I want what is best for my children. Always. And often times that means realizing that I don't have all the answers. Nooo, it would be way too easy if we did. Instead, our (meaning mine and hopefully yours) life buoys on the grace that our Heavenly Father provides second by second, moment by moment, and our journey moves forward as a result of learning from the mistakes we make along the way. And boy do I make a lot of mistakes.
Since I could remember, I have always been one of those parents that were against medication accept in rare cases. For the most part, I tried to mentally blame the parents-- because I obviously had angels for children that could do no wrong. Slowly, God began to change the circumstances in my life in order to break down that lack of humility, and he continues to do so each and every day. I make it no secret, that we have had our fair share of trials amongst the thousands of smiles, and I will admit that I have had to be led like a stubborn donkey a few times in order to do what was best in one of my children's lives.
Today marks one of those times----- in a monumental way. I started one of our children on Strattera for ADD. Now when I say I, of course I mean we, because John too has had a change of heart and mind. And we are both okay with this decision, as is our daughter, and we are excited at the potential our daughter has to be able to focus and improve the overall quality of her life as a result.
Some of her symptoms are:
Often does not give close attention to details or make careless mistakes in schoolwork, work, or other activities
Often has trouble keeping attention on tasks or play activities
Often does not seem to listen when spoken to directly
Often does not follow instructions and fails to finish schoolwork, chores, or duties in the workplace (not due to rebellious behavior or failure to understand instructions)
Often has trouble organizing activities
Often avoids, dislikes, or doesn't want to do things that take a lot of mental effort for a long period of time (such as schoolwork or homework)
Often loses things needed for tasks and activities (e.g., toys, school assignments, pencils, books, or tools)
Is often easily distracted
Is often forgetful in daily activities.
Yes, this is the same daughter that I thought had attachment issues, and while I can still admit that she may have very mild attachment issues, in my heart I know that she isn't doing 99% of what she does on purpose or for lack of attachment. And the doctor agreed.
And yes, it has taken three years to get here. And yes, I can hit myself up over the head because it took so long for us to get to this point, but you know what--- we have gotten to this point and I think it took this long for a reason. Now, our daughter trusts us enough to know that we aren't putting all of our faith in this medicine, and we have told her not to either. Imagine that kind of pressure. She also trusts that we have decided to move in this direction in order to help her feel better about herself and be able to better maintain the relationships she has instead of frustrating not only herself but the other people in her life (including me) who can easily misinterpret all of her actions as manipulative, laziness, or ditsy.
I wish I could say that things are definitely going to change-- but I have learned to take things day by day. I am not sure what tomorrow holds in terms of seeing an improvement, but at least today, a new door was opened.
And speaking of doors---- I so angrily almost shut the door on our progress we have been making with William. John and I both know that there is no such thing as too much attention you can give a child as long as it is constructive and loving and positive--- and if it is possible that it is just that easy to see an improvement in William's behavior, then we would be fools to not put forth the effort. And so we have. We have been reading with him more, letting him come in and wake us up early in the morning so we can go downstairs and supervise him making us eggs for breakfast and then eating together, and just having him be closer to us..... period. This has definitely made our relationship with our son stronger and better so that he is less defensive when he hears the way we see things--- but it has not helped with the outrageous initial reactions he has in social interactions that cause him to fly off the handle. Just last night at church, he was playing soccer with 10 other kids and he kept accusing them all of cheating so he would get the ball and not let them have it. This continued on, and he could not see that even if another child was cheating--- none of the other kids seemed to mind because they were all having fun instead. Needless to say, he had to come home with us instead of staying during kids church-- and that meant more one on one time with us. So yay for that-- but nay at the same time for his inability to see that having fun was more important than focusing on the rules.
So we came home, and spent time with him. And the night ended on a beautiful note. In the morning, William came to wake us up before anyone else was up so that he could make us eggs again for breakfast. I was feeling incredibly rushed having to get not only myself showered and dressed but Alex and Dennis too, so that we could get out the door by 7:15 ( to take Caleb and Annalynto the doctor) in addition to getting everyone else ready for school. In the midst of our hurried morning, I don't even know how, but William tripped over the little potty that Dennis had just used and quickly picked it up in a last stitch effort to set it back down. Instead he froze as the pee rained down all over the floor. When I saw it, I immediately yelled at him for not thinking on his feet and setting it down rightside up before all the pee dripped out.
