Posted tagged ‘Bible’

WHAT DO THE DISABLED FEEL LIKE LIVING IN A WORLD BUILT AROUND AND FOR AVERAGE “ABLED” BODY PEOPLE?

October 18, 2021

PSALMS 139:14

I PRAISE YOU, FOR I AM FEARFULLY AND WONDERFULLY MADE. WONDERFUL ARE YOUR WORKS; MY SOUL KNOWS IT VERY WELL

QUOTE BY: MARTINA NAVRATILOVA “Disability is a matter of perception. If you can do just one thing well, you’re needed by someone.”

Hi all it’s me, so I guess you can tell what this article is going to be about LOL, DISABILITIES AND THE WORLD OF DISABLED PEOPLE… I know all my regular readers/followers are probably a little confused and are probably like what the heck, why have two headers? Why have the inspirational quote below the scripture verse? How could you change the look of the beginning of your articles. The scripture verse as your main headline on every article was the-book-of-roo’s statement piece, that’s what made you stand out from all the other blogs out there. If your saying that let me just say I know! You are so right, and I promise after this article I’ll never change it again🙏 The thing is, with this particular article I just felt it needed that inspirational quote even more than it needed the scripture, I almost wasn’t even going to put a scripture verse but after I started actually writing the article I than realized it still needed a scripture too so that’s when I decided ok I’ll just give it 2 headers LOL. I don’t know why it needed both but I just felt that’s where the lord was leading me and as I always tell you all, I always want to do what he’s guiding me to and not just what I think will get me the most hits on this blog or what I think will get me the most popularity points. I want to continually do what I feel his heart (the lords) is telling me, and what I felt his heart was saying today was to make that quote by Martina Navratilova the focus of this article, why? Because I felt this articles focus had to be centered around disabilities and disability awareness.

First off before I get deep into this article and it’s purpose, let me give a little update on me. I think the last time I wrote an article for this blog was around my birthday (august), so let’s start there. My summer was great, except for that minor hiccup at the end of July, I been doing really well. I havent been to active cause of Covid-19 but I’m doing what I feel I can do safely without putting me or my family in harms way. I did get vaccinated and so did most of my family, but we do have my niece to think about, she is only 10 years old so she is unable to get the vaccine right now so because of that I’m also limited on my activities because now when I do things I mostly do things with her and so I not only have to worry about my health but I also worry about hers too, and I never want to do anything that’s going to put my life and health or hers in harms way, so I haven’t done much this past year. How am I doing otherwise you ask? I am doing great, I haven’t been in the hospital since July, thank you JESUS🙏That guy named Jesus is just awesome isn’t he? LOL 🤪 don’t get me wrong, my health hasn’t been perfect but it also hasn’t been awful, let’s say it’s been manageable and at times I’ll even go as far as to say it’s been good. Other than my health not much new to report just been trying to enjoy my family and my life with my family LOL. Covid-19 hasn’t made that easy but we’re getting by and making the best of things. Book is great, should be out around New Years (for real this time).

What have I been up to you ask? Well for one writing and finalizing my book, secondly I been working hard to get my YouTube channel off the ground, and also my podcast, and speaking of my podcast it is really why I’m here, well partly why LOL. I recorded a episode a few months ago during ADA Anniversary (American with Disabilities act) it was their 30th anniversary, and so I recorded a episode with a fellow disabled friend his name is Tim Randles. we called the episode: what do the disabled feel like living in a world built around and for average “abled” body people? We discussed how we both felt in our younger years especially and we talked about different things that we both went through, and struggles that we both dealt with. After we recorded this I went to upload it but I had issues getting the podcast episode uploaded. I worked on it for weeks but still nothing seemed to be getting me any closer, I still could not get this thing to upload and so I ended up scratching the whole episode. I said: well it’s way to late to upload it now this was supposed to be for ADA 30th anniversary but it’s now a month past the anniversary so oh well I guess it wasn’t meant to be heard, but deep down I was heart broken that I couldn’t fix this because deep down I knew how important it was that this episode was heard but after weeks of trying I said: oh well I give up and I moved on with my life LOL. Well all of a sudden at the beginning of October my friend (the same friend who I recorded the episode with) he said: hey you know it’s dwarfism awareness month and he ended up writing this whole article on his own blog about dwarfism and when he wrote what he wrote I immediately said to myself, oh my gosh! This is my second chance to upload that podcast episode. I immediately got working on it and finally after doing some digging around I not only figured out why I originally could not get this thing to upload, but also figured out how to get it uploaded, and by October 4th, I think it was the 4th, I had the episode uploaded for all to hear, THANK YOU JESUS🙏 so if you all want to go listen to that you can by clicking the link👇 or by going to whatever application you listen to your favorite podcast shows and search THE-BOOK-OF-ROO, or you can just type in Roo and it should pop up by just typing that too, and once you search you should see not only our name but also our logo.

