Guest guest Posted January 4, 2010 Report Share Posted January 4, 2010 Thanks for your input, Kim. I am also a psychotherapist, but do not generally treat children, and am relatively new to the world of lyme, so do not have a lot of experience in this area-yet. We are actually scheduled with Judith Levanthal, traveling from land to see her. I have also contacted the ins company to see what may be covered- no answers yet. We have been dealing with my son's issues since he was born, but only recently got the lyme diagnosis. I am hopeful the testing would give us some new info and insight and be able to identify what is lyme related and what is not. We have been to so many doctors and therapy providers over the years, I think I have become a bit skeptical that something can be offered that we have not already done or tried. I would really like someone to be able to tell me if the envt at my son's school is contributing to his stress (ie: large class size, noise level etc). In your experience, is this identified by the testing? I am wondering if I need to find someone who can actually go and observe him in class. Thanks, Dara > > Hello Dara, > As a Lyme-Literate psychotherapist working with children and families impacted by Lyme, I can't stress enough how important good neuropsych testing can be. Not only will you receive necessary info related to how the illness has affected brain function, but also critical insight into what accommodations and/or modifications may be of assistance with regard to social, emotional, behavioral, and/or educational functioning and planning. With regard to education, it is of utmost importance that children be educated in accordance with their particular abilities and needs.  IEP qualification and development should take place in concert with results of the neuropsych testing. Two leaders in the field are Drs. Leo Shea and Judith Leventhal located in NY and MA. Additional info about them may be found at http://www.n-e-t-s.org/Shea-Leventhal%20Role%20of%20Neuropsych%20Testing%20LD.pd\ f. Perhaps either doctor may recommend a LL provider in > your area if you are unable to travel to them.  Also, in terms of cost, it may be of benefit to research whether or not your particular insurance carrier would reimburse you for their services whole or in part, perhaps as an " out of network " provider. > All the best to you and your family, > Kim >  > > ________________________________ > From: darabeth2003 <dara.alewine@...> > > Sent: Sun, January 3, 2010 7:37:12 PM > Subject: [ ] neuropsychological testing > >  > Has anyone had neuropsychological testing for your child with LD? Did you find it helpful? > I have testing tentatively set up for my 6yo son with a lyme literate psychologist, recommended by our LLMD. I will do anything if it is helpful, but also reluctant for not wanting to put him through one more thing, it is very expensive, and not sure what she can tell me as far as recommendations that we are not already doing. He already gets a variety of therapies and has an IEP with some accomodations. > Anyone willing to share your experience? > Thanks, > Dara > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.