Guest guest Posted January 26, 2010 Report Share Posted January 26, 2010 Hi, Ivan. My daughter has been diagnosed with ocd and tourettes. She is almost 13 and was diagnosed with ocd at 6 yrs old, and a tic disorder a few months later. She didn't develop the vocal tics for about another year. She also claims to not have an actual obsession, but just a " weird " or " bad " feeling or not " feeling right " . I think this is sometimes called " just right " ocd. We have also been unable to separate rituals from tics. Her doctor has told us this is common in a diagnosis of ocd with tourettes or tics. For her, I believe that her problem is really more tic related, with anxiety thrown in. I know that she has ocd, as she has some issues with confessing, and lots of responsibility issues, but I think that these things take a backseat to the tics, which as I understand it, are pretty much a physical reaction that can not be controlled. We have done some habit reversal therapy for tics, with moderate success. My daughter also takes zoloft, but we did not see a dramatic change in her behavior/symptoms until we added tenex. It was like a miracle. While she has had some mild tics over the years, they have been manageable and fleeting, and her quality of life shot back up to where it was before this disorder began. She was a little sleepy when first starting the meds, but she adjusted to that quickly. She is definitely not sedated. The tenex has actually been helpful also, in that is counteracts some of the activating effects of the zoloft. I strongly suggest you give the tenex a try. My daughter takes 3/4 of a 1 mg tablet in the a.m and one at about 6 in the evening. Start out slow and see what happens. You can always stop the tenex, if it doesn't seem to be working, but from reading this post, I have the feeling that it could be very helpful. Good luck to you and your son. > New member here. My son Jake has been diagnosed with fairly severe > OCD starting end of Sept '09. (Jake's OCD may have been catalyzed > by watching his sister go through a disturbing depression at around > the same time -- which in itself was possibly due to my wife's > battling a brain tumor. Talk about a domino effect! > > Anyway, Jake's OCD is not " classic " in that 1) his repetitive > behaviors have no discernible " trigger " and can happen anywhere and > at any time(i.e.: no fears/anxiety about contamination, harm, > confessing, bad thoughts etc.); 2) He doesn't feel actual > obsessional anxiety when confronted by the OCD, only feeling > " weird " , which can last for hours sometimes if he doesn't perform > the ritual; and 3) his rituals seem to overlap with tic-like > behavior (throat clearing, pointing while saying " Oh yeah " ) In > addition, although never formally diagnosed with ASD, Jake may have > a " touch " of Aspergers. > > Jake has tried to engage in ERP therapy without meds, (Brady Case, > M.D. out of NYU Child Study program in Hackensack) but couldn't. > When he did seemingly perform the ERP, he said it was only > " pratice " and not " real life " so that the habituation process > really never happened. Dr. Case then put Jake on Zoloft about 8 > weeks ago and Jake is currently up to a dose of 150mg. The 150 mg > has been for about 1 week. We have not seen any imporvement of > symptoms although we have been told that we need to try an SSRI at > the responsive dose for 8-10 weeks for OCD. > > Mansueto, PhD out of the Washington D.C. area has written > about a subset of OCD called " tourettic OCD " which seems to fit > Jake like a glove. Some the treatment implications of tourettic OCD > is that it generally does not respond as well to SSRIs and it > generally does not respond as well to classic ERP and the cognitive > behavior therapy may have to be tweaked. > Does anyone have kids with this harder-to-treat subtype " tourettic > OCD " and if so, what treatments have worked? Any providers who > specialize in this subset in the New York City tri-state area? Our > treating psych has suggested that we contemplate augmenting the > Zoloft with either an alpha agonist (Clonidine or Tenex) or an > atypical antipsychotic in low doses. We really don't want to sedate > Jake (either augmenting med) or expose him to the potential insulin > resistance that may accompany the atypical antipsychotics but he is > really in distress. > > To say the least we feel overwhelmed and would appreciate any > experience/wisdom/comments. Sorry for the long post. > > Ivan > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 27, 2010 Report Share Posted January 27, 2010 Ivan, I'm so sorry to hear about all your family has been going through. It certainly does sound like a domino effect. I don't know anything about Tourettic OCD, but I do know that SSRIs often take longer than a week at an effective dose to show significant improvement. I imagine you may find someone on the listserve who can provide information or you might try contacting Dr. Mansueto himself to see if he can recommend anyone in your area. I'm glad you found us. (mom with OCD, 9 yo daughter w/OCD) > > Subject: Tourettic OCD in 9 year old boy > To: > Date: Tuesday, January 26, 2010, 10:34 PM > New member here. My son Jake has been > diagnosed with