Showing posts with label Autism. Show all posts
Showing posts with label Autism. Show all posts

Monday, March 30, 2015

Update....

Through the months, many have asked why I do not blog anymore. In all reality, lack of time was my primary reason, however, after spending so much time catching everyone up via email and FB, I think blogging is less time consuming!

I'm going to change things up a bit and just do a brief outline with more details coming later. I'll break down the individual points into more detailed blogs later.

Also, I'm going to veto keeping the children's individual blogs updated and put all the information here. You'll be able to search the blog via keywords though.... so if you are here looking for info on diabetes, just search for that word.


First, let's address the children.

My eldest is in his second semester of college and is doing great. Due to his Aspergers, we had to obtain him a tutor that would prevent him from doing too good of a job. Yes, you read that right. He would fixate on making his work perfect, and in 3D modeling perfection can be very time consuming. His tutor tells him when it's an "A" grade and time to move on. Well, his tutor is very helpful in other ways as well, but that was our initial reason for acquiring a tutor.


In addition, his Type 1 Diabetes is still difficult to manage. It's never easy having Type 1, however the Aspergers means he's unable to make executive judgement calls when it comes to managing his diabetes.   Due to his being so skinny, his CGM (Continuous Glucose Monitor) isn't effective and gets false readings regularly. I'll explain this more in a future blog.

Also, another diagnosis of chronic depression and anxiety has come on board resulting in our finally opting for medication. We're only on week two, so we'll see how it goes.


My middle child, as always, is excelling. I'd lose my mind without her. She has so much responsibility yet takes it in stride. She is a straight A student this semester and is working towards her dreams. Her dreams, although the same since 2 years old, have changed. Instead of being a veterinarian working with abused and neglected animals, she intends to be an Animal Behaviorist rehabilitating abused and neglected animals. Yeah....that's MY GIRL! :) I have no doubt the change in her interest came as a result of our having to put down a dog that had killed two dogs and injured two others. Rehabilitation services would have costed us $5k that we didn't have, and didn't seem to be able to raise. It impacted our entire family deeply and was the stimulus to alter her focus.


My youngest, well, he's still high maintenance. He's always moving though has slowed down some due to a back injury. Raising him is a tough job, and many days I'm dumbfounded by his perfect logic. Of course, perfect logic doesn't fit into this society so it's often difficult for him to comprehend what is considered appropriate and what is not. I often hear him say that he wishes he were not Autistic. :( Again, more details later.

Now, as for me......... I have a new diagnosis that consists of nerve damage in my arms/hands due to inflammation within the elbow. It's very painful and driving, typing, writing and any repetitive hand/arm movements make it worse (another reason I've not blogged as much). I have to have an EMG done, which is a test I swore a decade ago I'd never have done again. It's painful, and no fun, but we have to determine the extent of the nerve damage to determine how to proceed.

Nothing else has really changed health wise. My MCTD still kicks my butt. I still have to spend entire days in bed and watch my house fall apart. I still end up in pain that is so bad I would crawl into the Grim Reaper's embrace should he appear beside my bed at those times. I still look for the beauty in every day and cling to that beauty as my "happy thought". I still laugh about it, cry about it, and wonder why I can't remember what it felt like not to be in pain.

However, I graduate this May. It took longer then it should have, and lots of extensions from various instructors, but I did it. Yep, I'll be graduating college! I also am going to be starting my own business since my health and my children do not allow me to work a 9-5. I have an investor that will make this possible and I'm beyond psyched.

Also, I've been in a dating relationship for almost a year. You may have seen me write about dating with chronic illnesses, and/or dating with children with special needs. Maybe you've read what I've written about dating when you suffer from PTSD due to past abuse. Let me assure you, it is not easy.  However, I feel that I have grown more in my time with him then I have in the last couple of years. I've written before about how I felt I had hit a plateau in my personal growth as I wasn't able to put what I'd learned into practice. Well, now I have and it is a hard road. Yet, nothing that I've ever had in life that was good came easy.


