Guest guest Posted January 24, 2000 Report Share Posted January 24, 2000 Not to push any panic buttons, but does she have any other twitches or tics? That winking sounds like a tic...but before you get too concerned about tourette syndrome, I should remind you that most people have a tic or two and it doesn't mean they have Tourette Syndrome. Just wondering. BTW, remind me again, how old is ???? Take good care, In a message dated 1/24/00 12:45:21 AM Eastern Standard Time, GPesses@... writes: << I've been noticing that for the past several weeks, has been " winking " with her left eye - not all the time, just every now and then. We meet with the new dr this week, but I thought hearing ideas from all of you would give me some direction when I bring this up. Currently, is on 60 mg of Prozac. Any suggestions? >> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2000 Report Share Posted January 24, 2000 << I've been noticing that for the past several weeks, has been " winking " with her left eye - not all the time, just every now and then. We meet with the new dr this week, but I thought hearing ideas from all of you would give me some direction when I bring this up. Currently, is on 60 mg of Prozac. Any suggestions? >> Is this the only tic that has? How old is she? If you are not seeing any other tics this may be no big deal and may go away. Knowing what is and is not a tic can be tricky. Before my son was diagnosed with TS I was surpassed to find that coughing, throat clearing and sniffing can be tics. Many children have transient tics which are no big deal and go away. Let's hope that's all this is. Patti in So Cal Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2000 Report Share Posted January 24, 2000 My son had this same tic about 2 months ago. It lasted for about 2 - 3 weeks and then disappeared. He has never been diagnosed with tourettes but I have noticed that he does have some occasional ticcing - both motor and vocal. Eliz in WI Tics > From: GPesses@... > > I've been noticing that for the past several weeks, has been > " winking " with her left eye - not all the time, just every now and then. We > meet with the new dr this week, but I thought hearing ideas from all of you > would give me some direction when I bring this up. Currently, is on 60 > mg of Prozac. > Any suggestions? > > --------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 25, 2000 Report Share Posted January 25, 2000 Winking can certainly be a tic, my daughter has had a few tics that were short-lived and which began at OCD onset. For months they would come and go, Kellen says they are OCD and feel just the same as OCD, for what that is worth. I was surprised to find that they bother her as much as any other aspect of OCD, since they seemed (to me) so low-level and " background. " More recently, she had an explosion of primarily body tics and her doctor put her on a low dose of Risperdal since ticcing at this level was interfering with getting to sleep, etc., and she was achey from doing them all day. The Risperdal has done a fair job of minimizing them. My understanding is many people with a primary diagnosis of OCD have some tics. Kathy R. in Indiana > From: GPesses@... > > I've been noticing that for the past several weeks, has been > " winking " with her left eye - not all the time, just every now and then. We > meet with the new dr this week, but I thought hearing ideas from all of you > would give me some direction when I bring this up. Currently, is on 60 > mg of Prozac. > Any suggestions? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 25, 2000 Report Share Posted January 25, 2000 Hi Kathy R-- What's interesting to me is how some docs will say that many people with a primary dx of OCD also present with tics, while other docs will say that many people with TS will present with OCD and/or other anxiety disorders. I'm supposing TS has been ruled out in your daughter's case? That she doesn't meet the diagnostic criteria for TS??? That might explain why she has a primary dx of OCD and not TS--just thinking/wondering out loud. Take good care, In a message dated 1/25/00 9:41:38 AM Eastern Standard Time, klr@... writes: << From: " Kathy " <klr@...> Winking can certainly be a tic, my daughter has had a few tics that were short-lived and which began at OCD onset. For months they would come and go, Kellen says they are OCD and feel just the same as OCD, for what that is worth. I was surprised to find that they bother her as much as any other aspect of OCD, since they seemed (to me) so low-level and " background. " More recently, she had an explosion of primarily body tics and her doctor put her on a low dose of Risperdal since ticcing at this level was interfering with getting to sleep, etc., and she was achey from doing them all day. The Risperdal has done a fair job of minimizing them. My understanding is many people with a primary diagnosis of OCD have some tics. Kathy R. in Indiana >> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 26, 2000 Report Share Posted January 26, 2000 Hi all, > From: DHu1017467@... > > Hi Kathy R-- > > What's interesting to me is how some docs will say that many people with a > primary dx of OCD also present with tics, while other docs will say that many > people with TS will present with OCD and/or other anxiety disorders. Yes, I guess both statements are true. I've been reading that some researchers think OCD and Tourette's are different expressions of