THE-BOOK-OF-ROO PODCAST LINK

As some of you know besides writing/blogging/vlogging and doing all the more serious things I do on social media I also have a tiktok page where I do more funny/quirky/silly things, things to just have fun and try to have something more childlike where I could focus on having a little fun and not be so serious. I also started the page because I wanted a outlet to show people they can be silly around people like me, and it’s ok to even mention our disability and maybe even acknowledge it😱

So when I made the page I purposely made every video title start with “the 2FT crippled lady” Now when I did that yes I purposely did it because I knew it be something that would catch people’s eye and catch them off guard a little, but never in a billion years did I think it would become the big deal that it’s becoming. About 2 months after I made the page a friend/family member came up to me and said: I like your videos but I’m not to happy that your calling yourself the “crippled” lady. I gave them my reasons for why I did that and also explained my views on that word and explained to them that the word was not a bad word. Well fast forward about 3 weeks and all of a sudden I started getting contacted by several people who follow me on tiktok and other social media pages, when I say several, I mean several, especially by DM (direct message) and all these people were saying the same thing, one woman even said to me, why do you have to use crippled why can’t you say unique lady, which like I said in my YouTube video👆 I find it is a little comical that people do not have a issue with 2FT lady, 2FT lady is not a issue at all, the only issue is crippled lady. I decided the only way to solve this problem was to face it head on, and so I made the YouTube video that is listed at the top of the page and I explain my views on this word “crippled”. Like I stated in the video, crippled is not a “bad” word, if you look up the word crippled it almost means the exact same thing as the word disabled, actually if you google the word crippled their explanation of that word is actually nicer sounding than the word disabled. The problem isn’t the word, or “words” it’s our outlook on the word and so I will continue to use the word “crippled” until people feel more comfortable about it. Like I said in the video, being disabled is not a terrible thing, yes there are aspects to it that are terrible but it in it self isn’t. I have still been able to live a very fulfilling life and my disability has not stopped me from doing anything I’ve wanted to do. Yes some things I’ve had to work harder than the average person but I’ve still been able to accomplish everything I’ve ever dreamed up.

No matter if your disabled or not I can almost guarantee that you all have had struggles, you all have had an ability that didn’t come perfectly, you have all been crippled in one way shape or form in your lives, you may not realize it but you have. Maybe your scared to ride a bike, maybe you have panic attacks, maybe you have financial issues, marriage issues, issues with your children, those are all forms of being crippled, just because my crippled-ness is more visible doesn’t mean it’s any different, the word isn’t the problem, the problem is us for giving that word so much power! Me being crippled is just a small piece of who I am. I am strong, courageous, and wonderfully made. That’s really all I have for today but after your done reading this reach out to me in the comments on this blog or on YouTube or in any of my various other social media pages and let me know your outlook on the word “crippled and let me know if you learned something from this article, as always thank you for reading this and for supporting me, I truly do appreciate it and am grateful for each and every one of you🙏 I love you all God bless and remember keep shining everyone! 😘

