Depression and any kind of mental health problem is so real. But it’s not talked about, we act like it’s not real: as if they are trying to get more love. But really people with mental health problem are not acting they do need help. Depression and mental health does need to be talked about!
Lately I have been reading like crazy and that is why I haven’t been writing.. I have moved to Pueblo and sometimes I get down because I get lonely,, I wonder if I made the right decision for me. But it will get better, once I have my own house.
Starting over can be hard but it could be what is needed to grow yourself, in so many ways. But it also gives you anxiety, I’m in that in life, I want this I know it will be great for me, but right now it’s a little hard.. I’m not sure what to do each day. I know it will get better but now I’m going through anxiety but I am not giving in.
Today is Mental health day. I like to think I stand to help people with mental health problems… It’s a difference that most people don’t understand. I understand that having depression or bipolar it’s not something you can help! I am going to try to help stop the way others view mental health because it’s not right.
Someone somewhere is dealing with depression, but hiding it because if you have a difference you get out casted. Depression is not something to take lightly it could get to where they could take their own life. When we can do something to help them feel loved and needed.. Don’t let depression tran you a way from them. Be there, because your friendship and love might be the only thing that helps!
Depressed hurts it not only hurts the one who has it but also everyone who loves them.. it’s hard to know what to do if someone you know is going through depression; you may not know what to do to help them without them realizing that you are aware of their depression. As I learn more about people who have depression, most people don’t want to talk about it but you can tell by the way they act: as if nothing matters or they don’t want to do anything. Also if they don’t care about themselves! You can tell, but it’s hard to know what to do or tell them.. Depression is like your mind takes over and we don’t understand why people are pulling away and hiding: but we want to help we want to find a way of being there for them when they feel alone. Just be there it could be all that is needed!
My summer day is getting busy with my trip which I have been thinking about forever now. As a person with a disability and needing to go with me and everything else I have to an idea about if I can get into. Sometimes my cp, can make a trip in a way challenging but I have an amazing team who help me experience everything without even a second thought.. we are going to Chicago for my best friend, so I am so thankful to my other best friend who is giving up her weekend so I can spend time with a friend.
I’ve been thinking about this idea that if you have a difference you are looked at or people thought of as you can’t do much, or people just don’t try to understand what you going through. Maybe you are in a wheelchair and you get locked at as you are a child, why? Or you have depression and or mental health problems, you have to deal with all the bad things that people can say to put you down. I want to change the world sees people who are different!
This month is CP awareness month it is a part of me. I think it has made me who I am, I want to help people to understand that just because I have CP doesn’t mean my life is not amazing! I do everything just like anyone but I need help. Living with cp can be hard, especially when the kind is not like most, I have to work harder to find the right things which will help me do the things I love. But I am happy the way I am!
Why do people want to take their own lives? Here is my thoughts. We all have our difference but many people don’t understand that just because you can’t seesee a difference doesn’t mean that they don’t have a difference. Someone who has depression, you can not see it and they might not tell anyone about what they have. They may have had a harder time telling someone because people don’t know how to act towards someone who has depression. So they hide it in when they need someone for help in the time they need it the most. If the people who have depression felt understood and loved maybe it would help,
Mental health has a bad stigma around it, just because it’s not easy to understand or know how to help people with mental health problems. I want to change the way we think about mental illness, I understand that having any kind of mental illness is not something that you can make up : like a disable it something that they can’t help. I don’t know a lot about mental health but I am learning because I think it could help more people who are hiding thier illness because of the stimga others have made about mental health..
We all have hopes and dreams.
We are going to be different from each other
Through we are the same.
But you don’t want to talk me because I have a difference!
We are not that different from each other!
How can I help people with depression you may ask, I am a happy person! I am, but I also know what it’s like to be different or have people not understand you. Depressed can be hard to handle at times, especially if you are alone and people tran you away because of it! Even though it is not something you can help, like my cp there are stuff that you can’t help. The feeling of being lonely and maybe it’s harder because your depression can make it harder time telling others what you are feeling. Not being able to talk to someone could make depression wrost on you. I want to help people who feel lonely.
Love can be hard sometimes but it’s worth it! It is the most important thing we can give maybe even the one thing that could save someone’s life! Love helps depression you might be asking? Yes it does help! Just knowing that you have someone who wants you in their life could mean the world to someone when they are going through depression and wanting to end their own life. Just LOVE!
