It has been a long haul through the first semester of college for Keegan (you can find him and I on AspieLife on FB). College opened up a whole new set of stressors we had not encountered yet. Anxiety attacks, meltdowns, and panic! However, I am proud to say Keeg passed with all As and Bs.
Keeg has picked up a few more diagnosis since he started college, the most recent being Eosinophilic Esophagitis. However, that new diagnosis explains the uncontrolled vomiting he had as a child every time he ate, the choking he's had for years, and so much more. You can read about it on WEbMD.
Keeg hasn't posted on this blog but he has posted on the FB AspieLife page along with others. Feel free to catch upthere !
Saturday, January 3, 2015
Asperger Suicide SCREAMS
It came to my attention most recently that the blog posts that receives the most views across all my blogs is the one I posted about a local 14 year old teen with Asperger Syndrome that committed suicide.
It has also come to my attention most recently that the majority of the people reading that blog post are those with Aspergers contemplating suicide. The second runner ups are their parents.
My heart is breaking. I am the mother of two on the Autism spectrum. I have seen so much heartache and pain.
When I was a young teen, even though I did not have Aspergers, I attempted suicide. I remember that hopelessness. I felt like I was all alone in the world and no one else could understand.
BUT YOU ARE NOT ALONE!!!
If you have Aspergers and are thinking about suicide, YOU ARE NOT ALONE. Because right now there are others from ALL OVER THE WORLD that are logging onto the internet, punching some words into a search engine, and coming to read the blog posts because THEY ARE ALSO SUICIDAL.
I can't say I understand Aspergers. I wish I did. As a mother I wish it so very much. I would love to understand why my sons feel and think the way they do. But there is hope. There is always hope. Even if the hope is only that you aren't alone.
Please, don't commit suicide. You are beautiful. You are put here, on a planet you feel is alien, to teach neurotyps like me what I am supposed to be.
Join us on Facebook at AspieLife. My son started this FB group to bring together not just those on the Autism Spectrum, but also those that love them and care! He said that all the groups were either for people on the spectrum, or were for those that loved someone on the spectrum but all that seemed to do was alienate us farther apart. He wanted somewhere that we could all share, and talk, and CARE. A place of acceptance and support. So, he created AspieLife. Please, come join us there and know you are not alone.
If you are a parent, sibling, friend, spouse, girlfriend, boyfriend, workmate, etc of someone on the Spectrum and YOU CARE then please join us on AspieLife.
You are not alone. Any of you. Regardless of how you feel, what you think, what you've done, what you will do......... I LOVE YOU.
It has also come to my attention most recently that the majority of the people reading that blog post are those with Aspergers contemplating suicide. The second runner ups are their parents.
My heart is breaking. I am the mother of two on the Autism spectrum. I have seen so much heartache and pain.
When I was a young teen, even though I did not have Aspergers, I attempted suicide. I remember that hopelessness. I felt like I was all alone in the world and no one else could understand.
BUT YOU ARE NOT ALONE!!!
If you have Aspergers and are thinking about suicide, YOU ARE NOT ALONE. Because right now there are others from ALL OVER THE WORLD that are logging onto the internet, punching some words into a search engine, and coming to read the blog posts because THEY ARE ALSO SUICIDAL.
I can't say I understand Aspergers. I wish I did. As a mother I wish it so very much. I would love to understand why my sons feel and think the way they do. But there is hope. There is always hope. Even if the hope is only that you aren't alone.
Please, don't commit suicide. You are beautiful. You are put here, on a planet you feel is alien, to teach neurotyps like me what I am supposed to be.
Join us on Facebook at AspieLife. My son started this FB group to bring together not just those on the Autism Spectrum, but also those that love them and care! He said that all the groups were either for people on the spectrum, or were for those that loved someone on the spectrum but all that seemed to do was alienate us farther apart. He wanted somewhere that we could all share, and talk, and CARE. A place of acceptance and support. So, he created AspieLife. Please, come join us there and know you are not alone.
If you are a parent, sibling, friend, spouse, girlfriend, boyfriend, workmate, etc of someone on the Spectrum and YOU CARE then please join us on AspieLife.