Hey all don’t forget about my Patreon Campaign. A Patreon Campaign is basically a partnership. There’s different dollar amounts you can commit to giving. There’s one as low as $5.00 and what I like about this program is, it is not just about giving, it’s about giving and receiving. To all those who commit to giving. There are different prizes/gifts you all get in return for giving. For example: Anyone who commits to donating $50 a Month. I will send you a THE-BOOK-OF-ROO magnet, a OI CAN DO ALL THINGS wristband and I will give some Perfectly Posh Products. That’s just the $50 level reward but there’s some other great rewards on the site too plus anyone who joins no matter how much they commit to giving. They will automatically be among the first to receive my book. So check it out.  Patreon Page Click here

THE-BOOK-OF-ROO has options now! If you all are looking for a way to reach me on a more personal level, or maybe want to send a cash donation you can do that now. Please send any cards/Letters/Gifts to this PO Box. PO BOX: THE-BOOK-OF-ROO

4496 Mahoning Avenue #911 Youngstown, OH 44515

Please remember you can still also donate by clicking the donate button that is located at the bottom of this and all other articles located on THE-BOOK-OF-ROO.

I THINK THATS IT FOR TODAY. THANKS FOR READING AND SUPPORTING ME AND THE-BOOK-OF-ROO. GOD BLESS AND PLEASE REMEMBER KEEP SHINING FOR CHRIST. BECAUSE HE NOT ONLY LOVES YOU, BUT ADORES YOU. ALSO PLEASE REMEMBER IF YOU NEED PRAYER I AND THE-BOOK-OF-ROO READERS ARE HERE TO PRAY. JUST STOP BY OUR PRAYER PAGE AND POST YOUR PRAYER REQUEST AND I PROMISE WE WILL PRAY 😇 ALSO PLEASE REMEMBER AS I SAID EARLIER, RUNNING THIS WEBSITE AND WRITING/PUBLISHING A BOOK DOES ALL COST MONEY. SO IF YOUR FEELING LED PLEASE DONATE TO MY SITE. ITS VERY EASY TO DO. WE HAVE MANY OPTIONS NOW BUT THE EASIEST OPTION IS JUST TO CLICK THE “DONATE” BUTTON AND FILL OUT THE FORM. PLEASE KNOW I AM GRATEFUL FOR EACH AND EVERY DONATION THAT COMES IN NO MATTER IF ITS THROUGH THE PATREON PAGE, PO BOX OR PAYPAL. GOD BLESS, I LOVE YOU ALL AND MORE IMPORTANTLY JESUS LOVES YOU. KEEP ON SHINING FOR CHRIST ❤️

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ROO YOUR 2FT TALL CRIPPLED LADY DOING A VLOG/BLOG & SHARING WHAT WISHBONE DAY IS.

May 8, 2021

1 PETER 3:9

DO NOT REPAY EVIL WTH EVIL OR INSULT WITH INSULT. ON THE CONTRARY, REPAY EVIL WITH BLESSING, BECAUSE TO THIS YOU WERE CALLED SO THAT YOU MAY INHERIT A BLESSING

Hi all it’s me, I’m back! Did you miss me? Hehehehe 🤪 this is going to be another short and sweet blog because I said most of what I wanted to say in my Vlog, which you can watch the Vlog at the link above 👆 the Vlog is mostly me talking about what wishbone day is and why the day is so important and special to me and my family and the entire O.I (Osteogenesis Imperfecta) community. I had such a good day and I truly do thank everyone who made it so special for me, you all are amazing and I’m so blessed to have you all, not many disabled people are as blessed as I am. There are so many people in the disabled community who do not have that, so many families give up their children who have O.I and so many people who don’t even have a support system, God blessed me beyond what I could have ever imagined when it comes to that stuff. Most of my family is whole heartedly in this fight called O.I right along with me, they are there not only cheering me on and uplifting me, but also caring for my every need, no matter if it’s a physical need or emotional, they are whole heartedly there with me and I truly do know how blessed I am for that. I have been in so many hospitals where I look around at the other patients and their so alone. One of the last times, not the last but one of the last, I was in the hospital getting ready for a very, very minor surgery and I had both my parents on each side of my bed and they were both arguing about which one got to take me into the operating room. Than I happened to look over in a bed next to me and there was this young boy sitting there, no older than 12-13 and he sounded very bitter, very angry and very alone and I happen to over hear the woman talking that was with him. She happened to be a caseworker and he was in foster care and he was having a pretty major surgery and you could just see how alone, terrified and lost this kid was and of course because he was scared he kept lashing out at the caseworker, but honestly the caseworker was so rude and selfish, and so, let’s get this over with so I could go home attitude that I would have lashed out at her too. It was all over her that she did not care one ounce about this kids well being, all she cared about was getting the job done so she could go home, and it broke my heart because all that kid wanted was for someone to act like they gave a crap about him, all he wanted was to be thought of. I don’t think he was even desiring love at that point, all I think he desired was for someone to show him compassion.