But it was too late. As soon as it came out of my mouth, I regretted it.
Ugh......... an apology just doesn't quite feel adequate to me. Of course, it has to be, but I knew better. And somehow saying I was feeling stressed and rushed is really no excuse.
I am going to work on this---- I need to. Just as much as I expect William to work on his issues.
Lord, help us both.
P.S. Thank you blogreaders for the the wonderful suggestions to look into ADHD and spend more time with our son. I am always open to ideas and differing opinions--- and will even post them all if they are written with respect. Truly... thank you.
31 inspiring thoughts:
Christine,
My nine year old daughter was diagnosed with ADHD and is on Vyvanse and has been for about a year and a 1/2 now . We tried Stratera but it did very little for her and suppressed her apetite too much. And she cannot afford to lose any weight. I feel that by putting her on the medicines we made the best decision for her.
She had a lot of the symptoms you spoke about, but she was also lying, stealing and her grades dropped from A-B's to D's. After starting the Vyvanse, we immediately saw a difference in her behavior. Her grades went up and the lying and stealing stopped. She was more able to concentrate. Before the medicine, when she tried to talk to us, you could tell that her mind was working 10 times faster than she could get the words out and this caused a lot of frustration on her part. She also sees a therapists at school who keeps up with her progress, and talks with her at school about her actions and such.
I feel for you and will be praying that she does as great as my daughter has on the medicine.
Sincerely,
Trisha Woodcock
Christine, I have those same moments of regret also. They KILL me. But you know what? A few months ago my own mom was voicing her own regret over all the yelling she did at us (four kids) when we were small. I was shocked. SHOCKED! I remember a few times, but i knew they were not undeserved, and the thing I remember most about my mom. MOST? How much she loved us all. She was very verbal, and physical with her love. That is seriously all i remember. She was so glad to hear that. So I take that to heart when I have my regrets.
Jill
Oh Christine! I hear you on the medication front. When Curtis was in the neuro facility we refused all medications. He was there for 5 months and the attending Dr. sat us down and was very blunt and told us he would never leave the facility without other methods of help. So...we jumped in even though it was horribly uncomfortable and let our son starts on some medication. We are so glad we did. It does help him, but didn't make it all better. It was a help in the time of his storm. I am so appreciative of your candidness. I learn from you because you let the Father work in your heart. I need to work in the some of the same situations you have posted about recently. Love you girl!
This is not meant to be mean spirited but I have to giggle sometimes. You have a beautiful family you are fun and on the run making sure every detail is met. When I hear that you fussed at someone over the potty of pee, it becomes REAL you are human, you are a real person, you make mistakes like all of us do, maybe the difference is, is that you put it all out there for us to read.
As for putting one of the kids on ADHD med's GOOD FOR YOU!!! 2 of my children are on it, and it has made life so much easier not only for them but for us too. It helps them function more saftely and I am very happy about it.
You are a wonderful parent....
I think that you waited and tried other things for the past 3 years shows how committed you are to helping your daughter. Our child psychiatrist always said that medication is the last thing to do, and I agree with him whole-heartedly.
You actually going with the decision to medicate eventually is probably the best thing now. I do hope and pray that this will work out for all of you for the best.
I have two on ADHD meds. They would not otherwise be able to succeed in school. That is just the way it is. One would also drive people crazy because he is also asperger's. Without the meds he starts antagonizing others and the autism symptoms seem so much worse. They cause him to have trouble coping and then the ADHD on top of that. Whew.
You have to do what you feel is best for each child. ANd sometimes along the way that might change. But do what works for now.
I agree that medication can be a good or a bad thing, and it may not be immediately apparent which it is. I did not like Strattera, and really have only met one person who it worked for, for a short time. I think that if strattera works for a child, then it should be used, as it is the only ADD med I ever took that did not effect my sleep.