Today is suicidal prevention day, because of what I want to I think it’s should be written about. Depression anxiety is real and in my view it is seen as something we can just look over as if somebody just made up that they are depressed. Its not; the way I understand it, it is as if your mind takes over your thoughts and feelings and you can’t help your feelings when you are depressed. I am a happy person so me writing about this is kind of weird, but first a few of my dearest friends go through depression and anxiety on a daily bread and I know that people out there are very understanding which makes you want to hide it, but what is most needed is to know you are loved! This is what I am working on my blog facebook page/group to be about. Less suicides if they know that they are loved, is my own views on this but maybe this is more needed to help. But that is how I want to make a difference.
Having a difference that everybody can see I think can be a little easier, than the differences you cannot see. Having a disability all my life, I have learned how to explain to others what my disability is and if they are open to differences I have a new friend. But that is not always the case because people are afraid of something new, yes I have a wheelchair I don’t talk well but I can get people to get comfortable with my disability. So if you have a mental illness I think it’s harder for others to understand what you are going through. This month is mental illness awareness mouth, each day there is someone who has to hide who they are just because others don’t understand how mental illness can just take over the body and you don’t can’t get out of it, it’s not you. People who have mental illness might just need someone to understand them just be a friend. Is not something we can’t help we can. If we take the time to understand how mental illness works.
Its starting to get cold out, what do you like do when weather changes? The days it’s too cold to get out of the house, your comfort zone; it’s not just the weather that go through changes, we do too. We try to keep it hidden, because of everything from others would say to pick on us, even though it is not our doing, difference or illness is not something we can control but people don’t understand differences even if we are all different. They don’t understand your life may be your life can be because of an bad experience that has been hard to deal with, or maybe you may have an illness, or a disability, that others don’t get because it’s new to them. Growing up with CP and now trying to live as normal as I can but I still get the look like I’m not to do something just because I use a wheelchair. What is the big deal I don’t walk, I used to let others thoughts get to me, but now I know where I taking my life and what the people who are in my world think about me and is what helps me when others are trying to put me down. Maybe it would help you.
This morning I was at an event for the disability community, thinking that I could do some networking and meet new people; it didn’t end up that way, it felt as if people are afraid of differences even though we all have a difference. I think I can make friends easily, but I don’t. Once people know what disability I have then they start to talk to me; because I move all the time and my speech is not that good, its hard to meet people. Having a difference in which people can see even before they talk to you can put you down, but you have to show them you’re more than your difference!
Depression can be lonely. Its hard to know how much to help; or not to say the wrong thing. These thoughts we all, even me and I want to help people who depression not because I know about it; but I could help being their happiness back or just even just be there when its really needed. I feel like depression is an illnesses that people ran from, just they don’t understand , don’t think they know what to say. Here is the way I say it, its not about knowing what to say but first just be there nothing else could help them more than knowing that someone is always there! Just knowing that they are loved and someone is there ready to talk or be a friend whom no one else will.
My week away was amazing and needed too. I am tired but I loved every moment of it, as you know having a difference that others can see and then think that you are not capable when you know are, can be hard. But there at camp it was what can you do. I had to think of goals each day that I thought I have do; I wanted to walk everybody which I did! I even did some walking on the ropes course which was hard but fun then I zipped down the best part! We rafting I loved so much, I loved everything getting to meet new friends and feeling like I was not disabled and nominal, I worked hard but had a great week.
I have been in a wheelchair all my life, so something about knew I couldn’t do. Such as getting to the top of a mountain! There are many others that I didn’t think I could get to do, I have done a lot for myself that others didn’t think I could do; but this weekend I’m going to get to be on top of a mountain WHAT? You might be saying me too! Most things I have found a way around it so I can have a normal life. But getting to the mountain what? Really, my friend is a mountain climber and knows that I may not have had a opportunity for something like this, so we have started an organization to get people out who do not get to go on hikes because of their differences or just don’t think they can. This is a huge thing for me and others like me to I will write a blog on the experience next week.