Than after I experienced that I went to surgery and when I came back there happened to be this beautiful little girl in a bed right across from me and she was no older than 7-8 years old and she had just come out of a even more major surgery, such a big surgery that she was on a ventilator, but she was very much awake and knew everything that was going on, and when she woke up from her surgery she was looking all around the room and started getting really anxious and so the nurse tried to calm her down by telling her she’s ok and that her mommy would be back as soon as she could but she had to go to work. This little girl was terrified and again was alone and had no one, and I know as your all reading this your probably starting to get all judgmental and probably saying: how dare that mother choose work over being with her baby girl, but you see the thing is it’s easy for us to judge, but we don’t know that families full story. I know the child’s home and mothers work was over an hour in a half from the hospital because I heard the nurse say it. That mother kept calling the hospital every five minutes so I know it was killing her not to be there. We don’t know why she chose work over her kid, maybe she’s a single mom, maybe she has more than one child, maybe she has to work her butt off to pay for her daughters medical needs, again we don’t know the full story but I can promise you she wasn’t absent just because she was a bad mother. So your probably asking yourself now what is my point to bringing up these kids stories? My point is not everyone is blessed enough to be born into a family that’s going to be able to be there the way we need or desire. I was blessed because my parents were an amazing team, they had an incredible partnership and so when one was down and maybe not able to juggle all those balls that parents who are raising disabled children have to juggle, the other one was right there to catch those falling balls. I never once went to a single surgery without either of them, they both were always there holding my hand.

Average, “abled” body people do not realize the things us disabled people have to deal with, from insurance, to education, to jobs, to medical things, to bills, to finding ways to pay for medication and equipment that we need. I mean for example, I can’t even easily go out and visit people in their homes like I used to because even that is becoming a huge challenge and people always think it’s me just trying to be lazy or pull the sick card but it’s not! Not only is it a challenge for me to go out because physically it drains the life out of me, but also it can become very stressful, not only is it stressful because of my medical problems but it is also becoming stressful because most houses and even buildings are not totally wheelchair accessible, especially in Ohio, heck not even our streets are accessible, and so that has become a major challenge, especially when visiting people at their houses. A lot of people say to me, well you figured out ways to do it when you were younger so why can’t you figure out ways now? But here’s the thing, when I was younger my family and friends were also younger LOL. It was very easy back than because if for example, I wanted to go visit someone at their house and they had steps. My family and friends would just carry me and my chair right into the house, but that’s not possible anymore because even though I never got any taller, I still got heavier LOL. I used to only weigh anywhere from 15-20 pounds, where now I weigh 39-42 pounds, that’s a huge difference, it’s a lot easier to carry 15 pounds up stairs than it is to carry 40 pounds, and people can’t carry my chair in anymore because my chair, with me and my oxygen weights close to 200 pounds, you try lifting 200 pounds. The chair is 100 pounds, the oxygen tank is another 15-20 pounds, the 2 bags I have strapped to the chair weights probably another 15-20 pounds, it literally has all my supplies that I need to survive and than my body weights 40 pounds so add that all up, that’s like 180-190 pounds! So there’s no way 60 something year old people could lift that, especially when one of those people are battling a terrible, debilitating form of arthritis. I love when people suggest for my 65+ year old parents just carry me into the house like I’m a toddler, number one thats not even possible anymore because of the fact that I weigh 40 pounds, I’m to heavy to even just lift, secondly I’m on oxygen so your not only asking for them to carry my body but than also my tanks, which I also than have to unstrap because their literally strapped onto my wheelchair and let me tell you, taking that a part is not easy, secondly where am I supposed to go if I’m carried in? Am I supposed to sit on my parents lap the entire time like I’m a little kid. I mean you all do realize how degrading that even is for people like myself, we’re not kids. I’m almost 35 years old! Do you really think I’d be comfortable sitting on my mommies lap still? Get real, I love my mom but come on people LOL.

