There are a few sayings and things my children seem to live by and that annoy the heck out of me. See if you recognize any of them:
1. I didn’t make the mess so I’m not cleaning it up. Well pretty much 95% of the mess isn’t mine either but if I can clean up after you, you can clean up after each other.
2. Are you sure I have to go to school? Yep its my peace and quit time.. oh and they teach you all the things you swear you already know.
3. People who make bills should go to jail. They are stealing our money. While I tend to agree sometimes; its just the way the world works.
4. I didn’t get another turn on the computer like Michael did. You can insert any of the children into this equation. What I cant get them to understand is while we try to make things as fair as possible, there is only so many hours in a day and sometimes its just not fair.
5. When are you going grocery shopping? There is no food to eat. I love this one as we always have food. We just don’t have junk food. Or the fast throw in the microwave types of food. There is plenty of veggies in the fridge to snack on.. or You can actually cook something to eat.
6. When are you giving us our allowance. You already owe us the last few weeks. Your allowance isn’t an automatic thing. Its called doing your chores every day without being asked. So as of today I owe nothing as you have done no work.
7. I’m bored. There is nothing to do. There is plenty to do. You just don’t want to do it. You can wash dishes, scrub the bathroom, clean your room, or do some laundry. You could also get your brothers and sister to play a game, read a book, or go for a walk.
8. Mom where is my…..? I am not the keeper of your items. You are responsible for your own items. I am only responsible for you.
9. I have it worse than you because…. For whatever reason my children feel they must debate with each other why they have it worse and there forth should have more privileges than the others. Again we are back to the lesson life just isn’t fair. I have yet to convince any of them that there are people out there who have it worse than they do.
10. Mom I need ……. Every day my children come to me swearing they need this or that. Right now my youngest wants an Xbox 360 and my daughter wants minutes on her cell phone. This is where I get to talk about money doesn’t grow on trees and if they did their chores and saved their money then they could get what they want.
For some reason my lessons that come with these sayings always seem to go in one ear and out the other. So come tomorrow we will be going through the list again I’m quite sure and while I’m giving my lessons I’ll be wishing for a miracle.
Sometimes its a pain being a single parent, making all the decisions and facing the consequences of those decisions whether good or bad. Being a single parent to a child with mental illness, I’ve found out those decisions are even harder to make because there is a greater amount of error possible. I’ve found myself stuck several times in a catch 22. Damned if I do and Damned if I don’t. At those times I feel like I’m rolling a dice to see where I land. I try to make the best decisions I can for my children. I seek a lot of advise from my mom and from my son’s counselor. At times I think I annoy them with my doubts, but that isn’t my worry. My children are my worry. My mom is strong in her Christian belief. So a long time ago during one of her talks she says, “Aimee remember God doesn’t give us more than we can handle” My reply was ” I wish God didn’t think I was so strong”
The hardest decisions for most families are financial, education, and beliefs. For a family with a single parent with a mentally ill child it includes medicines, therapy, and doctors. Financial for me personally is a very hard one. I live below poverty. Up till about 4 years ago I worked a minimum wage job and barely made ends meet even with my son getting SSI. About 4 years ago Joey had a very bad set back. I missed so much work; I ended up quitting to make it easier on both my job and myself. At the time we were on medicaid, food stamps, and SSI. Joey’s counselor brought us applications for other programs to help, but we never qualified for most of them. Joey isn’t listed as Mentally Retarded. While he has the diagnosis of Asperger’s Syndrome, it isn’t the main problem. We weren’t homeless so we didn’t qualify for housing assistance. We scraped by. 2 years into it I had enough and tried to go back to work. When I worked we lost medicaid, because though I made 7.15/hour and worked 20 hours I made to much and lost medicaid and food stamps. They add in SSI into the family budget. I couldn’t afford Joey’s medicine so I quit working again to get assistance with his medicine. I can’t tell you how many times I’ve had utilities disconnected to borrow money to have them turned back on. Again we didn’t qualify for energy assistance, because we weren’t on a housing program. I am currently looking for ways to make money from home, because I can’t afford to pay someone to take care of Joey and he must be supervised at all times. The Childcare program only goes to the child is age 12 and the adult care program doesn’t start until age 18.. so that puts us in a bind. I do babysit and do other odd jobs like housecleaning as I can get them. So financially its very difficult.
