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My older son had outbursts pretty severely. I recommend the book " The

Explosive Child " by Ross Greene. Also, once he went through puberty he really

calmed down behaviorally. You didn't say how old your daughter is. Pam :)

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It is so good to know that we are not the only ones. I have three other

children and she just makes everyone so upset. this morning she " lost it "

because

she didn't want her hair brushed. I just feel like I need to get away from her

sometimes because I feel like I am going to completelly have a nervous

breakdown.

I just wish that there was some way that we could help her get control of

herself.

Thanks for the advice ,

erica

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I have talked to her dr about her not sleeping so many times I feel like i am

just repeating myself every month when we go in. See, at school she is so

well behaved and when we go to the dr. she couldn't be any better, it is just at

home. I don't get it. I have tried everything I can think of.

erica

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My 9 1/2 year old son has these diagnosis and is on a boat load of meds.

There are a lot of good books to read that give great suggestions on how to

handle things before the melt down. The last medication added to our son was

depakote for mood stabilization and out of all his medications this is the

one I have seen the most results from so far although he always seems to

still get major angry with me especially in the morning no matter what I say

We also see a chiropractor which was recommended by his psychiatrist which

has helped. I didn't think it was making a difference till we missed a week

and he had an unbelievable bad week end. Not sure what will happen when we

are done with all the sessions for that or if he will be seen regularly for

maintenance.

I know the walking on egg shells well and there are certain things in life

that set him off that we can't avoid and I dread those events. We are

planning on a 2 week vacation like we normally do this summer and if I could

get over the guilt of not taking him I think I would because I know that he

will make it miserable. He loves vacation and the beach but such stupid

things set him off. It's not fair to the other kids I know dealing with this

but I just can't leave him behind.

You're not alone and that has helped me knowing there are other parents out

there dealing with this.

Suzanne

-- ( ) hello, new to group

hey everyone, how are you? I really need help. My daughter has as. and

adhd and odd, she has these fits where we litterally have to restrain

her, she doesn't sleep and we have tried everything! She is on

concerta and seraquil in the morning and mirtazapine( remeron) at

night . The concerta is helping her so much at school. Her grades are

awsome, but at home she is a different child. I feel like I can't take

anymore. We are walking on egg shells just so that we don't upset her

and throw her into one of her " meltdowns " .

Does anyone else have any of these problems or some suggestions to

help us ? I am desperate!

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Subject: ( ) hello, new to group

hey everyone, how are you? I really need help. My daughter has as. and

adhd and odd, she has these fits where we litterally have to restrain

her, she doesn't sleep and we have tried everything! She is on

concerta and seraquil in the morning and mirtazapine( remeron) at

night . The concerta is helping her so much at school. Her grades are

awsome, but at home she is a different child. I feel like I can't take

anymore. We are walking on egg shells just so that we don't upset her

and throw her into one of her " meltdowns " .

Does anyone else have any of these problems or some suggestions to

help us ? I am desperate!

Hi! Do you have any local resources available to you? It sounds like you

might look into finding a behavioral specialist - someone who can come in

and assess her behaviors and figure out a behavior plan that works. If she

isn't sleeping, that is probably a huge reason she is so grouchy or

unreasonable. Talk to the med doc about her sleeping problems. She needs

to get to sleep!!

Roxanna

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Hi!

I feel you! My daughter is almost 7 and she sounds very similar to

yours. Although she has a hard time everywhere not just at home, home

seems to be the worst. I think that is typical with most kids though,

they are alway worse with their mothers than anyone else.

Sometimes I just don't know how I'm going to make it through a morning

with her without losing my mind or strangling her. I worry about days

that I have alone with her, I'm freaked about this summer because I

just can't handle her for an entire day by myself, I do it when I have

to but I know it isn't good for either of us. I know thats awful to

admit as a mother but its the truth. The best thing for me is to get

some time away even just to have one other person to share the duties

with husband, grandma, aunt, etc. I don't know how some of you guys

homeschool, I would absolutely lose my mind! But I know too how

different all these kids are.

My daughter doesn't sleep either and we just recently tried Clonidine

and its been working awesome! I posted here about it a couple weeks

ago to see if anyone had tried it and I got a flood of positive

responses. I can't tell you how wonderful it is for everyone to get a

full nights sleep.

Keep us posted!

Rechelle

>

> hey everyone, how are you? I really need help. My daughter has as.

and

> adhd and odd, she has these fits where we litterally have to restrain

> her, she doesn't sleep and we have tried everything! She is on

> concerta and seraquil in the morning and mirtazapine( remeron) at

> night . The concerta is helping her so much at school. Her grades are

> awsome, but at home she is a different child. I feel like I can't

take

> anymore. We are walking on egg shells just so that we don't upset her

> and throw her into one of her " meltdowns " .

> Does anyone else have any of these problems or some suggestions to

> help us ? I am desperate!