You are not alone. Any of you. Regardless of how you feel, what you think, what you've done, what you will do......... I LOVE YOU.
Thursday, August 7, 2014
T1D Aspie College Fund
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: Courses start August 18th so I'd like to have my needed supplies by then!
Monday, December 30, 2013
From Highs To Lows
Keeg has truly been struggling. It breaks my heart and I wish that I could help him. He had an Aspie breakdown today. In addition to his health concerns, we've had a very traumatic outside force wreaking havoc on our life and the stress has been considerable.
Keeg's last visit with his endo showed that his A1C has dropped to 5.2. While seemingly ideal, it actual means that he is having way to many lows. His doctor has decreased his Levimir to 100 units at night, yet he is still waking from his low sugars (50s to 60s).
The endo stated that this is considered his "honeymoon" stage. The stage where it appears the pancreas is suddenly working and creating insulin. She stated that it doesn't last long, and soon we'll be battling highs again.
Keeg also has an inner ear infection and feels terrible, so he doesn't want to eat. He is alternating between excessive overwhelming hunger, and the desire not to eat at all. No good for fluctuating sugars.
We are still awaiting his appointments with his many other specialists.
We are embracing the positive and happy moments and using them as the sails to pull us into tomorrow.
With love,
his mom
Keeg's last visit with his endo showed that his A1C has dropped to 5.2. While seemingly ideal, it actual means that he is having way to many lows. His doctor has decreased his Levimir to 100 units at night, yet he is still waking from his low sugars (50s to 60s).
The endo stated that this is considered his "honeymoon" stage. The stage where it appears the pancreas is suddenly working and creating insulin. She stated that it doesn't last long, and soon we'll be battling highs again.
Keeg also has an inner ear infection and feels terrible, so he doesn't want to eat. He is alternating between excessive overwhelming hunger, and the desire not to eat at all. No good for fluctuating sugars.
We are still awaiting his appointments with his many other specialists.
We are embracing the positive and happy moments and using them as the sails to pull us into tomorrow.
With love,
his mom
Thursday, October 17, 2013
Update: Immunology, New Insulin, and more...
First, my apologies. So many of you have asked me for updates on Keeg. In all truth, after our visit with immunology, I shied away from blogging. Putting into words all I felt at that time was a bit to much. Now though, I've had some time to process and deal, and now is the time to share.
Keeg visited his immunologist. We had more labs run (ALOT) and are still waiting results. We have been referred (again) to an allergist, hematology, and geneticist. As soon as lab results come back, we will lay out a plan for immunotherapy. Basically, the docs want to start manipulating his immune system to see if they can get it to quit attacking his own body. I don't have a lot of details, but will at a future visit. Hopefully, the worst case scenario is just that.... a scenario and not reality. Worst case being that he is Type 1 Diabetic because his immune system attacked his own pancreas, as it may do other organs.
Keeg is having difficulty swallowing. It feels like something is stuck in his throat. Food does get stuck in his throat. He's been tested for cilia dysfunction previously, but it looks like we'll be referred back to the ENT to test again. It's a horrible battle. He has to count his carbs for his meal, take insulin based on those carbs, then eat the amount of food he counted carbs for. However, when he gets to where he can't swallow, it results in his having taken to much insulin. He has to take his insulin BEFORE he eats, so inability to finish his meal really messes up his sugar level!
Keeg stays tired. Although we had hoped this would clear up in a few weeks due to diabetic management, it appears that his immune system is still wreaking havoc. He is so weak, tired, even lethargic at times. Apologetic....a thousand times a day he apologizes for not being able to help, for needing assistance, or for just being unable to play and have fun.
Today was our endochronology visit. Keeg has had to come off his Lantis pen because it burns him so terribly bad. There is another long acting insulin pen out, but insurance won't cover the pen. So, we came home with actually syringes and vials of insulin today. First dose is in half an hour. I'm nervous, but don't want him to know. I've never stuck a syringe in anyone before! Thank goodness my friend is here and that she is a CNA and former EMT. I don't know how I'd do it if it were just me!
Keeg's A1C has dropped from 12 (yes, it was 12!!!!) to 8.5. So, we celebrated a bit when we heard that one! Yay!