fairly severe OCD starting end of Sept '09. > (Jake's OCD may have been catalyzed by watching his sister > go through a disturbing depression at around the same > time -- which in itself was possibly due to my wife's > battling a brain tumor. Talk about a domino effect! > > Anyway, Jake's OCD is not " classic " in that 1) his > repetitive behaviors have no discernible " trigger " and can > happen anywhere and at any time(i.e.: no fears/anxiety about > contamination, harm, confessing, bad thoughts etc.); 2) He > doesn't feel actual obsessional anxiety when confronted by > the OCD, only feeling " weird " , which can last for hours > sometimes if he doesn't perform the ritual; and 3) his > rituals seem to overlap with tic-like behavior (throat > clearing, pointing while saying " Oh yeah " ) In addition, > although never formally diagnosed with ASD, Jake may have a > " touch " of Aspergers. > > Jake has tried to engage in ERP therapy without meds, > (Brady Case, M.D. out of NYU Child Study program in > Hackensack) but couldn't. When he did seemingly perform the > ERP, he said it was only " pratice " and not " real life " so > that the habituation process really never happened. Dr. Case > then put Jake on Zoloft about 8 weeks ago and Jake is > currently up to a dose of 150mg. The 150 mg has been > for about 1 week. We have not seen any imporvement of > symptoms although we have been told that we need to try an > SSRI at the responsive dose for 8-10 weeks for OCD. > > Mansueto, PhD out of the Washington D.C. area has > written about a subset of OCD called " tourettic OCD " which > seems to fit Jake like a glove. Some the treatment > implications of tourettic OCD is that it generally does not > respond as well to SSRIs and it generally does not respond > as well to classic ERP and the cognitive behavior therapy > may have to be tweaked. > Does anyone have kids with this harder-to-treat subtype > " tourettic OCD " and if so, what treatments have worked? Any > providers who specialize in this subset in the New York City > tri-state area? Our treating psych has suggested that we > contemplate augmenting the Zoloft with either an alpha > agonist (Clonidine or Tenex) or an atypical antipsychotic in > low doses. We really don't want to sedate Jake (either > augmenting med) or expose him to the potential insulin > resistance that may accompany the atypical antipsychotics > but he is really in distress. > > To say the least we feel overwhelmed and would appreciate > any experience/wisdom/comments. Sorry for the long post. > > Ivan > > > > > ------------------------------------ > > Our list archives feature may be accessed at: http://health.groups.yahoo.com/group// > by scrolling down to the archives calendar . Our links > may be accessed at http://health.groups.yahoo.com/group//links > . Our files may be accessed at > http://health.groups.yahoo.com/group//files > . > Our list advisors are Gail B. , Ed.D.(http://www.ocdawareness.com ), Tamar Chansky, Ph.D.( http://www.worrywisekids.org ), and Dan Geller, M.D. ( > http://www.massgeneral.org/doctors/doctor.aspx?ID=18068 > ). You may ask a question of any of these mental health > professionals by inserting the words " Ask Dr.(insert name) " > in the subject line of a post to the list. Our list > moderators are Castle, Judy Chabot, BJ Closner, and > Barb Nesrallah. Subscription issues or > suggestions may be addressed to Louis Harkins, list > administrator, at louisharkins@... > . Our group and related groups are listed > at http://health.groups.yahoo.com/group/ocdsupportgroups/links > . IOCDF treatment providers list may be viewed at http://www.ocfoundation.info/treatment-providers-list.php > . > NLM-NIH Drug Information Portal may be viewed at > http://druginfo.nlm.nih.gov/drugportal/drugportal.jsp?APPLICATION_NAME=drugporta\ l > . IOCDF recommended reading list may be accessed at http://www.ocfoundation.org/Books.aspx . IOCDF > glossary of terms may be accessed at http://www.ocfoundation.org/glossary.aspx > . IOCDF membership link may be accessed at http://www.ocfoundation.net/membership/ . Drugs.com > pill identification wizard may be accessed at http://www.drugs.com/imprints.php . Mayo Clinic > Drug and Herb Index may be accessed at http://www.mayoclinic.com/health/drug-information/DrugHerbIndex > . Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 27, 2010 Report Share Posted January 27, 2010 Ivan, Have you explored the possibility of PANDAS? My dd's ocd is exactly as you describe Jake's. She feels a need to repeat (till it feels normal) but has no obsession to go with it. Our last psychologist suggested PANDAS and I began researching it this fall, after seeing my dd suffer off and on for 3 years. When I read " Saving Sammy " , I was convinced as her behaviors were so similar to his. We've since started her on Augmentin XR as well as Zithromax and her symptoms are slowly abating over time. It's been 2.5 months since she started them. She has gone from crisis mode to enjoying many parts of her day. She still struggles daily with reassurance questions and some repeating behaviors but the improvement has been drastic and I'm convinced that one day she'll be cured. I keep harping about it on this board when new members join because I'd hate for anyone to miss checking out this possibility. A great place to research and ask questions is www.latitudes.org Often SSRIs do not work for kids with PANDAS. PANDAS can also cause attention issues and these kids have a difficult time working through exposures. Please look into it. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 30, 2010 Report Share Posted January 30, 2010 -- Thanks for the response. I'm so happy for you and your daughter that she's doing much better. Questions: Did your daughter try exposure-response prevention therapy at any time, either before or after the meds? If so, did the meds help her engage in this therapy? You mentioned habit-reversal therapy as not being much of a help. Was this attempted before or after the meds? How long has your daughter been on Tenex? How long do you plan on keeping her on the Tenex? Thanks again, Ivan -------------- Original message from Quattlebaum : -------------- > Hi, Ivan. My daughter has been diagnosed with ocd and tourettes. > She is almost 13 and was diagnosed with ocd at 6 yrs old, and a tic > disorder a few months later. She didn't develop the vocal tics for > about another year. She also claims to not have an actual obsession, > but just a " weird " or " bad " feeling or not " feeling right " . I think > this is sometimes called " just right " ocd. We have also been unable > to separate rituals from tics. Her doctor has told us this is common > in a diagnosis of ocd with tourettes or tics. For her, I believe > that her problem is really more tic related, with anxiety thrown in. > I know that she has ocd, as she has some issues with confessing, and > lots of responsibility issues, but I think that these things take a > backseat to the tics, which as I understand it, are pretty much a > physical reaction that can not be controlled. We have done some > habit reversal therapy for tics, with moderate success. My daughter > also takes zoloft, but we did not see a dramatic change in her > behavior/symptoms until we added tenex. It was like a miracle. > While she has had some mild tics over the years, they have been > manageable and fleeting, and her quality of life shot back up to > where it was before this disorder began. She was a little sleepy > when first starting the meds, but she adjusted to that quickly. She > is definitely not sedated. The tenex has actually been helpful also, > in that is counteracts some of the activating effects of the zoloft. > I strongly suggest you give the tenex a try. My daughter takes 3/4 > of a 1 mg tablet in the a.m and one at about 6 in the evening. Start > out slow and see what happens. You can always stop the tenex, if it > doesn't seem to be working, but from reading this post, I have the > feeling that it could be very helpful. Good luck to you and your son. > > > > > New member here. My son Jake has been diagnosed with fairly severe > > OCD starting end of Sept '09. (Jake's OCD may have been catalyzed > > by watching his sister go through a disturbing depression at around > > the same time -- which in itself was possibly due to my wife's > > battling a brain tumor. Talk about a domino effect! > > > > Anyway, Jake's OCD is not " classic " in that 1) his repetitive > > behaviors have no discernible " trigger " and can happen anywhere and > > at any time(i.e.: no fears/anxiety about contamination, harm, > > confessing, bad thoughts etc.); 2) He doesn't feel actual > > obsessional anxiety when confronted by the OCD, only feeling > > " weird " , which can last for hours sometimes if he doesn't perform > > the ritual; and 3) his rituals seem to overlap with tic-like > > behavior (throat clearing, pointing while saying " Oh yeah " ) In > > addition, although never formally diagnosed with ASD, Jake may have > > a " touch " of Aspergers. > > > > Jake has tried to engage in ERP therapy without meds, (Brady Case, > > M.D. out of NYU Child Study program in Hackensack) but couldn't. > > When he did seemingly perform the ERP, he said it was only > > " pratice " and not " real life " so that the habituation process > > really never happened. Dr. Case then put Jake on Zoloft about 8 > > weeks ago and Jake is currently up to a dose of 150mg. The 150 mg > > has been for about 1 week. We have not seen any imporvement of > > symptoms although we have been told that we need to try an SSRI at > > the responsive dose for 8-10 weeks for OCD. > > > > Mansueto, PhD out of the Washington D.C. area has written > > about a subset of OCD called " tourettic OCD " which seems to fit > > Jake like a glove. Some the treatment implications of tourettic OCD > > is that it generally does not respond as well to SSRIs and it > > generally does not respond as well to classic ERP and the cognitive > > behavior therapy may have to be tweaked. > > Does anyone have kids with this harder-to-treat subtype " tourettic > > OCD " and if so, what treatments have worked? Any providers who > > specialize in this subset in the New York City tri-state area? Our > > treating psych has suggested that we contemplate augmenting the > > Zoloft with either an alpha agonist (Clonidine or Tenex) or an > > atypical antipsychotic in low doses. We really don't want to sedate > > Jake (either augmenting