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Need Care Foundation, 1507 Guest Street, Greensboro, CA (2026)

12/24/2023

🎄🎁 **Special Christmas Message from Need Care Foundation** 🎄🎁

Dear friends,

As the holiday season approaches, we, at Need Care Foundation, are filled with joy and gratitude. It is a time to reflect on the blessings we have received throughout the year and extend our love and support to those who need it the most.

Christmas is a time of hope, love, and togetherness, and it is our mission to ensure that every child with disabilities in Liberia experiences the magic and joy of this festive season. We are a nonprofit organization dedicated to providing care and support to persons with disabilities, with a special focus on children. Our commitment extends to the most vulnerable populations, including the underprivileged, the less fortunate, and the most marginalized.

At Need Care Foundation, our motto, "Transforming rejected lives today for a better future," embodies our belief that every life is precious and deserving of care, compassion, and opportunities. We strive to create a society where individuals with disabilities are embraced, empowered, and given the tools they need to thrive.

This Christmas, we invite you to join us in making a difference. Your support can help us bring smiles to the faces of children who have faced rejection and neglect. Together, we can provide them with access to education, healthcare, rehabilitation, and inclusive opportunities that will transform their lives and give them hope for a brighter future.

Let us come together as a community, spreading love, kindness, and generosity this Christmas. Your support, whether through donations, volunteering, or spreading awareness, will make a significant impact on the lives of those we serve.

On behalf of the entire Need Care Foundation team, we extend our warmest wishes to you and your loved ones. May this Christmas season be filled with love, joy, and peace. Together, let us create a world where every person with a disability is embraced and empowered.

Merry Christmas and a Happy New Year!

12/09/2023

🌟 Welcome to the Need Care Foundation! 🌟

We are thrilled to have you join us on our journey of transforming the lives of persons with disabilities and the less fortunate in Liberia and around the world. At the Need Care Foundation, we believe in the power of compassion, empathy, and collective action to bring about positive change.

Our mission is to create a more inclusive and equitable society, where everyone, regardless of their abilities or socio-economic background, has the opportunity to thrive. We are dedicated to providing care, support, and resources to those in need, empowering them to lead meaningful and fulfilling lives.

Through our various programs and initiatives, we aim to address the unique challenges faced by individuals with disabilities and those living in poverty. From education and vocational training to healthcare and community development, we are committed to making a lasting impact and breaking barriers that hinder progress.

But we can't do it alone. We rely on the support and generosity of individuals like you who share our vision of a more compassionate world. Whether it's through volunteering, fundraising, or simply spreading awareness, every contribution, big or small, makes a difference.

Join us in our endeavor to create a society where everyone is valued, respected, and given equal opportunities. Together, we can create a ripple effect of change that will touch countless lives and inspire others to take action.

Thank you for being a part of the Need Care Foundation family. We look forward to embarking on this incredible journey with you, as we strive to make a positive impact and transform lives.

07/25/2023

I have reached 600 followers! Thank you for your continued support. I could not have done it without each of you. 🙏🤗🎉

06/16/2023

On this special occasion of The Day of the African Child, it is essential to focus on the unique and beautiful children living with albinism in Africa. These children face numerous challenges, including discrimination, social exclusion, and even physical harm. However, they also bring a light and a joy to our communities that is truly inspiring. It is our responsibility as a society to ensure that these children are protected, valued, and empowered to reach their full potential.

Albinism is a congenital disorder that affects the production of melanin, the pigment that gives color to the skin, hair, and eyes. Children with albinism have little or no melanin in their skin, making them more susceptible to sunburns and skin cancer. In addition to physical challenges, children with albinism face discrimination and social exclusion due to their appearance, which can lead to psychological harm.

The discrimination and violence against children with albinism are alarming in Africa. Witchcraft beliefs and superstitions in some African cultures have led to the kidnapping, mutilation, and killing of people with albinism. The body parts of people with albinism are believed to bring good luck and wealth, which has led to a thriving black market for their body parts. This negative attitude towards albinism has created a hostile environment for children living with the condition.