He and I work. We are good for each other and when we set our minds to it, we make an amazing team. He gets along well with the children.

He doesn't understand me. He's had an easy life. He wears beautiful rose colored glasses that leave me amazed, dumbfounded and even infuriated at times. Yet, his rose colored glasses are helping me to remember that life isn't difficult for everyone and that is a big part of why some can't understand the struggles of others. His rose colored glasses keeps me from hating mankind.

His rose colored glasses also help me to see things from a perspective I was never afforded. He believes in things I deemed impossible before I was even out of elementary school. He tells me that he is a realist and I believe in fairy tales. Yet, in my mind, I see him believing in fairy tales and I the realist. You see, we balance each other out and each bring to the table something that the other hasn't been exposed to.

I always thought I had to be with someone that had been through horrible things. How else could he understand me? Yet, this relationship has taught me that I was wrong. Don't get me wrong, he's not perfect, and he has plenty of baggage from his past relationships that he is working through as well. However, at the end of the day, he doesn't have to understand me to love me. He doesn't have to understand me to support me. Just as I love him and support him yet can't understand how he can wear those beautiful rose colored glasses, he can love and support me without understanding why I view life as a dark journey where one must actively seek the beauty.

Opposites may not attract, but they can co-exist together. It's a difficult journey, but, in our case, is having the most magnificent results.

More updates coming soon. I know that there are many that come to my blog because they want to know they are not alone. Those that come just to read my struggles with chronic illness. Those that come to read about raising children with special needs children. Those that come to read about PTSD. I know that I clammed up over the last couple years, and left a lot of people feeling abandoned. I didn't speak out much about what caused that to happen and in all reality, not quite sure I want to now.

However, I will make my best effort to be there NOW. I can't change the past....but I am always changing my present and future.

As always, to all those that are recovering from substance abuse, have survived rape, gang rape, domestic violence, child abuse, molestation, religious abuse and the like.... you CAN move forward and have good things in life. Keep your chin up. You are worthy.

To those battling chronic pain and chronic health conditions.....you too can have good things in life. Don't give up. Fight the fight with every breath. You are stronger than you believe.

This one is for the full time single parents raising children with special needs......that would be the parents that do not get time off when their child visits the other parent, nor do they get child support, nor do they have family support to assist.....there doesn't seem to be many of us out there. Our lot in life is unique. No one else can understand what we go through and each time we hear people tell us we are an "inspiration" or "a superhero" or "amazing", we secretly want to punch them repetitively in the face. Remember that you aren't alone. I'm here and I know your struggles. I know the tears you cry, the times you hide in your shower, and the times that you are certain you will die from exhaustion. If you, like me, suffer from your own health issues on top of it.....well, we are a very elite group that are scattered around the globe. Just remember, you aren't alone. Never alone. There are always those that look up to the sky and wonder if anyone else knows what they feel like. And the answer to that, my dear friend, is yes.




*****All photos courtesy of Rena Linder******

Monday, January 5, 2015

Aspie Curtain


All my life I have struggled to belong.
Always being told your doing it wrong. 
Most of my thoughts I kept inside.
Never really knowing who to confide.
Knew every answer never had to study.
No true friend just the occasional buddy.
Always in trouble for speaking out of turn.
Proper social skills so hard to learn.
Eye contact was a troubling thing.
I'd rather just hum, whistle or sing.
Then one day a thought came to be.
Asperger's syndrome is this part of me.
Looking back all the signs were there.
My life became oh suddenly clear.
For this is me I am now so certain.
Out from behind this Aspie Curtain.


Guest Blog
January 5, 2014
By Aspie Santa


Thursday, August 7, 2014

T1D Aspie : College Dreams




Check out what this guy's dreams and ambitions are!

