Mothering › Forums › Parenting › Special Needs Parenting › *~SPD support thread- January~*
New Posts  All Forums:Forum Nav:

*~SPD support thread- January~* - Page 3

post #41 of 57
kalynnsmom, I'd for sure explain to her why your daughter does this, and either tell her yourself that her comment hurt your daughter's feelings or have your dd do it if she wants. bravo for your dd's resourcefulness!

can anyone tell me what kind of therapies help kids who are really over responsive?
post #42 of 57
Quote:
Originally Posted by furfeet View Post

can anyone tell me what kind of therapies help kids who are really over responsive?
lots and lots of heavy work, physical activity, relaxation training, being outside in nature, sensory soothing activities (like swimming, baths, sandboxes, playdough, legos, etc), supplements like melatonin & GABA and EFT.
post #43 of 57
Hi! I am so glad to find this thread. What great support! I am a mommy of 3 fabulous kiddos. 18yr DS,12yr DD,and 15 months DD (SPD dx @ 13months).
I do believe now that 12 yr DD is also SPD.

I finding that having a SPD 15 month old the most chanllenging thing I have ever done. I find my self frustrated and compeletely drained. I am a Early Childhood Educator (now SAHM) and by nature expect a certain amount of control. I have none!!! I find myself staring at a screaming ,fit throwing child and have no idea how to soothe her. Brushing and joint compressions help when she allows me to come near her. Her new favorite thing is to stomp her feet and yell at me when she asked something. She wants to be left alone. She will climb up into my lap but at her own desire. I have to talk and play with her from a distance. I find giving her verbal warnings when things are about to change (transitions) has helped some.
My DH has a hard time understanding and how it affects everything she does. He can not stand the crying.
As she gets older I am noticing more and more SPD behaviors that were not present 3 months ago.

I posted another thread, it explains some other issues we are dealing with.
http://www.mothering.com/discussions....php?t=1192085

Just surviving the ride!
post #44 of 57
i forgot to mention weighted blankets and vests too for OR kids.

lots of info is really good for transitions. in the AM i tell DS what to expect for the day. i give him lots of warnings when things are going to change. now that he can tell time it helps a lot. he is better able to time his own transitions. i find that OR kids are really rigid and want things done their way. when they get surprised (which is often) they dig in their heels and resist everything. i call it the reflexive no. when DS was 2-3 he had some of the most monumental tantrums i have ever seen in a kid. but i am happy to say he's grown out of them. he can still be explosive, but at least it's not 45 minutes of kicking and screaming until he passes out.
post #45 of 57
Quote:
Originally Posted by umami_mommy View Post
i call it the reflexive no.
I sometimes wonder how much of A's spd he got from me. I have had to teach my kiddos that if they want something or to do something out of the norm they need to ask me and wait for an answer because if they demand an answer immidiatly it will be no. I have no idea why I do that. If they give me a while I usually say yes but to change things up on the fly drives me crazy and I resist with all my being. I like your term "reflexive no" and plan on using it as explanation in the future.
post #46 of 57
my DH has a reflexive no also. he is also OR. it's for sure inherited.

they both are driving me nuts today
post #47 of 57
My son is four and is in OT for SPD right now...we'll start feeding therapy soon as well. I look forward to relating to other mamas who deal with SPD children!
post #48 of 57
just posted this thread...

http://www.mothering.com/discussions...8#post15055908

any input would be great!
post #49 of 57
Quote:
Originally Posted by umami_mommy View Post
lots of info is really good for transitions. in the AM i tell DS what to expect for the day. i give him lots of warnings when things are going to change. now that he can tell time it helps a lot. he is better able to time his own transitions. i find that OR kids are really rigid and want things done their way. when they get surprised (which is often) they dig in their heels and resist everything. i call it the reflexive no. when DS was 2-3 he had some of the most monumental tantrums i have ever seen in a kid. but i am happy to say he's grown out of them. he can still be explosive, but at least it's not 45 minutes of kicking and screaming until he passes out.
I am new to SPD, can you help me understand why it is associated with difficulty with transitions?
post #50 of 57
"reflexive no".... now that's a great way to put it! yes, we got that here for sure!

my daughter's actually more of a "reflexive throw yourself on the floor backwards, kicking your heals into floor and scream 'NO!!!!' " heh but reflexive no is an easier way to put it lol
post #51 of 57
Quote:
Originally Posted by mamatoni View Post
I am new to SPD, can you help me understand why it is associated with difficulty with transitions?