>

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Rechelle,

It is so good to hear that I am not the only one out there! I completelly

hear yah when you say you dread being alone with her all day. I feel the same

way. My husband is a Marine and I am so deathly afraid of the next time he

deploys. Last time he was gone for 8 months and we have three other children and

we

had the military police at our house, I don't know how many times. Sometimes

I called them because I couldn't take it anymore and I had nowhere else to

turn. I thought maybe they could scare her into behaving, but as we all know

that

worked for maybe 10 minutes.

I dread waking her up in the morning for school because I don't know what

her mood is going to be and what may set her off that day. God forgive me, but I

love my daughter very much, but sometimes I really don't like her. Do you

feel the same way?

We have tried Clonidine. It worked awsome for about a month then it just

stopped working.That seems to be the biggest problem, she becomes amune (sp?) to

her meds so quickly. The only one that she hasn't had a problem with is the

concerta. But that just makes it easier for her to study. I wish that we could

just find something that would make her sleep. I don't think my husband and I

have had a full nights sleep for over a year, and we are just so darn tired.

I swear, her dr. must think we are drug happy because everytime we go in I am

asking for something else to help her. I even go in, in tears begging her to

help. She just tells me that we will get it figured out and to remember that

she is there for my daughter not my husband or myself.

Well, enough rambling, it is so good to know that we are not alone in this.

Thank you for responding to my message. Maybe we could keep in contact. Kinda

help eachother.

erica

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We only saw the behaviors at home for the longest time and I was told that

was where my son felt safest and because of unconditional love. It was just

this fall that things started falling apart at school and then the things

that have happened makes me want to scream.

Suzanne

-- Re: ( ) hello, new to group

I have talked to her dr about her not sleeping so many times I feel like i

am

just repeating myself every month when we go in. See, at school she is so

well behaved and when we go to the dr. she couldn't be any better, it is

just at

home. I don't get it. I have tried everything I can think of.

erica

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Guest guest

My daughter has sleep problems when her yeast is high. I have had her tested

and she has very high yeast but treating yeast can be very complicated. The

following site has some good info you yeast/autism issues. Until we started

treating her yeast she rarely if ever slept like a typical child. Read up more

on the yeast/sutism link.

http://www.danasview.net/yeast.htm

rechelle5us <rechelle5@...> wrote: Hi!

I feel you! My daughter is almost 7 and she sounds very similar to

yours. Although she has a hard time everywhere not just at home, home

seems to be the worst. I think that is typical with most kids though,

they are alway worse with their mothers than anyone else.

Sometimes I just don't know how I'm going to make it through a morning

with her without losing my mind or strangling her. I worry about days

that I have alone with her, I'm freaked about this summer because I

just can't handle her for an entire day by myself, I do it when I have

to but I know it isn't good for either of us. I know thats awful to

admit as a mother but its the truth. The best thing for me is to get

some time away even just to have one other person to share the duties

with husband, grandma, aunt, etc. I don't know how some of you guys

homeschool, I would absolutely lose my mind! But I know too how

different all these kids are.

My daughter doesn't sleep either and we just recently tried Clonidine

and its been working awesome! I posted here about it a couple weeks

ago to see if anyone had tried it and I got a flood of positive

responses. I can't tell you how wonderful it is for everyone to get a

full nights sleep.

Keep us posted!

Rechelle

>

> hey everyone, how are you? I really need help. My daughter has as.

and

> adhd and odd, she has these fits where we litterally have to restrain

> her, she doesn't sleep and we have tried everything! She is on

> concerta and seraquil in the morning and mirtazapine( remeron) at

> night . The concerta is helping her so much at school. Her grades are

> awsome, but at home she is a different child. I feel like I can't

take

> anymore. We are walking on egg shells just so that we don't upset her

> and throw her into one of her " meltdowns " .

> Does anyone else have any of these problems or some suggestions to

> help us ? I am desperate!

>

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Subject: Re: ( ) hello, new to group

I have talked to her dr about her not sleeping so many times I feel like i

am

just repeating myself every month when we go in. See, at school she is so

well behaved and when we go to the dr. she couldn't be any better, it is

just at

home. I don't get it. I have tried everything I can think of.

erica

Well, you could always video tape the problems to show the doc. Or find

another doc who does believe you. My two take meds for sleep and this can

be a common problem for kids with AS/HFA.

Roxanna

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Subject: Re: ( ) hello, new to group

that's not a bad idea, I will definatlly try that. Is your child on meds at

night for sleeping problems? If so, what knds have worked/ not worked?

erica

We've used clonidine with great success for sleep issues.

Roxanna

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  • 1 year later...
Guest guest

Contact your Early Intervention 0-3 years old. You can also get a

referral from your pediatrician. Early Intervention will come to your

house and evaluate your child for speech and if he qualifies you can

get speech therapy for him.

Usually at 18 months a child has between 25-50 words. Do a search on

developmental milestones and you can get a better idea if he is meeting

his milestones not just for speech, but fine/gross motor also. Have

you had his hearing checked?