However, despite these challenges, children with albinism have proven to be some of the most resilient and creative members of our communities. They have found ways to overcome their challenges and bring joy to those around them. Their unique beauty, strength, and resilience are a source of inspiration and pride for us all.

As a society, we must take the responsibility of protecting and empowering children with albinism. Education is crucial in breaking down stereotypes and misinformation that fuel discrimination and violence. Communities must be educated about albinism and the challenges faced by children with the condition. We must advocate for policies that protect children with albinism and hold perpetrators of violence accountable.

We must also embrace children with albinism as members of our communities and celebrate their unique beauty and talents. We must provide them with equal opportunities in education, employment, and other areas of life. By doing so, we can empower them to reach their full potential and contribute positively to our societies.

In conclusion, on this special occasion of The Day of the African Child, let us celebrate the strength, resilience, and beauty of all children, including those with albinism. We must commit ourselves to creating a world where every child can thrive and shine. It is our responsibility to protect, value, and empower children with albinism to reach their full potential. Happy Day of the African Child!

06/13/2023

On this special occasion of International Albinism Awareness Day, I, Dakpannah U-Thant Nicholas Smith, Advocate for the Rights of Persons With Albinism, would like to extend my warmest greetings to all persons with albinism and their allies worldwide.

This year's theme, "Inclusion Is Strength," resonates with the core values of our society. We firmly believe that every person, regardless of their skin color, deserves to be treated with respect and dignity and to have equal opportunities in all aspects of life.

Sadly, many people with albinism face discrimination, stigmatization, and violence due to their unique skin condition. Therefore, it is essential that we advocate for their rights and promote their inclusion in society.

As we celebrate this day, let us pledge to work together to create a world where persons with albinism can live without fear and achieve their full potential. We must continue to raise awareness, educate the public, and advocate for policies that protect the rights of persons with albinism.

Finally, I would like to express my gratitude to all the individuals, organizations, and governments that have supported our cause over the years. Your solidarity and commitment are essential to our success.

Once again, I wish you all a happy International Albinism Awareness Day.

06/12/2023

International Albinism Awareness Day is celebrated on June 13th every year to raise awareness about albinism and to promote the rights of people living with albinism. This year's theme is "Inclusion Is Strength" which emphasizes the importance of including people with albinism in all aspects of society. In this article, I will discuss the significance of International Albinism Awareness Day and the theme of inclusion.

Albinism is a genetic condition that affects the production of melanin, the pigment that gives color to the skin, hair, and eyes. People with albinism have little to no melanin, which results in pale skin, white or light-colored hair, and light-colored eyes. Albinism is a rare condition, and it affects people of all races and ethnicities. However, people with albinism face many challenges, including discrimination, stigmatization, and social exclusion.

International Albinism Awareness Day is an opportunity to raise awareness about these challenges and to promote the rights of people living with albinism. It is also a chance to celebrate the strength and resilience of people with albinism and to recognize their contribution to society. The theme of inclusion is particularly relevant this year because it emphasizes the importance of creating a society that is inclusive of people with albinism.

Inclusion means recognizing the value and worth of every individual and creating an environment where everyone can participate and contribute. In the context of albinism, inclusion means ensuring that people with albinism have equal access to education, healthcare, employment, and other opportunities. It also means challenging the stereotypes and misconceptions that surround albinism and promoting a more positive and accurate image of people with albinism.

Inclusion is not just a moral imperative; it is also a practical necessity. When we exclude people with albinism from society, we miss out on their talents, skills, and perspectives. When we include them, we create a stronger, more diverse, and more resilient society. Inclusion is strength because it allows us to harness the full potential of every individual and to build a society that is better for everyone.

On International Albinism Awareness Day, we should celebrate the progress that has been made in promoting the rights of people with albinism and recognize the work that still needs to be done. We should also acknowledge the courage and resilience of people with albinism and the contributions that they make to society. Most importantly, we should recommit ourselves to the goal of creating a society that is inclusive of all people, regardless of their differences.