Allow me to introduce myself. My name is Keegan. I turned17 years old a month ago. I have Aspergers which is a form of Autism. I also have Type 1 Diabetes, which was diagnosed September, Friday the 13th, of last year. Since I was 4 years old, I've had serious immune system issues that specialists have not been able to accurrately diagnose. Since they haven't been able to diagnose me, you can't treat an undiagnosed illness. That means that I can't really get the help I need. For me personally, it means I get exhausted easily and sometimes end up in hospital for large amounts of time. I get sick easily also. Something really cool is that I have Situs Inversus Totalis. This means that all my organs are on the opposite side. For all you Trekkie fans out there, Situs Inversus plus Aspergers means I'm a Vulcan because with Aspergers I think very logically. I also suffer from migraines (from mind melding too much). I have severe allergies to everything environmental (everything that has to do with outside such as trees, flowers, grasses, hays, molds, etc). Except penicillin.
Because of my Aspergers, I don't have common sense. So I joke around with everyone about it. When I do something that doesn't makee sense, people say, “It's not rocket science” and I say, “If it was rocket science, I'd get it!”
Because of Aspergers and my health issues, I have a hard time concentrating and I get distracted easily. I also stay pretty weak. This makes it hard for me to get a job, attend a full course load in college, drive, and take care of my own needs.
My dreams are to go to college so that I can have the knowledge to create video games. I want to create fun video games that will help people with special needs develop the skills they need in real life. For example, a game that will teach them to interact with neuro-typicals. Or, the game might help them to undersand facial expressions (we have problems with that). I want the games to be an exciting game that you'd find on a top seller list.
Also, as I sale these games, I will donate a percentage of profits to different non-profit organizations that help kids with special needs such as Aspergers, Type 1 Diabetes, Cerebral Palsy, etc.
As of today, I am OFFICIALLY enrolled in college. I have enrolled in an Associates Degree progam in Simulation and Game Design. I am excited. But, I don't have everything I need for college. Our family does not have the money needed to get my stuff for college. I also have a pell grant but it's not enough to cover everything I need. It will cover tuition costs though.
In addition to tuition, I also need the following:
*Basic school supplies (binder, notebooks, pencils, pens, sketch pad, etc)
*A computer that ideally will have an i7 processor, a nVidia 850 graphics card, and at least 16gb ram. This is needed because of the work we'll be doing in class on the computer.
*Transportation costs to get back and forth to the campus
*An external hard drive to back up all data
*Books for courses
I feel kind of bad for asking people for money because I never do. I am used to living on what little funds we do have so I can't really get the stuff I want or need. I really want to go to college because it will be something I can do that will help me make money and that I can do while resting (so I don't get to worn out). I will also be able to make money so I can help others instead of people offering to help us.
Any amount of money will be of help. Thanks in advance for helping out. Once able, I will always help people out.
Any extra funds that are left over in my educational fund when I'm done with my degree will be donated to anybody else I find that has special needs and needs help with college.
Thank you for your help in following my dreams.
Sincerely,
 Keegan Duffy


