This ruined her life and her family’s life in general, as parents were not having enough money of taking her to hospitals for treatment.

Yet she was feeling unbearable pain and spending sleepless nights.

But after Aphromoth vested covered and published her story, they got money from well-wishers and took her to hospitals.

Now her condition is no longer worse like before, and they hope that with more treatment she’ll even have a normal life.

A campaign was created in different good samaritans contributed to saving the girl’s life, and they were given money to take the girl to a more advanced hospital.

This is the update.

Is the family’s one and only daughter who was born normal, but after only three months into this world, her skin started changing mysteriously.

Parents started taking her to nearby hospitals but could not help.

The skin was aching too much, making the daughter spend sleepless nights and the whole skin later became like this.

Due to this illness, she started working at eight years and even her ears were kind of affected.

The skin of the young girl developed a bad smell that would make people and other children omit and go away from her.

The skin became stiff as hard as a tree that cutting her nails is no longer possible with an ordinary nail cutter.

Whenever pain increases, they have to get a stone or something else hard saw us to rub it on her skin.

Despite having sad health problems, she has a lot of dreams to achieve and she is sure that one day she will make it, being the reason she wakes up and goes to school daily to learn, as she aspires to be a doctor and who focus on treating skin diseases, as she knows how it feels suffering and battling with such diseases, and she of course put in more efforts, which is why she’s one of the smartest pupils in this class and parents are so proud.

Coming from school is always a big distance and mostly on too much sunshine.

That might also be one of the reasons her condition keeps getting worse and worse.

Since she’s the only child here at home, she helps in some activities regardless of being sick, like fetching water and more activities to help her parents.

Parents were scared and say that after their daughter became like this, they’re afraid of producing another one.

They add, they tried whatever possible way of solving this issue, but were told only advanced treatment would help, and that meant a lot of money.

Yet the family lives under extreme poverty.

That was our first visit to the family and they urgently needed support so as to take the poor girl at the hospital, as they are low-income honors and cannot afford the girl’s treatment.

After a year since we visited today, we took a long journey back to this far village and visit the family to see if maybe there’s an improvement and know more about what has been going on since the day we left.

The man says our first visit was a blessing, as a few people who saw their story on afromax tv showed them some love and care by calling them asking how they are, telling them not to worry and, of course, sending them some money to buy her some painkillers and more, which really helped them, and they thanked all those people who took time and had to do something for this family.

They also took the vein at the hospital and was given some medicine that she’s applying on her skin.

He reminds us of how the gut skin changed and how it all started from.

Since they took her to hospital and gave her some medications.

They have hope, given that the illness is slowly calming down as by now she can at least sleep and rest, contrary to last time where she could have sleepless nights due to too much body pain.

It was a music combination recently

And she’s still suffering from their skin illness, but parents admit that she had started recovering story by slurry, but there is still a long way to go for her to fully get rated, recover and have the normal skin, which means a lot more money for her to recover.

After airing and publishing her story, a campaign was created on Givinglifecom and their goal was to help this family that lived under extreme life conditions to get money for the daughter’s advanced treatment, and many people worldwide contributed and today will bring all funds gathered with.

This money comes up, and i believe that it will not take long, as what delayed the whole treatment process was lack of enough money, and now the problem is solved.

He says the 14 year old will be taken to an advanced hospital and not be treated.

The 42 year old takes this time thanking people who are helping them to save their daughter’s life, which has never been the same due to the skin abnormalities, and they finally got the support they wanted.

He adds that a lot is still needed for the ghost treatment and you can keep helping them by contributing on the giving life’s link, phone in description and being in top comments.

Divine also thanks.

Anyone who contributed to saving her life has been challenged by fellow children who remind her that she looks different to them and other more discouraging comments, but since they have given their money, she says it’s just a matter of days, as she was soon betrayed and have a normal, good looking skin.

If you expect that life owes you something, you may be setting yourself up for massive disappointment.

That’s because life can sometimes be quite unfair.

However, the key ingredient that makes everything else possible is hope.

It’s your hope for a better future that motivates you to make great sacrifices in the present.

Thank you for watching.

I’m Elijah, and this is afromax english.

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