As far as education is concerned, we have been blessed to live in the school district that we do. Our school is awesome. Joey loves school. They treat each child like they matter. The school is very involved with every pupil from the principle to the classroom aides. Our school has helped up get Joey where he needs to be. Our yearly IEP meetings have at least 10 people involved in them. The principal or vice is always there, as is the school counselor, one general ed teacher, the special ed teacher on record, every therapist, the students case manager if they have one, and the do everything in their power to get the parent there. I can’t not sing enough praises for our school system. They have backed us in so many ways. Joey use to fight going to school. He had so much anxiety. The school helped eliminate that anxiety and he goes without any problems now. The hardest decision I’ve ever made for education was what classes to put him in.
Since my child strongly doesn’t believe in anything, teaching our Christian beliefs is a challenge. Joey had a hard time with the difference between fantasy and reality. He was taught at one point that fantasy was what you couldn’t see and reality is visual. So unfortunately, he believes that God is a fantasy. We don’t let that hinder our talking about God and the bible. We just don’t make a big deal about it. It works for us.
Medicine, therapies and doctors all go together really. Its extremely hard deciding which way is best. One problem is after we decided we usually have to get approval from Medicaid ( which is stupid a lot of the time). Anther is learning what different types of meds do and how they react with one another. Being up to date on side affects and follow up appointments. It makes your mind spin. One major error on our part had my son dealing with a sever allergic reaction called Stephen Johnson. He was in the hospital for a week and then took a month to heal. He was lucky. It could have been worse. Hes had to be hospitalized once because a med did the exact opposite thing and caused him to go psychotic and attempt to hurt himself and his doctor. So medicines can bad reactions and then there are the medicines like Zyprexa that really help him. Therapies can help as long as the child receives something from it. Joey once did brush and joint therapy and it would make him more agitated. His brother had the opposite it calmed him. Joey does great in group therapy because it gives him a chance to socialize and to learn that others deal with some of the same issues. We learned through trial and error though that he needs someone to attend with him to keep him focused. Doctors all I can say is that if your doctor doesn’t understand your child it won’t go over well. Joey talks in code a lot. He vocalizes what he feels. examples: anxiety= “There is a tornado in my stomach” a migraine= “someone is hitting me with a hammer” and indigestion= ” Someone is tearing apart my insides” We have had some good doctors who take the time to talk to Joey and understand him. We’ve also had some bad doctors and I’ve had to fight to get him moved from their care. Always trust your instincts where your child is concerned. You truly know them better than others.
Decisions are hard and many have lasting effects. Just use the best judgement you can and don’t beat yourself up about the bad ones. Just learn and move on to the next one. Don’t be afraid to seek advice or help and be willing to put it all out on the line. No one can truly understand what you are going through if you aren’t willing to share your dirty laundry. Have patience and always remember to take a few minutes out of the day for yourself. Just know if you aren’t truly alone in this mess. Others are facing similar things.
After much anxiety (both for Joey and myself), Joey attended his first semi formal dance. I was so proud to watch him do another milestone in a young persons life. As with most schizo-affective people, Joey has problems completeing daily living skills including taking a shower. On the day of the dance not only did Joey take a bath, but he did so without even being asked. I helped him fix his hair. He was so grown up in his suit. He was on his best behavior. He needed to be reminded very few times about what was socially acceptable. He went to the dance with his sister and her friends. They were wonderful with him and helped him be comfortable in the crowd. He even got his first slow dance as a girl in his class asked him to dance. He was so excited he talked about it over and over again for 3 days.