PS. My courses start on the 18th and I hope to have all supplies before then!
- See more at: http://www.youcaring.com/tuition-fundraiser/t1d-aspie-college-fund/215548#sthash.ijQ1bBlD.dpuf
Allow me to introduce myself. My name is Keegan. I turned17 years old a month ago. I have Aspergers which is a form of Autism. I also have Type 1 Diabetes, which was diagnosed September, Friday the 13th, of last year. Since I was 4 years old, I've had serious immune system issues that specialists have not been able to accurrately diagnose. Since they haven't been able to diagnose me, you can't treat an undiagnosed illness. That means that I can't really get the help I need. For me personally, it means I get exhausted easily and sometimes end up in hospital for large amounts of time. I get sick easily also. Something really cool is that I have Situs Inversus Totalis. This means that all my organs are on the opposite side. For all you Trekkie fans out there, Situs Inversus plus Aspergers means I'm a Vulcan because with Aspergers I think very logically. I also suffer from migraines (from mind melding too much). I have severe allergies to everything environmental (everything that has to do with outside such as trees, flowers, grasses, hays, molds, etc). Except penicillin.
Because of my Aspergers, I don't have common sense. So I joke around with everyone about it. When I do something that doesn't makee sense, people say, “It's not rocket science” and I say, “If it was rocket science, I'd get it!”
Because of Aspergers and my health issues, I have a hard time concentrating and I get distracted easily. I also stay pretty weak. This makes it hard for me to get a job, attend a full course load in college, drive, and take care of my own needs.
My dreams are to go to college so that I can have the knowledge to create video games. I want to create fun video games that will help people with special needs develop the skills they need in real life. For example, a game that will teach them to interact with neuro-typicals. Or, the game might help them to undersand facial expressions (we have problems with that). I want the games to be an exciting game that you'd find on a top seller list.
Also, as I sale these games, I will donate a percentage of profits to different non-profit organizations that help kids with special needs such as Aspergers, Type 1 Diabetes, Cerebral Palsy, etc.
As of today, I am OFFICIALLY enrolled in college. I have enrolled in an Associates Degree progam in Simulation and Game Design. I am excited. But, I don't have everything I need for college. Our family does not have the money needed to get my stuff for college. I also have a pell grant but it's not enough to cover everything I need. It will cover tuition costs though.
In addition to tuition, I also need the following:
*Basic school supplies (binder, notebooks, pencils, pens, sketch pad, etc)
*A computer that ideally will have an i7 processor, a nVidia 850 graphics card, and at least 16gb ram. This is needed because of the work we'll be doing in class on the computer.
*Transportation costs to get back and forth to the campus
*An external hard drive to back up all data
*Books for courses
I feel kind of bad for asking people for money because I never do. I am used to living on what little funds we do have so I can't really get the stuff I want or need. I really want to go to college because it will be something I can do that will help me make money and that I can do while resting (so I don't get to worn out). I will also be able to make money so I can help others instead of people offering to help us.
Any amount of money will be of help. Thanks in advance for helping out. Once able, I will always help people out.
Any extra funds that are left over in my educational fund when I'm done with my degree will be donated to anybody else I find that has special needs and needs help with college.
Thank you for your help in following my dreams.
Sincerely,
 Keegan Duffy


