Guest guest Posted December 9, 2001 Report Share Posted December 9, 2001 I bet its gonna look great tho Kim!!! Shaye Digest Number 551 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 29, 2002 Report Share Posted January 29, 2002 MyH has been diagnosed with apraxia since he was almost three and from preschool until now he has been mainstreamed in a regular classroom. He gets pulled out for speech everyday and OT twice a week other then that he is with other children the rest of the day.His school has always mainstreamed all of the kids together and the only kids that have their own teacher or aid is if they are autistic or a behavior problem and then they are only in the class room for a certain amount of time a day. Hope this helps.Oh,I told everyone that was being evaluated for his speech and comprehension level.He was tested and passed everything with flying colors. He was over the 30th percentile which they have to be below to qualify. He was in the 67th percentile.Does anyone know what this means.I know it is not the same as percentage.Thanks Gretchen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 8, 2004 Report Share Posted April 8, 2004 Hi Arlene, Nice to see you here aswell as the Best Bet Diet Group Copaxone can be stopped straight away as far as I know. I was on copaxone for 11 months up till around the end of February. I am not on LDN yet but I wanted to stop copaxone well before I started LDN as I don't like using a cocktail of drugs. I stopped copaxone without even talking about it with my neurologists as I knew he wouldn't see it the way I do. The reason why I stopped copaxone was because it was not doing me any good and I feel diet alone is controling my MS far better. I stopped overnight and had no problems. Infact it's now around 6 weeks on since I stopped copaxone and I've noticed positive things, my head feels clearer...diet alone had made my head clearer the last year but since stopping copaxone I feel more alert again...maybe not related but its' something which has definately happened and remained six weeks on since stopping copaxone. Also since last November I was getting shooting pains in one side of my head, which I presumed was Trigmental Neuralgia....it was really getting me worried at times and would strike so unexpectadley. The funny thing is I've not got a shooting pain in my head since I stoppped copaxone either....and even weirder is I remember someone else here saying this happened to them to when they stopped copaxone. by the way I've had troubel for ages trying to get a script for LDN from my Neuro and GP, and since being on a waiting list with Dr. Lawrence I should be starting it now shortly. I think it will be far easier determinng whether LDN is helping me with copaxone gone out of my system. Regarding restarting copaxone if LDN doesn't work for you, this can be done fine ! I know a few people who at one stage were on copaxone then chaged to another drug and ended up going back on copaxone again sometime later. Message: 14 Date: Wed, 7 Apr 2004 07:35:07 -0700 (PDT) From: Arlene Lizotte <alcha508@...>Subject: Re: Copaxone and LDNI have a question I hope someone can help with. I have been taking Copaxone for about a year. I started on LDN Monday and would like to quit the Copaxone. I just wanted to know if I have to wean myself off or can I just quit taking it? Also does anyone know, can I quit it for a while and go back to it, if the LDN doesn't work for me?My neuro wants me to keep taking it, b/c he says if I stop I may get worse (as if I haven't already on it, LOL)Any input would be appreciated.Arlene Messenger - Communicate instantly..."Ping" your friends today! Download Messenger Now Quote Link to comment Share on other sites More sharing options...
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