Keeg watched a friend making a huge breakfast of hashbrowns, biscuits and gravy, sausage, eggs, toast, etc. He ran outside, sat on the steps, busted out crying and yelled, "I hate diabetes". Our friend took him to the grocery store and worked to find a way to feed him a breakfast of thing she liked, while keeping it in his carb limit. It's difficult.
We have found that Quinoa is great for him. He gets to eat what appears to be a large quantity of food, it fills him up, and it's super yummy and good for us!
We are still learning. We still goof up often (like those times we get to busy running errands and don't have food to eat). We discovered that cheesecake is a dessert that he can have, which is good because who doesn't like homemade cheesecake? And contrary to a certain Yankee's opinion (you know who you are), cheesecake with Splenda is AWESOMENESS.
We have weeks lined with specialist appointments, testing, and more. I'm holding onto my faith that God will come through and provide me with the computer jobs I need so that we can make some much needed money. He has always provided before, and I'm sure he will now.
As some of you know, we've been fostering dogs that are pulled from gassing shelters. It's been therapeutic for our family..... seeing abused, neglected, rejected and abandoned dogs. Also, dogs that have such a wide variety of health issues. Their unconditional love, in the midst of their pain at human's hands is an inspiration in itself. It has helped our family to be acutely aware of the pain many suffer, and how we can make a difference. It helps to take the attention from our own pains, health issues, financial problems, and more. Saving dogs lives touches you in a way that nothing else can.
Despite all our family battles now, we are together. We love each other. We are a team.
Nothing else really matters.
Keeg visited his immunologist. We had more labs run (ALOT) and are still waiting results. We have been referred (again) to an allergist, hematology, and geneticist. As soon as lab results come back, we will lay out a plan for immunotherapy. Basically, the docs want to start manipulating his immune system to see if they can get it to quit attacking his own body. I don't have a lot of details, but will at a future visit. Hopefully, the worst case scenario is just that.... a scenario and not reality. Worst case being that he is Type 1 Diabetic because his immune system attacked his own pancreas, as it may do other organs.
Keeg is having difficulty swallowing. It feels like something is stuck in his throat. Food does get stuck in his throat. He's been tested for cilia dysfunction previously, but it looks like we'll be referred back to the ENT to test again. It's a horrible battle. He has to count his carbs for his meal, take insulin based on those carbs, then eat the amount of food he counted carbs for. However, when he gets to where he can't swallow, it results in his having taken to much insulin. He has to take his insulin BEFORE he eats, so inability to finish his meal really messes up his sugar level!
Keeg stays tired. Although we had hoped this would clear up in a few weeks due to diabetic management, it appears that his immune system is still wreaking havoc. He is so weak, tired, even lethargic at times. Apologetic....a thousand times a day he apologizes for not being able to help, for needing assistance, or for just being unable to play and have fun.
Today was our endochronology visit. Keeg has had to come off his Lantis pen because it burns him so terribly bad. There is another long acting insulin pen out, but insurance won't cover the pen. So, we came home with actually syringes and vials of insulin today. First dose is in half an hour. I'm nervous, but don't want him to know. I've never stuck a syringe in anyone before! Thank goodness my friend is here and that she is a CNA and former EMT. I don't know how I'd do it if it were just me!
Keeg's A1C has dropped from 12 (yes, it was 12!!!!) to 8.5. So, we celebrated a bit when we heard that one! Yay!
Keeg watched a friend making a huge breakfast of hashbrowns, biscuits and gravy, sausage, eggs, toast, etc. He ran outside, sat on the steps, busted out crying and yelled, "I hate diabetes". Our friend took him to the grocery store and worked to find a way to feed him a breakfast of thing she liked, while keeping it in his carb limit. It's difficult.
We have found that Quinoa is great for him. He gets to eat what appears to be a large quantity of food, it fills him up, and it's super yummy and good for us!
We are still learning. We still goof up often (like those times we get to busy running errands and don't have food to eat). We discovered that cheesecake is a dessert that he can have, which is good because who doesn't like homemade cheesecake? And contrary to a certain Yankee's opinion (you know who you are), cheesecake with Splenda is AWESOMENESS.