Being in a wheelchair you would think it would be easy to be seen! It’s not; I was at the hospital visiting a friend and I realized that another friend of mine worked there, so we went to see if she was in. I was rolling down the hall way of the hospital with my father and friend staying to one side so others could pass through thinking that way I won’t ran into anyone. So I thought, , now I don’t expect people to move out of my way, though my body does not always listen to what I want to do. But I always try to make others can get by me. So as we were walking I don’t think anything about that the other people were gone to close to my wheelchair before moving over to the other side even though I was on the side; my friend saw and said people are just walking like you’re not there. I get out of two reactions from others who don’t know me, first is very helpful; second is ignoring me because of my disability. Why is being in a wheelchair such a big thing it is the way I can get around!
Today is mental illness awareness day, depression, suicide and many others disabilities in which nobody can see. The hardest difference to talk about, there are many different thoughts on this topic; even if you deal with depression it may be different in your life than anyone else. It is so different for everyone, for some talking about it helps them, others just hide it. I don’t know very much about mental illness but it’s one topic I want to help.
As you know; I am working on becoming a online mentor, I want to help in different topics including disabilities, depressed and bipolar depression. I am disabled , people can see my difference and I can explain why I am the way I am but it still hard for people to us my CP. But the two other differences I want to help in or just be a support in depression and bipolar; you don’t see if someone is dealing with it. I can understand that whoever has either of bipolar or depression; first it is the easy to tell someone second you feel different and from my experience people don’t see differences even though we all are different! But if you have a differences you can face loneliness and much more hard things than your difference, I get it all the time I may not be a doctor, but I understand what it’s like to a name called just because of something I can’t help. But back to bipolar; this is what it is ‘’ What Are the Symptoms of Bipolar Disorder?
In bipolar disorder, the dramatic episodes of high and low moods do not follow a set pattern. Someone may feel the same mood state (depressed or manic) several times before switching to the opposite mood. These episodes can happen over a period of weeks, months, and sometimes even years.How severe it gets differs from person to person and can also change over time, becoming more or less severe. Symptoms of mania (“the highs”):
- Excessive happiness, hopefulness, and excitement
- Sudden changes from being joyful to being irritable, angry, and hostile
- Rapid speech and poor concentration
- Increased energy and less need for sleep
- Unusually high sex drive
- Making grand and unrealistic plans
- Showing poor judgment
- Drug and alcohol abuse
- Becoming more impulsive
During depressive periods (“the lows”), a person with bipolar disorder may have:
- Loss of energy
- Feelings of hopelessness or worthlessness
- Not enjoying things they once liked
- Trouble concentrating
- Uncontrollable crying
- Trouble making decisions
- Needing more sleep
- Appetite changes that make them lose or gain weight
- Thoughts of death or suicide
- Attempting suicide’’ https://www.webmd.com/bipolar-disorder/guide/default.htm.
Here is an over view of bipolar depression, I know I couldn’t fix this or depression, but if we start learning about it, I might be able to help someone with either depression and or bipolar diseases.
I have Cerebral palsy the crazy kind I like to tell people! I’m always moving and not because I want to, its uncontrollable yeah I make fun of myself half the time! I am hard to understand, I like to think I don’t give up easily, its can get hard but I have to keep going because I know I have the best support team batting with me! I live on my own but I have a roommate and caregivers that came and go through the day. Like anyone my age I am in the place in my life, I’m still trying to fugue out what I want to do with my life but I know CP is not keeping me down! Cp day is March 25th.
Have you ever imagined your life different? If you are in a wheelchair; you will understand this more. I am in a wheelchair and need help getting out of the chair; I am on my own half of the day. Nominally its ok; I can get my work done or just have some time to myself but what happens if I need to go,,,, or if I need to get out of my chair; I cannot! I could probably find a way but I can’t go P on my own, that is the only thing about being home alone that sucks! I was talking to a friend about how I could not imagine how if I could walk and just go wherever I wanted to, I could not see myself as an able-body! I guess because my CP has always been a part of me, it would be weird to think about me walking! Its just me, not saying that I am just cp but it is the only thing I know. Having people help me though my day though life!
