Anonymous wrote:My daughter (3.5) has just been diagnosed. Currently at a private preschool that has been so helpful in allowing push-in support and teacher training. My daughter still has two more full school years before kindergarten. It’s all still overwhelming to me! I am currently focusing on making sure the preschool she’s in next year (whether we continue at current school or switch) will support fade-in’s at the start of the school year. Can anyone offer me optimism on what happens after that? Will we need that same support into prek and then k, or will she outgrow it, or does it just depend?
Anonymous wrote:My daughter has selective mutism and we send her to a small private school with experienced teachers - similar to Beauvoir but different city. We've been blown away at the progress she's made. All the faculty and staff know her and have gone out of their way to make her comfortable. She will be in 5th this year and at school you would not notice a difference between her and the other children.
She was diagnosed at 4 years old and still gets triggered in some environments, school is not one of them. When she was diagnosed I made an appointment with the HOS, dean, principal, and her 2 teachers. Ever since then, the school ensures the right mix of kids in the class and teachers that will be best for her (and all the other students). Please take the time to get this right for your daughter; our progress has been amazing.
I'm not sure any public school has the capacity to do this for all the students they have. My other children are bright social kids and benefited from this thoughtful class selection too. One of the teachers at the school told me "I believe all children have a special need". She was trained as a GT teacher, but at the time was teaching 2nd grade.
Anonymous wrote:My child will be starting kindergarten next year (2024). She is receiving therapy for selective mutism and has made great progress, but I want to do everything possible to make her transition to kindergarten successful. Her therapist recommends that we do "sliding in" sessions before school starts.
In an ideal world, what this looks like is DD and I would be in the classroom playing, I use strategies to make sure DD can be verbal there, then the teacher comes in, sits to the side, we make sure DD can be verbal with the teacher there, then prompt the teacher to get closer and eventually ask DD questions. The goal is to get DD comfortable being verbal with the teacher. We would ideally do two or three of these sessions. Probably at least 15 minutes each.
Can something like this be done in the real world in MCPS/public school systems?
Anonymous wrote:Anonymous wrote:Anonymous wrote:Anonymous wrote:Is she on Prozac? If she is not on a small dose of Prozac, may I ask why?
Ds had it and Prozac was a life saver. At a young age small dose can require the brain chemistry and then child develops better social behaviors and talking becomes what is normal for the kid.
DD was diagnosed very young - around 2.5 - which is too young for medication. She has responded fairly well to PCIT-SM therapy, and I suspect it's because of that her therapists have not yet recommended medication. However, we have experienced progress and then plateaus where she is verbal but not fully verbal in school. Some of it may be our fault for not being as diligent as we could be with exposures and playdates. We are looking forward to building our skill set during the parent training component of the camp and also getting tips from the other parents. I really appreciate your comment because it is a reminder to ask about medication. Anxiety definitely runs in our family and I myself recently started an SSRI which has been a game-changer for me personally.
Micro dose of Prozac for a few weeks before school started and then weaning off w/n 6 months plus requesting he be assigned a low key experienced teacher (versus high energy rapid fire talking teacher) and having him visit the classroom the week before school started 2x greatly helped more than therapy or the selective mutism summer camp. We paid for an advocate to assist us before our meeting with the school to present our request at the 504 meeting the prior April before DS started K. Also the cost of the psychologist who wrote report after observing ds in prek class and answering questions over the phone. Thankfully the microsdose worked and was a life changer for us.
who can prescribe prozac in DMV area. DS is 2.8 months.
Anonymous wrote:Anonymous wrote:Anonymous wrote:Is she on Prozac? If she is not on a small dose of Prozac, may I ask why?
Ds had it and Prozac was a life saver. At a young age small dose can require the brain chemistry and then child develops better social behaviors and talking becomes what is normal for the kid.
DD was diagnosed very young - around 2.5 - which is too young for medication. She has responded fairly well to PCIT-SM therapy, and I suspect it's because of that her therapists have not yet recommended medication. However, we have experienced progress and then plateaus where she is verbal but not fully verbal in school. Some of it may be our fault for not being as diligent as we could be with exposures and playdates. We are looking forward to building our skill set during the parent training component of the camp and also getting tips from the other parents. I really appreciate your comment because it is a reminder to ask about medication. Anxiety definitely runs in our family and I myself recently started an SSRI which has been a game-changer for me personally.
Micro dose of Prozac for a few weeks before school started and then weaning off w/n 6 months plus requesting he be assigned a low key experienced teacher (versus high energy rapid fire talking teacher) and having him visit the classroom the week before school started 2x greatly helped more than therapy or the selective mutism summer camp. We paid for an advocate to assist us before our meeting with the school to present our request at the 504 meeting the prior April before DS started K. Also the cost of the psychologist who wrote report after observing ds in prek class and answering questions over the phone. Thankfully the microsdose worked and was a life changer for us.
Anonymous wrote:It will be.tough for a SM kid in an mcps kindergarten. Even with a great teacher and administrative support, there will be 20 plus kids in the class. Your quiet non disruptive child won't get much in the way of attention or accommodations. The SM kids i have encountered have been very entrenched in not speaking....it can last for many years.
Anonymous wrote:Reviving this thread, as I have a rising Kindergartner with SM. Some posters have mentioned private schools with experience in SM. Would people be willing to share names of specific schools? I thought DC would be fine in MCPS, but now I'm starting to worry. The class sizes of our local school's K are larger than I thought. I'd like to explore other options.
Anonymous wrote:Anonymous wrote:Anonymous wrote:Hi op - I am facing the same situation and wondering how kindergarten went. Was your daughter in pre-k? We just received an official diagnosis and she will be starting K in the fall. She’s always been in full time daycare / preschool and she can talk but very quietly in the classroom (is totally fine on playground). I don’t think her case is extremely severe but I am worried about her ability to communicate and learn in K and ask to go to potty…
Hi! So our DD will start K this year. She no longer has SM after working with a SM therapist, SM camp and doing lots of exposures and setting up a reward system for brave talking . She does still have anxiety, so still want to do an extra visit to meet the teacher if possible but are pretty hopeful she will be fully verbal.
I would definitely lean into treating the SM. SM is both very impairing and treatable. Get the Overcoming Selective Mutism book - I found it so helpful.
Which camp did you do?