med) or expose him to the potential insulin > > resistance that may accompany the atypical antipsychotics but he is > > really in distress. > > > > To say the least we feel overwhelmed and would appreciate any > > experience/wisdom/comments. Sorry for the long post. > > > > Ivan > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 30, 2010 Report Share Posted January 30, 2010 Hi BJ-- I appreciate your response and I hope that your son is doing better. You mentioned that it took about 6 months for his meds to reach a helpful level. What meds/doage was he on? Jake has been on Zoloft for about 10 weeks now, and he his psych dr. has slowly increased him to where is now on 150 mg (this dosage for about 2 weeks). We really have not seen an improvement, and he still cannot enage in the ERP therapy. Take care, Ivan -------------- Original message from " svdbyhislove " : -------------- Welcome, Ivan. I'm not familiar with Tourettic OCD, but remember reading that Tourettes and OCD, often go hand in hand. At one point, a psychologist diagnosed our son with Tourettes, but I'm still not sure if that was correct, since those with OCD often can have tics that come and go. Someone in here once shared the criteria for Tourettes. Seems like they said the tics have to be ongoing for at least a year in order for it to be considered Tourettes, which hasn't been the case for our son. Our son's current psychologist also thinks he might have mild Aspergers. It can be hard to sort it all out sometimes. Especially when the disorders can share traits. It does seem that often treating kids who are comorbid can be much more complicated. I can share with you that the last time our son was put on meds, it took 6 months for him to reach a level that was helpful to him. But, we did notice improvements along the way too. Are you noticing any improvement at all? I thought the same as , that you could be dealing with some " just right " OCD, when you describe that he doesn't have the typical anxiety attached. Our son had some OCD that was like that. It actually seemed the easiest for him to overcome with the ERP. We had health issues in our family too, that were anxiety producing. It's horrible when you already have a kid pre-wired with an anxiety disorder, in a situation that is stressful. It just seems to make everything worse. I hope your wife is recovering and okay now. I can imagine that you are overwhelmed. It is the worst when they are really suffering. Have you found anything that helps him? For instance our son was able to distract himself sometimes, with video games, his computer, or even TV, to get a small break from the constant bombardment of thoughts. Please keep in touch and let us know how things are going. I hope the medication kicks in soon and you start to see an improvement. We usually noticed a difference, from a med increase, within 2-3 weeks. BJ > > New member here. My son Jake has been diagnosed with fairly severe OCD starting end of Sept '09. (Jake's OCD may have been catalyzed by watching his sister go through a disturbing depression at around the same time -- which in itself was possibly due to my wife's battling a brain tumor. Talk about a domino effect! > > Anyway, Jake's OCD is not " classic " in that 1) his repetitive behaviors have no discernible " trigger " and can happen anywhere and at any time(i.e.: no fears/anxiety about contamination, harm, confessing, bad thoughts etc.); 2) He doesn't feel actual obsessional anxiety when confronted by the OCD, only feeling " weird " , which can last for hours sometimes if he doesn't perform the ritual; and 3) his rituals seem to overlap with tic-like behavior (throat clearing, pointing while saying " Oh yeah " ) In addition, although never formally diagnosed with ASD, Jake may have a " touch " of Aspergers. > > Jake has tried to engage in ERP therapy without meds, (Brady Case, M.D. out of NYU Child Study program in Hackensack) but couldn't. When he did seemingly perform the ERP, he said it was only " pratice " and not " real life " so that the habituation process really never happened. Dr. Case then put Jake on Zoloft about 8 weeks ago and Jake is currently up to a dose of 150mg. The 150 mg has been for about 1 week. We have not seen any imporvement of symptoms although we have been told that we need to try an SSRI at the responsive dose for 8-10 weeks for OCD. > > Mansueto, PhD out of the Washington D.C. area has written about a subset of OCD called " tourettic OCD " which seems to fit Jake like a glove. Some the treatment implications of tourettic OCD is that it generally does not respond as well to SSRIs and it generally does not respond as well to classic ERP and the cognitive behavior therapy may have to be tweaked. > Does anyone have kids with this harder-to-treat subtype " tourettic OCD " and if so, what treatments have worked? Any providers who specialize in this subset in the New York City tri-state area? Our treating psych has suggested that we contemplate augmenting the Zoloft with either an alpha agonist (Clonidine or Tenex) or an atypical antipsychotic in low doses. We really don't want to sedate Jake (either augmenting med) or expose him to the potential insulin resistance that may accompany the atypical