These are just some of the challenges that disabled people face that society really has to open their eyes to. After that cop in the George Floyd case was sentenced I told all my friends, no matter who or what race they were. I was so excited to see justice was served and I was so excited to see some light shining on the way people of different races and especially the African American community are treated. I told my friends I really pray we achieve equal rights finally, but that African Americans and asians and even the LGBTQ community and every other community out there that’s fighting for the right to be treated as a equal. I feel your pain, I truly do, and I’ll be honest, when I said that, especially to a lot of the African American community, they got very upset and I think they thought because I was a white Girl I couldn’t possibly understand how they felt. They said I nor my family or friends knew what it was like to be murdered just because of the color of their skin and to a certain degree their right, but here’s the thing. Just like they keep telling me and all white people to educate ourselves they need to do the same and educate themselves on the disabled community. Because the reality is we were murdered, we may not have been murdered for the color of our skin but we were murdered for the fact that we looked and acted different. They basically treated us like caged animals, especially in the 30s-40s 50s 60s and even a little in the 70s. We were not only being murdered but were being locked up in literal cages and treated like we were a friggen monkey at the Circus, if you don’t believe me look it up for yourselves and no I’m not just referring to what hitler did to us, even though that was awful enough all by it self, somewhere around 40,000 disabled people were murdered by him, but not only was that awful but there are tons of other stories just like that where people murdered us and treated us like animals, and the sad part is a lot of it was said to have been done all in the name of science. There’s a great movie called breathe and it’s about this man who developed polio and the story was based on a true story. I won’t give the movie out plot out, but there’s a part in the movie where hospitals and society tell this man that he has to live the rest of his life in a medical facility, in the movie they told him and his wife that they didn’t have a choice, it was the law. If you were disabled and needing medical care you were automatically put in a facility and every single person just accepted that, until this man. This guy was one of the first to realize that even if you were disabled it didn’t mean your life was meaningless. This particular guy was not only young but he also had a wife and his wife just had a baby literally right when he started getting sick so he knew even though he was disabled he still had a future, he had his wife and more importantly his child and so he fought for the right to go home and fought for the right to be a father to his child. He made the doctors and hospitals figure out ways to run his equipment at home and he just enjoyed what time he had left at home with his wife and supposedly that’s where it all started, that’s where Doctors and the medical community started opening up their eyes to the fact that disabled people were not just some brain dead mutant lifeless pile of flesh but that we were living breathing human beings and we had desires, thoughts, feelings and dreams just like the rest of society.

So why bring all this up? Well for one to educate you all and to open your eyes to see that your not alone, no matter if your fighting racism or any of the other things I previously mentioned your not alone, and we not only feel your pain, but we desire to be respected and seen just like you all, but the difference with us is the fact that we’re a much smaller community than you all so we are overlooked and not heard the way most of you are heard and so that’s why, instead of fighting and debating one another about whose pain is deeper, let’s instead come together and help support each other, hold each other up and fight for each other’s right to be respected and seen. We the disabled community need you abled body people we need you to be loud with us and show the world that we are important too.

