It's Not The Witches & Wizards, It's A Genetic Disorder 

I don't know who amazes me most. Is it Ms Adeola, Miss Oluchi Sonia or Sign Language guy. Everything is amazing. You're doing a great job not just only exposing Nigeria's government inadequacies, you're creating awareness about things I have never seen or heard about before.

Thank you for including the Deaf community in your initiative. This is really amazing

Muscular dystrophy Also called: MD Muscular dystrophies are a genetically and clinically heterogeneous group of rare neuromuscular diseases that cause progressive weakness and breakdown of skeletal muscles over time. The disorders differ as to which muscles are primarily affected, the degree of weakness, how fast they worsen, and when symptoms begin. Wikipedia Symptoms: Increasing weakening, breakdown of skeletal muscles, trouble walking Treatment: Pharmacotherapy, physical therapy, braces, corrective surgery, assisted ventilation Prognosis: Depends on the particular disorder Specialty: Neuromuscular medicine

Adeola, thanks for the sign language, it is high time every video start having this. Also for bringing awareness to MD

I used to have a neighbour who is living with this condition. However, we were made to believe that it was the devil's attack on her especially because she wasn't born that way. This is another eye-opener for me. Thanks for sharing, dear namesake 😊

I love Queen's positive approach to this condition & to life in general. I pray that a lasting solution or a cure will be found as soon as possible. More awareness is needed for our country people.

Amazing.Queen is an amazing woman who did not allow Mascular Dystrophy to define her.keep living life girl u r a warrior nd I love you

This is so informative especially in rural Africa where we tend to attribute things we fail to comprehend as witchcraft. I have heard people blame others for their child's condition and even attack or even kill for witchcraft allegations.

Watching this makes me so emotional. Today makes it 9 years that my lovely son passed as a result of spinal muscular atrophy. It's a genetic disease.

I understand totally what you are going through, the stigma is real. I went through the same thing as I live with young onset Parkinson's disease.

You are doing an awesome job ma🙌😊 hey oluchi, I see you, for years I had been made to believe that the condition afflicting my sister and I, instead of pursuing medical assistance my parents were busy going from various churches and native doctor, sadly before they realized what it was damaged has already been done😭😭😭😭

Adeola this another level with signed language. You're thinking progressively. Well done Ade

My heart felt sympathy for anyone going through a different situation. I can't imagine how hard this is.

2 of my uncles have this disorder and for years I was made to believe it was a bad choice they made when in secondary school that caused it, I never knew, unfortunately one has passed on, may his soul rest in peace, please bring more awareness to this, may God bless you.

@Oluchi thanks for educating and for your bravery towards life, you didn’t allow MD to define. More Grace and Strength.

Thanks for the awareness @Adeola, This is indeed a welcome development, and public awareness to educate every human the nature of genetical disorder. And to our interpreter, Thank you for bridging the gabs by promoting inclusion in providing sign language for the deaf.

This is a brilliant video and as a health care professional talking about issues like this is an important part of having a good quality of life for the citizens.The government should put in place measures to support your quality of life.

Thank you for bringing the awareness, and thank you, Oluchi Sonia, for sharing your story ❤

Thank you for educating all of us 😍

Adeola, I believe you can be influential enough in getting Oluchi a remote job (work-from-home).

Thanks so much Adeola for putting this message out there! I respect you alot!!

Thank you for shedding light on this topic and many others. Thank you for bringing awareness to the masses.

Thanks for creating awareness about this.

Thanks Adeola for educating a lot of people about this condition. God bless you

Weldone Collins this is amazing

There's this amazing girl who graduated from my uni that had this experience suddenly. We rallied around her for a while. Thank Adeola for shedding light on this.

Wow thank you for your video Adeola, thank you to that lady for sharing her story

I love the video very educative and may I add the sign language was like a cherry on top of the cake because I know sign language and was able to understand what was being said. Thank you Mrs. Adeola ❤

The mutations are usually inherited, but in some cases they occur spontaneously.

Thank you so much for sharing my Coach, Queen story. I hope people can learn more about some genetic diseases or disorders and stop attributing everything to spiritual attack. I live with Heterotopic Ossification and mehn,i ate and drank all manner of things.😂

Thank's Adeola from bringing up this lady's story. I've been watching her for some years now on the social media but never understood what was wrong with her. I wish she can attend one of pastor Kumuyi's GCK crusade, I'm sure if she can have a faith that the Lord can bring her back to normal, she will be according to her faith. once again Thank you Adeola

Thank you Adeola. Thank you.

Thank you Adeola ❤ for educating us on MD disorder

Thanks for enlightening us on this issue

I have a family friend with this disorder, she struggles to walk for long a once vibrant lady.