the same basic disorder and that they exist along a continuum--from OCD only on one end to Tourette's only on the other, with mixtures of symptoms in between. My daughter's contention that " it's all the same stuff " (tics, bad thoughts, compulsions) would fit with this theory. > > I'm supposing TS has been ruled out in your daughter's case? That she doesn't > meet the diagnostic criteria for TS??? That might explain why she has a > primary dx of OCD and not TS--just thinking/wondering out loud. I believe one of the diagnostic criteria for Tourette's has the tics continuously present for a year or more, which isn't true of my daughter at this point. She only had shortish periods of tics more off than on for almost a year, and they were very subtle. Only this past couple of months did she develop many tics that were much more intense and bothersome, this is why she was started on the Risperdal, which has helped quite a bit. Kathy R. in Indiana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 26, 2000 Report Share Posted January 26, 2000 hi patti-- I just joined your tourettes list and was looking for a little more info-- i see no archives, but is there some secret place I might not know about? When I joined the OCD parenting list, I read thru months of archives and found them really helpful-- any ideas? Thanks much Ellen in NY Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 26, 2000 Report Share Posted January 26, 2000 Well to be more specific, the DSM-IV says tics must be present for at least a year with no more than a three month period between episodes. If more than three months pass between tics, then the counting sort of begins again, for those TS psychiatrists who are really picky--and ours are! From what I understand, TS is on the Autism, Aspergers spectrum...with Autism at one end and TS at the other end of the spectrum. Somewhere in there, no doubt, is OCD..I'm pretty much convinced of that. Take goodcare, Diaan In a message dated 1/26/00 10:05:45 AM Eastern Standard Time, klr@... writes: << I believe one of the diagnostic criteria for Tourette's has the tics continuously present for a year or more, which isn't true of my daughter at this point. She only had shortish periods of tics more off than on for almost a year, and they were very subtle. Only this past couple of months did she develop many tics that were much more intense and bothersome, this is why she was started on the Risperdal, which has helped quite a bit. Kathy R. in Indiana >> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 30, 2000 Report Share Posted January 30, 2000 Charlene - I will do my best to explain ERP. It stands for Exposure and Response Prevention and is the preferred therapy for OCD. It is preferred because it is nonmedicating and long lasting. It actually teaches a person to face their anxieties without performing the ritual or compulsion. Once a person learns this technique, they are usually (hopefully) able to " boss back " future OCD related anxieties and rituals by creating their own exposure tasks. Many people are then able to decrease or even come off of medication. Some people use ERP before trying meds and are able to avoid them completely. There are quite a few good manuals out there that teach a person how to do this themselves but it is best if you can find a good therapist who is an expert in the field. ( The books are good for additional support.) The experts are hard to find, however, and as many members have discovered, there are a lot of therapists out there who claim to know how to treat OCD but really don't. If you decide to pursue this, you may want to call the OCFoudation and ask about therapists in your area. Last summer I was traveling 250 miles one way to have my son treated by an expert - it was well worth it. That's it in a nutshell. There are quite a few parents on this list that know their stuff in regards to this therapy. Good luck. Eliz in WI. tics > From: Charleen.Bower@... > > Thanks for the warm welcome Eliz in WI! Hearing from people who understand > first hand really makes a difference. My circle of friends are wonderful, but > no one has a child with these challenges. While they have always been very > tolerant when with Gavin, their well meaning advice to me shows their lack of > understanding. I can tell that deep down they really feel things could be > different. > > As for your question about Gavin's tics, we have a whole list of them that > come and go with a mind of their own. Throat clearing/coughing , jaw snapping, > shoulder and hand clenching, blinking, mouth and nose twitching, facial > scrunching. Once last year, and once again this year, we had a period of two > weeks or so that his body movements were so severe that he had the appearance > of someone with palsy. (It is interesting to note that both times these > episodes happened about two weeks after a strep throat. The neurologist was > sure that it was TS and not chorea that sometimes follows strep infections.) > Then we have the OCD type activities, repeating words, rubbing the paper after > each letter (as if brushing off non existent crumbs), going over the same > letter, etc. > By the way, what are ERP techniques? This is just the first time I will show > my ignorance. I have so much still to learn. > > Charleen in town > BLOOM WHERE YOU ARE PLANTED > > --------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 20, 2001 Report Share Posted October 20, 2001 Excuse me everyone, Can somebody tell me what is the meaning of " tics " ? Shinta Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 21, 2001 Report Share Posted October 21, 2001 Tics are repeated involuntary motor movements (such as eye blinking). Original Message ----- From: A R i E <askari@...