Tina

>

> hello i am a new comer to this group and i have a 20 month old son

that

> doesn't talk or have much interest in it. he jibber jabbers, but no

> words yet. i was wondering if that is even normal? I have friends and

> alot of family all on my butt on why he isn't talking? Everyday I am

> getting asked from several people if my son is talking yet, so I am

> courious of i need to start being concerned? I am getting a bit

> fusterated on what to do. I am a stay home mom and feeling liek i am

> not doing enough. can i get some advise and ideas on this. Thank you

> soooo much.

>

> Tara B

>

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Get him evaluated by Early Intervention in your state. It's free. He

should be saying something by now. It's free and if there is nothing

wrong they will tell you. Generally he should be saying a few words now

and have 50 words by age 2. I had my son evaluated at 20 months. It has

been slow going because speech is not natural for him but it is the best

decision I ever made. You will cry and be scared but it is worth it and

there is so much hope, especially getting to it early.

God Bless!

Liz

Tara wrote:

>hello i am a new comer to this group and i have a 20 month old son that

>doesn't talk or have much interest in it. he jibber jabbers, but no

>words yet. i was wondering if that is even normal? I have friends and

>alot of family all on my butt on why he isn't talking? Everyday I am

>getting asked from several people if my son is talking yet, so I am

>courious of i need to start being concerned? I am getting a bit

>fusterated on what to do. I am a stay home mom and feeling liek i am

>not doing enough. can i get some advise and ideas on this. Thank you

>soooo much.

>

>Tara B

>

>

>

>

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  • 1 month later...
Guest guest

Hi, I'm and my son is Owen, 4 1/2 mos old, and he was just

diagnosed with plagiocephaly on friday and he got a head ct today, and

unfortunately the appointment for physical therapy isn't until August

(soonest they could get us in). Is there anything we can do ourselves

to help him while we wait? Thanks!

-

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That sure is a long time to wait. Go to this website and it pretty

much gives you the exercises that the Therapist will give you.

http://www.neckexercises.info/

It is on the Plagiocephaly website.

>

> Hi, I'm and my son is Owen, 4 1/2 mos old, and he was just

> diagnosed with plagiocephaly on friday and he got a head ct today,

and

> unfortunately the appointment for physical therapy isn't until August

> (soonest they could get us in). Is there anything we can do

ourselves

> to help him while we wait? Thanks!

> -

>

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Welcome !  Does Owen have Torticollis?  If so, There are stretches you can do - and most of your PT will be done by you - But honestly He needs to be seen by a PT who can evaluate him. Did you get x-rays of his neck to look for bone abnormalities? If there is an abnormality(though rare) PT can actually cause harm.

If Aug. is the 1st you can get in to see a PT then call a different one. Look for one that treats kids w/ Torticollis. Also, Call you ped. They may have a handout with the stretches diagramed for you.

HTH!

 Jen and Luli - 18 mo.

Left Tort - Right Plagio - Hanger Band Grad - CA

tallulah jayne

www.babiesonline.com/babies/j/jens5th/

Hello, New to Group

Hi, I'm and my son is Owen, 4 1/2 mos old, and he was just

diagnosed with plagiocephaly on friday and he got a head ct today, and

unfortunately the appointment for physical therapy isn't until August

(soonest they could get us in). Is there anything we can do ourselves

to help him while we wait? Thanks!

-

AOL now offers free email to everyone. Find out more about what's free from AOL at AOL.com.

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  • 10 months later...
Guest guest

Welcome Lori,

Our son was also diagnosed late. He was almost 17. He is now 18 and

graduating high school. He has plans for a local college. Keep reading

and you may find it very helpful.

Ginny

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Did he have a lot of food issues? In hindsight yes. I mentioned the

possibility a few times, but as often as we moved with the military,

it didn't get handled. I feel bad about that.

>

> Crohns can be hard to manage. I feel for the poor guy. Did he have a

> lot of food issues growing up?

>

>

>

>

> >

> > Hi, I'm Lori and I live in West Texas with my AF husband, two sons 17

> > and 20, and three cats and special needs dog. My oldest son has

> > Asperger's syndrome that was not diagnosed until he was 15, and he has

> > also been recently diagnosed with Crohn's disease. I am wondering how

> > many of your kids may have other medical type issues, especially

> > autoimmune? Or if there is a family history of that? I ask because of

> > the new research and our own situation. Thanks, Lori deep in the heart

> > of Texas

> >

>

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According to several studies from different sources, there is a

definite correlation. I do understand trying to get diagnosed, because

it took many years for me to get diagnosed with Lupus/UCTD.

>

> About the autoimmune connection...thats interesting. My Mom has RA,

and MS runs in our family as well. I have some sort of autoimmune

thing going on I think, that I am trying to get diagnosed right now

(very frustrating, WHOLE different subject ;)) and I have a son with

AS. I wonder if there may be a connection?

> thanks,

> kate

>

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