
Our daughter, Elora, is a young child living with Apert syndrome, a rare congenital condition that affects the development of the skull, face, hands, and other parts of the body.
She deserves the opportunity to receive the specialist medical care she needs, but getting that care has become a financial challenge for our family.
We are reaching out for help—not because we have given up, but because we are determined to do everything we can to give Elora the medical attention and future she deserves.
Every donation, no matter how small, can help us take another step toward getting her properly evaluated and treated.
Elora is a precious child who has brought so much love and meaning into our family. Despite the challenges associated with her condition, she continues to grow and face each day with strength.
Living with Apert syndrome means that her medical needs cannot simply be addressed with routine care. She needs appropriate specialist assessment to understand her current condition and determine what treatments may be necessary.
As her family, our greatest concern is making sure we do not lose valuable time simply because we cannot afford the medical investigations and specialist care she needs.
Elora has been diagnosed with Apert syndrome, a rare genetic condition that affects the normal development of the skull and facial bones and can also affect the hands and other parts of the body.
Because Apert syndrome can involve different medical systems, proper evaluation may require several specialists and investigations.
We therefore need to obtain the appropriate medical assessments so qualified doctors can determine the best course of treatment for Elora.
At present, our family is trying to arrange the medical investigations and specialist consultations required to properly assess Elora's condition.
One of our concerns is that Elora has experienced episodes of breathing difficulties, sometimes lasting for several days. We need appropriate medical evaluation to understand the cause and determine whether further treatment is required.
Unfortunately, access to the specialist care Elora needs is not readily available where we live, which means that we may have to travel to obtain some of the necessary investigations and consultations.
We do not want to make assumptions about what treatment Elora will ultimately require. The purpose of the medical assessments is to allow qualified healthcare professionals to properly evaluate her and recommend the appropriate treatment.
We have been communicating with the World Craniofacial Foundation regarding Elora's situation.
They have asked us for additional medical information to help them understand her condition, including information such as:
These investigations and specialist evaluations are important because they can provide a clearer picture of Elora's medical needs and help determine what treatment options may be appropriate.
We are therefore seeking assistance to obtain the medical documentation and specialist evaluations that have been requested.
Our family has been doing what we can to care for Elora, but the cost of medical investigations, specialist consultations, transportation, treatment, medication, and related expenses is beyond what we can comfortably afford at this time.
The situation is particularly difficult because some of the specialist services and investigations Elora may need require us to travel.
We are asking for financial assistance so that lack of money does not prevent Elora from receiving the evaluations and treatment she needs.
Our initial fundraising goal is $15,000.
This is an estimated overall target intended to help cover Elora's medical investigations, specialist consultations, medically recommended treatment or surgery, medication, transportation, accommodation, and other necessary expenses.
The exact cost of Elora's treatment cannot yet be confirmed because some of the recommended investigations and specialist evaluations still need to be completed.
We will therefore use the funds according to her actual medical needs and the recommendations and quotations provided by qualified healthcare professionals.
Medical tests and investigations — $1,500
This will help cover laboratory tests, imaging such as CT or MRI where medically recommended, cardiology evaluation, and other investigations requested by her doctors or specialists.
Specialist consultations — $1,000
This will help cover consultations and assessments with the appropriate specialists, including craniofacial and other relevant medical specialists.
Treatment/Surgery reserve — $8,000
This amount will be reserved for medically recommended treatment or surgery if specialists determine that it is necessary. The exact cost will be established through medical assessment and hospital quotations.
Medication and medical supplies — $1,000
This will help cover prescribed medications, medical supplies, and necessary follow-up care.
Travel and transportation — $1,000
This will help with transportation for Elora and an accompanying parent or guardian when travelling to hospitals, specialist centres, and medical appointments.
Accommodation and meals — $1,000
This will help cover accommodation and basic meals when medical appointments, investigations, or treatment require us to stay away from home.
Additional medically necessary expenses — $1,500
This provides a small reserve for additional investigations, consultations, transportation, medication, hospital-related expenses, or other necessary costs that may arise during Elora's treatment journey.
We want to be transparent that these are estimated allocations, not official hospital quotations. The exact costs will become clearer as Elora undergoes the recommended medical assessments.