Holidays are always rough around here. Joey does so much better on a schedule and during the holidays those schedules go right out the window. Christmas Eve we had some extended family over for dinner and so that the kids could have christmas together. The way our families work is I have all 4 of my children on Christmas Eve and then thier fathers get them Christmas Day. We have been doing it this way for years since my family always did things Christmas Eve together and my ex’s families do thier gathering on Christmas Day. Anyways… So Christmas Eve went over well. Joey recieved a tracphone, a remote control car, a 8 gb flash drive for his videos, an mp3 video player, Night in The Museum 2 DVD, and Axe body wash and body spray. He loved everything. He got a cheap cell phone for 2 reasons.. One if he loses it Im not out a lot of money and 2 he never uses the phone for some reason so we are gonna use it as therapy. Joey and I made a deal I would upgrade his cell to a nicer one if he keeps track of it and does his chores to keep minutes on it. I am hoping the cell will give him more confidence in answering the phone and to use the phone to call others. His Mp3 video player was yet another coping skill we utilize. His other mp3 broke so I needed to replace it.. So as a present I upgraded it to include videos. I have learned over the years to try to make Christmas and birthday presents double as coping skills. Since coping skills play a huge part of our lives it only makes sense to get him the best that I can afford. So Christmas in Joey’s eyes was a huge success.
We are now facing the new year and what surprises we have in store for us. We have been working on our goals and thinking about past achievements. Its a time to be reflective and hopeful at the same time. Its a time I take every year to remind my children that dreams are important in your life. You need something to reach for. Dreams can be big or small. So take time to Dream and remember anything is possible if you try.
I was reading an article today about a mother who was afraid her child would end up as a mass murder because she needed help with him and unable to get it. I was flabbergasted at some of the points of the article, but it made me realize to many people have no idea where to turn when thier loved ones start showing signs or of getting the help that is so desperately needed until damage is already done.
I was blessed to have found help as early as I did. I thank God every day for putting me in touch with the right people. That isn’t to say that everything was easy because it never is and I didn’t always get the help or answers I needed, but I have learned a lot. I’m taking the time right now to offer some words of wisdom from a parent who has been where you are and who is still traveling down the uncertain highways of caring for someone who suffers with a mental illness.
Number One: Seek help from a mental health agency. Don’t look just for a psychatrist, or just a therapist, or just a social worker, or just any one person. You need a team. I personally suggest a case manager to begin with. Our local Mental Health Center has an Intensive Youth Services department. My son has a case manager from there who not only works closely with my son and myself, but also there office has a staff meeting with the psychatrist and they go over all the kids’ files. This is a god sent for those days you find yourself calling the crisis line because the person calling you back may not know you personally but they know the case and how to direct you in the right direction. The psychatrist is kept up to date on what is going on to be able to say.. Hey get them in the office, or maybe we should try this instead. So when you do go to your appointment you don’t feel like you have to remember every little thing. These services will also help implement a safety plan/ or crisis plan and they will also set goals. Pick someone both you and your loved one are comfortable. If your not comfortable with who you got a assigned to don’t be afraid to say hey we need someone different. You need to be comfortable to tell them all your dark secrets. I don’t know where we would be if we didn’t have these services for Joey.
Number Two Find some sort of support system. I can’t not stress enough how much this will mean to you as you go down this long road. It doesn’t matter if its a support group online or close friends and family. Just find a natural support system that you can count on. Thier will be days that you will need to bend an ear; either to vent or just ask for advice, or even a sounding board. There will be days you will offer to lend your ear to focus on another’s problem so that you might come back to your own later.
Number 3 Realize its a trial and error process. Every person is different and that include mental illness. Its a huge trial and error. One being diagnosis, your loved one may get a few diagnosis because he/ she fits them then as time goes on they are revised and changed. With new symptoms and with new research things are changing all the time. Another part of this is that you will problable go through lots of trials with medicines. Different people react with different medicines. Just make sure you are talking with your nurses and doctors about everything. Little things matter and sometimes those little things are the clues you need. A good thing to start is a journal so that you can see whether you are truly making progress or not.
Number 4 For the safety of the person, yourself, and other family members stick up for yourself and don’t be afraid to let your voice be heard. The best piece of advise I’ve ever recieved is “No one knows your child better than you” so if you no something is wrong don’t let others sweep it under the rug. Take the article I mentioned at the begining . The mother said her child was going after her with a knife threatening her. After she manuevered the situation to where she was in control, she took her son to the er. The er said he seemed calm they didn’t have a bed there and sent them home with a potent drug. Now I’ve been in a similar instance where my child was not safe. I was lucky I was told by the mental health proffession what to expect and what my rights were. That mother had the right to say ” my son needs help now. he needs placement. I know my hild and what he has gone through and what he is currently going through”. Even if the place doesn’t have a bed they must find a bed in another facility or atleast give you the numbers to other places. You have the right to recieve assisance and make sure you and all your family members are safe.
