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.
@DuduyemiHood2 ай бұрын
Thank you for including the Deaf community in your initiative. This is really amazing
@matthewosasu2 ай бұрын
Adeola, thanks for the sign language, it is high time every video start having this. Also for bringing awareness to MD
@patternsamazing2 ай бұрын
The sign language is actually unnecessary. KZbin already has a subtitle function, everything she is saying can be read on the screen. Videos can also be slowed down if they are too fast. This will make reading easier for anyone who cannot read fast enough. Adeola, teach people how to use this function, it is right there.
@healthythrivingfamily98202 ай бұрын
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.
@CExcel2 ай бұрын
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
@kingilo54052 ай бұрын
Adeola this another level with signed language. You're thinking progressively. Well done Ade
@farmthings19892 ай бұрын
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.
@BlessingEbeye-qj4go2 ай бұрын
Well done Adeola and please stay strong guys
@dammiesuzy2 ай бұрын
Thank you for bringing the awareness, and thank you, Oluchi Sonia, for sharing your story ❤
@Mavelcreativestudio2 ай бұрын
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😭😭😭😭
@LadyJaneAnams2 ай бұрын
Thank you my darling sister for this topic. This is real indeed.
@annekanem37552 ай бұрын
@Oluchi thanks for educating and for your bravery towards life, you didn’t allow MD to define. More Grace and Strength.
@samueloseyomom47062 ай бұрын
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.
@chinyererachel2 ай бұрын
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.
@queenideas2 ай бұрын
Oh so sorry dear, please don’t give up. I pray God heals you too in Jesus name, Amen.
@chinyererachel2 ай бұрын
@@queenideas We won't give up 🙏🏽. You are really one of the strongest people I have seen.
@heavenandhellisreal2 ай бұрын
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 ❤
@NdifrekeKeresifon2 ай бұрын
My heart felt sympathy for anyone going through a different situation. I can't imagine how hard this is.
@iphieashley32212 ай бұрын
❤❤❤❤
@NdifrekeKeresifon2 ай бұрын
@@iphieashley3221 thank you
@adeolao.sam-oladapo76082 ай бұрын
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 😊
@blessinggambo14272 ай бұрын
My neighbor presently has this condition too, exactly like this lady's own, her stated when she was in secondary sch, she graduated since 2009 no job uptil date cuz of her condition.. It's painful honesty.
@biochar.2 ай бұрын
I can only imagine how worse you people must have made her feel with your deeds and actions. I trust Nigerians with their f00lish religiousness.
@peterillah79442 ай бұрын
Satan can inflict the disease on someone who was initially okay.
@queenideas2 ай бұрын
@@blessinggambo1427oh, is she in Nigeria?
@blessinggambo14272 ай бұрын
@@queenideasyes
@blessedwithbeautycreative25192 ай бұрын
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.
@MomentsWithFikayomi2 ай бұрын
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.😂
@mosesena2 ай бұрын
Thank you for educating all of us 😍
@justeatplantsnike2 ай бұрын
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.
@oluwatobiadegoke132 ай бұрын
All is well with you in Jesus' name 🙏🏾
@justeatplantsnike2 ай бұрын
@@oluwatobiadegoke13 ,Amen. Thank you.
@LouisOsas2 ай бұрын
So sorry
@iheomanwakpadolu25762 ай бұрын
It's OK. May he continue to Rest In Peace 🙏
@olaolaitan78342 ай бұрын
Prayer up for you and your family 🙏🏽
@YvonneJack2 ай бұрын
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
@ElizabethMomoh-f1w2 ай бұрын
Weldone Collins this is amazing
@biblemysteriespuzzle2 ай бұрын
Thanks so much Adeola for putting this message out there! I respect you alot!!
@damilolaisaiah236628 күн бұрын
Wao Adeola Well done. Many Including me don't know about this. The lord is her strength
@Jennifer-Ihuoma2 ай бұрын
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
@akolawoleomoba35322 ай бұрын
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.