Thank you Collin for bridging the communication gap. It’s commendable

Thank you for this awareness creation on MD.

😢 sending you warm hugs and love 💕

It is a great series. Keep it up. We need to awareness

Thanks for sharing. I hope a cure comes. Education and Enlightenment are important. There should be a quota for people with disabilities. I agree with Queen.

Thank you for the education Adeola

Thank you Adeola and Oluchi for bringing exposure to MD. The stigma is what makes MD even more difficult to live with. At least with exposure and education people are able to have a better understanding.

Thanks Adeola for doing a series on disability. Nigerians are very uneducated on disabilities. As a person who has a disability it is super hard being a Nigerian. The things said at you alone makes you wonder.

You're an amazing human being. You're able individual. I pray that Nigeria will do better when it comes to supporting and including people with disabilities. Thank you for the sign language. I also hope there will be a law that protect disabled persons against discrimination in the near future. You're very right that government needs to make it a mandatory for all buildings should have disabled persons access, which includes ramps.

Thank you Adeola for this information. God bless you

First From Cameroon 🇨🇲 🇨🇲 🇨🇲

Very educative video.

Great video love u Oluchi stay strong ❤❤❤

Thank you make it accessible with sign language interpreter for Deaf people like me we appreciate e🎉

Welldone Adeola. Always a pleasure to see you on set, doing good as usual. It reminds me of the focus of my tv shows when I was much younger. God bless you real good in Jesus name 💖 amen

Nice video, thanks for d sign language too

thank you for creating awareness

This is really educating

It was so heart breaking to hear the part of when she went for an interview. These are the things the government of Nigeria should look into by ensuring facilities are in place to accommodate these issues. It's a shame all they do is think of enriching themselves.

Oluchi stay strong,you are beautiful

Thank you Adeola

Very enlightening

My sister Chinoye lives with it

In a lawful country this lady is suppose to get the job, they highest priority! But Nigeria is lawless and without empathy

I love your channel, God bless you ma

Oluchi my school mate😢 we use to call her hot stepper back then in school, we didn't know it was a condition. It is well with you in Jesus name my dear

Well done my sister. If you live in a developed country, you will know about this illness.

God! This is the first time I've heard this.

Hi Mrs Adeola!!!

There should be more awareness on such disorders. Nigerians are quick to judge what we don't understand

Thank you

Ma Adeola please do about NF too. Thanks

Adeola , there is a medication for it. It can also be treated surgically. It is similar to Myasthenia Gravis

My sister na witchcraft... having a name doesn't rule out witchcraft...

Wow! So many things that people are dealing with in this life o😢

I love you stay blessed

Please apply for the United States Visa. I think there's a visa category for you. Adeola will help you with that

education is important.

Hmmn! Oh, my God!

Because there's a diagnosis does not mean a disease is not demon sponsored.

Hmmmnnn!!! It is well

My daughter I advise you to go to SCOAN for deliverance for your healing you will be healed by the grace of God Almighty but because we don’t have faith we can see the other side of life please try God first and you see with God everything is possible my dear daughter

Lou Gehrig disease. It is very common in the USA .it is a progressive disease and I wish the young lady all the best .

Good morning my love ❤🎉

Jesus can dissappear this thing. 🙌

Ignorance of so many medical defects make people assume a lot especially in Africa and Nigeria in particular.

Please, does it come with pains? I'm just wondering if, in addition, they also suffer pains. That will be terrible 😢

Duchenne Muscular Dystrophy

I believe that this too can be heal. What God cannot do does not exist

Come to GCK. Jesus will definitely heal you. He has done it for countless number of people with more severe cases. #GCK

To me, this is still abnormal.

She shouldn't stay in an upstairs house for easy access

Pls somebody should direct her to papa j.

I was a caregiver to someone that had this.She was born normally but now she is like a vegetable.

Very sad

Nigeria is so backward, why would people with challenges can't work.

Jesus can do it

Motor nurone desease

What's the different between this and Autism and Celebral Palsy? Can someone help please

OOO GOD !!!!! Why did GOD created this kind of problem na ?.

Adeola, stop trying to be too smart. The enemy can strike any child of destiny before they are born with genetic disorder. It was never God's plan for any child to suffer. This is a subjective matter. Thanks

But traditional this can easily be cure, there’s a name for it Yoruba called roomo lowo roomo lese. Please correct me if I wrong.

This is marvelous Cyril, and I know the feeling , I understand the struggle, it never been easy even for a day, thank you ma'am for giving us the platform🙏 @adeola fayehun