 We award them, we give them 100,000 just to say thank you for the good work they are doing. We award them, we give them 100,000 just to say thank you for the good work they are doing. We award them, we give them 100,000 just to say thank you for the good work they are doing. What exactly has been going on today? We award them, we give them 100,000 just to say thank you for the good work they are doing. We award them, we give them 100,000 just to say thank you for the good work they are doing. We award them, we give them 100,000 just to say thank you for the good work they are doing. We award them, we give them 100,000 just to say thank you for the good work they are doing. We award them 100,000 just to say thank you for the good work they are doing. We award them 100,000 just to say thank you for the good work they are doing. We must transform the young people who are still the young people who are not up to date at the moment. What changes is to find the young people who are sick because of the disease in the country. That's one of the biggest challenges. The biggest challenge might be dangerous to anyone Maybe we face this problem due to sankak 아 ^^ Never had its impact would I say We Bulgarian 방송 have had some issues But people have admitted their problem So ni kisha fika uko, one of the biggest challenge, for example nishokia panende wajir, manzewe na ame ziti. Tukia na bia na anza. So the biggest challenge ni mu pata ni him. So ni wama ni kia na na anza. Anava kumiza wakite. So the biggest challenge ni mu face most of the time when as our foundation, when we go to those villages, ame uko machinani, wana je pata maneka uko maneka apokotsam, buhurubusi ya kule nani kabisa. Ukshengia kule nani wana pata there are some cultures who still believe that giving back to a child who has any form of disability is a curse. Na bada kuna zile cultures na ame ni om tuak zeliwe wana skia, anatupo uko inje, anatupo komstuna fitu kama hivyo. So kaziangu muhimu kwa ni kusensitize hawa zazi. Kaziangu wanda na local chiefs. I talk to local chiefs na ame bia if you know any child, any story that you know around the area, kama kuna umtom is around any form of disability, kindly tuan bia. Si ufanya kitne tuan medical camps like during the week. So kama tumenda apokotsama, sada rili kutakwa na medical camp, but during the week tuan fanya sensitization around the villages. Kwa ambia tuwa tuwei. On sada rili takwa usweli flani. Kama kuna umtoto, tafadali milete jmamosi na tuan apiana pamphlets, flyers, tuan ambia letinim toto. Uksha letua, kuna kituna fanyanga in itua medical, wana fanyu akama medical inspection to confirm the level of disability that they have. Nakukonfirm to how it can be resolved. And from there to try to chukwa numbers out, chukwa all the information that we need, our towa nakuja wana letua pakijabe, then surgery is performed on them. But the most important thing in kwa ambia the nation, nama kwa ambia wana inchuku inje, if you know anyone who has any form of disability, usiai o gopati because I'm the one with disability, maybe hauna persa na bitu kama iso. Talk to us, people like us, we know how we can help you and how such challenges they can be, kus kuna well wish us, nma prana na ukuja na biminda kusahidi amtutu yote tu, apati surgery. Na una pata aku willing ataku, kulipi amtutu apati surgery. Na uku na mtuko nyumbani, tengi na una feel how na you persa ya kumita hospitali. So, speak up, talk to your local chiefs, talk to your hospital, talk to any organization. Mimi kama unizapata handoliangu on social media, just inbox me, I normally help so many kids who are born with disabilities. Sajari labda ina cost how much because tu na elewa apani kijabe and most of the kwa na elewa kijabe ina koga very very expensive. How much does it cost? Okay, in general you can't, where's the quantify, kus you see there are very different forms of disabilities, physical disabilities, kus na pata muntu maybe akuna club food, na mngine maybe akuna mkuna mimi mifunji kanandani, kakika vibai, akuna korekta vibai, na mngine meza liwa, mkuna nifupi na vitu kama iso. So you see all these things, because lalma tongizwa chumandani na mkuna iku level na iingine, all these things vary. But most of the time, we normally tell people that those who want to give is in between 60,000 to 120,000. But the salary can be even exceeding that amount. But you see you remember at the end of the day as much as the doctors are doing this through funding and all that. Badu kuna some costs here and there that is nafa kulipu and all that. But as a parent, that is not your cost. That