We have weeks lined with specialist appointments, testing, and more. I'm holding onto my faith that God will come through and provide me with the computer jobs I need so that we can make some much needed money. He has always provided before, and I'm sure he will now.
As some of you know, we've been fostering dogs that are pulled from gassing shelters. It's been therapeutic for our family..... seeing abused, neglected, rejected and abandoned dogs. Also, dogs that have such a wide variety of health issues. Their unconditional love, in the midst of their pain at human's hands is an inspiration in itself. It has helped our family to be acutely aware of the pain many suffer, and how we can make a difference. It helps to take the attention from our own pains, health issues, financial problems, and more. Saving dogs lives touches you in a way that nothing else can.
Despite all our family battles now, we are together. We love each other. We are a team.
Nothing else really matters.
Saturday, September 21, 2013
Sleep Deprivation, Low Sugar, Migraines and more
It was after 4a.m. before Keeg's sugar started coming back up. I'm exhausted. With my own health issues, sleep is so very important to keep me from flaring. Yet, sleep didn't exist but for a few hours.
Keeg has a migraine today. His sugar is still running in the 80s, even after food. He is also exhausted. Although he slept, it doesn't appear he was rested from it.
I know that in time all this will get easier, but right now it is HARD.
My heart aches for Keeg. He is trying so hard to put on a brave front and smiling face. Yet, he is consumed with one thing only, trying to eat.
I have a thousand wishes, and all of them revolve around my children and I being healthy. That's what I wish we could have.
I'm having a hard time finding the beauty today.
Keeg has a migraine today. His sugar is still running in the 80s, even after food. He is also exhausted. Although he slept, it doesn't appear he was rested from it.
I know that in time all this will get easier, but right now it is HARD.
My heart aches for Keeg. He is trying so hard to put on a brave front and smiling face. Yet, he is consumed with one thing only, trying to eat.
I have a thousand wishes, and all of them revolve around my children and I being healthy. That's what I wish we could have.
I'm having a hard time finding the beauty today.
Friday, September 20, 2013
Low Sugar
I haven't updated simply because I can't find time. Tonight I'm exhausted and just want to sleep. Yet, Keeg's sugar tested 89. At 80 I have to actively get his sugar higher. So, I'm trying to stay awake to test again. We haven't dealt with low sugar yet. To say I'm scared is an understatement.
Keeg has had an anxiety attack, or more, each day. Trying to count carbs, juggle insulin, get full, and remember all the info we learned is taking it's toll on both of us. Add to that midnight and 3am checks....I'm exhausted. He sleeps through his midnight and 3am checks and insulin, but I have to make sure I'm up. My alarm now requires me to do math problems with no snooze option, just to make sure I don't sleep through the alarm.
My two best friends, one of which is a CNA has come to stay with us until we get it all under control. Having them here gives me a security I wouldn't otherwise have.
My dear, recently deceased friend has a young niece with Type 1 Diabetes. Her mother has shown me amazing support and I couldn't do it without her. Just knowing she is here for me means so much.
You may recall, the last blog post stated that I knew eventually that someone would say something about his checking sugar and taking insulin in public. Well, it happened. You can read everyone's responses to the situation here:
Response to "Don't Do That In Public"
Please keep us in your thoughts, prayers, positive vibes.
Keeg has had an anxiety attack, or more, each day. Trying to count carbs, juggle insulin, get full, and remember all the info we learned is taking it's toll on both of us. Add to that midnight and 3am checks....I'm exhausted. He sleeps through his midnight and 3am checks and insulin, but I have to make sure I'm up. My alarm now requires me to do math problems with no snooze option, just to make sure I don't sleep through the alarm.
My two best friends, one of which is a CNA has come to stay with us until we get it all under control. Having them here gives me a security I wouldn't otherwise have.
My dear, recently deceased friend has a young niece with Type 1 Diabetes. Her mother has shown me amazing support and I couldn't do it without her. Just knowing she is here for me means so much.
You may recall, the last blog post stated that I knew eventually that someone would say something about his checking sugar and taking insulin in public. Well, it happened. You can read everyone's responses to the situation here:
Response to "Don't Do That In Public"
Please keep us in your thoughts, prayers, positive vibes.
Subscribe to:
Posts (Atom)