PS. My courses start on the 18th and I hope to have all supplies before then!
- See more at: http://www.youcaring.com/tuition-fundraiser/t1d-aspie-college-fund/215548#sthash.ijQ1bBlD.dpuf
Allow me to introduce myself. My name is Keegan. I turned17 years old a month ago. I have Aspergers which is a form of Autism. I also have Type 1 Diabetes, which was diagnosed September, Friday the 13th, of last year. Since I was 4 years old, I've had serious immune system issues that specialists have not been able to accurrately diagnose. Since they haven't been able to diagnose me, you can't treat an undiagnosed illness. That means that I can't really get the help I need. For me personally, it means I get exhausted easily and sometimes end up in hospital for large amounts of time. I get sick easily also. Something really cool is that I have Situs Inversus Totalis. This means that all my organs are on the opposite side. For all you Trekkie fans out there, Situs Inversus plus Aspergers means I'm a Vulcan because with Aspergers I think very logically. I also suffer from migraines (from mind melding too much). I have severe allergies to everything environmental (everything that has to do with outside such as trees, flowers, grasses, hays, molds, etc). Except penicillin.
Because of my Aspergers, I don't have common sense. So I joke around with everyone about it. When I do something that doesn't makee sense, people say, “It's not rocket science” and I say, “If it was rocket science, I'd get it!”
Because of Aspergers and my health issues, I have a hard time concentrating and I get distracted easily. I also stay pretty weak. This makes it hard for me to get a job, attend a full course load in college, drive, and take care of my own needs.
My dreams are to go to college so that I can have the knowledge to create video games. I want to create fun video games that will help people with special needs develop the skills they need in real life. For example, a game that will teach them to interact with neuro-typicals. Or, the game might help them to undersand facial expressions (we have problems with that). I want the games to be an exciting game that you'd find on a top seller list.
Also, as I sale these games, I will donate a percentage of profits to different non-profit organizations that help kids with special needs such as Aspergers, Type 1 Diabetes, Cerebral Palsy, etc.
As of today, I am OFFICIALLY enrolled in college. I have enrolled in an Associates Degree progam in Simulation and Game Design. I am excited. But, I don't have everything I need for college. Our family does not have the money needed to get my stuff for college. I also have a pell grant but it's not enough to cover everything I need. It will cover tuition costs though.
In addition to tuition, I also need the following:
*Basic school supplies (binder, notebooks, pencils, pens, sketch pad, etc)
*A computer that ideally will have an i7 processor, a nVidia 850 graphics card, and at least 16gb ram. This is needed because of the work we'll be doing in class on the computer.
*Transportation costs to get back and forth to the campus
*An external hard drive to back up all data
*Books for courses
I feel kind of bad for asking people for money because I never do. I am used to living on what little funds we do have so I can't really get the stuff I want or need. I really want to go to college because it will be something I can do that will help me make money and that I can do while resting (so I don't get to worn out). I will also be able to make money so I can help others instead of people offering to help us.
Any amount of money will be of help. Thanks in advance for helping out. Once able, I will always help people out.
Any extra funds that are left over in my educational fund when I'm done with my degree will be donated to anybody else I find that has special needs and needs help with college.
Thank you for your help in following my dreams.
Sincerely,
 Keegan Duffy


PS. My courses start on the 18th and I hope to have all supplies before then!
- See more at: http://www.youcaring.com/tuition-fundraiser/t1d-aspie-college-fund/215548#sthash.ijQ1bBlD.dpuf

Monday, March 10, 2014

Peter Lanza and Asperger Syndrome

Just once I'd like to see the media portray Asperger Syndrome AS IT ACTUALLY IS. I have to give props to Adam Lanza's father, Peter Lanza when he stated , "Asperger's makes people unusual, but it doesn't make people like this."

However, at the same time her refers to those with Asperger's as being "arrogant". He states that all the kids in the Tech Club at the high school are "weird and smart". He stated that Adam thought "he could control her (his mother) more than he could control me."

Adam's mother stated that, "“While Adam likes to believe that he's completely logical, in fact he's not at all, and I've called him on it."

A psychiatrist that Adam saw, Paul J. Fox, implied that home school equated with "isolating him from his peers."

The reporter, Andrew Solomon, commented on "violence by autistic people" when there is an invasion of personal space and then follows the statement with a comment on committing crimes.

Lastly, the reporter stated, "Both Autism and psychopathy entail a lack of empathy."

So, where do I, the mother of two children on the Autism spectrum stand? Where do I, the mother of a teenage boy of Aspergers, other of an 8 year old with High Functioning Autism, and friend to many adults and children Aspies stand?

First, I have yet to meet a child with Asperger Syndrome that is arrogant. Let's take a moment to define "arrogant". Google defines it as, "having or revealing an exaggerated sense of one's own importance or abilities." Yet, this article goes on and on about how Adam felt that he couldn't do anything right. How he was frustrated and helpless at his inability to complete tasks he should have been able to do, tasks his peers could perform. NOTHING in the article, or anything I've read about Adam portrayed arrogance. Show me just ONE child with Asperger Syndrome that is "arrogant". Just show me one!! You'll be hard pressed to do that.

Peter Lanza also said that Adam felt he could control his mother. Yet again hasn't all the information about Adam show that he felt no control at all? Again, show me one child with Asperger Syndrome that seeks to control others. It doesn't happen. They want to be able to control their own environment, just like neurotypicals. Yet, Asperger Syndrome makes it more difficult to do that.