is not your cost. Your cost as a parent is utu mitu kuna mtoto na itrajiku sayidiwa, then of course, guys will come together, look for ways to make sure that umta atapata surgery. My aim is to make sure that in future, kuna eradication of all atone is not a disability that can be corrected. You know, kuna zilezen yun na jwa ini more of neuro, but kumana zileza physical disability that can be things like clubfoot. I don't think in the next like 10 years Kenya should be, we should be witnessing children who are working in clubfoot. Ya. Pengine ni ulize kwa de center, pakasa sayivi mekua able kupafumia surgery ambazoz mekua successu kwa watotu kamaunga pivi. Inaia alone is more than 2000 children. Inaia alone So, you can imagine because, okay, I don't work at kwa, but my foundation works closely with kwa. Ya. So, miimi peki amu kama through Malaika Disability Foundation, the children that ni meleta apa every year is more than 500, 600 every year. Ya na san? And you see, at the end of the day, kwa alone, them they have more than 2000 kids that they support every year. Ya na san? Izi ni shida badotu na zifes around. So, when you travel, okay, na wuku inje machinani kabisa, you'll find most of these kids, na sometimes you can't even blame the parents, because na pata ana information, na piya na guba de stigma, na piya the parent mu ni na pata at the end of the day, akona a lot of responsibilities to do as a parent. Because, on me just sometimes, na samangati, oh, uya na chikuwa tota, miwa feature, miwa fungia na meanda, but if you go to those women, wawanzu kumbiya story, na kumbiya, miwa na fungia kaziya kibaruga. Na umtota ni kimwa change haizi jitege meya. Na nenewa, na bini ni umfungi e, kumana, siizi shinda, umta na itaji, na zima ni, na, I must take care of the child 24 hours. Yes. But sasa, ata kama na take care of the child, ni kona tuangi na kama wa tano, na na zima wa kule, na mii miwe peke hangu, na na zima ni fungia kibaruga, na ni pate unga. Ni pate unga. So you end up understanding some situations, I don't advocate for it, but you understand some situations, and then you advise them to do something that is correct, the right way to do it. Onambiya if there is, and that's why, najianga ma children's centers, ma children's homes, ma technical schools around the country. That's another thing that what you move on. I'm going to those villages, na make sure, na gana county government, na gana utunye, donors, we buy land, we build a a vocational home for these kids, so that at the end of the day, there's someone who's taking care of them. You understand? As a mother, mimi yana za kwa na mleta, pa kama take care na mleta, na mwacha apu, kuna kia give us who will take care of the child, mama na kibarua ya ke, and then mtu na shuguli ke wa. How in us, we've said every, na kwa gana 2,000 people with disability. Nationally, we're more than, we're going, how do you go about this? Maybe you know, nesa yanda upate waku more than that. Mama, kuna wale wana, nesa takawa saidike, lakini muna labda, hawafaiku, kusaidika io time. So how do you deal with such cases? There's a roster. There's a roster. So by time, there's a full calendar, whereby we do medical camps. And we've divided so many regions, like, na sama kama say, na central, na course, na ifo, na san. So by time, na course region, we know in the course region, if this month, we are taking care of course, na eastern. So we know this month is course in eastern. So, kuna a very good schedule that you may power, because these are hospitals that have been running for so many years. So they have the experience on how, they know how to, to prepare the schedule and the program itself. So, sometimes, wana konga more than 2,000. But, irai mean that, adakama konga more than 2,000, wazishu guli kewa. Because we have doctors in this hospital, we have equipment in this hospital, and we have very good caregivers in this hospital. And we have the wads, and we have, just a very good facility, that take care of these kids. But at the same time, we, irai mean that we, we don't call out for, guys will wish us to come and contribute whatever they feel like. Because sometimes, kama jana ni negatu post-TV, mama fila ni negatu, in less than 2 minutes, alikwasha tumapesa, akantumia, misi jake ya ni ni, ya empesa kanambia, this confirmation, I can't make it for the work tomorrow, but I hope the money that I've sent, will help the children. So that's what we do. Okay, pengina ni ulize, you know, we've seen, you know, many people, let me just say a few people come up with organizations, kama hi ya kwa yama