> <autism > Sent: Saturday, October 20, 2001 8:30 AM Subject: Re: tics > Excuse me everyone, Can somebody tell me what is the meaning of " tics " ? > > Shinta > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 22, 2001 Report Share Posted October 22, 2001 In a message dated 10/21/2001 4:05:07 AM Eastern Daylight Time, askari@... writes: Excuse me everyone, Can somebody tell me what is the meaning of "tics" ? according to my medical dictionary, a tic is a repeated, uncontrolled, purposeless contraction of muscle or group of muscles, most commonly in the face, shoulders, or arms. Â Typical tics include pointless blinking, mouth twitching and shoulder shruggi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 20, 2001 Report Share Posted December 20, 2001 Hi Cornelia, Here are a few questions that I have: 1.) Does your son have seizures now or has he outgrown them? 2.) Is your son on any Prescription Medications at the present time? 3.) Is your son on any type of Special Diet for his problems? 4.) Does your son take any Vitamin or Mineral Supplements? Take Care, Sharon Myers [ ] Tics Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 21, 2003 Report Share Posted February 21, 2003 STOP the bethanecol that is a bad reaction > I recently added bethanecol and an amino acid blend to my son's > supplements and he got a huge case of tics. Tons of tics. Any advice? > thanks Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 21, 2003 Report Share Posted February 21, 2003 THANKS!!!! I didn't know bethanecol could cause tics. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 10, 2003 Report Share Posted March 10, 2003 Hi ! Now Carol has even more to explore to try to help her son -sensory tics -lyme and tics - strep and tics -that should be at least 6 cents worth at 2 cents a pop. Some of the links I found below that may help I never would have known to search for in regards to tics (MD-parents like you are good to have around!): Strep and tics Treatments Reduce Strep-Triggered Symptoms of OCD and Tics in Some Children National Institute of Mental Health (NIMH) researchers report that some children whose symptoms of obsessive-compulsive disorder (OCD) and tic disorders were worsened by a common strep infection have been successfully treated with plasma exchange (PEX) and intravenous immunoglobulin (IVIG). Dr. Swedo and colleagues at the National Institutes of Health reported their findings in the October 2 issue of Lancet. " http://www.nih.gov/news/pr/sept99/nimh-30.htm Lyme and tics " Psychiatric.Two studies from different institutions found that children with Lyme Disease may develop late problems with visual and auditory attention. These children may be mistakenly diagnosed as having primary attention deficit disorder as opposed to attentional deficits secondary to a systemic infection. Other findings in children include new onset phobias (e.g., fear of the dark, separation anxiety), depression, listlessness and irritability, oppositional behavior, obsessive-compulsive behaviors, and/or Tourettes Disorder. " http://www.columbia-lyme.org/flatp/lymeoverview.html " The impact academically is most significant. These children have fall-off in academic performance, difficulty learning new material, problems with short-term memory, problems with word finding, and a number of them have lost reading skills. Frequently, these children may present with a picture of ADD or may have an underlying ADD or ADHD that is made worse by the Lyme. Incidentally, Dr. Pietrucha noted that children with Tourette's may also have a worsening of their tics when they have been ill with Lyme disease symptoms. A case report published in Lancet indicated that a child with Tourette's who was found to have concurrent CNS Lyme disease experienced a remission of the Tourette's after the Lyme disease was treated. " http://www.medscape.com/viewarticle/412987? WebLogicSession=Pm1eQ2bGDEokShuTCSaWgh0C0bPEtvooYaTduWlBav6eqZGNOBn9| 1142142660663020111/184161393/6/7001/7001/7002/7002/7001/-1 Sensory tics " Like many other aspects of this site, this page is put together from anecdotes and personal experiences. " http://au.geocities.com/jones_kacm/tictypes.htm http://au.geocities.com/jones_kacm/5_senses.htm (I added the school / stress ones too since I believe that is a possiblity as well) Stress and tics " Management of a tic disorder should explore possible stresses in the child's life at home and school. Stress can exacerbate tics which in turn, often impacts on the child's self-esteem. Helping the child and parents to devise strategies to deal with stress, and providing reassurance and monitoring are the mainstays of management. " http://www.sch.edu.au/articles.asp?type=3 & doc=30 " Dr. Preston Herrington, Pediatrician Margie noticed that since her five-year-old son, , had started school, he developed a new habit of frequently pulling at his own ears. Everything from an ear infection to developing a " tic " crossed her mind. After consulting with her physician – she learned it was neither – it was simply a way was calming himself as he adjusted to the changes from being at home with mom to starting school. Childhood habits like