Guest guest Posted February 6, 2009 Report Share Posted February 6, 2009 I live in NY and we also have BC/BS Preferred PPO. Our insurance does cover therapy. Did you try calling the insurance company yourself? Maybe this speech therapist is mistaken? > > I just got a call from the SLP who evaluated my son last week and > diagnosed as mod-severe Apraxia of Speech (age 3 1/2). She said the > insurance won't cover his speech therapy. We have Blue Cross/ Blue > Shield PPO. I don't think the coverage gets much better than that! The > SLP said we could pay out of pocket at $120 per week. We would be > driving an hour each way to speech, so she suggested a one hour > session, once per week. I have the Kaufman Workout Book and Cards at > home...but I don't feel like I am doing him a lot of justice working > with them. I am so frustrated and unsure of how to help our. Our local > school district is difficult to work with and has some really weird > loopholes you have to jump through to get speech. I honestly don't > trust them with him. Please help...should I take him to see > Kaufman? I live in Southern CA...what is a mom to do? Help Please!!! > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 6, 2009 Report Share Posted February 6, 2009 Good to know that they are covering speech for other children with Apraxia. We have been told by the insurance company that it is not medically necessary. Even though he is 2 years behond on expressive language and less than 10% intelligible speech... My mom works in the insurance " world " so we are going to call them together today to find out about the appeal process. In the meantime - my hubby agrees we must pay out of pocket to get him the help he needs, even though that will be a huge cost each month. We are also considering a trip to see Kaufman to find out more about how to work with him at home. I am determined not to let an insurance company dictate whether my son will ever speak or not. That is silly! Thanks to you all for letting me vent my frustrations! Leah > > > > I just got a call from the SLP who evaluated my son last week and > > diagnosed as mod-severe Apraxia of Speech (age 3 1/2). She said the > > insurance won't cover his speech therapy. We have Blue Cross/ Blue > > Shield PPO. I don't think the coverage gets much better than that! The > > SLP said we could pay out of pocket at $120 per week. We would be > > driving an hour each way to speech, so she suggested a one hour > > session, once per week. I have the Kaufman Workout Book and Cards at > > home...but I don't feel like I am doing him a lot of justice working > > with them. I am so frustrated and unsure of how to help our. Our local > > school district is difficult to work with and has some really weird > > loopholes you have to jump through to get speech. I honestly don't > > trust them with him. Please help...should I take him to see > > Kaufman? I live in Southern CA...what is a mom to do? Help Please!!! > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 6, 2009 Report Share Posted February 6, 2009 > > I just got a call from the SLP who evaluated my son last week and > diagnosed as mod-severe Apraxia of Speech (age 3 1/2). She said the > insurance won't cover his speech therapy. We have Blue Cross/ Blue > Shield PPO. I don't think the coverage gets much better than that! The > SLP said we could pay out of pocket at $120 per week. We would be > driving an hour each way to speech, so she suggested a one hour > session, once per week. I have the Kaufman Workout Book and Cards at > home...but I don't feel like I am doing him a lot of justice working > with them. I am so frustrated and unsure of how to help our. Our local > school district is difficult to work with and has some really weird > loopholes you have to jump through to get speech. I honestly don't > trust them with him. Please help...should I take him to see > Kaufman? I live in Southern CA...what is a mom to do? Help Please!!! > We were in a similar situation with BC/BS PPO, except in NJ. After several appeals and the usual agonizing " well that's what the benefits say " , we were able to get coverage by getting a PDD-NOS diagnosis. Don't know if Cal. works the same, but it may be worth a try, good luck.... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 6, 2009 Report Share Posted February 6, 2009 From what I understand it's all how the script for s/t is worded. Our insurance does not cover speech therapy for a delay but apraxia is not a delay it is a nuerological disorder. YOu should find a speech therapist who has plenty of experience with apraxia and then she or he should know how to get the coverage. My insurance does not cover s/t but we get coverage if the proper codes are used. Ex. oral motor weakness, feeding issues, also your nuero or dr. who wrote the script needs to use the right codes. From what I understand the script should never say developmental delay. Also, a child with apraxia needs more s/t then once a week. Take what you can get from the school just make sure it is the right kind of therapy. My 2 1/2 year old gets therapy 5xs a week. Good luck. -------------- Original message from " Leah " <kaiserfamily4@...