Life gets busy the days can seem so short when you are busy. I’m getting ready to host Ms. Wheelchair Colorado this Saturday though I love it it’s a lot of work. Let’s just says it’s hard work but it’s rewarding. From being a constant 7years ago; and I still think how could I be Ms. Wheelchair Colorado 2010, thinking back on that your it was probably the best year in the way it helped me to understand that my wheelchair is just a way for me to get around! I already knew that, from my family and friends but that year helped! Seeing others with the same challenges as you, and just learning from them made me want to do more and not just be taken care of. I could make differences I would have to work for it but after being around women in wheelchairs was what I needed! The Ms. Wheelchair organization is not about how you look but what you do! I love that so much a pageant like that doesn’t exist; not only that but having people like you is very helpful. This is why each year I want to give more women the same opportunity.
Having a physical disability but just physical can be hard there is so many thoughts that people who see somebody like me. I am not saying that any kind of disability is not hard but for me in what I have done and what I see most of the time it’s not easy. My CP is just physical but others who don’t know me think it’s more, and that so gets to me every time, even though I know it’s coming! Do you feel like that? I think even if you don’t have a disability you can get that. So how do you not let it got to you? Love you are first, knowing that there are people who need you, who love you for you! Tried to not let them put you down isn’t easy without knowing you have a family and friends who don’t judge you.
Childhood with a difference can be hard on everyone. Not because it’s the child but because there is so much people think they need more than a normal child. I am saying that some child who are disabled nothing more but every disability is so different in more ways than people think; trying to group all disabled children into the same class doesn’t seem right to me. I think there could be a other way to see it a child can or needs more help. Some people who have disabilities could do more than people think. It may be a little different but they can, just learn them and go from there!
What do you think of when you think of disability? There are several different ideas about what people with disabilities but mostly it’s what you cannot do, its not because they don’t care they just don’t know any different. Having a wheelchair and getting that look of oww sorry about that you’re in a wheelchair or baby talk like I don’t understand. Every time I meet someone new, I am still not used to it. Its me, I can do anything and no I am not a kid just because I don’t walk. It like I have to walk to think! I have a lot that I can do just in a different way. It happens all the time and I want to change that view. I will!
I just saw a post about breaking the silence towards mental illness and I couldn’t agree with that more! I don’t deal with depression or mental illness but I know people who have and I want to be a person could may be change the way we think about it; just like I want to do for the disability community. Because I don’t like the way its looked at. In a way it is like saying to me; why don’t you walk? Its not something people can help; maybe something happened that left a bad impact on them, or it just is. I know there is much more that is a mental illness I’m still learning but this important to me. I don’t think depression well enough supported; maybe I can’t do much but I will try to.
One of my other things I am involved with is an organization that helps woman in wheelchairs feel empowered. “The mission of Ms. Wheelchair America is to provide an opportunity of achievement for women who happen to be wheelchair users to successfully educate and advocate for the more than 54 million Americans living with disabilities. Unlike traditional beauty pageants, Ms. Wheelchair America is not a contest to select the most attractive individual. It is instead a competition based on advocacy, achievement, communication and presentation to select the most accomplished and articulate spokeswoman for persons with disabilities. The selected representative must be able to communicate both the needs and the accomplishments of her constituency to the general public, the business community and the legislature.’’. I was honored to be Ms. Wheelchair Colorado 2010 and I still cannot believe the judges choose me. But anyway now I run it in Colorado and I get to give other woman in wheelchairs the same experience and may be change their life; because I know it did for me. Ms. Wheelchair American is not about how you look but more about what you do with your disability and your community. I loved everything about my year, this group is not something you do once and then you forget about it; no it is people who can understand what it is like to be in a wheelchair and still want to have a life. Friends that I still talk to! Each March Ms. Wheelchair Colorado has a pageant to find a new Ms. Wheelchair, if you know anyone who is interested please let me know!
Yesterday I wrote about how if you have a disability you are basically can’t get a job. There’s a lot that could mess up your benefices that the government gives you. If you’re disability is physical only you can understand that the idea of working is not that early to do not you cannot work but because the help you have to every day could be taken from you. So we end up creating new ways to have a normal life, or not trying! I don’t know about you guys, but it seems wrong. People with disabilities should not feel like they can’t work or own a house because of the government. I know many people who are the same problem I am; how do we live on the money we get from the government it’s hardly eat for anyone to live on, especially if you have a home or just starting to live independently and having a few pay mouthy payments you cannot make it. So coming up with others to make everything work is hard to where we have to make do. All through its helps us, it’s all makes us not trying to better ourselves. Not to want to be able to be independent, get a job or have a life. The government wants to help the disabled people but I would like to see something that would let us want to get a normal life.