Number Five Remember you are human. I sometimes forget that I don’t have to be the strong one all the time. I forget its ok to lose it once in a while. The fact is there will be times where you will be frustrated, upset, angry, not sure if you can keep fighting, and having feeling of guilt. Its all perfectly normal. No one is going to look down on you for losing your cool or for asking for help. Just remember two things. One you are your loved one’s best advocate because no one cares more for that person. and Two on days that look very dark just think of all the good things that you have witnessed. All the challenges met and conquered. Realize that it will get routine. Some days better than other but you will find routine.
Number Six Utilize Coping skills. One of the best things for us is the use of coping skills. Coping skills can be anything. Utilize those things that help calm your loved one. One of the funniest for us is food. My son always starts getting upset when he is hungry, yet for some reason he won’t voice he’s hungry sometimes. So when I notice him getting agitated I offer him a snack. Another is for him to reorganize his cards. Anything that will calm the situation should be used as long as its not dangerous to someone
Well for tonight those are my words of wisdom. I know I will have more advice from things I’ve tried or have been taught but for now my brain is shutting down. Keep your head up. If you have any questions please feel free to ask.
Its 7:52 am and all I can think is. YES ITS MONDAY!!!. Most people I know dread mondays. Back to work or school you must go. I, on the other hand, welcome in the structured days of sanity for my house. You see one of the most important things to a child with schizo-affective disorder is STRUCTURE. Thier thoughts and emotions are so jumbled that they need the routine of every day life to stay as close to identical as possible. So the weekends are our roughest time, because a major part of every day doesn’t happen. The kids don’t go to school. For an example of a weekend here, I will describe my less than stellar performance this past weekend.
Saturday morning my youngest two (who deal with thier own issues) went out to play. I played on my online game while my two teenagers slept in. Joey woke about 10. Sami, his sister a few minutes later. We only have one working computer and one tv with a dvd player. I can’t afford cable.. Anyways so Sami asked me to use the computer. I make the kids rotate with eachother for time on the computer. Each child gets one hour. Sami wasn’t on but 15 minutes, before Joey starts getting upset and growling. I ask Joey what is wrong and he launches into a long inaccurate rant about “hes asked for hours for a turn on the computer. When are we eating? Every body needs to shut up we are making to much noise” Now after having dealt with Joey for years I know I need to redirect him to get him to calm down and focus. So I start with feeding him. Every thing I suggest and ultimately make for him is disgusting. I suggest he play the playstation or watch a movie. I mistakenly suggested he could clean up his mess in my living room. HE procedes to tell me that he didn’t make the mess. That it was one of the boys. (This is extremely common because while Joey did make the mess he doesn’t remember it so he figures he didn’t do it) Joey continues to rant. At this point its about 12. (All I can only say I’m human )I lost it. I yelled back and told him everything that makes me frustrated. His sister and two brothers who had both came home by then got pulled into it. I felt bad afterwards but hey sometimes its what they need. Joey was apologetic and says, “mom all you had to do was ask”. Now you have to understand I do ask Joey and the kids to help around the house and such. Joey just never remembers. Luckily he wont remember mom losing it on Saturday. Well at this time I give him his turn on the computer. For the next hour, It was peaceful. No headaches no hassles. Afterwards Joey just decides to get his dirty clothes and put them in the washer. He doesn’t remember how to use the washer but he does get his dirty clothes together. Plus he got out his suit and got it ready for next week’s school dance he’s going to. Life is calm for about an hour or two, then Joey loses it again. He walked to our kitchen (for what I have no idea still) and came back to the livingroom angry. He starts his rants about everything again. This time adding in the rants about us never having money, or having a car, about he doesn’t care about the neighbors upstairs and he will just kill everyone. Again I work on calming him down while deflecting my son Michael (who is Adhd and PDD-NOs) from causing more grief by telling everyone what is the correct and incorrect ways of doing anything. I must say I threatened them with the lose of everything they hold dear. Not a good threat dealing with Joey. He freaked out. He thought I was gonna take away all his coping skills stuff. (I’d be dead before I would ever let anyone do that to him or myself) Finally night arrived. The fight over taking a shower or not began. Of course Joey won that one. He’s 6’3″ tall and weighs about 220. I can not pick him up and put him in the shower anymore.. Daily life skills are the hardest thing for Joey. After the battle of wills about the shower, it was the battle of wills on medicine. I must say I am excellent at winning that one. I won’t give up and I think he knows that. An hour later my house is quiet as all three of my lovely sons are fast asleep and only my night owl teenage daughter is up talking to her friends. Most nights like Saturday I lay in bed replaying the day wondering.. Was my choices right? Did I screw something up more? Are the kids safe? So that was my Saturday. Sunday ran along the same lines. Though for some reasons all three boys thought it was bash mommy day. And I heard everything I do wrong. Main one being I don’t have a job. They sounded like they were repeating everything thier fathers ever said about me.
