing the Abernathy’s story far and wide so they can get as much help is possible are all greatly appreciated! Thank you for reading, praying, contributing, and for sharing. May the Father above bless you abundantly. Thank you so much for reading our story and learning more about us.

Update Detail Story #1

April 6th, 2025

Now for the details:
In early 2015, Kaleigh had the most beautiful and seemingly perfect home birth with her 4th child, her first son; but soon after his birth, the situation became traumatic as Kaleigh began to hemorrhage massively, nearly causing her to lose her life. The rest of that story is a longer story for another time, filled with the immense praise and thanksgiving to the Heavenly Father for preserving Kaleigh’s life, but the aforementioned traumatic event set up the perfect storm, which is why we come to you now with this petition for help.
A few days after the hemorrhage, Kaleigh started experiencing many bizarre, frightening, and extreme symptoms. As the postpartum period went on, and according to her blood work, she had recovered from the hemorrhage, but she wasn’t doing well in the slightest, and as days and weeks went on, she continued manifesting new symptoms; the list grew to a staggering 7.5 pages to present to her doctor.

Kaleigh could no longer read anything, including simple picture books to her children. She couldn't look at a screen; neither could she listen to the radio or to people having conversations. She had gait problems, too weak and lacking coordination to pick up her feet to walk; she could barely shuffle. She couldn't drive. She also could hardly ride in a car. The neurological and cognitive issues were so severe that when she had to be in a vehicle, Kaleigh had to cover her face with many layers of blankets because the light from the sun and the motion of things passing by would make her extremely weak and increasingly sick.
Kaleigh’s health had declined so dramatically -she had become so sick, so ill, and so fragile - that she was completely incapacitated; heartbreakingly for her, her oldest children (then 7 and 8 years old) had to take over all mothering chores, including rocking the newborn baby.

Even basic, everyday tasks became excruciating; Kaleigh was too debilitated that brushing her teeth or hair and bathing were exhausting and excruciating. When she could muster the energy to do these things, she would have to stop many times throughout and rest, and then it would take days for her to recuperate. Kaleigh was so weak that a walk to the bathroom had her constantly strategizing how to catch herself if her legs should completely give out so that she would sustain the least amount of damage to her body.
Kaleigh suffered daily with chronic fatigue and profuse and unrelenting pain, arthritis in almost every joint, and muscle pain from head to toe.

She also suffered with severe neurological symptoms, including: extreme brain fog, word loss, dizziness, shaky vision, feeling like she was falling even when lying down, extreme light, motion, and sound sensitivity, POTS, tremors, bad short and long term memory loss to the point that, at times, she would forget the words she was told the moment they were spoken to her. At just 30 years old, manifesting these symptoms and more, which affected all of her bodily functions, systems, her organs and tissues, Kaleigh was told she was in the early stages of Parkinson's disease.

After almost a year of doctors consultations and assessments, and myriad laboratory tests to determine why Kaleigh had not recovered from the birth trauma, it was confirmed by her family doctor that she was suffering from Chronic Lyme Disease (specifically NeuroBorreliosis/ Neurological Lyme/ Autoimmune Lyme). Kaleigh’s doctor said that her condition was so severe that there was nothing she could do to help her medically and that Kaleigh would have to seek alternative care elsewhere.

Shortly after receiving the Lyme diagnosis, Kaleigh ended up with a surprise pregnancy that further complicated her already severe health condition, in part because numerous Lyme treatments are not safe to do while pregnant or breastfeeding. As with all pregnancies, Kaleigh’s 5th put more stress on her body and immune system and took nutrients from her to grow this precious life, which made her even sicker. Already so weak and not having recovered from her previous pregnancy, what should have been a wondrous time turned into a very scary and stressful pregnancy.

Kaleigh's doctor told her she was worried she wasn't going to make it through the labor; her midwife told her she was concerned that she could deliver the baby, but that her body was so weak that she would hemorrhage again. It had been just over a year since Kaleigh had been so close to death, and now, being told that it was likely to happen again, but this time being so much weaker, the situation seemed dire and frightening.

As the midwife had predicted, Kaleigh experienced a severe hemorrhage once again, but not quite as severe as the first; and still, the stress of the pregnancy and birth exacerbated the Lyme, causing Kaleigh’s health to spiral further downward to the point that she could no longer function without help. Over the course of three years, her husband, Michael, often had to stay home from work for Kaleigh and their 5 small children. When he was at work, they had to pay for in-home care.

About 2.5 years after this birth, Kaleigh had some small improvements. She could take short, slowstrolls on the porch or right in the front yard, but no more. She was still unable to do any chores or anything that resembled “normal” activities representative of a healthy life; and yet this was still an improvement to the time of such utter infirmary that only allowed for her to stare at the wall or out the window, day after day, week after week, month after month, and year after year…. The simple ability to go outside and see plants and hear birds was nourishing to her soul.

Tragically, at this time, Kaleigh was bitten by another tick, which manifested the tell-tale bulls-eye rash that is common for many with Lyme Disease; and while not everyone who has Lyme will present with this rash, if you do experience this symptom, it absolutely means you do have Lyme. So, Kaleigh had gotten Lyme disease again on top of being devastatingly sick with Lyme already. The significance here is that being bitten again means that you can acquire new strains of the bacteria along with different co-infections, which compound any previous illness, including the current case of Lyme.

Despite the small gains Kaleigh had made, symptoms came roaring back; she was in and out of the ER regularly with symptoms resembling a heart attack and stroke (often at the same time). MCAS was exacerbated at this time, causing Kaleigh to manifest allergies to anything that had a smell, natural or chemical, including food. If she smelled someone's toothpaste, mouth wash, soap, laundry detergent, hairspray, etc. she would break out in hives. Her throat would tighten, her hands and toes would turn blue, she would tremble uncontrollably, and her heart rate would increase significantly; this made it to where she had no safe place to go.

Kaleigh spent years in terror, concerned about manifesting symptoms or acquiring new ones. She was unable to spend time with anyone else but her immediate family to keep symptoms to a minimum. No one could visit, and she couldn't go anywhere without a special mask to block possible allergens and a wheelchair. Anytime she had to leave, she had to be aware of the location of the nearest hospital.
The new infection also exacerbated POTS to the point that Kaleigh was unable to stand upright or walk standing upright for 3 years. To go to the bathroom, she would have to walk bent over with her head at or below her heart. This was extremely uncomfortable and went on to cause increasing musculoskeletal damage.
Once again, Michael needed to be there for his extremely ill wife, and due to the severity of Kaleigh’s condition, he was barely able to work for the better part of two years. In that time, the Abernathys ended up having to sell their home to try and keep themselves afloat financially. They moved into a converted school bus in an attempt to move to a healthier environment and cover medical care, and here they have lived (in their bus) as a family of 7 since 2020 (more than 4.5 years).

Before Kaleigh was reinfected, after she had suffered so severely and now understood the seemingly innumerable symptoms of Lyme, it became obvious that she had probably had Lyme for over 3 decades. She was now aware that the things that had appeared normal to her all of her life were, in fact, not normal.
It was at this time that it became clear that all 5 children were experiencing symptoms of Lyme.

The CDC has recognized that a mother can pass Lyme disease to a baby in utero. It seems that all of Kaleigh's precious little ones had acquired Lyme during pregnancy and had been sick for their whole lives. The children have also been bitten by many ticks individually, so they could have gotten new infections, compounding their issues, just like Kaleigh did.

CONTINUED ON NEXT UPDATE

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