twisting or chewing hair, grinding teeth, tugging on ears, and nail biting sometimes are confused with tic behaviors. Nervous habits like these are controllable behaviors that develop in times of stress. They are common in school-aged children as they adjust to new routines, new schools, and new friendships. Nervous habits are often outlets for pent-up energy. Do not worry about them unless they are done compulsively. Sometimes a change of scenery, a gentle awareness discussion, or relaxation exercises will help break the habit. Childhood nervous habits usually stop when the child learns more effective ways of comforting himself while coping with stress. Tics, on the other hand, are involuntary muscle movements that are physical problems, not psychological ones. Motor tics include eye blinking or squinting, shrugging the shoulders, grimacing, repetitive coughing or shaking the head. Vocal tics include tongue clicking, clearing the throat, sniffing, coughing, or saying words out of context. In rare cases, children may curse or say unpleasant things that they do not mean. Those behaviors are not used to calm a child as with a nervous habit, because they are not in the child's control. While their presence may seem as if the child is experiencing stress, they generally are not direct responses to stress or anxiety. They can happen randomly.... " http://www.lifecoursehealth.com/LifeCourse/Columns/ColumnsDetail.asp?ColumnID=37 " The most common tic disorder is called " transient tic disorder, " which may affect up to 10 percent of children during the early school years. Teachers or others may notice the tics and wonder if the child is under stress or " nervous. " Transient tics go away by themselves. Some tics do not go away. Tics which last one year or more are called " chronic tics. " Chronic tics affect less than one percent of children and may be related to a special, more unusual tic disorder called Tourette's Disorder. " http://www.puberty101.com/aacap_tics.shtml Note to Carol: Carol -I just noticed when I cut and pasted part of your mesage to include here that I missed in my last message to you about your son no longer receiving any therapies. Talk to your son's former case manager at the school and see if you can work out with them a schedule to bring him in to the school for the therapy sessions -and perhaps a class or two he enjoyed -if there was one? If you pull your child out of school and it's not agreed upon/worked out with the school in the IEP -they may not be responsible -however you could work it out now I'm sure. Being that your child was such a good student, and being that he was having regressions that were alarming in the school -I would talk to your school about working something out. If they are not open to this -I would speak to a special ed attorney or advocate in your state/area. Your child's entitled by law to a free and appropriate public education in the least restrictive environment -I'm sure there is a way to work things out so that your son could continue to at least receive therapy. Who knows -perhaps he can gradually work back up to being in school full time again? Remember " no child left behind " -it's the law. Best wishes to all of you! ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 10, 2003 Report Share Posted March 10, 2003 I'm in here for my daughter who has apraxia, but my son has a chronic tic disorder. We've seen the neurologist and had the strep test done. Thanks, Suzi > i'm pretty new to the group and have noticed a lot of parents e- > mailing in that their kids have " tics. " it sounds like some of > these " tics " are really sensory symptoms, as opposed to true tics, > which are pretty fixed neurologic patterns. if your child truly has > tics, he should be worked up by a neurologist, and also checked for > strep and lyme. otherwise i've heard several success stories of > these so-called " tics " being treated by OT - and it works! > > my 2 cents. > leslie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 11, 2003 Report Share Posted March 11, 2003 In a message dated 3/11/03 9:30:40 AM Eastern Standard Time, anncrow@... writes: > abmd group abmd group,whats that? Jennie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 11, 2003 Report Share Posted March 11, 2003 thankyou to everyone continuing to respond. Ann, I know that some people are really affected by yeast (my sister-in-law's life was changed when as a teenager someone finally diagnosed yeast as the problem and she was treated) and as someone else said, it could be a PART of the difficulty, but made an excellent point that at first I wasn't thinking about and that is that the behaviors definitely correlate with stressful environments (outside- the- body factors, rather than internal factors) and it can't be the school lunches (ha!) since in some group situations he has not been in this school or had a school lunch. This also would apply to the person (sorry can't remember your name) who recommended it may be an aminoacid type problem, wouldn't it? In the fall when people were responding to Suzi about her son I did have Micah tested for strep in the blood, thinking maybe that could be it. Suzi, your idea was a fabulous one, although of course, now too late as since we have homeschooled the behaviors have drastically reduced and I sincerely hope that they will disappear completely again as they have in the summer (although since I am still pushing him in a sense to