Anyways Back to why I love Mondays. Monday morning while the kids drag a little they all get ready and go to school. For the next week its peaceful but busy time between 7:50 am and 2:45 pm. I have a lot of things to do while the kids are at school. I have to clean my house. Continue to do what I can online to make money. Deal with more government paperwork to make sure Joey gets on the waiting lists for different programs to help with his life skills. Call therapists, email teachers.. the list just go on. But while im doing that I’m not trying to keep WWIII from breaking out in my house.
While I am doing all I must do, Joey is in his routine at school. He does good in that routine also. He takes a shower there between first and second period. He has teachers and aides that assist him through out the day. Schools are very structured and for Joey its calming. After school its mostly steady around the house. Some days can be bad but for the most part we have a strict schedule that helps keep Joey calm.
So bring on Monday mornings and the time to rejuice my engines…
Hi. I’m Aimee. I started this blog because I find little on the subject of raising a child with a diagnosis of Schizo-affective disorder. I hope that this blog will help others who are faced with many of the same struggles we face every day. It is also my way to vent out some of the frustration that comes along with this diagnosis. For those of you who aren’t raising a child with a special needs, I hope you are able to understand the struggles we parents of special need children face and are atleast willing to say “I am here for you even though I don’t understand the struggles you face”.
I am gonna start by telling everyone the history of my descent into the world of parenting a child with special needs. It all began Feb. 16, 1998 when my son, Joey, came into this world. Bless his little soul, I had no labor pain. I woke up that day to the feeling like I had to push. I was rushed to the hospital, and not even thirty minutes later he came screaming out. Let me repeat.. I HAD NO PAIN WHATSO EVER. Any mother would say that was very very rare. Much later I would start to say, “Now I know why I had no pain, its because life was gonna be hard enough later on” So Joey came out at 7lbs 7 oz. The first couple of years of his life were easy enough. He had hearing problems at 2 but that was corrected with tubes. At 3 he never went to sleep, so that was our first round with medicine. We had a wonderful doctor at the time. He listened to what we had to say and prescribed my son a medicine he would only take for 30 days. He believed at the time it was just a chemical imbalance and that righting that would fix the problem. And we believed it had. We didn’t have any other real problems until Joey was in kindergarten. Joey’s father and I had seperated before he was born and divorce when he was three. I had a second husband and Joey’s father had married again also. My husband and I lived in Evansville, Indiana at the time. Joey’s father lived in the smaller city of Mt. Vernon, In. We thought that the huge classrooms in the Evansville schools were the problem so Joey and his sister went to stay with his dad in Mt.Vernon where they had smaller classrooms. Joey had problems all through first grade and was diagnosed with ADHD and put on medicine. My husband and I decided to move back to his hometown of Lawrenceburg Indiana and we took Joey with us and our other 2 sons. Our daughter decided to stay with her dad where she was comfortable. In second grade Joey’s teacher noticed he was having problems and recommended he recieve counseling from our local Community Mental Health Center (something to this day Im very very thankful for). Joey’s first counselor was Andy R. He saw Joey at school and met with me once a month to tell me about his progress. Andy recommended Joey be put into a program called Intensive Youth Services. It is also ran by CMHC only instead of the case manager seeing him at school they would see him at home, or where ever was convient. At the end of 2nd grade we had tried so many ADHD medicines none really worked and several he was allergic to. Because of his baby brother had so many medical issues we had moved into my mother-in-law’s at the time for the extra help with childcare. That year I think I spent most of it in the hospital with one child or another. Any ways, so third grade for Joey started at a new school. It was aweful. He had a horrible teacher who didn’t understand anything we were going through. She actually told my son he was gonna fail third grade. She refused to listen to anything his case manager Amy D said. Actually blamed me. Well Amy and I discussed it. I removed my son from that school and re enrolled him back at Aurora Elementary. (A school district he is still in and will remain so.) 2 weeks later his teacher and I met and she couldn’t believe the difference. He was getting A’s an