Are you disabled and wanting to work or be independent? Do you need the services for the government? You want to have a full time job to be able to have a home just as everyone else. But you can’t; because if you have a job earning some extra money, the government will take away the services you need such as home care. For someone like me who needs aids daily and other services I want to get a job but I can’t! It can be announcing because I know I have to have help from the government but I also want to do more with my life than just hanging around. I think that there should be a way to have some kind of job but still get what you need. If you are in the same boat I am; what do you think?
Having being born with CP, I think having a disability is not a big deal I am still able to do everything I want to. But there have been times when I am out with family or friends and I can’t get in places, lucky I have amazing people who find a way to get me in! Sometimes it’s not that easy! The disability community have the ADA to a lot of public places they should be accessible and mostly they are. There some places that aren’t, especially older buildings and some state buildings are not accessible nor many sidewalks; they may have a ramp but then you find a light post really where some of who uses a wheelchair would be able to get on to the sidewalk I have seen it many times. The ADA does help and it has given the disability community a lot; though as far as accessibility it would always more to work on.
I have cerebral palsy, so reading this letter someone wrote thanking their CP was pretty awesome! I would do the same thing; yes my cp can be hard and annoying most of the time but I know that I would be different if I didn’t have a disability. Yes I have to work harder than most, I need help with everything. I know I can’t get a normal job that annoyed me, its more because I could lose the help I need daily, I have work harder at something simple as getting people to see me without my cp. But am I happy with what I have who I am and all those quotations; yes I am!
Having a physical disability can be hard sometimes but you can explain to people how to help you or you know what works for you. A disability that can be seen you are able to teach others and also bring awareness to it. But a mental illness is not that easy to explain. Here is a reason why I think it’s harder to tell others about mental if you have depression or some kind of mental illness; I think people think it’s all in someone’s head that you have depression but as I read more about mental health is not just in their hands. Sometimes it is something that they can’t control or even something from their past that has left hurt that they don’t think they feel they can let go of. Or maybe that is just a disability. This article about someone who is sacred to tell her story just because others don’t see that having a mental illness is a disability. https://themighty.com/2017/05/scared-my-mental-illness-makes-me-hard-to-love/.
This is one reason I want to help people who feel like they can’t talk about mental health.
I have cerebral palsy so this article I like and agree with the message that having any kind of disability is not something to be afraid of or having others make fun of. Its a difference that people un-sure of, but we can teach others about different disabilities and maybe we could change the way having a disappearing is seen.
I think this article is awesome, it gives decisions of all the difference kinds of CP because there are so many ways that CP, its not one type but even knowing what kind someone has it can every from person to person. I have Ataxia is the least common form of cerebral palsy. Ataxia means ‘without order’ or ‘incoordination’. It is not a common type which can be hard sometimes; when I need to tell people about it, or I just say I have the crazy kind!
‘Ataxia is the least common form of cerebral palsy. Ataxia means ‘without order’ or ‘incoordination’ Ataxic movements are characterised by clumsiness, imprecision, or instability. Movements are not smooth and may appear disorganised or jerky. The incoordination seen with ataxia occurs when a person attempts to perform voluntary movements such as walking or picking up objects. Ataxia causes an interruption of muscle control in the arms and legs, resulting in a lack of balance and coordination.’
I haven’t done this in a while; what I’m thankful for. I just got home from an amazing week at camp. I love this camp its like I don’t have a disability. That camp is made for the disabled so everything I could do or they would find a way for me. I did things I don’t think I can do like walk through a ropes course, or rock climb! It just feels awesome going to a place where you’re not looked at as different, when in everyday life that is what you get more than I can say. I move a lot I can’t talk readily or people don’t understand what me, but there is not a big deal!
My CP can be so tight and in doing excise or anything else can be so hard, but I keep going yesterday was an tighter day. I had to go to project walk and nominally it helps. But not yesterday, I have so much that I’m excited for that it makes me tighter then normal. CP is not the same every day well least mine isn’t, that is what is the hard part of my cerebral palsy. But it’s what I have to deal with to keep moving forward, all that to say there are many people who have it hard, and may not think they could be supported but you are; your journey may be hard but you are not alone! Don’t hide you!