perform difficult tasks like writing and reading I don't expect them to...in other words, the environment here at home isn't completely stressfree either). It would be fascinating to compare notes with how your older son does if you do decide to homeschool. Did they have a name for his tic disorder or did they just call it that " tic disorder " because I do think they could diagnose my son with that as well. Did they prescribe any meds and did they help at all? Micah is still involved in an after school group at the school called Destination Imagination (formerly, Odyssey of the Mind) which lasts one more week. It will be interesting to see what happens with the tics that are left once he does not go to the school at all. Tracie, good news is: I was finally able to get on medicaid and next week he starts private OT and private pool therapy (probably short-term so I can do carryover in the lake this summer). I am not sure if medicaid will pay for it, however, since our state's new governor is considering therapy as one of the aspects of medicaid to cut back on. Still, I found a local agency which has some funds that may be able to back me up a little (one year, when Micah was three, the COST of the private therapy he got EQUALED the amount of my husband's YEARLY SALARY.....so to me (his therapy totaled between 3 and 4 hrs. a week) that is INSANE and I understand why the medical field is such a mess and why taxes should not have to pay those exorbitant amounts). So I continue the hassles of trying to get therapy and the academic work to my son while maintaining his emotional health at the same time. ....interesting about Khalid going to Sylvan! I got some materials on them a couple of months ago and lodged it in my brain for later on down the road....if Micah wants to go to college I think it would be excellent college prep. Well, all, thanks again for all your thoughts. I especially appreciated the detailed one from , whose child sounds an awful lot like mine, except again for the good skills in reading.....it could be the gifted IQ but I think probably just that his reading ability isn't effected by the disability ( the dr. told me that usually NLD isn't diagnosed until round fourth grade because that is when the subtle meanings or 'reading between the lines' make it really difficult for NLD kids) because Micah also has a high IQ in the verbal section, although not in the gifted range. he definitely has the huge discrepancy though. I think it is so ironic that a child having so much trouble with talking and communicating can also score so high on the " verbal " range of an IQ test! What I found most interesting was the fact that he too has been diagnosed with both global apraxia and nld....now I know three kids that have both. Any body else out there?????? And what state are you in? Thanks again to everyone, Carol Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 11, 2003 Report Share Posted March 11, 2003 They are talking about tics at the abmd group if anyone is intrested. My 2 cents Ann Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 11, 2003 Report Share Posted March 11, 2003 Jennie it is another group abmd is a Autism Biomedical Dicussion group. From the first page that come up with your groups there is a fill in blank that says join a group if you put in abmd it will take you right there. It is very intresting My 2 cents Ann Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 11, 2003 Report Share Posted March 11, 2003 My daughters tics are seizure related. She has eye tics or rhythmic blinking which is a seizure. -- [ ] Re: tics Hi ! Now Carol has even more to explore to try to help her son -sensory tics -lyme and tics - strep and tics -that should be at least 6 cents worth at 2 cents a pop. Some of the links I found below that may help I never would have known to search for in regards to tics (MD-parents like you are good to have around!): Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 11, 2003 Report Share Posted March 11, 2003 Carol, They just diagnosed with a chronic tic disorder. The funny thing is lately, we can't notice the tics at all. I did put him on the fish oil, and that seemed to help. However, I took him off the fish oil and he is doing okay still. I think a lot of it is stress, and I think the stress level is a lot less now than it was in the beginning of the school year. He is not on any meds because we didn't think the tics were bad enough. never noticed them, so we didn't want to make a big deal out of it. I'm just reading a lot about tic disorders and tourettes to see what natural things help. I do think he has some personality quirks that I am a little concerned about, but he is an 8 year old boy and they all seem a little quirky. Suzi >Suzi, your idea was a fabulous one, although of >course, now too > late as since we have homeschooled the behaviors have drastically reduced > and I sincerely hope that they will disappear completely again as they have > in the summer (although since I am still pushing him in a sense to perform > difficult tasks like writing and reading I don't expect them to...in other > words, the environment here at home isn't completely stressfree either). It > would be fascinating to compare notes with how your older son does if you do > decide to homeschool. Did they have a name for his tic disorder or did they > just call it that " tic disorder " because I do think they could diagnose my > son with that as well. Did they prescribe any meds and did they help at > all? Micah is still involved in an after school group at the school called > Destination Imagination (formerly, Odyssey of the Mind) which lasts one more > week. It will be interesting to see what happens with the tics that are > left once he does not go to the school at all. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 11, 2003 Report Share Posted March 11, 2003 Hi Suzi and all! Just wanted to clarify -I didn't put Dakota on the oils for the tics -it was to try to help his attention and focus due to all his teachers and neurodevelopmental MD's since 3 years old in " normal " preschool " highly suggesting " that Dakota had ADHD or ADD or CAPD or something depending on whether it was from an MD or a teacher. Years later at the First Apraxia Conference sponsored by CHERAB I had a chance to speak with Dr. AJ about her views and research in the UK on why higher EPA may be better while most in the US only talk about the DHA. http://www.pufanewsletter.com/pufa/Pufa22.pdf http://archpsyc.ama-assn.org/issues/v57n7/fpdf/ylt0700.pdf Dakota clearly was struggling to focus or stay on task for any amount of time -not just at school -at home too. Even for things he wanted to do. The higher EPA added to the ProEFA worked great for him and it was noticed -and still is. It was around that time however that my husband gave the higher EPA with the ProEFA to Tanner as well during a weekend trip when I had to stay home and we all noticed another surge in Tanner's speech. (you start getting greedy for more and more of those surges) To be honest I don't remember if the change of the O3/O6 oil formula had anything to do with Dakota no longer having tics. I have to say I don't think so -but that didn't cross my mind back then. It was clearly school related since it subsided during the weekend and school breaks and came back full force when back in school again. And -Dakota loved school and loved his teachers and friends. The focus problems and " tics " were observed by his teacher -the school psychologist -and Dr. Sinha at that time. I don't believe anyone viewed the movements as anything but stress related actions -and the word " tics " was not used - " nervous behaviors " was. (I used the word tics however when I spoke to the school because that's what they looked like to me) Some of this story is in the archives somewhere -or some about the ADHD and oils is at Speechville http://www.speech-express.com/alternative-therapy/efa-faqs.html Boy! Carol you were looking for " someone " to relate -and instead found more than a few someones that do! (so do we include tics on the list of associated or related disorders that may run in the families of children with communication impairments or what?!) Should stress related -temporary tics like temporary stuttering be called " developmental tics " ?! Or once a child has them -he has them- even if he no longer has them? Suzi what does you doctor say about them stopping? ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 11, 2003 Report Share Posted March 11, 2003 There are different kinds of tics. There are some that are temporary and only last a few months. is considered a chronic tic disorder because his lasted over a year. I'm still not sure what the difference between a chronic tic disorder and tourette's syndrome. I thought the main difference was that for tourette's they had to have a vocal tic. I know that last year started snorting for several weeks (it really bugged me). Snorting is considered a vocal tic. After the snorting, he started jerking his head. I also think he has some eye blinking tics. That's about it. I tried the ProEFA because we don't eat much fish, and I was curious to see if it would help with 's tics. That's when the tics got better, and then they eventually stopped. I've taken him off the ProEFA to see if the tics come back. They haven't, yet. Suzi I don't remember if the change of the O3/O6 oil formula > had anything to do with Dakota no longer having tics. I have to say > I don't think so -but that didn't cross my mind back then. It was > clearly school related since it subsided during the weekend and > school breaks and came back full force when back in school again. > And -Dakota loved school and loved his teachers and friends. The > focus problems and " tics " were observed by his teacher -the school > psychologist -and Dr. Sinha at that time. I don't believe anyone > viewed the movements as anything but stress related actions -and the > word " tics " was not used - " nervous behaviors " was. (I used the word > tics however when I spoke to the school because that's what they looked > like to me) > > Some of this story is in the archives somewhere -or some about the > ADHD and oils is at Speechville > http://www.speech-express.com/alternative-therapy/efa-faqs.html > > Boy! Carol you were looking for " someone " to relate -and instead > found more than a few someones that do! (so do we include tics on > the list of associated or related disorders that may run in the > families of children with communication impairments or what?!) > > Should stress related -temporary tics like temporary stuttering be called " developmental tics " ?! Or once a child has them -he has them- even if he no longer has them? Suzi what does you doctor say about them stopping? Quote Link to comment Share on other sites More sharing options...
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