I now take Vyvanse, and it has worked very well for me. Any type of ADD medication can cause weight loss, and I think maybe stunt growth as well, so it is important that she be monitored, as she may have little or no appetite and may forget to eat if not reminded.
I hope the medication helps her.
Didn't your pediatrician ever suggest testing your daughter for ADD? Has the pediatrician talked about testing William because of his social skills?
Whoever said that being a parent is easy?
Glad to hear that things are going better for your daughter and you have some answers for what some of the problems were.
As for medication, I feel that when it is recommended by a doctor and serious discussions have taken place, then it probably is right. After all, a doctor knows far more than I do as I don't have 4 years of med school, 5 years of internship and residency and many years of experience. My BS in business doesn't hold a candle to it.
Same here Trisha.. My 8 yr old son is on Vyvance for the past year and WOW WOW what a improvement!! He gets all B's & A's, and can follow through on things... He is skinny to begin with and the problem I did have was the same as Trisha. He lost his apetite around lunch time. I use Carnations Ins. breakfast to help throughout the day and night...
Hope it helps! Be patient!!
Stacey NY
Christine, Like yourself I am reluctant to medication. However earlier in the year we put our son on Concerta! And it is like night and day! He has done so much better all the way around in life. Sometimes we have to do what is best for the child. You are an amazing Mom and inspiration to us all..
NIkki
You know what Christine, thanks for posting on these topics. I know you have before its just this time I find myself in a similar type of situation. I often find myself snapping at my daughter for things that she should know. (For one example, You don't dish out scalloped potatoes onto your plate with your cupped hand...for goodness sake can she not see the spoon sitting in the dish?!?!)
She is a completly different child from one setting to the next. Angelic and sweet at Church, Dis-organized and rude at school, passivly manipulitave with strangers and at home goes between all and then some. :) She also lets down her guard and we often see the real girl, who is just lovely.
Sorry this is getting long...I just wanted to let you know that I am trying to work on the same things. Having more patience, not saying the first thing that comes to mind when something like the potty incident happens, spending more valuable one on one time with her. What adds another aspect (As posted on my blog) is that we are expecting a baby within 3 weeks or so and dealing with the "I want to be the baby" aspect in her behavior too. *Sigh* I am sure you can imagine :)
Catherine Wishart
Thanks for always keeping it real BTW. Its encouraging to know other people are working on the same things! :)
Thank you for posting AND for all those who have commented so far. I really thought we were the only family that hesitated at ADD medicine. After 3 years of trying everything under the sun we relented and tried Vyvanse. It has made a world of difference in our house. Since we are new to this, I am curious what kind of follow-up other doctors are doing with your kids? Currently we are seeing the doctor every 3 months to evaluate how things are going. Is this normal? To often, not often enough?
When you describe William I feel as if you are describing my friends son. She has torn her hair out countless times, regretted actions, etc. She's had him looked at for Aspergers, etc, which he does not have. He does have a sensory disorder though. The encouraging thing is that as he gets older he is improving. He's in year 5 now, so about 10-11 years old. He is exceptionally competitive, and still doesn't cope with sporting events if he doesn't win. But he's learning to manage his reactions over time. Keep up the hard work. You're doing the right thing.
Our daughter is on Strattera and it has been positively life-changing for her! I've heard that some don't have good results with Strattera, but we're in the camp who LOVE this medication! Hope it is the same for your child, but if not, don't hesitate to tweak the dosage or try something else. If you've got any questions feel free to ask!
Lori
Mom to 8 great kids, soon to be 9!
www.youbelong.net/hays
Hey ...you are human..try not to be too hard on yourself. As you've given many parents advice...look to the Lord. Have faith in Him...which you do.
Meds are not the worse thing..my child would not even be able to function in the outside world without his.
God bless
To err is human - to post about it and focus on improving is a true inspiration. I need your strength. Please pray for me; our family is collapsing and we all need as many prayers as you can muster. Especially for Olga who we will be unable to adopt as a result. PS - Concerta is what worked wonders for us - I believe I read it has much better results with girls.... which be warned the hormones do a job on the ADD and medication - it is a constant balancing act.