antipsychotics but he is really in distress. > > To say the least we feel overwhelmed and would appreciate any experience/wisdom/comments. Sorry for the long post. > > Ivan > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 30, 2010 Report Share Posted January 30, 2010 Kerry-- I hope your daughter is doing much better. Jake's OCD with tics did seem to have a sudden onset but then again, he observed his sister go thpough a very distubing major depression at around the same time. Jake's strep titers came back normal, although some other members suggested that a negative titer doesn't necessarily rule out PANDAS. Interestingly, Jake, in 2005, 2006 and 2007, had a rapid and severe facial and head cellulities where half of his face literally " blew up " and he had to be agressively treated with antibiotics. These infections all ocurred in September of each year and September (in 2009) is when we started to notice his OCD/tic symptoms. What I'm not sure of is if this can still be PANDAS or some other autoimmune attack of his brain when the last known infection ocurred 2 years beofre his sudden OCD/tics. Thanks, Ivan --------- Tourettic OCD in 9 year old boy To: Date: Wednesday, January 27, 2010, 3:34 AM New member here. My son Jake has been diagnosed with fairly severe OCD starting end of Sept '09. (Jake's OCD may have been catalyzed by watching his sister go through a disturbing depression at around the same time -- which in itself was possibly due to my wife's battling a brain tumor. Talk about a domino effect! Anyway, Jake's OCD is not " classic " in that 1) his repetitive behaviors have no discernible " trigger " and can happen anywhere and at any time(i.e.: no fears/anxiety about contamination, harm, confessing, bad thoughts etc.); 2) He doesn't feel actual obsessional anxiety when confronted by the OCD, only feeling " weird " , which can last for hours sometimes if he doesn't perform the ritual; and 3) his rituals seem to overlap with tic-like behavior (throat clearing, pointing while saying " Oh yeah " ) In addition, although never formally diagnosed with ASD, Jake may have a " touch " of Aspergers. Jake has tried to engage in ERP therapy without meds, (Brady Case, M.D. out of NYU Child Study program in Hackensack) but couldn't. When he did seemingly perform the ERP, he said it was only " pratice " and not " real life " so that the habituation process really never happened. Dr. Case then put Jake on Zoloft about 8 weeks ago and Jake is currently up to a dose of 150mg. The 150 mg has been for about 1 week. We have not seen any imporvement of symptoms although we have been told that we need to try an SSRI at the responsive dose for 8-10 weeks for OCD. Mansueto, PhD out of the Washington D.C. area has written about a subset of OCD called " tourettic OCD " which seems to fit Jake like a glove. Some the treatment implications of tourettic OCD is that it generally does not respond as well to SSRIs and it generally does not respond as well to classic ERP and the cognitive behavior therapy may have to be tweaked. Does anyone have kids with this harder-to-treat subtype " tourettic OCD " and if so, what treatments have worked? Any providers who specialize in this subset in the New York City tri-state area? Our treating psych has suggested that we contemplate augmenting the Zoloft with either an alpha agonist (Clonidine or Tenex) or an atypical antipsychotic in low doses. We really don't want to sedate Jake (either augmenting med) or expose him to the potential insulin resistance that may accompany the atypical antipsychotics but he is really in distress. To say the least we feel overwhelmed and would appreciate any experience/wisdom/ comments. Sorry for the long post. Ivan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 30, 2010 Report Share Posted January 30, 2010 Hi, Ivan. He is currently on 60 mg of Celexa, which doesn't sound like much compared to the 150 mg of Zoloft, but the mgs per dosage is not the same for the two meds. For Celexa, that is considered the max (according to some docs). It took 6 months for him to stabilize on the meds and reach maximum benefit because we took it slowly, trying to find the right dosage without over medicating. As we were slowly raising the dosage (usually 10 mg at a time) we saw improvements all along. It got gradually better. Sometimes it was minute improvements, so we would have to up it again. We usually waited for 3-4 weeks, after an increase, to see how he responded. Then when he got to 60 mg, we sat there for a while to see how he did. He was doing ERP therapy through most of that too, so was receiving the benefit of that too. Eventually, the two together worked. I was just reading in Aureen Wagner's book that if they reach maximum dosage, it is recommended that they wait for 4-6 weeks before deciding the medication is not working. For some, they have to try different medications because one won't work for them, but another does. We were lucky that the first one we tried, worked. It's all so individual, unfortunately. Wouldn't it be nice if there were concrete answers that worked for everyone. <sigh> I know it is really rough during that wait. I'm so sorry you are in that place. We've been there more than once