So how do we do that you might be asking? Well number one educate yourselves, secondly be loud, just like you all helped us be loud on wishbone day, be loud every day. Write our governors, our president, and everyone else who will listen and also share articles like this, share vlogs and support us, and if your in the work place and a disabled person comes in asking for a job, actually interview them and take them seriously, give them the respect to at least try to see beyond their disability.

I just wanted to touch on one last thing before I end, I read an article in our local news paper, actually my mom pointed it out to me, but anyways, in the article it was talking about how so many people are fighting on social media outlets because they feel their being silenced and I think it’s so sad because so many Christians are feeling that way too, but here’s the thing. I don’t think anyone’s deliberately silencing anyone, I just think we’re letting are imagination get the best of us. What I think their doing is trying to control the madness, and what I mean by that is their trying to control the fake news. There are so many conspiracy theories out there and they are just trying to shut those down. For instance so many people were spreading rumors that covid was fake and because so many people started sharing these conspiracy theories, people than started to believe in them and because people were believing them, those theories were than killing more people, I know for a fact this virus is real, I have lost some of my friends to this virus, I also almost lost a man who is like an uncle to me so I whole heartedly know it’s real. The whole capital riot, that all was put together by using social media, where again people were murdered and that all could have been avoided if the owners of social media just controlled things better, so now that’s what their trying to do. Unfortunately they don’t have a radar that can just tell them this dudes normal and that dudes a wack job, trust me I’m sure they would love to have a radar like that, but unfortunately they don’t. All they have is algorithms. What that is, is a program that tracks everyones moves, it tracks what words we use, how we use them, what kind of articles we post, and what it does is than calculates everything and if, for example you post an article that has been shared 500,000 times and yet they have gotten 300,000 reviews saying this article is fake news, than that program automatically shuts that article down and it can no longer be shared, because to the computer program it’s a site that is considered potentially harmful to its users. That’s how all this works it’s not “social media” shutting stuff down exactly, but honestly it’s you and me, because theirs people on the net who purposely keep reporting certain things so that it looks like it’s social media shutting stuff down, but in reality its “trolls” (computer hackers/nerds) putting all that in motion to make these conspiracy theories look more real and justifiable, and the reason president trump got booted off most of social media is because he likes to fight back, which sometimes yes can be a good thing, but some times you have to learn the right ways to fight back. I don’t like to get into politics but the fact he made fun of a person with a disability was heart breaking to me and it’s heart breaking to see so many people who call themselves Christians and who say they support me but than also are supporting a person who straight up mocked a person for having a disability. I would like to ask you, if it was any other human making fun of a disabled person, and let’s go a step further, let’s make it personal, if this person was making fun of me would you all still be justifying the behavior? And please don’t tell me he wasn’t making fun of a disabled person because he was, he was bending his fingers and hands and talking like he was slurring his words because he was mocking a man who was disabled. I have bent arms, when I talk my words don’t come out clear, I don’t slur my words but because I have a bent jaw and no top teeth I definitely have a lisp and my words sound all muffled when I speak, I know this about myself, I’m not ashamed of it. I am someone who has almost died a dozen times so do you really think I’m going to care about my looks or the sound of my voice LOL, HECK NO! I have been through hell and back keeping this body of mine kicking so I’m going to love every ounce of it no matter what and I’m going to see myself the way christ sees me, but my original point to saying all that is, would any of you who know and love me be ok with someone mocking me like that? I already know the answer is no you wouldn’t be ok with that, so my real question is if we wouldn’t be ok with that in any other way, shape or form, than why are we trying to convince ourselves that trump mocking.another disabled person is ok?