B’s and the sweetest boy. Christmas break came and then we all started seeing a difference. His teacher called me and said he was spacing out and having these aweful headaches. He was acting different and he would purposely get in trouble so he wouldn’t have to go out to recess. I took him to the doctor. He was diagnosed with petit mal siezures and CMHC was seeing him more often. In April that year, We were in the doctors office when Joey started yelling. He swore up and down someone was behind him talking. At the time he was in a chair up again the wall in a room with only the doctor and myself. His doctor asked a few pointed questioned and we finally learned Joey heard voices. He had auditory hallucinations. As far as we could tell hes always heard them. He just never knew no one else heard voices in thier heads. CMHC were still observing him. As long as he wasn’t a danger to himself or others, he was ok. May because our first big problem. Joey came home and met with Amy telling her that the voices wanted him to hurt someone in his class and he would have done it too just to get them to shut up. Only the teacher didn’t have the object in her desk. Immediately Amy and I took him to Cincinnati Children’s Hospital were they admitted him into the acute psych ward. It was a scare time. Joey didn’t do good the first few days. Amy and I went to the first of 4 family sessions and when Joey came in he got so mad he through a table across the room. Well that was the end of that meeting. The second one went more smoothly. At the third meeting they had test results for me. They had done extensive testing on Joey and I got the shock of my life then. My beautiful boy was diagnosed with Asperger’s syndrome, General Anxiety Disorder, Intermiddent Explosive disorder, Sepration Anxiety Disorder, and Psychosis- Not otherwise specified. The last was because at his again he couldn’t be diagnosed with a specific psychosis. After several family outings and all to make sure he was safe to come home, Joey was discharged with a list of medication and a whole new set of doctor appts and therapies. Life went on for a year without any major upsets we had our daily struggles, but with CMHC’s help we got through it.
Then Joey went into 5th grade and all hell broke loose again.The hallucinations got worse and daily life was a struggle. We never knew what it was going to be like to wake Joey up to get ready for school. He would act out as soon as he woke up or he would get up fine, get ready for school then have a panic attack before walking into the school building. Joey’s communications skills were awful and so figuring out the problems was a mission and a half. An example of his communication skills: He went to the school nurse and reported, “I have a tornado in my stomach.” Took several questions before we realized he was talking of the feeling you get when your anxious.
Joey had several stays in acute units over the months of Aug through November. We were searching for help and answers and not really getting anywhere. It was all so frustrating. The acute cares weren’t cutting it. Most were actually more problematic than helpful. I remember one we went to, decided yes Joey fit the criteria of admittance to the acute unit. That was a Monday night. Tuesday morning I got a call asking for permission to do a battery of test on him, which I ok’d. Then Wednesday morning I got a call asking me how soon I could be there to pick up my son as he was being discharged. They never tested him, or had a single family session. A few weeks after that, Joey had a psychotic break. His aunt woke him up for school and all seemed fine. Twenty minutes later I go to make sure he was ready and he just lost it. He was uncontrollable. He was 10 and a scrawny little guy, yet all that adrenaline helped him knock over 8ft solid oak bookcases. It was the very first time I ever had to call 911 to get help in controlling my son. When it started his aunt, her fiance, and myself were there trying everything we knew to calm him down and keep him safe. Two emts and a police officer showed up. 5 of us were holding him down trying to keep him and everyone else safe and to get some sort of calming medicine into him. Even with that many adults holding him down, he still managed to get loose enough to punch his aunt in the face. When we were able to restrain him to a gurney, he was taken to our local er. His casemanager, at the time, met us at the er. Joey was consious the whole time. I was told they were just waiting on a place to accept him as a patient. About 30 minutes into our er visit, Joey looks over at his case manager and ask her where she came from and where he was. This was the first recording of what we came to know as blackout episodes. He didn’t remember a thing that happened from the time he went to bed the night before to that point in the hospital. Joey was transported about 2 and half hours later to a facility.