and it is the worst! Is there anything you can do to help distract him? Electronics helped our son, sometimes. Video games, his computer, even the TV would help sometimes. I got pretty good at Kart. <grin> We even played marathons of board games to try to keep his mind occupied, while waiting day after day for the meds to finally kick in. On the especially rough days, he would sometimes need to take Klonipin too, to cope. So many days I felt like I could finally breath again, when he would go to sleep. I knew his mind was at rest and I could relax a little. I hope the med kicks in for you soon. BJ > > > > New member here. My son Jake has been diagnosed with fairly severe OCD starting end of Sept '09. (Jake's OCD may have been catalyzed by watching his sister go through a disturbing depression at around the same time -- which in itself was possibly due to my wife's battling a brain tumor. Talk about a domino effect! > > > > Anyway, Jake's OCD is not " classic " in that 1) his repetitive behaviors have no discernible " trigger " and can happen anywhere and at any time(i.e.: no fears/anxiety about contamination, harm, confessing, bad thoughts etc.); 2) He doesn't feel actual obsessional anxiety when confronted by the OCD, only feeling " weird " , which can last for hours sometimes if he doesn't perform the ritual; and 3) his rituals seem to overlap with tic-like behavior (throat clearing, pointing while saying " Oh yeah " ) In addition, although never formally diagnosed with ASD, Jake may have a " touch " of Aspergers. > > > > Jake has tried to engage in ERP therapy without meds, (Brady Case, M.D. out of NYU Child Study program in Hackensack) but couldn't. When he did seemingly perform the ERP, he said it was only " pratice " and not " real life " so that the habituation process really never happened. Dr. Case then put Jake on Zoloft about 8 weeks ago and Jake is currently up to a dose of 150mg. The 150 mg has been for about 1 week. We have not seen any imporvement of symptoms although we have been told that we need to try an SSRI at the responsive dose for 8-10 weeks for OCD. > > > > Mansueto, PhD out of the Washington D.C. area has written about a subset of OCD called " tourettic OCD " which seems to fit Jake like a glove. Some the treatment implications of tourettic OCD is that it generally does not respond as well to SSRIs and it generally does not respond as well to classic ERP and the cognitive behavior therapy may have to be tweaked. > > Does anyone have kids with this harder-to-treat subtype " tourettic OCD " and if so, what treatments have worked? Any providers who specialize in this subset in the New York City tri-state area? Our treating psych has suggested that we contemplate augmenting the Zoloft with either an alpha agonist (Clonidine or Tenex) or an atypical antipsychotic in low doses. We really don't want to sedate Jake (either augmenting med) or expose him to the potential insulin resistance that may accompany the atypical antipsychotics but he is really in distress. > > > > To say the least we feel overwhelmed and would appreciate any experience/wisdom/comments. Sorry for the long post. > > > > Ivan > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 31, 2010 Report Share Posted January 31, 2010 Ivan: Did they say what caused the facial celluities? It appears the most common cause of it is strep or staph infections. It still sounds like PANDAS to me. I'll keep you posted on whether or not the antibiotics work. As far as I know my daughter has not had any strep infection since the OCD came out. She did have a Chicken pox vaccine on 12/1/ and the tics started shortly thereafter. From what I understand, the antibiotics may still work even though we now have been dealing with this for over a year and are just starting antibiotics and steroids. Kerry  From: ivanchai2 <i.diamondatt (DOT) net> Subject: Tourettic OCD in 9 year old boy To: @ yahoogroups. com Date: Wednesday, January 27, 2010, 3:34 AM New member here. My son Jake has been diagnosed with fairly severe OCD starting end of Sept '09. (Jake's OCD may have been catalyzed by watching his sister go through a disturbing depression at around the same time -- which in itself was possibly due to my wife's battling a brain tumor. Talk about a domino effect! Anyway, Jake's OCD is not " classic " in that 1) his repetitive behaviors have no discernible " trigger " and can happen anywhere and at any time(i.e.: no fears/anxiety about contamination, harm, confessing, bad thoughts etc.); 2) He doesn't feel actual obsessional anxiety when confronted by the OCD, only feeling " weird " , which can last for hours sometimes if he doesn't perform the ritual; and 3) his rituals seem to overlap with tic-like behavior (throat clearing, pointing while saying " Oh yeah " ) In addition, although never formally diagnosed with ASD, Jake may have a " touch " of Aspergers. Jake has tried to engage in ERP therapy without meds, (Brady Case, M.D. out of NYU Child Study program in Hackensack) but couldn't. When he did seemingly perform the ERP, he said it was only " pratice " and not " real life " so that the habituation process really never happened. Dr. Case then put Jake on Zoloft about 8 weeks ago and Jake is currently