Like I told a few of my friends, if you want to support trump great go ahead I’ll support you, if you want to fight back and help him get on social media again, great more power to you, but until that moment happens just calm down, stop getting yourselves so upset that your making yourselves sick, and stop throwing a tantrum and stomping your feet on the ground like a 5 year old and saying on social media, I’m not coming back on my page till Trump is back! Really guys? Like really? You really think that’s going to achieve what you want. There’s certain rules everyone has to abide by in the world of social media, it’s not just trump, we all have these rules. When I was a kid? I lost one of my accounts for not following the rules and I was warned just like he was warned, but I ignored the warnings and eventually lost my account and that’s exactly what happened here. He broke the rules, it took me 2 years before I could get my account back,so what their doing to Trump is not uncommon and it’s not because he’s “trump”, if anything their trying to treat him like they would anyone who breaks the rules, trust me even though they don’t agree with his political views, it’s killing them to ban him, you know how much money their losing, trust me their desire to make their millions trumps (no pun intended) their desires to stand for their political views. So instead of being so angry that you throw a tantrum do your research and make sure the outlets your going to, to read this research is reliable sources, and once you do, if your still frustrated and angry and if you still feel your being smothered and silenced than just fight back. Humble yourselves enough to be still and know he is God and he will work all things together for good and he will teach you that some times the best ways to fight back and shine his light is just to be still and love, live out love, it’s easy to love those who love you back, but can you be loving to those who you may think doesn’t deserve it? That’s what being a Christian really is and I’m sorry to say but most Christians are failing this challenge and it’s breaking the Lords heart. So do what 1 Peter 3:9 says. Let’s really be what we’re called to be!

Wow this Vlog/blog was much longer than I anticipated sorry, but once I started writing I just felt the Lord telling me to add more and more LOL. I hope you all have the patience to read all this LOL. God bless, I Love you all and you will be seeing me again real soon 😘

Hey all don’t forget about my Patreon Campaign. A Patreon Campaign is basically a partnership. There’s different dollar amounts you can commit to giving. There’s one as low as $5.00 and what I like about this program is, it is not just about giving, it’s about giving and receiving. To all those who commit to giving. There are different prizes/gifts you all get in return for giving. For example: Anyone who commits to donating $50 a Month. I will send you a THE-BOOK-OF-ROO magnet, a OI CAN DO ALL THINGS wristband and I will give some Perfectly Posh Products. That’s just the $50 level reward but there’s some other great rewards on the site too plus anyone who joins no matter how much they commit to giving. They will automatically be among the first to receive my book. So check it out.  Patreon Page Click here

THE-BOOK-OF-ROO has options now! If you all are looking for a way to reach me on a more personal level, or maybe want to send a cash donation you can do that now. Please send any cards/Letters/Gifts to this PO Box. PO BOX: THE-BOOK-OF-ROO

4496 Mahoning Avenue #911 Youngstown, OH 44515

Please remember you can still also donate by clicking the donate button that is located at the bottom of this and all other articles located on THE-BOOK-OF-ROO.

I THINK THATS IT FOR TODAY. THANKS FOR READING AND SUPPORTING ME AND THE-BOOK-OF-ROO. GOD BLESS AND PLEASE REMEMBER KEEP SHINING FOR CHRIST. BECAUSE HE NOT ONLY LOVES YOU, BUT ADORES YOU. ALSO PLEASE REMEMBER IF YOU NEED PRAYER I AND THE-BOOK-OF-ROO READERS ARE HERE TO PRAY. JUST STOP BY OUR PRAYER PAGE AND POST YOUR PRAYER REQUEST AND I PROMISE WE WILL PRAY 😇 ALSO PLEASE REMEMBER AS I SAID EARLIER, RUNNING THIS WEBSITE AND WRITING/PUBLISHING A BOOK DOES ALL COST MONEY. SO IF YOUR FEELING LED PLEASE DONATE TO MY SITE. ITS VERY EASY TO DO. WE HAVE MANY OPTIONS NOW BUT THE EASIEST OPTION IS JUST TO CLICK THE “DONATE” BUTTON AND FILL OUT THE FORM. PLEASE KNOW I AM GRATEFUL FOR EACH AND EVERY DONATION THAT COMES IN NO MATTER IF ITS THROUGH THE PATREON PAGE, PO BOX OR PAYPAL. GOD BLESS, I LOVE YOU ALL AND MORE IMPORTANTLY JESUS LOVES YOU. KEEP ON SHINING FOR CHRIST ❤️

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