”No one wants to be discriminated against. No matter who you are, you have the same rights to life and equality as everyone else. This is the purpose behind the 2010 ADA Standards for Accessible Design. These standards as issued by the Department of Justice and the Department of Transportation ensure that Americans with disabilities have the same rights of access to public buildings as every other citizen of the United States.”(http://accessadvocates.com/why-the-2010-ada-standards-for-accessible-design-mean-equal-rights-for-you.)
Think about this; as if someone discriminated against when there is nothing wrong with you, you are able to do everything but someone doesn’t like something about you. That what someone with a disability feels like what we get discriminated just because we are different. We are all different the only difference between someone with a special need and the able-bodied is, year not see their disability.
what goes through your mind when you’re out and you see a parking spot for wheelchairs? Do you take it? Thinking you just have to run in for quick minute no one will notice. Like the person with a wheelchair won’t need in the time you are in the store; you may have that thought that wheelchair uses can wait or just park somewhere else. But the thing is when you have an accession van, or just a wheelchair; you are going to need the extra room to get out.those parking spots have a reason for being wider; even helping someone to get out of a car you are going to need the room. It’s not there for anyone or just for a quick stop!
Before I got my accessible van, I would need to have someone put my chair together than get me out and in the chair, my mom and I had a car park too close to the car, my mom thought we had enough room to get me in but as we tried; mom and I ended up on the ground between the two cars because there wasn’t enough room for me to get in.
This article tells more about why the disabled parking shouldn’t be a just quick run in opposition.
Last Thursday it was a great sunny day outside so I decided to go for a walk with my dog Simba. I had just got a new phone holder for my wheelchair, I wasn’t used to it yet and it didn’t have the sticky stuff that I use on everything I use because of my movements it helps if stuff does not move. But my mom and I thought with the kind of holder it is I would be fine. So I started on my walk with Simba, I went a longer way because I was enjoying being outside; my foot pad had dropped off my chair I was trying to pick it up myself because there was not one around and when trying I dropped my phone. I saw a car drive by I got them to stop and they came over to help, now I was moving a lot and they tried to hand me my phone but I couldn’t hold on to it, so they thought I couldn’t have a phone or be out on my own. So they started texting the first person in my message box I had no idea that they had texted my friend who is in an another state, they got her freaked out that something happened to me. Then they called my mom and said they found me that was all oh and where to come, the other lady called 911! While I am saying I could walk home (I do this all the time) they had my phone which has a talker app I use if I need to have people understand what I am saying but I couldn’t, they could understand me some; but when I could go on. They said they knew I could get home but they would not let me go like a was a chance that couldn’t be on their own, so just as I could see my mom walking towards me the fire truck came I started crying thinking they would take me away, like my mom couldn’t take care of me. Don’t know why I thought that but I did! So the firemen saw my mom and I and that I wasn’t hurt, he said that the ladies made this bigger than it needed to be.
I think the didn’t know anything about disabilities and I was moving so much, thinking that I was hurt but if they knew what I was saying they shouldn’t have called the firefighters just asked me what I needed.
I have a disability, I need to be on med-aid to help pay for the help I need daily and my wheelchair and others things I need. But I also want to have a job I am not one to stay home and think that became I’m disabled I don’t need to work. When you are on mad-aid you can’t work a lot or you’ll stop getting the benefits. So how could you work when you know the things that help you live a normal life might not be there if you get a job and start bringing in money; I think that they (med-aid) should help us want to work; shouldn’t let think we can’t work. Yes if we can pay for all we need out of our money than it would be different. But when people with disabilities have the thought that you shouldn’t work because of losing benefits, you wouldn’t want to get a job but if your benefit group were helping you to get to where you don’t need them it would better than making us more disabled.
Ever notice how what you have a difference or a disability, the looks you get or people think of you as an hero just because you have a disability? I get it a lot. Its not right; just because we have a disability doesn’t mean we are heroic. We were born with it or something happened we have a disability. To be a hero is more than just being disabled or because we are different, a hero is someone who always puts others first!