up to a dose of 150mg. The 150 mg has been for about 1 week. We have not seen any imporvement of symptoms although we have been told that we need to try an SSRI at the responsive dose for 8-10 weeks for OCD. Mansueto, PhD out of the Washington D.C. area has written about a subset of OCD called " tourettic OCD " which seems to fit Jake like a glove. Some the treatment implications of tourettic OCD is that it generally does not respond as well to SSRIs and it generally does not respond as well to classic ERP and the cognitive behavior therapy may have to be tweaked. Does anyone have kids with this harder-to-treat subtype " tourettic OCD " and if so, what treatments have worked? Any providers who specialize in this subset in the New York City tri-state area? Our treating psych has suggested that we contemplate augmenting the Zoloft with either an alpha agonist (Clonidine or Tenex) or an atypical antipsychotic in low doses. We really don't want to sedate Jake (either augmenting med) or expose him to the potential insulin resistance that may accompany the atypical antipsychotics but he is really in distress. To say the least we feel overwhelmed and would appreciate any experience/wisdom/ comments. Sorry for the long post. Ivan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 31, 2010 Report Share Posted January 31, 2010 Yes, most likely she will continue on antibiotics prophylactically. From: [mailto: ] On Behalf Of i.diamond@... Sent: Saturday, January 30, 2010 10:51 PM To: Subject: RE: Tourettic OCD in 9 year old boy -- I'm sorry that you and your dd have had to suffer for the last 3 years and I hope that her healing will continue unabated. Jake's strep titers came back within " normal " ranges, both for ASO and anti-deoxyribonuclease-B. I believe either you or another member mentioned that PANDAS may still be present even w/o elevated titers. Also, although Jake had serious facial cellulitis infections in 2005, 2006 and 2007 (all ocurring in September of those years) his onset of OCD/tic symtpoms didn't occur until 2009 (although interestingly, in September as well). When your daughter completely heals, will she continue on the antibiotics prophylcatically? Thanks Ivan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 31, 2010 Report Share Posted January 31, 2010 Hi, Ivan. My daughter has done erp. This began just a few weeks after starting medication, basically as soon as we could get an appointment with the therapist. We consistently did it for about 6 months (with the therapist), and then off and on until about 2 years ago, which was probably the last time she formally met with her therapist. However, I feel that she probably does erp every day on her own. She has issues, and she figures out ways to deal with them. I don't think this would be possible for her, at least in the beginning, without medication. She was quite manic, and even suicidal when this all first began, which is very scary in a 6 year old child. She couldn't really focus on anything, until we began the medication. So, I do believe that it was instrumental, in our case, of facilitating the success of erp. Maybe with an older child, they could understand what was happening and why, but for a first grader, we just had to get her calmed down in order to help her. The habit reversal therapy was to help with tics, not the ocd. This was after the meds, and was fairly recently suggested to us by our doctor, maybe 2 years ago. My daughter didn't really seem interested in following through with it, which is why I think we had only moderate success. Also, I believe there is evidence both pro and con for this therapy as a solution for tics. I'm not sure how I feel about it, because my daughter has always explained the tics to me as something that physically just has to be done, more like a sneeze, and less like an impulse that can be stopped. We tried the habit reversal for a squeak tic, which then made my daughter begin a whistle tic. Not sure which was worse. She's a great whistler now, though! (haha, sometimes you just have to laugh at it in order to get through) Both tics have since disappeared, and she has had no noticeable tics for at least the past year. Her anxiety is a little worse, though. My daughter has been on tenex for 7 years. I plan on keeping her on it as long as it is helpful. She is almost 13, so is aware of her medication. We have discussed tapering the meds at sometime in the near future, to see how she does. According to what her doctor feels is best, we may begin with the tenex, or maybe the zoloft. She's doing so well, and is at such a crossroads of growing up, I hesitate to rock the boat. She has no negative side effects that we know of from either medication, so right now, we are just staying the course. I hope your child and your family find some relief soon. My daughter, my husband, and my sister, all have ocd, and are all happy, functioning individuals after varying degrees of trials and tribulations, so please know that your son can be helped, and hopefully all will be well. > -- > > Thanks for the response. I'm so happy for you and your daughter > that she's doing much better. Questions: Did your daughter try > exposure-response prevention therapy at any time, either