Adam's mother stated that Adam felt he was completely logical, which he wasn't. Yet, the majority of children on the Autism spectrum are VERY logical and take everything VERY literal. If you stop to look at things from their literal perspective, then it is VERY logical. The more time you spend with those that are on the Autism spectrum, the more you realize that it is us, the neurotypicals that aren't logical. It is us, the neurotyps, that use phrases that do not make sense (it's raining cats and dogs). It is us, the neurotyps, that base our decisions on emotions, that will change plans at the last second, and that can leave tasks half finished without skipping a beat. Which of us, the neurotyps or Aspies are more logical?

I won't even respond to the comment Paul J. Fox made implying that homeschool equates isolation. If the general public hasn't wizened up to this myth by now, than that's on them.

Violence by autistic people when entering their personal space.......... Yes, some children on the spectrum can not tolerate you're entering their personal space. Some children on the spectrum have no concept of personal space. I'm mother two children that exhibit both (one is the first, one is the latter). In this respect, they are just like some neurotyps I've met. Come on, we know the guy or gal that stands to close when speaking to us. We also know the guy or gal that will not allow you to hug them or get close to them physically. Asperger Syndrome is no different then neurotyps in being one way or the other. The difference comes in how that information is processed by the brain. Yes, my youngest child will resort to what could be deemed "violence" when you move into his personal space and stay there. He will invariably, after communicating his intense discomfort in a variety of ways (verbal and/or non-verbal cues), push you away from him. If you come back, he may hit you. Yet it is impulsive, he doesn't think it through, he doesn't plan it, and he doesn't even do it in a way to cause damage. It is as much reflex as your jerking away your hand from a hot flame to avoid pain. Being in their personal space causes them pain and they are reacting accordingly. Yes, there have been cases of police officers stepping into a person with Autism's personal space while speaking to them in a very loud and raised voice, and the person striking out in an attempt to restore their personal space. However these were also cases where the law enforcement officer was unaware of the person being on the spectrum and approached them in a way that frightened, confused, and seriously terrified the person. Still, shouldn't the reporter be more specific? Why would the reporter imply that Asperger syndrome is synonymous with criminal violence? The reality is that studies have not empirically shown that there is a higher prevalence of violence among those with Asperger Syndrome. What has been proven is that more males with Asperger Syndrome show violence than women with Asperger Syndrome but this is simply because there are many more men with Asperger Syndrome then women. Many specialist have verified that Autism Spectrum Disorders DO NOT result in higher criminal activity.

"Both Autism and psychopathy entail a lack of empathy." Really? Where oh were did this research come from? It has been determined that studies done regarding empathy and ASD did not utilize testing tools to accurately measure empathy. People with ASD think and feel differently then neurotyps and therefore the tests that register empathy in neurotyps did not give an accurate result when tested on those with ASD. A study that was done addressing this states that, when tested with a way that truly represents those on the spectrum and empathy, the measurements are comparative to neurotyps. Of course, I've seen my child cry for HOURS because he made a comment that someone took offense at. A comment that was purely logical and meant to cause no harm or disrespect. I've seen the empathy in those tears.

Unfortunately, there will always be those that jump on what the media states and bases their assumptions on that. There will be those that, due to the media's portrayal of Asperger/ASD, will believe that Autism equates violence.


I will not be one of those. Please, join with me in refusing to accept what is portrayed by media as fact and instead determine to dig for the facts yourself and see the truth in all matters.  

Saturday, November 16, 2013

To My Children



                  
First, I want to address this to my lovely, beautiful, intelligent daughter Keara....

Keara, I have made so many mistakes in life. So many mistakes in your life. Some of the worst decisions I've made in life concerned the men I chose to share parts of my life with. The results to you have often been disastrous. You've learned not to trust men and to always look for the other shoe to fall. You've learned that men will use you to get what they want, then discard you. You've learned that men will stick around while it benefits them, but when things get hard and they can no longer have all they had before, they will leave. These things you've learned, not because all men are this way, but because these were the men I brought into your life.

