Guest guest Posted December 2, 2003 Report Share Posted December 2, 2003 Dear , Wow. Poor Luke, poor you. It's so awful when school falls apart because then everything else seems to follow. We were in your shoes last year - thankfully (knock on wood) things are going much, much better this year. Annie used to take only .5 mg Clonidine (half a tablet - I hope I'm remembering the mg. right). It really helped her knock out. But she only takes 18 mg Concerta, and I remember that when we tried to raise that she was up all night. Our pdoc stopped the Clonidine because she said it only stays in their system for four hours, so unless we wanted to dose it continually during the day it wouldn't help her tics. It seemed to ME that it was helping her tics, even during the day, but this could have been from the increased sleep. At any rate, we solved the tic issue with increasing the Risperdal. She still has some, but right now they are barely noticeable. Sleep is so important for kids. When Annie gets a full night (9-10 hours) she is a different person. I used to wonder last year whether her school problems were from not sleeping well, or what. What seemed to help us the most with the school problems were a) a different teacher because of the decreased stress, and switching to Lexapro. She seems more capable of remembering things this year, and is doing all her homework on her own. That could also be from an added year of maturity though. If increasing the Concerta doesn't help, could you try a different ADHD med? I can't remember what you've done in the past. Have you tried Strattera? Adderall? It seems to me that there must be a point at which increasing the dose of the stimulant has to just keep the kids from sleeping, at which point they definetly won't concentrate. Keep in touch. I'd like to hear how things go for you. Best wishes, in NV mom to Annie (11, on Lexapro, Concerta and Risperdal) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 2, 2003 Report Share Posted December 2, 2003 In a message dated 12/2/2003 8:48:04 AM Pacific Standard Time, msmichelle@... writes: > I meet with the principal this Thursday, and would sure appreciate > any support and advice you can lend so that I can feel a little more > confident going into that meeting. His issue is getting Luke to > school on time. I'd suggest asking your doc to send a letter. Our doc typed up a letter for me in her office, saying that the severity of 's OCD and depression were interfering with school, and that she recommended " home hospital " . Perhaps if your doc described what it's like to get a compulsive kid up and moving and out the door, it would help. Also, if the princ. sees that it's either allowing you to do some homeschool or having to cough up some district funds for tutoring, he might see the light about partial homeschooling, since it wouldn't affect his budget. Good luck. We're in CA and I'm grateful that the school has been extremely cooperative. Suzanne Suzanne Stone 480 Lomer Way Milpitas, CA 95035-5933 Weekenders Independent Team Leader and Fashion Coordinator Weekenders.... The Clothes You Love to Live In. www.weekenders.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 2, 2003 Report Share Posted December 2, 2003 Hi - we are trying clonidine right now, too. Be very careful in changing the dosage - it does affect blood pressure, and our p-doc has us titrating up very slowly over a month, starting with 1/4 of a 0.1 mg tablet at night, then 1/2 tablet at night, then adding 1/4 tablet in the morning to the 1/2 at night, changing every 5 days and checking our son's blood pressure often. We are going to start giving it 3x a day this week. Haven't seen any real changes in behavior or tics yet, but at least it hasn't made his ocd any worse. Here is some helpful info on clonidine I found on the web - originally from the TSA - it is so frustrating that it takes so long to know if these medications are helping or not, isn't it! regards, Sandy http://www.texaschildneurology.com/Tourette.htm Clonidine Clonidine (Cataprese) is an imidazoline compound with alpha- adrenergic agonist activity. In low doses it " down-regulates " alpha- adrenergic neurons in the locus ceruleus, decreasing the release of central norepinephrine. Since 1979 it has been considered to be of benefit for the treatment of TS although the response rate is lower than that of either haloperidol or pimozide. In general it is of advantage because of the low incidence of side effects associated with its use. Perhaps of greatest importance is that it does not have the potential of causing tardive dyskinesia. Clonidine has been approved by the FDA only for use in hypertension, but clinicians can prescribe it for TS without special government approval as long as they understand its indications and share the basis for their decision with the family and child. In addition to reducing the simple motor and phonic symptoms in TS, clonidine seems especially useful in improving attentional problems and ameliorating complex motor and phonic symptoms. In general, clonidine is started at low doses of 0.05 mg/day and slowly titrated over several weeks to 0.15-0.30 mg/day. Since clonidine has a 6 hour half-life it is important that patients take small doses 3 to 4 times each day. (An alternative to multiple doses is the transdermal patch that needs to be changed only once a week.) Doses of 0.4 mg daily are not infrequent, but doses above 0.5 to 0.6 mg/day are more likely to lead to side effects. When the medication is working effectively, patients may experience the need for their next dose by sensing an increasing anxiety, frequency of symptoms, or irritability. Unlike haloperidol, which may lead to clear improvement within a few days, clonidine tends to have a slower onset of action. When larger doses are used earlier, improvement may occur sooner, but there may be more sedation. With slower titration to therapeutic levels, clonidine may take three weeks or longer to show a beneficial effect. The patient may experience a reduction in tension, a feeling of being calm, or a sense of having a " long fuse " before tics are reduced. A gradual decrease in complex motor tics and compulsions also may precede clear improvement in simple tics. In the most successful cases, attentional, behavioral, and complex phenomena seem more responsive than the simpler tics. Evaluation of the medication's effectiveness may not be possible before three to four months. When there is a positive response, improvement may progressively appear over many months and up to a year or more later. Patients gain confidence in themselves, adjust better to school, feel less irritable, and have fewer tic symptoms. Those therapeutic benefits reinforce each other. The major side effect of clonidine is sedation, which appears early in the course of treatment and especially if the dose is increased quickly, but which tends to abate after several weeks. A few patients have dry mouth, although it is experienced less often by children than by adults. There are occasional reports that patients feel that things are " too bright, " perhaps because of the impairment of pupillary contraction. At high doses, there may be hypotension and dizziness, particularly if clonidine is given at high doses quite early or if it is increased to over 0.4 or 0.5 mg/day. At lower doses, blood pressure is not clinically affected, although a fall of several mm mercury in diastolic and systolic pressure can be detected. Slight prolongation of the PR interval on the electrocardiogram has been noted, but this has not been considered to be of significance. Increased irritability, nightmares, and insomnia have also been reported. When clonidine is withdrawn, it should be tapered gradually. ********************** Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2003 Report Share Posted December 23, 2003 Kelley, I am so happy that the medication is working so well for your daughter. I can't imagine struggling for that long with the sleep issue. We have had trouble with our son's sleeping patterns from infancy until now. I've read everything I could find re: helping one's child to sleep and it hasn't proven fruitful. Nevertheless, we're going to keep on trucking and once I change my mindset and accept the fact that medication may be part of the answer, I'll get more educated about clonidine. It is so difficult for me to come to terms with the need for medication... but the day will come. in AZ Quote Link to comment Share on other sites More sharing options...
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