before or > after the meds? If so, did the meds help her engage in this > therapy? You mentioned habit-reversal therapy as not being much of > a help. Was this attempted before or after the meds? How long has > your daughter been on Tenex? How long do you plan on keeping her on > the Tenex? > > Thanks again, > Ivan > -------------- Original message from Quattlebaum > : -------------- > > > Hi, Ivan. My daughter has been diagnosed with ocd and tourettes. > > She is almost 13 and was diagnosed with ocd at 6 yrs old, and a tic > > disorder a few months later. She didn't develop the vocal tics for > > about another year. She also claims to not have an actual obsession, > > but just a " weird " or " bad " feeling or not " feeling right " . I think > > this is sometimes called " just right " ocd. We have also been unable > > to separate rituals from tics. Her doctor has told us this is common > > in a diagnosis of ocd with tourettes or tics. For her, I believe > > that her problem is really more tic related, with anxiety thrown in. > > I know that she has ocd, as she has some issues with confessing, and > > lots of responsibility issues, but I think that these things take a > > backseat to the tics, which as I understand it, are pretty much a > > physical reaction that can not be controlled. We have done some > > habit reversal therapy for tics, with moderate success. My daughter > > also takes zoloft, but we did not see a dramatic change in her > > behavior/symptoms until we added tenex. It was like a miracle. > > While she has had some mild tics over the years, they have been > > manageable and fleeting, and her quality of life shot back up to > > where it was before this disorder began. She was a little sleepy > > when first starting the meds, but she adjusted to that quickly. She > > is definitely not sedated. The tenex has actually been helpful also, > > in that is counteracts some of the activating effects of the zoloft. > > I strongly suggest you give the tenex a try. My daughter takes 3/4 > > of a 1 mg tablet in the a.m and one at about 6 in the evening. Start > > out slow and see what happens. You can always stop the tenex, if it > > doesn't seem to be working, but from reading this post, I have the > > feeling that it could be very helpful. Good luck to you and your > son. > > > > > > > > > New member here. My son Jake has been diagnosed with fairly severe > > > OCD starting end of Sept '09. (Jake's OCD may have been catalyzed > > > by watching his sister go through a disturbing depression at > around > > > the same time -- which in itself was possibly due to my wife's > > > battling a brain tumor. Talk about a domino effect! > > > > > > Anyway, Jake's OCD is not " classic " in that 1) his repetitive > > > behaviors have no discernible " trigger " and can happen anywhere > and > > > at any time(i.e.: no fears/anxiety about contamination, harm, > > > confessing, bad thoughts etc.); 2) He doesn't feel actual > > > obsessional anxiety when confronted by the OCD, only feeling > > > " weird " , which can last for hours sometimes if he doesn't perform > > > the ritual; and 3) his rituals seem to overlap with tic-like > > > behavior (throat clearing, pointing while saying " Oh yeah " ) In > > > addition, although never formally diagnosed with ASD, Jake may > have > > > a " touch " of Aspergers. > > > > > > Jake has tried to engage in ERP therapy without meds, (Brady Case, > > > M.D. out of NYU Child Study program in Hackensack) but couldn't. > > > When he did seemingly perform the ERP, he said it was only > > > " pratice " and not " real life " so that the habituation process > > > really never happened. Dr. Case then put Jake on Zoloft about 8 > > > weeks ago and Jake is currently up to a dose of 150mg. The 150 mg > > > has been for about 1 week. We have not seen any imporvement of > > > symptoms although we have been told that we need to try an SSRI at > > > the responsive dose for 8-10 weeks for OCD. > > > > > > Mansueto, PhD out of the Washington D.C. area has written > > > about a subset of OCD called " tourettic OCD " which seems to fit > > > Jake like a glove. Some the treatment implications of tourettic > OCD > > > is that it generally does not respond as well to SSRIs and it > > > generally does not respond as well to classic ERP and the > cognitive > > > behavior therapy may have to be tweaked. > > > Does anyone have kids with this harder-to-treat subtype " tourettic > > > OCD " and if so, what treatments have worked? Any providers who > > > specialize in this subset in the New York City tri-state area? Our > > > treating psych has suggested that we contemplate augmenting the > > > Zoloft with either an alpha agonist (Clonidine or Tenex) or an > > > atypical antipsychotic in low doses. We really don't want to > sedate > > > Jake (either augmenting med) or expose him to the potential > insulin > > > resistance that may accompany the atypical antipsychotics but > he is > > > really in distress. > > > > > > To say the least we feel overwhelmed and would appreciate any > > > experience/wisdom/comments. Sorry for the long post. > > > > > > Ivan > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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