 I am so very sorry my beautiful daughter. I am so sorry that my own dysfunction has already altered your beliefs about this world. I am so sorry that I didn't deal with my own issues long before you came into this world, so that you would not be tainted by them.

 Keara, I know that all men aren't this way. I know that there are good men out there that will stand by their woman, be there for them, love them, and know them better then they know themselves. You've seen these examples. Maybe they didn't all start out that way, but they chose to be that way at some point. There aren't many that we know, but there is Dennis with Laura.. There is Opa with Oma. Although it hasn't panned out yet, I believe that John will be in this category as well with Mickey.

Keara, you deserve a man that knows you better then you know yourself. A man that takes the time to learn all your secrets, not to hold them against you, but to be there to support you when you free them. You deserve a man that cherishes you so much that any harm that comes to you would come to him as well. A man that puts your interest and well being above all else. You deserve a man that will go out of his way to make sure he knows what you need, without your ever having to ask for it. You deserve a man that truly, unconditionally, beyond a shadow of a doubt, loves you for all time to come.

Keara, let my mistakes not be in vain. Please, take your time. No man will ever be able to validate you, increase your own self esteem, or make you feel truly accepted. No man has the power to make you feel worthy, beautiful, or OK. There is not a man on the planet that can ever make  you feel "good enough". These things are within you already and I pray that you delve deep inside and find these things long before you start looking for the man to marry. You have your whole life ahead, and the decisions that you will soon start to make regarding dating and marriage will impact every aspect of your entire future life. Choose well my beautiful child. Learn from your mother's mistakes and do not repeat them.

I want you to watch a video my beautiful dove. I want you to notice, not the time, or energy, or money that the man put into this video but instead, how well he already knew the woman he was asking to marry him. He knew what she liked, what she wanted, what was important to her, how to make her laugh and how to make her cry. He knew HER.

This my love, this is what I want for you one day.. I love you Keara, and I am so sorry that your perception of what love truly is has been so warped by my own choices and dysfunction. You and your brothers are my everything. You three have taught me what unconditional love and unconditional forgiveness is. I wish I had known these things before I became a mother, yet without you three I would have never known. I love you sweetheart, and want  you to have the most amazing life filled with true, unconditional love, unconditional forgiveness, and unconditional respect.
                         





                                                                                                                                                      










As for my two boys, I want so much more for you then you've seen. I want you to grow up to be the men that God created you to be, not the type of men I've allowed into your lives. You both have so much to give and such huge hearts.

Keegan, your health issues have enabled you to have a compassion for those that others ignore. Your Asperger Syndrome has given you insight that others will never have. You are so very perfect and you don't even see it. You are the most loving, compassionate, humble, and amazing teen that I know and I am so flipping proud to be your mother. Remember, no one else reflects on your self worth. You were created a child of God and are exactly what you are supposed to be. Embrace who you are, it is so very beautiful and I hope you never lose sight of it.

Pookie, I think that your love of women is already pronounced and well known. :-) I have no doubt that you'll charm the socks off of the ladies. Remember son, a woman is a delicate and strong version of you. Your respect is of upmost importance. Respect her always and she will blossom and grow to be all that God created her to be. You are to be her protector. Remember to know her better then you know yourself and love her always.

I love both of you and I am sorry that your lives have been so difficult. As I told your sister, learn from my mistakes and go on to live a beautiful life full of unconditional love, unconditional respect, and unconditional forgiveness.

I love you three so very much. Always remember that, even after  I am gone. I will live on in you each time you show respect, love and forgiveness. In those things I will reside with you forever and be with you,  long after my physical body fails me.

I love you three so flippin much, there are just no words to express it.

Your mother always,

Melissa

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