If the actual costs differ from these estimates, we will adjust how the funds are used according to her medical needs and provide updates to supporters.
We have not simply waited for someone else to help us.
We have been seeking medical assistance, contacting organizations that may be able to support children with craniofacial conditions, and trying to obtain the investigations required to move Elora's case forward.
We have also reached out to organizations such as the World Craniofacial Foundation to explore possible assistance and treatment opportunities.
However, obtaining the requested medical investigations requires money that our family is currently struggling to provide.
That is why we are now asking the wider community for help.
We want to be completely honest about where we are in Elora's medical journey.
We have documentation confirming Elora's Apert syndrome diagnosis, together with the medical information currently available to our family.
However, we do not yet have every investigation requested by the World Craniofacial Foundation.
Additional laboratory work, cardiology evaluation, and head/brain imaging such as CT or MRI may still need to be completed or obtained, depending on the doctors' recommendations.
We are not presenting medical documents that we do not have, and we will not claim that a test has been completed when it has not.
As additional medical reports, test results, prescriptions, hospital documents, and treatment recommendations become available, we intend to keep appropriate documentation and provide updates to supporters as much as possible while respecting Elora's privacy.
Our goal is complete honesty and accountability.
We know that not everyone can make a large donation. That is okay.
A small contribution can help pay for a medical test. Another donation can help with transportation. Someone else may help with medication or a specialist consultation.
And if you cannot donate, sharing Elora's story may be just as valuable.
The more people who see her story, the greater the possibility that someone who can help will find us.
We are asking you to stand with Elora and our family as we work to get her the medical evaluation and care she needs.
Please donate if you can. Please share her campaign. Please help us give Elora a better chance at the care she deserves.
Thank you for taking the time to read Elora's story, for caring about her journey, and for considering helping our family.
Every donation. Every share. Every prayer. Every act of kindness brings Elora one step closer to the care she needs.
Click the Pray button to let the fundraiser owner know you are praying for them.
Fundraiser created byEzekiel Orumgbe
Fundraiser funds will be received by Ezekiel Orumgbe

Fundraiser created byEzekiel Orumgbe
Fundraiser funds will be received by Ezekiel Orumgbe
Our daughter, Elora, is a young child living with Apert syndrome, a rare congenital condition that affects the development of the skull, face, hands, and other parts of the body.
She deserves the opportunity to receive the specialist medical care she needs, but getting that care has become a financial challenge for our family.
We are reaching out for help—not because we have given up, but because we are determined to do everything we can to give Elora the medical attention and future she deserves.
Every donation, no matter how small, can help us take another step toward getting her properly evaluated and treated.
Elora is a precious child who has brought so much love and meaning into our family. Despite the challenges associated with her condition, she continues to grow and face each day with strength.
Living with Apert syndrome means that her medical needs cannot simply be addressed with routine care. She needs appropriate specialist assessment to understand her current condition and determine what treatments may be necessary.
As her family, our greatest concern is making sure we do not lose valuable time simply because we cannot afford the medical investigations and specialist care she needs.
Elora has been diagnosed with Apert syndrome, a rare genetic condition that affects the normal development of the skull and facial bones and can also affect the hands and other parts of the body.
Because Apert syndrome can involve different medical systems, proper evaluation may require several specialists and investigations.
We therefore need to obtain the appropriate medical assessments so qualified doctors can determine the best course of treatment for Elora.
At present, our family is trying to arrange the medical investigations and specialist consultations required to properly assess Elora's condition.
One of our concerns is that Elora has experienced episodes of breathing difficulties, sometimes lasting for several days. We need appropriate medical evaluation to understand the cause and determine whether further treatment is required.
Unfortunately, access to the specialist care Elora needs is not readily available where we live, which means that we may have to travel to obtain some of the necessary investigations and consultations.
We do not want to make assumptions about what treatment Elora will ultimately require. The purpose of the medical assessments is to allow qualified healthcare professionals to properly evaluate her and recommend the appropriate treatment.
We have been communicating with the World Craniofacial Foundation regarding Elora's situation.