Knowing what I know about the ADA ( Americans with disabilities act), this article about what some states are doing to better life for so many people with disabilities I hope that Colorado and the whole world could think like this. The ADA is there to help people with disabilities have a normal life but like with anything the ADA could use an update. There are a few states that are the disabled community are working in changing some laws in the ADA to better fit the community who needs it.
You have a difference you are disabled.You want to have a normal life, you have worked hard to go to school to get a job which you can do. Your disability is what people see before anything else, what you can’t do. Your disability should not be what they think about when they are interviewing you or anyone that is knowledge about the work, but word disabled has been looked at badly that people don’t think, that being disabled could just mean different; we are all different from each other! Yes I know it just one way to look at it, but it makes since just read it more closely you will understand; or maybe when you are disabled it seems right. If we can see your disability or not no one is normal or the same so why do we think that having a disability that you can see is a big deal because it’s not; people who are disabled are just like you only thing is, you can see our difference.
This a great article about how to teach children and all people that people who have a disability doesn’t mean you have to run from them. We have a seeable disability, but you know that we are all disability in some way.
when I was ms. wheelchair 2010, my goal was to help teach families of children with disabilities, that him or her can do more than you think don’t limited them. Schools and dr’s may tell you their kind of disability but you should see how your child learns and behaves before knowing that the child needs special education, see the child before the disability. This article looks at some things that may help in that;
5 ways to improve the lives of children with a disability
by Chris Lenart | Dec 29, 2015 | Improving kids’ lives | 0 comments
Children with a disability have to be in a supported and have the same opportunities that the other kids have. For this discussion, I am going to focus on the child with a disability who is high functioning in terms of education. What I am going to say does not apply to all kids with disabilities. I am going to give you five points to think about today.
1. Allow the kids with disabilities to learn by making mistakes.
What I mean by this is that sometimes parents try to protect their child with a disability so that they don’t allow the child to fail at something. I feel that the parents want to protect them altogether because they are a person with a disability. My point is this – what will happen to the person with a disability if their parents are not around? Will they know what to do when they have to make a critical decision. When I moved into my condo almost six years ago, my dad and I had fights about how I was handling my money. Yes, I didn’t manage my money wisely, but I needed to learn the hard way. Everyone has to go through the hard times and learn from their mistakes.
2. The kids had not been taught something the right way so they don’t have learn the right way when they are on their own.
What I mean by this is that I have heard from people who have a disability that they didn’t learn math or reading properly in school. I think that this is a huge disgrace because it was not their fault from not learning at school. Basic math and reading are essential thing that you need every day. Sometimes I feel sorry for the person, but after the person says that they were cheated on their own education over and over, it gets tiring. We are living the best era of humanity because we have the internet to learn from.
3. The person with a disability can be more independent with proper technologies.
I see people with disabilities in a manual wheelchair and having a person pushes them around. If that person was me, I would go nuts. Where is the independence with having a person pushing you all around. Beside that, I know people who have a disability, can not work a computer by themselves. This blows my mind because they want to be independent. As kids who have a disability grow up, technology will get better. So why not help them learn to use technology for their benefit now. Google is working on a car that drives by itself. Technology is unlimited so we have so much to look forward in the next ten years.
4. Kids who have a disability have to have all of the opportunities that the other kids have.
In the school system and community, there are so many activities that kids have. But they don’t allow kids who have a disability to join. So there are activities that are set up for kids who have a disability. This is good to a point, but the kids with disabilities need to be with kids around their neighborhood. Integrating all kids together is the most important thing to do. The kids are most likely in the same school. If they are out of the school environment, they can socialize more. The friendship will grow at school and in the neighborhood.
5. To be a family, everyone has chores including the child who has a disability.
This might sound harsh to a point, but let me explain. Say the family has three kids and two have a weekly chore to do. Will the kid who has a disability learn responsibility? Maybe. Now if the child who has a disability has a chore, they will learn responsibility. Let’s say the child does not have the ability of doing a chore by themselves. Maybe allow the kid to work with their sister or brother. This way they learn responsibility that I feel many people who have disabilities are lacking these days. I hope that I have given you some food for thought. I don’t want to sound too harsh but after living on my own and seeing how other people with disabilities act, I have gotten to a point where I don’t like what I see.