I apologize that it’s taken me so long to write the second post in this Series. These posts have been difficult for me to write for some reason, but we’re wrapping up our Early Intervention Services now and I wanted to share our experience in case it helps anyone out there. You can read Part 1 here.
. . . . .
A case worker from Early Intervention contacted me within days to schedule an appointment to visit us at home. Olive was 16 months old at the time. During our hour-long meeting, she observed Olive playing and we discussed our concerns. She suggested that we have Olive evaluated by a speech, occupational, special instruction, and a physical therapist. Each evaluator subsequently contacted us to set up individual meetings in our home.
T H E E V A L U A T I O N S
Olive was present for each of the evaluations. They observed her doing some of the things we were concerned with like not responding to her name, not looking when we pointed, lack of eye contact, obsessively playing with her shoes and cars, etc. We asked tons of questions and they offered a lot of great advice. For instance if your child has a problem with making eye contact, you can hold a toy in front of your nose so that they have to look at your eyes. They also identified things that we had no idea were considered issues, like how Olive always sat in a w formation on her legs, which was very common with kids with low muscle tone. She usually stuck her tongue out which was another indicator of low muscle tone. She also stuffed her mouth full of food only to gag on it, which was a sensory issue because she couldn’t feel the food unless her mouth was very full.
All the evaluators were so knowledgeable, we learned so much just from the evaluations themselves. I was very hopeful about getting Early Intervention services if it meant getting to work with therapists as excellent as they were, but we wouldn’t know if we qualified for services until our second meeting with our case worker.
The evaluators submitted their reports to our case worker, and then we set up an appointment to go into her office to develop an ISFP (Individual Family Service Plan), where a service coordinator would approve which services we would receive. They are required to initiate services within a specific time frame, so everything happened relatively quickly. But since we had to coordinate 6 different meetings and pull Olive out of daycare for each one, it took us about a month to get through it all.
G E T T I N G A P P R O V E D F O R S E R V I C E S
Once we arrived at our case worker’s office, we went over the reports the individual evaluators submitted. In order to qualify for services, Olive had to show a 33% delay in one area, or a 25% delay in 2 areas. The evaluations honestly sounded much worse than I expected! They were particularly concerned with her speech regression — she stopped using words she had been using for months. Although a speech delay is not necessarily indicative of a larger problem, kids with delays usually present with speech delays.
Our case worker acted as our advocate, and the service coordinator determined just how much services we received. We were approved for 30 minutes of speech, 30 minutes of occupational therapy, and 30 minutes of special instruction once a week. Olive did not qualify for physical therapy, but that was the one area where we weren’t concerned because she continued to make progress even if she was delayed (she eventually walked at 18 months).
Shortly after we were approved for services, our assigned therapists contacted us to set up appointments. Although services can be provided at your child’s school, our daycare didn’t really have the space for it so we opted to have all our services done at home. We are extremely lucky to work from home, so that we were able to be present for her therapy sessions. In the end, 3 sessions a week required a big time investment on our part because we had to pull Olive out of daycare and take a lot of time off of work. We have no regrets though because the sessions were so short, the most helpful part of them was learning from the therapists so we could work with Olive on our own time.
O C C U P A T I O N A L T H E R A P Y
Our occupational therapist hit it off with Olive right away and we could tell that she was going to be awesome. She worked with Olive on things like her fine motor skills, life skills like getting dressed/feeding herself, behavioral issues like tantrums, and sensory issues. Often I would just ask her tons of questions throughout the entire session because she was such a fountain of knowledge! Olive received occupational therapy for about 6 months until our therapist suggested that we stop because she had made so much progress, and her fine motor skills were at or above her age level. I was so sad to say bye to her because she was such a great therapist.
S P E E C H T H E R A P Y
Olive bonded quickly with our speech therapist as well. She was friendly and fun, but after a couple months of sessions, we decided it just wasn’t working out. It was a really tough decision because we really liked our speech therapist as a person, but we requested a different therapist because this was the area where we felt Olive needed the most help.
You can request to work with specific therapists, so we requested a speech therapist that our occupational therapist recommended. That speech therapist was great. She used a combination of toys and apps to work with Olive on things she should have mastered at that age (like animals and colors), and provided us with tons of resources on other ways we could work on Olive’s speech. Even though Olive’s expressive language eventually caught up and seemed to be on par with kids her age, her receptive language appeared to be far behind where it should have been. Olive had trouble understanding basic questions and commands that she should have mastered given the level of her expressive language. But she finally started to catch up at the beginning of this year. Olive was recently tested by our speech therapist and her speech is now within the average range for kids her age (30 months). I met with our case worker yesterday and she suggested that we stop speech therapy services based on Olive’s most recent evaluation.