In conclusion, International Albinism Awareness Day is an important occasion to raise awareness about albinism and to promote the rights of people with albinism. The theme of inclusion is particularly relevant this year because it emphasizes the importance of creating a society that is inclusive of people with albinism. Inclusion is strength because it allows us to harness the full potential of every individual and to build a society that is better for everyone. Let us celebrate International Albinism Awareness Day by promoting inclusion and recognizing the value and worth of every individual, regardless of their differences.

03/16/2023

Zahid Hussain Kori writes
Pakistan Albinism Society - PAS

Short Story

Pakistan Albinism Society - PAS

Albinism, And Living in These Situations.

it's difficult to live and survive with Albinism and it will become more difficult if you belong to a poor family. Albinism is a rare genetic condition People with albinism also have a number of eye problems including impaired vision ( even after wearing glasses ) Photophobia ( sensitivity to light ) and may even demonstrate involuntary movements of the eye. This story is about these people whom you are seeing in pictures. Here an area of Pakistan Hyderabad called Gulistan-e-Sajjad Where both mother and son beg to survive. they both are sitting on the road under the sun and sky, Because of this, their skin is damaged, They are totally unaware about the consequences of Albinism, their lives are at high risk.

03/16/2023

Albinism Is Never A Curse! (Poem by Preston Nwiiga).

Model: Esther Estyshiny Odukoya

Each and every moment I walk in fear because I do not know who will take away my life.
It is not like I am a fugitive No! But because I am an albino,
Some do not even want to seat next to me,
Eating with me is like they are feeding on vomit,
They do not want to rub shoulders with me, as if a am a curse from God,

But listen to me even as I speak with tears in my eyes,
My tears shall no longer be in a bottle, I am spitting out the bitter truth.
Let the silence be broken now, we will no longer be silent like a rock cost hit by the waves.

Segregation is bad; we are humans like you are
God created man in his own image and likeness, of which we all know.
Why kill albinos for rituals, why discriminate and laugh at us?

Love us, care for us and here our cry.
To all the parents out there, remember that having an albino child isn't a case but a full blessing from God, and to all those who kill albino children please change for a better because God is not a God of discrimination but a God of love to everyone....
Blessed are those that are close to people living with albinism.
Remember we are not ghosts but normal people just like you.

Kindly share your thoughts and questions with us in the Comments Section

03/16/2023

WHY DO YOU CALL ME ALBINO?

For many people the term “albino” brings to mind images of a person or animal with a pale complexion and pink eyes. The term “albinism,” by contrast, is less commonplace or recognizable to people who may not know a person with the condition.

We all know that words can be powerful, so how do you say that someone is an albino without being disrespectful?

In the albinism community, opinions vary on the use of the word albino. While some find it extraordinarily offensive, others feel the label carries neutral or even empowering connotations. Many people with albinism agree that their feelings depend on the context or intent in which the word is used. The term can be derogatory when said mockingly or with malice, or it can be used innocently by someone who means no offense or is just curious.

Some people with albinism grew up in families or communities that used the word albino often and learned at an early age that there was no shame or negativity in referring to themselves as such. Others may have found that they were only called albino when they were being teased. Some describe their negative association with the word as being as offensive as a racial slur.

Some children and adults with albinism may use the term albino proudly and may feel empowered by “taking back” a once offensive word. By showing the world that they are comfortable calling themselves a word they once found hurtful or derogatory, the word “albino” loses all the power and shock value that it once claimed. By taking personal ownership of one’s condition, many people with albinism find that words like albino can no longer hurt them. Of course this is a very personal decision, and not all people with albinism feel comfortable using or hearing the term.

Although there are many people with albinism who are at peace with the term albino, when dealing with any condition, it is best to put the person first. For instance, say, “A PERSON WITH ALBINISM” rather than “an albino” or “an albino person.”
The rationale for this person-centered language is to do just that: put the person ahead of the condition. When a person is referred to as an albino, he or she is essentially being reduced to and defined by nothing more than their condition. It’s as though the world looks at that person and sees only the condition of albinism. In this way, it can feel like a dehumanizing label.

To most in the albinism community, the term “person with albinism” will always be a kinder, gentler, less shocking term. Regardless of the context, the word albino can sometimes be an ugly, jolting word to many, especially when heard unexpectedly. If you’re ever unsure, just ask. Every person with albinism will have personal experiences and opinions about the label.