i can only talk about my experiences but you have to have a certain about of flexibility in order to transition. my DS and DH both tend to be rigid and inflexible and so transition is difficult. any change takes a shift in focus, energy and attention. this is hard for people with sensory modulation disorders (three of the types of SPD).. change creates a sensory experience that is difficult to modulate. clear as mud?
post #52 of 57
thank you for the info on therapies, it's funny those are my ds's favorite activities, besides the weighted stuff. He freaks if anything is "on" him even if it's just his little bro when they're wrasslin'

as for transitions, ds has a horrible time with them, especially when he was at school. I think it's because to him, it seemed really jumbled and out of control. Lots of talking, movement, change, and it would just overload him.
post #53 of 57
other things that can help: blowing up balloons, sucking pudding or yogurt through a straw, blow pens. weighted medicine balls. pushing against a wall or adult. (resistance is the key here)

HTH!
post #54 of 57
Anybody still around? After a good month or so, things have been tough lately. Just feeling defeated and worried about the future (school, social issues as DD gets older). And feeling not-so-supported by most of those I've chosen to share DD's dx (now articulation disorder in addition to SPD)with....really ignorant and silly comments like saying that she has a speech delay b/c she's an only child and 'has so many adults who do things for her'. Um, ok.

Just feeling and needing to connect with mamas who understand.
post #55 of 57
Quote:
Originally Posted by beachbaby View Post
Anybody still around? After a good month or so, things have been tough lately. Just feeling defeated and worried about the future (school, social issues as DD gets older). And feeling not-so-supported by most of those I've chosen to share DD's dx (now articulation disorder in addition to SPD)with....really ignorant and silly comments like saying that she has a speech delay b/c she's an only child and 'has so many adults who do things for her'. Um, ok.

Just feeling and needing to connect with mamas who understand.
DS (nearly 4) has the same diagnosis -- articulation disorder and SPD. Apparently they often go hand-in-hand, though research hasn't figured out why yet. Regarding both speech and behavior, I got stupid comments about ds's older sister being so articulate that she spoke for him, or that it was because he's my youngest, so we baby him.

To which I say: Piffle.

Unless a person has lived with us, 24-7, for at least two weeks, they simply don't know the ins and outs of ds's needs. I do, and sometimes that means it looks like I'm being too tough on him and sometimes it looks like I'm being too easy on him. He's always changing and I'm always figuring things out, but I still know what works and when for him better than anyone else and quite frankly, if anyone feels the need to say something snarky when he's having a rough day, they can suck it.

General update on us:

DS is seeing an OT twice a week and it's made a huge difference. He's rejoined a number of activities that he couldn't handle sensory-wise just six months ago and he's learned a lot of coping skills and more socially-appropriate and safe ways to meet his sensory needs. Having someone come to our house just to play with him is also really fun for him and he loves having that special activity to look forward to, though he does resist some of the exercises she asks him to do. We're working on increasing his stamina -- he really fluctuates in energy levels and it makes it hard for him to keep up with the world around him sometimes.

His sleep has hit the toilet again, but we figured out why after the first week. He's teething! Somehow I completely blanked out those last sets of molars and mentally assigned teething to babyhood, despite my experience to the contrary with dd. Never even thought about it in relation to my almost 4-year-old. Once those teeth finally break through, I'm hoping the sleep comes back and he stops chewing on everything in sight.

Oh, and clothes? Clothes are The. Enemy. "Mama, I don't want to get dressed. I hate getting dressed." No kidding, sweetie. I got that one figured out somewhere during week 2 of the daily screaming fit and 45-minute saga around picking out a pair of pants. Last year it was the Snow White ballgown that he wore every day for 5 months. Now it's footie pajamas all the time, or "bootiful" clothes that feel good. This definition changes hourly, of course.
post #56 of 57
I'm feeling better today. Thanks, earthmama. Glad to hear the OT is helping so much. And about the 'bootiful' clothes. My DD is all about the 'FAAAAAAAAAAAANCY' clothes, too. She gets so mad, though, when she wears a tutu out in public and people call her a princess. She asks me to make signs for her to wear that say 'I am NOT a princess!' LOL!

OT, but if you have any articles on articulation disorder and SPD, I'd love see them. DD's articulation is due to oral motor issues because of low muscle tone. She's in the 14% percentile for articulation.

How's everyone else doing?
post #57 of 57
I posted a new thread for us!
New Posts  All Forums:Forum Nav:
  Return Home
  Back to Forum: Special Needs Parenting
Mothering › Forums › Parenting › Special Needs Parenting › *~SPD support thread- January~*