@veraaddoyobo84822 ай бұрын
Which government?
@peterugwu35422 ай бұрын
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.
@Nijaman242 ай бұрын
Thank you for shedding light on this topic and many others. Thank you for bringing awareness to the masses.
@felixtochukwuezechukwu2 ай бұрын
Thanks Adeola for educating a lot of people about this condition. God bless you
@hillsongcovers21732 ай бұрын
Adeola, I believe you can be influential enough in getting Oluchi a remote job (work-from-home).
@AyodejiOmotola2 ай бұрын
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
@BeyondBarrier20232 ай бұрын
Thank you Collin for bridging the communication gap. It’s commendable
@AgathaNjoku-k5p2 ай бұрын
Thank you Adeola ❤ for educating us on MD disorder
@Tara......2 ай бұрын
Thanks for creating awareness about this.
@Remi-j7z2 ай бұрын
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.
@Otherworldly232 ай бұрын
Wow thank you for your video Adeola, thank you to that lady for sharing her story
@chidmania84852 ай бұрын
Thanks for enlightening us on this issue
@deafwomenass.ofnigeriaabuj48602 ай бұрын
Thank you make it accessible with sign language interpreter for Deaf people like me we appreciate e🎉
@Angela-hm3xt2 ай бұрын
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.
@jpwithout2 ай бұрын
It is a great series. Keep it up. We need to awareness
@arionuigwe98642 ай бұрын
😢 sending you warm hugs and love 💕
@Funnymama742 ай бұрын
Thank you for this awareness creation on MD.
@OrganicEntertainments2 ай бұрын
First From Cameroon 🇨🇲 🇨🇲 🇨🇲
@Creativeifi2 ай бұрын
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.
@eakpan12672 ай бұрын
No cure for genetic disorders. They can only be managed.
@yemisiaderuku2902Ай бұрын
I think also awareness and education on Narcissism is very important So that people don't continue to fix people they can't help
@emmanuelskilful24892 ай бұрын
Great video love u Oluchi stay strong ❤❤❤
@OgheneroEwurhie-mm2cc2 ай бұрын
Thank you for the education Adeola
@annekanem37552 ай бұрын
Thank you Adeola for this information. God bless you
@chukwudozieokolo50152 ай бұрын
Thank you Adeola. Thank you.
@beea.94352 ай бұрын
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.
@GodsLovisaltimateАй бұрын
May God heal you and heal you completely IJMN🙏🏾
@commscompany15022 ай бұрын
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.
@olatunjiridwan49302 ай бұрын
Nice video, thanks for d sign language too
@janeottahsworld81192 ай бұрын
Oluchi stay strong,you are beautiful
@princeaghamiogie71542 ай бұрын
Very educative video.
@oluwasinaayomitoyin4552 ай бұрын
This is really educating
@elokaoduah90182 ай бұрын
thank you for creating awareness
@rotimiamzat83012 ай бұрын
I have a family friend with this disorder, she struggles to walk for long a once vibrant lady.
@kevisifyАй бұрын
Bless her heart.
@P.Rum-bb3qq2 ай бұрын
The mutations are usually inherited, but in some cases they occur spontaneously.
@mjbaba10002 ай бұрын
Thank you Adeola
@Ebisidor_Daria2 ай бұрын
I love your channel, God bless you ma
@euniceaniekwejesusbabyanie76282 ай бұрын
My sister Chinoye lives with it
@euniceaniekwejesusbabyanie76282 ай бұрын
She is so intelligent and hardworking , but is is limited my this disorder
@totsin2 ай бұрын
Hi Mrs Adeola!!!
@oluwatobiadegoke132 ай бұрын
God! This is the first time I've heard this.