S P E C I A L I N S T R U C T I O N
Special Instruction therapists focus on cognitive and social interaction, and meeting developmental goals. Olive did not hit it off with our special instruction therapist at all. She was scared of her, cried through the sessions, and the therapist just could not engage or bond with Olive. We wanted to give it a fair shot so we did a couple more sessions, but Olive never warmed up to her so we requested a new therapist.
We now have a special instruction therapist that we love. He helped us finally get Olive interested in books. Before the age of 2, Olive was only interested in lift the flap books, and even then she wasn’t listening to the story — she was just focused on lifting the flaps. Our therapist taught us tricks, like asking about the images in the book and turning pages instead of reading the story. Just getting Olive interested in books was an important step; previously Olive would just throw them! Now Olive finally likes reading.
The Special Instructor therapist tested her 4 months ago and she was still below average in some areas. But a test earlier this month showed that she has caught up and is no longer behind in any area, so we’re going to wrap up special instruction therapy very soon as well.
W H A T D O E S A S E S S I O N L O O K L I K E ?
During a therapy session, it essentially looks like the therapist is playing with your child. They usually bring in toys and activities that are designed to work on areas where your child is delayed. For instance an occupational therapist might bring in a stacking toy to work on fine motor skills, and a special instruction therapist might bring in a doll and play food to engage in imaginative play. Sometimes it’s hard to know just how much your child is getting from each session because they’re so short and Olive only saw each of her therapists once a week. But I learned by just observing and asking the therapists questions. I also think it depends on finding a therapist that is a good fit with your child, so you need to advocate for your child if something isn’t working out.
W H E R E W E A R E N O W
Has Olive stopped doing all the things we were concerned with when we first started this process? She still walks on her tip toes regularly, she still doesn’t respond to her name at least half of the time, she is still very independent and engages in parallel play most of the time (except with her immediate family).
But her speech is on par with children her age, she makes sustained eye contact, she is extremely affectionate, and she even taught herself the entire alphabet (we had no idea she knew it at all!). I still worry about her to tell you the truth, but she seems to be on track and I’m amazed at how much progress since we first started services a year ago.
I have friends that were approved for EI and ones that were turned down, but there’s nothing to lose from seeking an evaluation if you’re concerned that your child may have a marked delay. We learned so much just from the evaluations themselves. These are therapists that work with kids with all kinds of delays every day, so they really know what they’re talking about. It was very reassuring to ask them about general delays as well as specific questions about Olive that our daycare teachers and pediatricians didn’t have the answers to.
Early Intervention is the best thing you can do for your child if they really do have a delay, so I think it’s incredible that programs like this exist at low or no cost to families. Overall I have to say that I’ve been very impressed with the Early Intervention system, the quality of the therapists, and the speed and responsiveness with which they got everything done.
In my next post I’ll share what we did to help Olive that was most effective!
Olive’s Early Intervention Journey part 2 of 3
1. Is My Child Delayed? by Mrs. Bee2. Pursuing Early Intervention by Mrs. Bee
3. The Best Things We Did For Dealing With Olive's Delays by Mrs. Bee
Early Intervention part 6 of 6
1. Guest Series: Raising a Child with Autism by Mrs. Bee2. PDD-NOS by Mrs. Bee
3. The Ups and Downs by Mrs. Chocolate
4. Early Intervention Evaluation by Mrs. Chocolate
5. Is My Child Delayed? by Mrs. Bee
6. Pursuing Early Intervention by Mrs. Bee
guest
Hi Bee,
I am so happy Olivia responded so well. We have our meeting this Wed. Our child was approved for speech therapy (she is a 18m old with no sounds) and was also suggested that we evaluated for OT because of sensory issues (bathing, stuffing food and gagging). Can I ask how long did Olivia did speech for (time/days/months)? Did she had any sounds at all? So far my LO has above average receptive but expressive she is a 6m old. So glad EI has worked for you. We are going in with really high expectations! Thanks and good luck!!
pomelo / 5628 posts
Thanks so much for sharing! I’d be really interested in hearing more about the apps and activities you used to work on speech.
admin / watermelon / 14210 posts
@nina – we have done therapy for the past year. she had words and sounds, but she experienced a regression before we applied for services and stopped using them.
she had speech for 30 minutes/week, once a week for a year.
