Forum Community Guidelines
Our forums provide support for people dealing with neurological and related issues. Everyone joining this community should find it a safe haven where they are treated with respect, civility, and understanding.
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You may have links in your profile as long as they do not violate our guidelines (above). Links within a post to online resources and articles are generally OK. Do not post links to other forum communities with the aim of soliciting other members to that community, thereby taking them away from this community.
When a guideline is violated
If you violate a guideline, you will be contacted by PM or email. We will try to resolve things amicably. We don’t like to ban members and rarely do, but this is an option.
Updated March 19, 2010
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Updated March 19, 2010
Hi,My 8 year old son was recently diagnosed with TS. After much research on how to let him know, we sat him down, explained that he had a neurological condition along with the details and let him know he could come to us with any questions. Over the past few months or so, he has noticed his tics when he looks in the mirror and has asked what they are (he also has slight ADHD and tends to forget the details we review). We let him know in a very matter-of-fact manner that what he was seeing is his tics and it's part of TS. Also important to note that I have directly asked him in the past if his tics bother him and he's always said "no." We did come to an agreement (prompted by him) that we don't call out his tics, that if we see him ticing a lot, we ask if something is bothering him.The doctor we are working with feels no medication is necessary because his life is not being negatively impacted in any manner. And honestly, we'd prefer to not have to introduce medication unless there are no other alternatives.In the last few weeks, his tics have increased. There are times when his entire face is ticing and sometimes to me it looks painful. The other day be mentioned that his tics were bothering him after I asked him if anything were bothering him. I sat down to talk to him about it and said that with TS, sometimes the tics will be worse than others. I also asked him questions such as if something was bothering him at school or if he was anxious about something...My husband and I disagree on the approach I took because my husband feels Im leading him to reasons whereas I feel Im trying to uncover if there's a reason why his tics were increasing. I don't know what is "right" in these situations or even if there's such a thing, so I would love feedback from those of you who have TS to understand what is helpful. If you were 8 years old again, how would you want your parents to deal with the times when they noticed your tics increasing?Thank you in advance for your insight!