>: -------------- I just got a call from the SLP who evaluated my son last week and diagnosed as mod-severe Apraxia of Speech (age 3 1/2). She said the insurance won't cover his speech therapy. We have Blue Cross/ Blue Shield PPO. I don't think the coverage gets much better than that! The SLP said we could pay out of pocket at $120 per week. We would be driving an hour each way to speech, so she suggested a one hour session, once per week. I have the Kaufman Workout Book and Cards at home...but I don't feel like I am doing him a lot of justice working with them. I am so frustrated and unsure of how to help our. Our local school district is difficult to work with and has some really weird loopholes you have to jump through to get speech. I honestly don't trust them with him. Please help...should I take him to see Kaufman? I live in Southern CA...what is a mom to do? Help Please!!! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 6, 2009 Report Share Posted February 6, 2009 Here are some archived messages about insurance for speech therapy. Make sure they are using the correct codes for insurance--stay away from developmental codes. I had BCBS HMO and didn't have any trouble getting speech covered by insurance. So call the SLP and ask her which codes she used for insurance and ask her to use the different ones mentioned below by Dr. Agin. Good luck, Tina /message/8923 Archive from Marilyn Agin, M.D. Medical Director CHERAB Foundation -Dear Kari, I wanted to respond to your insurance code question for apraxia. In the ICD 9 medical code book, #315.4 is Dyspraxia Syndrome. The confusion is that is that many of the #315 codes are developmental, but not this one. #784.69 is probably the safer code to use in that it comes from the section where the codes are neurologic. I am also adding to this a previous post (#263) which further elucidates this: One of the forces that most of our families with apraxic children have had to deal at some time or another is the medical insurers. If a medical professional or speech pathologist writes a report or a bill for submssion to the insurance company, here are some important tenets to follow: -Oral/verbal apraxia is a neurologic disorder so never use the word developmental or a code that is " developmental " in the report or on the bill. -Useful ICD codes for Apraxia of Speech are #315.40 or #781.3. The latter code is also one used for Hypotonia, Sensorimotor Integraton Disorder, and Coordinaton disorder, which may be associated with apraxia of speech. -If there is an associated expressive language disorder with the apraxia, which is commonly the case, use #784.6 which is " other symbolic dysfunction. " If #315.3, 315.31, 315.39, or 315.9 are used, these are developmental codes and may not be reimbursed. Often the insurance co. will ask your doctor to write a Letter of Medical Necessity of Letter of Predetermination. This needs to state the appropriate diagnosis and code number, state that the diagnosis(ses) have a neurologic basis and are not developmental, and intensive treatment by qualified, experienced speech and occupational therapists is required. Often you need to state the specialized nature of the therapy (PROMPT, oromotor, sensory integration, etc.) and explain why your therapist is more qualified than the one who is " in network " for provider. Have your therapists state their specialized credentials and certifications. -Define apraxia as a speech disorder where the brain signals that go to the muscles and structures of the speech mechanism are disrupted. -Without therapy, children do not outgrow apraxia of speech. Speech therapy is needed at least 4x week by experienced oral motor speech therapists. Without this therapy, prognosis for improvement is poor. -The provider may only provide therapy for 2 months or 6 months of therapy. Accept it and reapply with new goals set by your speech pathologist. Don't be discouraged by a rejection. That's what they want, They want to wear you down, but don't let them. This is your child and you have to continue the fight and go to the top person in the plan. If they tell you this is a preexisting condition, this is absolutely absurd when talking about a child. Be advised though, that some insurers are better than others. Some will never offer speech services unless your child has had a stroke or accident. (What a horrible thought). If you have a choice of insurers, make sure you choose one wisely. Look at the benefits before you sign up. Good luck! Marilyn Agin, M.D. Medical Director CHERAB Foundation http://www.apraxia.cc ============= Archive from Larry Laveman, MD Medical Consultant, CHERAB Hi Kari: The code 315.4 generally refers to motor delays, and indicates a developmental origen (the 315 prefix is used for developmental and learning disorders). Codes beginning with 7 generally refer to signs and symptoms, and most doctors and therapists are advised by their coding gurus to avoid them, as they can sometimes cause reduced reimbursement (we all want to get paid fairly...). Some insurances may not recognize the 784.69 code, and reject the claim on this basis. I am cautious in my practice to always give multiple dx codes, describing the full symptom complex of the child. Larry Laveman, MD Medical Consultant, CHERAB http://www.apraxia.cc archived message about insurance /message/42108 > > From what I understand it's all how the script for s/t is worded. Our insurance does not cover speech therapy for a delay but apraxia is not a delay it is a nuerological disorder. YOu should find a speech therapist who has plenty of experience with apraxia and then she or he should know how to get the coverage. My insurance does not cover s/t but we get coverage if the proper codes are used. Ex. oral motor weakness, feeding issues, also your nuero or dr. who wrote the script needs to use the right codes. From what I understand the script should never say developmental delay. Also, a child with apraxia needs more s/t then once a week. Take what you can get from the school just make sure it is the right kind of therapy. My 2 1/2 year old gets therapy 5xs a week. Good luck. > -------------- Original message from " Leah " <kaiserfamily4@...