laika, to just be able to help people with disabilities, sanasana wa toto. Is it that the government pengina hi ya fanya enough ama inakwadi? Government ikona, organization ikona into a national council for persons with disability, NCBWD. National council ikopale Westlands, na inafanya kaziake, we semati fanya kaziake, na inafanya kaziake, it's only that it's, we know, at the end of the day, it's already overwhelmed. The same way, there's public schools, the same with these public hospitals, but at the same time, we still have private schools and still have private hospitals. So the government is doing its work through national council, national council in afanya kaziake, but at the same time, we can't all depend on just the government. We, kama ukona hi yo, ume pewa kami misa hi, I only thank God because I'm using my platform, I'm using my brand, I'm using what God gave me, to be as a public figure to help other children. And you see, sometimes, whenever I go to those villages, they look at me and they're like, you're so believable, as in we, ume kwa na, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, na kujua, So I'm just calling upon the Senators, the Senators to make sure that such small issues come here, they just look at it and help most of the people who are living in disability. At the same time, there are issues whereby one of the biggest challenges I feel in this country towards the disability is if someone has physical disability, imagine every after five years they have to go and renew. So I don't get the point of, why should you go after five years? I always wonder, is the government expecting that Amira Kultafanika in between the five years? Because if someone has permanent disability, you know this person, like I said, for the rest of his life, come and compare when it comes to tax evasion and all those things. Make it permanent. It should not be renewed after five years. So that's all I'm just calling upon the government kindly. We can check on such things which is very important. At the same time, funding when it comes to children who are born with disability, how they're going to school and everything kindly pray and urge the government to look upon such. Okay. Of course, to nafahamu kumbawa, tumbo wanakuja, they come from different sides of Kenya. Is there a plan to set up something for them? Was that the union wakikuja? Because I don't understand kumbawa, pengeine he sayhemu, nizika kosa the hotels, the facilities, chukwa watu onberonakuja? So Pali Numa, behind this building, now that's where the main wads and the main theater is Kopaali. But where we are standing right now, these are new buildings as you can see. The new building that last year, was it last year? I think last year, because I worked closely with Kewa, when I came here, we came here with Silvia Molinge, at that time she used to work at Safaiko. So when we came, I told Silvia, the biggest issue of notice about this hospital is that when the children come and the patients, when they come, they have to come with a guardian. But the problem that is happening in this hospital is that there is a world in your town as we can see our children. Even the beds and everything, we can see our children. So when the guardian comes, they always struggle where to accommodate, where to go and sleep. Because in your town, for example, you find a kid from a place like Malindia, Meletua. Aksha letua, anambia, sajirita, ita fanya wakama, after 2 days, anakama, inebidiya lalea apa. After 2 days sajirika sa fanya wakama, ina dipena, Observation Editoria, ita tereksha angalia na ona. Umtoto, I thought she'll recover maybe after 2 days, but the complication that through the sajirika, you may notice that inebidiya kaya another 14 days. So you see those 14 days, it means the guardian should be staying here with the patient and the child. So that's when we came up with the idea that after funding we build to kajengahi, this ward near guardians. So while guardians, instead of struggling those days when they're taking care of the children, the guardians now they can come and live here. And I spoke to Sylvia, Sylvia at that time she used to work at Safaikom, and then now Safaikom Foundation decided to give us that 7 million to build this ward. How many months have you been living here? Last year, I decided to go in April. I can say 5 months. 