They have asked us for additional medical information to help them understand her condition, including information such as:
These investigations and specialist evaluations are important because they can provide a clearer picture of Elora's medical needs and help determine what treatment options may be appropriate.
We are therefore seeking assistance to obtain the medical documentation and specialist evaluations that have been requested.
Our family has been doing what we can to care for Elora, but the cost of medical investigations, specialist consultations, transportation, treatment, medication, and related expenses is beyond what we can comfortably afford at this time.
The situation is particularly difficult because some of the specialist services and investigations Elora may need require us to travel.
We are asking for financial assistance so that lack of money does not prevent Elora from receiving the evaluations and treatment she needs.
Our initial fundraising goal is $15,000.
This is an estimated overall target intended to help cover Elora's medical investigations, specialist consultations, medically recommended treatment or surgery, medication, transportation, accommodation, and other necessary expenses.
The exact cost of Elora's treatment cannot yet be confirmed because some of the recommended investigations and specialist evaluations still need to be completed.
We will therefore use the funds according to her actual medical needs and the recommendations and quotations provided by qualified healthcare professionals.
Medical tests and investigations — $1,500
This will help cover laboratory tests, imaging such as CT or MRI where medically recommended, cardiology evaluation, and other investigations requested by her doctors or specialists.
Specialist consultations — $1,000
This will help cover consultations and assessments with the appropriate specialists, including craniofacial and other relevant medical specialists.
Treatment/Surgery reserve — $8,000
This amount will be reserved for medically recommended treatment or surgery if specialists determine that it is necessary. The exact cost will be established through medical assessment and hospital quotations.
Medication and medical supplies — $1,000
This will help cover prescribed medications, medical supplies, and necessary follow-up care.
Travel and transportation — $1,000
This will help with transportation for Elora and an accompanying parent or guardian when travelling to hospitals, specialist centres, and medical appointments.
Accommodation and meals — $1,000
This will help cover accommodation and basic meals when medical appointments, investigations, or treatment require us to stay away from home.
Additional medically necessary expenses — $1,500
This provides a small reserve for additional investigations, consultations, transportation, medication, hospital-related expenses, or other necessary costs that may arise during Elora's treatment journey.
We want to be transparent that these are estimated allocations, not official hospital quotations. The exact costs will become clearer as Elora undergoes the recommended medical assessments.
If the actual costs differ from these estimates, we will adjust how the funds are used according to her medical needs and provide updates to supporters.
We have not simply waited for someone else to help us.
We have been seeking medical assistance, contacting organizations that may be able to support children with craniofacial conditions, and trying to obtain the investigations required to move Elora's case forward.
We have also reached out to organizations such as the World Craniofacial Foundation to explore possible assistance and treatment opportunities.
However, obtaining the requested medical investigations requires money that our family is currently struggling to provide.
That is why we are now asking the wider community for help.
We want to be completely honest about where we are in Elora's medical journey.
We have documentation confirming Elora's Apert syndrome diagnosis, together with the medical information currently available to our family.
However, we do not yet have every investigation requested by the World Craniofacial Foundation.
Additional laboratory work, cardiology evaluation, and head/brain imaging such as CT or MRI may still need to be completed or obtained, depending on the doctors' recommendations.
We are not presenting medical documents that we do not have, and we will not claim that a test has been completed when it has not.
As additional medical reports, test results, prescriptions, hospital documents, and treatment recommendations become available, we intend to keep appropriate documentation and provide updates to supporters as much as possible while respecting Elora's privacy.
Our goal is complete honesty and accountability.
We know that not everyone can make a large donation. That is okay.
A small contribution can help pay for a medical test. Another donation can help with transportation. Someone else may help with medication or a specialist consultation.
And if you cannot donate, sharing Elora's story may be just as valuable.
The more people who see her story, the greater the possibility that someone who can help will find us.
We are asking you to stand with Elora and our family as we work to get her the medical evaluation and care she needs.
Please donate if you can. Please share her campaign. Please help us give Elora a better chance at the care she deserves.
Thank you for taking the time to read Elora's story, for caring about her journey, and for considering helping our family.
Every donation. Every share. Every prayer. Every act of kindness brings Elora one step closer to the care she needs.
Click the Pray button to let the fundraiser owner know you are praying for them.

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