@chinyewadibia84032 ай бұрын
Very enlightening
@dancecultureredefined4622 ай бұрын
Wow! So many things that people are dealing with in this life o😢
@Iammeggysil2 ай бұрын
In a lawful country this lady is suppose to get the job, they highest priority! But Nigeria is lawless and without empathy
@victoroluwaseyi14592 ай бұрын
There should be more awareness on such disorders. Nigerians are quick to judge what we don't understand
@elizabethkuye91662 ай бұрын
Well done my sister. If you live in a developed country, you will know about this illness.
@iphieashley32212 ай бұрын
Ma Adeola please do about NF too. Thanks
@allen-bryanmodelspecialsch362 ай бұрын
Adeola , there is a medication for it. It can also be treated surgically. It is similar to Myasthenia Gravis
@eakpan12672 ай бұрын
Not the same. Might look similar.
@nkeriuka122 ай бұрын
Thank you
@nengiawari20112 ай бұрын
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
@militarybishop60532 ай бұрын
Please apply for the United States Visa. I think there's a visa category for you. Adeola will help you with that
@katewilcox86052 ай бұрын
Please, does it come with pains? I'm just wondering if, in addition, they also suffer pains. That will be terrible 😢
@uchenebo30622 ай бұрын
I love you stay blessed
@topeadebiyi57842 ай бұрын
Hmmn! Oh, my God!
@xtamemeАй бұрын
Wow.... This is.....
@Charlisco20002 ай бұрын
Good morning my love ❤🎉
@Afro_Updates2 ай бұрын
I know this condition is common in Northern Nigeria
@YourNeighbour-w5g2 ай бұрын
My sister na witchcraft... having a name doesn't rule out witchcraft...
@g1stconsult2 ай бұрын
Hmmmnnn!!! It is well
@lebiseyi57852 ай бұрын
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
@currenttrendtv89202 ай бұрын
Jesus can dissappear this thing. 🙌
@peikinwinner62552 ай бұрын
education is important.
@nnamdiikenna2 ай бұрын
What's the different between this and Autism and Celebral Palsy? Can someone help please
@ariesunicorn82252 ай бұрын
Ask Google
@obayemiolawale71842 ай бұрын
Autism and cerebral got to do with brain neurons disorder but this muscle weakness disorder. In a simple term.
@josephyndinakin17022 ай бұрын
Very different.
@czogg992 ай бұрын
Lou Gehrig disease. It is very common in the USA .it is a progressive disease and I wish the young lady all the best .
@hackademics96042 ай бұрын
Duchenne Muscular Dystrophy
@militarybishop60532 ай бұрын
Or Becker muscle dystrophy
@dcndiob43252 ай бұрын
Ignorance of so many medical defects make people assume a lot especially in Africa and Nigeria in particular.
@MaryMarisenАй бұрын
I completely understand. The stigma is unreal, especially when you don't " look " sick. I have Primary Progressive MS and it's not written on my forehead..... Our society needs a lot of education and government needs to step up for everyone on all levels. To my fellow people living with chronic incurable conditions, you are not alone and we are so much stronger than people can imagine ❤🫶🏽🫂
@antimol45932 ай бұрын
Because there's a diagnosis does not mean a disease is not demon sponsored.
@ubonggeorge45092 ай бұрын
Pls somebody should direct her to papa j.
@almakanu34562 ай бұрын
Very sad
@idemudiaosaze2622 ай бұрын
OOO GOD !!!!! Why did GOD created this kind of problem na ?.
@pst.davidabiodun25312 ай бұрын
Come to GCK. Jesus will definitely heal you. He has done it for countless number of people with more severe cases. #GCK
@currenttrendtv89202 ай бұрын
She shouldn't stay in an upstairs house for easy access
@a2spaceltd5542 ай бұрын
Jesus can do it
@watchforlifeАй бұрын
You people and your religious nonsense!!!! Let Jesus intervene and fix the economy and entire country as well.
@ekaetteelgba59972 ай бұрын
I believe that this too can be heal. What God cannot do does not exist
@frugael34652 ай бұрын
I was a caregiver to someone that had this.She was born normally but now she is like a vegetable.