The new facility admitted Joey and then signed us up to come back in for a family session in two days. When we went in, the onsite therapist recommended Joey be placed in a residential facility. Though the decision was very hard for me to make I ultimately agreed because something had to give before someone got seriously hurt.
Joey spent 10 months in residential care. While the begining was hard, I would never change it. You see the place he was out did amazing work. They were the ones to figure out that Joey was being treated wrong. For two years along with Joey’s Asperger’s and psychosis, he was being treated for uncontrollable anger. The sad truth was Joey wasn’t angry, He was severly depressed and didn’t know how to express his emotions. We also found out during his time in residential that Joey doesn’t just have petit mal seizures but he also has temporal lobe seizures. The hardest part about residential is the phases to go through before you can be discharged. Joey finally managed to get through it all in 10 months.
The rest of 6th grade and almost all of 7th grade ran smooth. The end of 7th grade we saw my son slipping again. Unfortuantaly we were seeing a psychatrist I didn’t care for at all. He decided to randomly change Joey’s medication because he felt his medicine wasn’t working. Problem was I refused to put my son on the medicine he was prescribed because it was extrememly dangerous. The medicine has warnings that death is possible with missed dosing or with the wrong dosing. That there was a very fine line between theraputic and lethal. My thoughts was some days it was extremely hard to get Joey to take his medicine; other days he’d simply hide his medicine nad not take it. I didn’t like the ramifications of missed dosing or wrong dosing. Any ways.. so we say Joey having more and more issues. Joey school days wer shortend. He went to school for 4 periods instead of 7. Over the summer Joey had 2 acute stays one for attempting suicide. 8th grade we saw Joey just slipping more and more. School was cut back to 2 periods. His hallucinations were sparatic. He wasn’t sleeping really. CMHC was seeing him 5 days a week. Then lucky for us, we got a new child psychatrist. Joey hit it off with her. He was actually talking to her and so the med changing began again. It was at this time, that I found out that Joey was misdiagnosed. Children like Joey are commonly misdiagnosed because at early stages it shows the same ways as ADHD. Also children under the age of 13 are very seldom ever diagnosed with schizophrenia. At that magical age of 13 Joey’s diagnosis became schizo-affective disorder, thought processing disorder, Asperger’s syndrome, and seizures.
Well there are some very big downfalls to having a child on medications. One is when they have an allergic reaction. In April of this year, Joey was diagnosed with mono. Our peditrician neglected to warn me that his natural immune system was extremely low and that any medicine we could decrease or stop while he had mono should be. Joey developed a very scary reaction called Stephen Johnson syndrome. It took us almost two weeks to find out what he had and by that time I almost lost my son. We had been in and out of the doctors office due to the mono. We went in on a friday because His mouth was severely swelling. Dr wanted an xray done of his throat. We didn’t make it to have the xray. Joey started having trouble breathing. He was transported by way of our local er to Cincinnati Children’s Hospital Medical Center. We were in the er there for about 15 minutes before he was diagonosed and transfered to inpatient. It was a scary week and half. It took yet another month for the insides to heal. They found out Joey was allergic to one of his medicine called Lamictal and with his immune system down, the reaction just took ahold.
Since our stay in the hospital, Joey is maintaining life, though he is between a rock and hard place where medicine is concerned. 9th grade has been an interesting year so far. Thankfully we have an awesome school and teachers who help him achieve his simple daily living goals.
That is just a very broad overview of our lives to this point. I wanted to give you a history so you have a basis for future posts. My hope is to reach other parents and children going through the same sort of things. So that others know they aren’t alone. Another hope is that I am able to teach aleast one person to better understand what its like for the families and the children themselves who face this stuff every day. To be totally honest another hope is that I might find other things to try or resources that I don’t know about to help my son.
I am a single mother of 4 beautiful children. My son is diagnosed with shizo-affective disorder. I haven’t found much on this topic, so I started this blog to let other parents with children who have mental health issues know they aren’t alone and also to get the word out about how our lives are.