>: --- ----------- > > I just got a call from the SLP who evaluated my son last week and > diagnosed as mod-severe Apraxia of Speech (age 3 1/2). She said the > insurance won't cover his speech therapy. We have Blue Cross/ Blue > Shield PPO. I don't think the coverage gets much better than that! The > SLP said we could pay out of pocket at $120 per week. We would be > driving an hour each way to speech, so she suggested a one hour > session, once per week. I have the Kaufman Workout Book and Cards at > home...but I don't feel like I am doing him a lot of justice working > with them. I am so frustrated and unsure of how to help our. Our local > school district is difficult to work with and has some really weird > loopholes you have to jump through to get speech. I honestly don't > trust them with him. Please help...should I take him to see > Kaufman? I live in Southern CA...what is a mom to do? Help Please!!! > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 6, 2009 Report Share Posted February 6, 2009 You need to find out how your SLP is billing your insurance company. Some terminologies are not accepted as medically necessary by ins. companies. My insurance does cover apraxia as it is termed as a neurologically based disorder not developmental. If developmental is anywhere on the billing, chances are your insurance will reject it. Hope that helps. > > > > > > I just got a call from the SLP who evaluated my son last week and > > > diagnosed as mod-severe Apraxia of Speech (age 3 1/2). She said the > > > insurance won't cover his speech therapy. We have Blue Cross/ Blue > > > Shield PPO. I don't think the coverage gets much better than that! The > > > SLP said we could pay out of pocket at $120 per week. We would be > > > driving an hour each way to speech, so she suggested a one hour > > > session, once per week. I have the Kaufman Workout Book and Cards at > > > home...but I don't feel like I am doing him a lot of justice working > > > with them. I am so frustrated and unsure of how to help our. Our local > > > school district is difficult to work with and has some really weird > > > loopholes you have to jump through to get speech. I honestly don't > > > trust them with him. Please help...should I take him to see > > > Kaufman? I live in Southern CA...what is a mom to do? Help Please!!! > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 6, 2009 Report Share Posted February 6, 2009 Grhhhhh!! I've been dealing with this off/on for a number of years for my dd on Spectrum and just didnt have the time to mess with it, so we sucked up and paid privately. We too are an hour from therapy and our schedule was grueling for awhile. BUT I just want to say APPEAL! Long ago I worked in managed care as a case manager and the folks who took the time to appeal, often won. Managed care was sooo bad and so many entities went belly up long ago that a lot of the therapy groups in our area dont take ins at all. They provide you with the claim form and codes and you submit. Grhhhh.. just more work. But I did want to say, APPEAL.. it's often the only way. I'm on another list for Spectrum kids with Kaiser ins and someone just posted that their Appeal was reviewed by IMR (Ind Med Review ) and Kaiser's denial was overturned. Her child will now get the ST, OT and ABA he desperately needs. I've been thru the ringer with our school system at times but ultimately we got some pretty good services. Now (in elementary) the ST pretty much sucks - too much group but it's ok. If you want to bounce ideas off me as to getting better services thru the school - feel free to shout.. You can PM me altho I'm sure many here have had tremendous experiences they can share. I'm in N. CA. The beauty for your child with his dx would be to get both in place as he's so young.... Good luck! Leigh > > I just got a call from the SLP who evaluated my son last week and > diagnosed as mod-severe Apraxia of Speech (age 3 1/2). She said the > insurance won't cover his speech therapy. We have Blue Cross/ Blue > Shield PPO. I don't think the coverage gets much better than that! The > SLP said we could pay out of pocket at $120 per week. We would be > driving an hour each way to speech, so she suggested a one hour > session, once per week. I have the Kaufman Workout Book and Cards at > home...but I don't feel like I am doing him a lot of justice working > with them. I am so frustrated and unsure of how to help our. Our local > school district is difficult to work with and has some really weird > loopholes you have to jump through to get speech. I honestly don't > trust them with him. Please help...should I take him to see > Kaufman? I live in Southern CA...what is a mom to do? Help Please!!! > 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.