I hope that the medicine works out for you all. And that you start to see improvement with William.
Peace.
Christine,
I have not been reading your blog for very long, but I believe you mentioned - or someone did - about William perhaps falling under the umbrella of Autism. Some of the things you describe about him sound so much like my 11 year old grandson who was diagonosed with Aspergers Syndrome at 4. He has peer problems also. He really doesn't really have a friend except for my daughters friends children. His worst time at school is recess and has been since he started school. The problem is the rules to all the games change - all the kids get used to that and really take no notice = just get on with the game. He on the other hand will know the rules and then they change. He get so frustrated and calls everyone "cheaters" and has a bit fit in the playground and has even gotten himself into a few fights over these games. This is just one of his frustrations. These children are quite rule oriented - they REALLY like everything to be the same and get frustrated when it's not. Even at home things are better when it is orderly and structured. He copes so much better. I hope this helps you. You are doing a great job with your children and you are wonderful parents.
Dear Christine,
14 yrs ago we put our son on Dexedrine and did not tell his slightly younger brother. Within 3 weeks, the brother said, "this is the first time when we ever cleaned the basement that you really helped!" It was true. Even a child could see the difference. I don't know how we could have made it through ages 16-18 without the meds. In college, he stopped taking them, flunked out, struggled emotionally...and then picked himself up, got a better major, is graduating this December and is poised to enter graduate school. He now takes his meds on his own, knowing that they are not a cure-all, but they help immensely. He also gets planning assistance from his fiancee, who sees his flaw as minor. We did worry about nutrition and growth, but he is now 5'11" and a perfect weight. I tease that it's "better living through chemistry!"
Sherry in Ohio
I too went screaming and kicking down the path of ADHD meds. for my son. We tried everything for well over four years, finally my Dr. said to me: "You don't have a problem giving PJ his insulin do you?" Our oldest son is diabetic since age 11, I told him of course NOT. Then he said "Well why are you expecting Joey to function with his chemical imbalance when you don't expect it of PJ?" I started sobbing because I realized I had been expecting something from my son that he was unable to achieve. Not UNWILLING, UNABLE, big difference.
He's tried all the meds, the only one that is working at this time is the short acting Ritilin, but that allows us long enough to get his schooling done. We still work very hard on behavior modification and choices, we have a majority of the day and evening to do that :o/
He has also been diagnosed with ODD and probably on the autism spectrum. We take one day at a time with lots of prayer.
Praying it all works out well for your children. Don't be so hard on yourself, we do what we do with the best intentions and love, as long as we seek God's will we have to give ourselves grace.
Years ago I was against skeptical about medicating kids with ADHD as well. Then I met my stepson. Even with meds he struggles, but they have improved his life tremendously.
Hi Christine! I would still strongly recommend reading 'Disconnected Kids' - I am really wondering if there is something to what this book suggests. It's down the biofeedback line, I believe. Or even checking into biofeedback. I'd be interested to hear what you think of considering this type option (William.) Wishing you the best!
I have 3 kids on medication for AD(H)D and I know it was a good decision. I know God will heal them one day, but in the meantime i don't want to get all the negative attention the had before the medication. They are so much happier now because of all the positieve attention they get, and playing is so much more fun when you can concetrate a little better.
Hello...I have never commented on your blog, Christine, but have been following it and your family for some time now...atleast 1 or 2 years..Sometimes I felt a bit like a stalker! lol..I found your blog thru your adoption videos on Youtube and found you here... I think your life interests and intrigues me on several levels - inicially due to your adoption adventures, always a dream of mine that I do not think will ever be realized for verious reasons - and also your large family, another dream. Also your stamina and attitude towards parenting impress me - I have 2 girls (ages 2 and 8) and sometimes feel overwhelmed so I often wonder "how you do it?!" : ) You obviously have alot of faith in your faith and that is a huge plus on all accounts....