@Mrs Green Grass: i’ll work up a list for my next post!
blogger / nectarine / 2687 posts
Thank you so much for writing this! I’m so glad Olive is doing so well and hope that she continues to make good progress!
guest
Yes, I am also looking forward to hear about apps and exercises for speech!
blogger / nectarine / 2600 posts
I really like reading this to see Olives journey especially since we are also in EI for Juliet now.
honeydew / 7295 posts
Thank you so much for opening up about this. I understand firsthand how difficult it can be. At such a young age our children are a big mystery and its hard to know what’s really going on but I agree wholeheartedly that EI can only help and never harm a child. The earlier the better. I kind f wish I had gone with my gut on my son and started him sooner because even though we are in the early stages I already feel so relieved. I felt so powerless before wondering if I was doing everything I could to help him and wondering if certain things I did might hinder him. Now I feel so empowered and like I have tools at my fingertips! Our son had his first session this week and he did so amazing! The therapist was funny and reminds me a lot of James Lipton from Inside the Actors Studio. They will have a few people work with him in the coming weeks and see who fits best. And it’s 100 percent free! I seriously implore all parents with any doubt not to hesitate. I am very excited for what lies ahead. Another thing my therapist said that I liked was that he likes to focus on treating the child not the “condition”. He isn’t focused on diagnosis at this point. I think a lot of people fear labels for their children and the stigmas that might be attached. Bravo and much love to your family. Olive sounds like she is a wonderful little girl and I’m so happy to hear that she is thriving.
blogger / persimmon / 1398 posts
Thank you for writing this! It’s really, really informative and I even picked up a few tips to engage Pint-Sized. THANK YOU!
blogger / pomegranate / 3044 posts
Thanks for writing this up! We were approved for EI for DS2 recently and just had our first OT meeting this week, and I feel like I learned so much. MD (vs NYC) seems to be more laid back, the most frequently you can get services is 2x a month (which is what we’ll get). They said they follow a parent teaching model, to just taking the time (about an hour) to work with the child and then give the parents tasks to work on.
GOLD / coconut / 8266 posts
Thank you for writing this. When R was recommended for EI I felt like no one on the boards or in real life had any experience with it. It was a very lonely and confusing time for me. But R has thrived with her PT and loves her therapist so I’m happy we went through with it. R gets 45 minutes of PT twice a week.
cherry / 131 posts
Like everyone else, I have to say thank you for writing this post. I have personal and professional experience with EI and children with special needs. Like SwedishFish stated, it can be lonely and confusing. It is great that you are willing to share your story, and help others going through this.
blogger / persimmon / 1225 posts
Thanks for the inside scoop, so much helpful and interesting information! Go Olive!
guest
Thank you for sharing your experience. I just wanted to comment that each state has their own version of an early intervention program and the requirements for eligibility are different. Serve states it is one area of 25% delay is eligible some states it has to be in different areas, etc.For people reading that are interested in having a developmental evaluation completed, please contact your state early intervention program for specific requirements and assessment procedures
guest
EI is crucial. I had it as a kid (PT/OT) and my mom is a paediatric SLP so we had speech too. My LO was evaluated when she was 10 months for being behind on her gross motor skills (I started pushing for that at 8 months) and although is still behind (just figured out how to transition from lying down to sitting and pulling up to standing, is cruising and is semi-crawling), PT has been amazing for her. My mom is a bit worried about her play and speech, but my mom babysits once/week and my mom can’t be anything but a clinician, so for now we’ll let grandma lead therapy. It seems to be working since LO has become more expressive and although does parallel play a lot of the time, she likes to show those around her what she’s doing.
blogger / pomegranate / 3491 posts
Thank you for this post – so so glad that the process has worked so well for Olive!
pomegranate / 3212 posts
My son’s best friend has down syndrome and has OT PT and occasional ST. Not only has his friend thrived with her therapist but we reap a to. Of benefits too! We do her exercises with her and hear about different toys or experiences that the thrrapists reccomend and its always awesome advice even for a “typical” child.
pomegranate / 3053 posts
Thank you for sharing your experience with EI. I’m glad to hear that Olive has thrived from it and hope that she only continues to make progress with all the tools you’ve learned through therapy.
blogger / eggplant / 11551 posts
Thank you for sharing your experience in such detail – it really was so fascinating to read. I won’t hesitate to pursue EI if I ever feel like J is delayed in any way. I can’t wait to read your next post in this series!
blogger / nectarine / 2010 posts
I find that the most frustrating part of the EI process so far has been the opened ended, “what are your goals for (speech, PT, etc)?” Um, I want him to be up to speed for his age, whatever that involves. I felt so frustrated that no one was telling me what “normal” looked like, so I was totally unable to come up with goals. I settled on things I thought might be helpful for preschool, but still feel rather unguided.
blogger / clementine / 998 posts
ThaNk you for being so open
guest
I just came across this as my 16 month old is also struggling with delays, mainly speech. He is in daycare but recently switched over to a new class and they wanted to wait and see. I’ve been concerned since he was 12 months and just didn’t know if I should continue waiting. After reading this, I called NYDOH as well and a service coordinator will be contacting me back. I really hope my son gets the help he needs. Thanks for the post. Without it, I wouldn’t even know these services are readily available to me!