© National Organization for Albinism and Hypopigmentation - NOAH
Elizabeth Lizzshiny Odukoya
Esther Estyshiny Odukoya

07/30/2022

Vision Considerations
People with albinism have vision problems that are not correctable with eyeglasses, and many have low vision. It’s the abnormal development of the retina and abnormal patterns of nerve connections between the eye and the brain that cause vision problems. The presence of these eye problems defines the diagnosis of albinism.
The degree of impairment varies with the different types of albinism. Although people with albinism may be considered “legally blind” with a corrected visual acuity of 20/200 or worse, most learn to use their vision in a variety of ways and are able to perform innumerable activities such as reading, riding a bike or fishing. Some have sufficient vision to drive a car.

07/30/2022

What Is Albinism?
Albinism is an inherited condition that leads to someone having very light skin, hair, and eyes. It happens because they have less melanin than usual in their body. Melanin gives skin, hair, and eyes their color. Except for vision problems, most people with albinism are just as healthy as anyone else.

What Are the Signs & Symptoms of Albinism?
Albinism (pronounced: AL-beh-niz-im) that affects the skin, hair, and eyes is called oculocutaneous (pronounced: ok-yuh-low-kyu-TAY-nee-iss) albinism. This leads to skin, hair, and eyes that are lighter than you would expect based on someone’s ethnic background or race. Symptoms vary based on how much melanin someone makes.

Signs and symptoms include:

pale skin
hair that is very light blonde, brown, or reddish
eyes that are pink, light blue, green, gray, or light brown
eyes that are sensitive to light
a “lazy eye” (called strabismus)
back and forth movement of the eyes (called nystagmus)
vision problems
Albinism that only affects the eyes is called ocular albinism. Sometimes albinism can be part of other medical conditions.

What Causes Albinism?
Most of the time, someone has albinism because they inherited the gene for it from both their mother and father. Having just one of the genes (being a “carrier") does not give you albinism. Most parents of children with albinism do not have any symptoms.

Sometimes, albinism is caused by a new gene change (called a mutation).

How Is Albinism Diagnosed?
Doctors usually diagnose albinism when someone has skin, hair, or eyes that are much lighter than other family members. They’ll also look for changes in the eyes to help make the diagnosis.

How Is Albinism Treated?
Most people with albinism are otherwise healthy. Treatments mainly include taking care of the eyes and skin.

07/28/2022

MAPUTO: A father who wanted to sell his three albino children for use in witchcraft rituals was arrested in Mozambique before being able to close the deal, police said on Monday.

Police in the northwestern region of Tete, said three children aged nine to 16 were rescued at the weekend after an anonymous tip-off. Their uncle was arrested alongside their father.

The pair allegedly planned to traffic the minors to neighbouring Malawi where they could be sold for the equivalent of about US$40,000, local police spokesman Feliciano da Camara told a press conference.

Both men deny any involvement in the case.

"Investigations were carried out and it was possible to rescue (the) three minors... from captivity," Câmara said.

Albinism, caused by a lack of melanin, the pigment that colours skin, hair and eyes, is a genetic anomaly that concerns hundreds of thousands of people across the globe.

Some sub-Saharan African countries have suffered a wave of assaults against albinos, whose body parts are sought for witchcraft practices in the belief that they bring luck and wealth.

On June 27, a court in Malawi sentenced a Catholic priest to 30 years and several other people to life over the 2018 murder of a man with albinism.

Judge Dorothy NyaKaunda Kamanga said Thomas Muhosha, who led a parish in Machinga, 100 kilometres (60 miles) northeast of Blantyre, had planned to traffic 22-year-old MacDonald Masambuka's tissue.

The killing occurred at the height of a spree that saw over 40 people with albinism in Malawi murdered and scores of others assaulted.

One of the five convicted was the victim's brother.

"The convicts took advantage of the deceased's psychological need for love," the judge said.
"They lured him into believing that they had found a prospective wife for him and that they should go and meet her – that ended up being his death trap."

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