But still , day to day life as a Mom is hard as I am sure you know 12 fold. I think you are amazing and enjoy reading the little details of each day. It amazes me that you even have time to do a blog...
So here I am, finally out of lurkdom. My name is Rita, age 39 , very happily married and have 2 girls and I live in seville Spain....pleased to meet you : )
I am so glad you seem to be making progress with William and your other daughter.....we do what we can and try our best always knowing that our decisions are based on our profound love for our kids. You are an example of how one person (or two - can´t leave out John) can change the world, a child at a time.
Abrazos.
Hi, Christine! We just found out our 17 year old son probably has ADD. We will be seeing a psychologist to determine if he should try medicine or some other form of therapy first. In talking to the school district's IEP facilitator, she gave me a helpful bit of advise. She said that it could be kind of scary for my son if the medicine does work. She said that a lot of kids don't like it and are scared because even though what they are now feeling would be "normal" to us, it won't be "normal" to them. And that can be a scary feeling. It would be as if our brains suddenly amped up to the speed their brains are normally at. Anyway, I thought that was kind of helpful to keep in mind if and when we try medicine. Good luck! I think the hardest part of any "brain" medication is the trial and error period of finding what works. God bless.
Hey Christine,
Thanks for you post, it is filled with things I can so relate too!!! I just blogged about how I hate giving Autumn all her medication but she needs them, it helps her be successful in life and that is my goal. I will pray for you, you are a great mom!
I commend you, Christine. This is a difficult decision. I used to think that all of these diagnoses were baloney. Not anymore. God brought me to the bottom of my pride and "knowledge about such things" when I came down with a debilitating clinical depression. I resisted taking meds for it for a long time. I didn't get better and my whole life was in danger (marriage, relationships with my kids, my life). I finally gave in. They really helped me a lot. This experience changed my opinion about a lot of things...including ADD and ADHD.
There will come times when well meaning Christians will challenge you about this decision. They will make you feel like a poor parent...and weak Christian. They will even quote scriptures to back up their arguments. Stick to your guns and don't let them sway you.
Thank you so much for posting about your daughter. I will be watching for posts on how the medicine helps your daughter as I feel that soon we may be faced with making the medication decision for our daughter. I started seeing little things in our daughter (5) the summer before last that is leading me to believe that she will eventually be diagnosed with ADD (she is predisposed biologically). I have done a lot of research b/c I want to do what is best for her and I love to read first hand stories from parents that I trust on things they do to help their child be the best they can be!
I dont understand alot about adhd but i do understand autism and the need as parents for us to think forward to try and engage what will happen next.
Im not going to pretend i am anywhere near good at this to be honest since Livvy died my patience disappeared. I am having to learn this all again.
Patience for ourselves and for our children xxx
I know I'm late to the party here, but I must chime in.
As a child, teachers suspected I had ADD. My parents refused to medicate me. I struggled through junior high, high school, and college.
I worked as an equities trader on wall street, and luckily, that job suited my ADD tendencies. Eventually I got married, had kids, and was still suffering.
5 years ago, I started Adderall. I cannot tell you the change it has made in my life. Until you understand what it's like to have an ADD brain, you just cannot understand. It's a living hell, and by helping her now...you are saving her from YEARS of disappointment. I'm telling you, I honest to God tried so hard, but just couldn't succeed. Now, with the Adderall, I'm normal...productive...and HAPPY.
So, congrats...really.
:)
This is in response to "lorihays" comment. Unfortunately we are the parents of a son we put on Straterra 2 1/2 yrs ago. For us it was not such a good experience, but he was put on it for a processing delay (not ADD) to help him focus better in school. Instead of making him focus better in school it made him "inward focus" so if he had a bad thought he couldn't get rid of it. He thought he was going crazy so he never told us (he was too embarrassed and ashamed) until it was so bad that he had developed tics from it and was slipping into a depression. Needless to say we weaned him off in a hurry and he isn't on anything.
I won't be offended at all if you don't post this comment, I know it's negative, but just felt I needed to say what our experience was. I hope it works great for your daughter.
Post a Comment