5 months? Yeah, 5 months. So we've been living here for 2 months? Yeah, this is like 5 months. Because I remember, when I was in Gangalia, I think in November last year. So you were living here last year? In general, it's more of like a ward. So it's just, we have 2 partitions. So they confirm exactly how many beds but I can look at the proposal, but I'll confirm how many beds it can accommodate. And I'll take you for a tour in Tayona. So eventually, as Malayika Disability Foundation, we made sure that Kewa received the funding and here is the progress of what we did. And when are you planning to launch it? Now that depends with the administration at Kewa because my work, as Malayika, is to look for funding. So we have funding and then it's our own responsibility because at the end of the day, it's their project and it's their facility. So I don't know what you're asking. But we're on breaking, so we're just waiting for the launch. So I'll confirm with the administration when they're planning to do the launch. Maybe to take you back to Dogu. What inspired you to have such whatever like what you're doing right now? I lost one of my eye in 2001 and after losing my eye, I discovered how much people who are living with disability face stigma and all that because my eye at that time before me for new year's operation, ilikuwa nga white. So everyone ilikuwa nga enda uto nga lebe, baya, uto nga shianga, umto nga haje, unu na kilamto nga ako, nga lewa, nga kututu even because of your eye. So me ni kajuliza, imagine me ni macho tu na ni jishotu moja, nga ni kandawa usi ni kafani operation, ni kamaikopo haiuni lakini, ni kani kani naona, but imagine in my position at that time rasi kwa ni manzam ziki. So by the time I became a musician I used to have that heavy heart knowing that people who are living with disability wanna face a lot of challenges and a lot of stigma. So that thing really inspired me and by the time I knew God has blessed me to a level whereby I can transform lives, I can connect people with such facilities and such programs I was like why can't I do it. So in 2012 is when I launched my foundation, Malaika Disability Foundation, by that time I used to be called Malaika Trust and I started by doing an event called Malaika Tribute Awards, whereby we used to award people who are living with disability who have done great things despite their challenges. Are you looking forward to the future Kuziru Disha? Ya, I think this year I'm planning December 3rd. Because when I say they are doing it's only during Covid-19 that they are doing well. I think last year but one the aim is mostly just to award people who are living with disability who have done great things in the society. When I come out and give us, I want to tell them that they are doing well in the hospital and in the house. So I want to come out we award them, we give them 100,000 just to say thank you for the good work they are doing. Some of them are doing well in the house. They are doing well in the hospital, they do well in the disability. They are giving me 200,000 para kana 10,000 for the examined and for the trophy and for the certificate just to recognize it's not a competition it's just call a tribute or what, we just pay tribute for the work that they are doing. Wow. Tumalizia to Pengine. Come to Mbaya to tackle kuchangia to help, what is the number to call, what is the pay bill, what is the till number and all those necessary details come to Mbaya Pengine. Anatakak kuchangia, to fund, kumafandi ni ake napia komton bayana taka wsijidizi. What is also dinambara maya nasa ka upiga? Okay. Nda kupatia… The Pbil' number ite kwa pachini. Dira pachini kwa screen. The Pbil' number At the same time you can visit okangiya peji yango Instagram any of my platforms you can Inbox me at the same time kuna weiji ya meleika disability foundation inu tyu meleika disability foundation on Twitter, Instagram, and Facebook inetroivo, and then piya kuna peji ya AICQ wa I see kwa Kenya on Twitter, Instagram and Facebook, you can just visit their platforms, and if you have an issue, most of the time they will respond immediately when it comes to things about disability. Arapi jyongu mu respond immediately, ispokwadru kwa mumitumu hampi tu mwa ptusengiri na misbe, agini kwa wapitumu hampi tu mwa disability. I'll respond. few times when it comes to the disability, this issue you're dealing with you and your child. we're not sure what's going on with him For now, I'm busy, I try to say it, but I'm busy. Just as to kwenna watia wadiyu, na我的 hendishah. Mwukarti utawadia, nintawadulisha. Nakini jagwey Ah, niko easy. Kusili wech, maia. Ah, maia. Mi niko seigo. Wrnge jula eh. Wadatana givgode, jula eh. Sisi wngasahi kwaizu, juina waka nujoードfiki. Juina waka nujo dazeba, hendishah. Wadze jula eh? I pronunciation is very good. Neshkorosan