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terry,

prayers and hugs to you!!! i cant imagine the thoughts that are going thru

your head!!!! i have never experienced this and hope i dont have too....but

i think one of the other list members daughters was in body cast, jamie

maybe???? i am not sure, i think shes a girl...my memory is bad..... goes

along with the gray hair, sagging boobs, and wrinkled eyebrows..... :-) i do

know that when my cousin got hit by a car and was in a body cast, they left

a whole down there and her mom just used big diapers and wiped her

constantly.... goodluck and please know you and matthew are in our

prayers......leah

>

>Reply-To: egroups

>To: egroups

>Subject: HELP!

>Date: Tue, 23 Jan 2001 06:40:53 -0000

>

>Hi all....

>A few months ago I mentioned that we were concerned about 's

>feet...they are flat and he walks on the inside of his ankles. Since

>then, we saw an Orthopedic doc who took some x-rays of his feet and

>his hips. He told us that 's feet " are flat " (duh!) and that

>he will prescribe orthotics. He also said that there is a problem

>with his hip. He referred us to an Orthopedic Surgeon in LA. We saw

>him today and he says that 's femur (leg bone) is malformed

>and so is his pelvic bone that forms his hip joint. He says that

>it " probably " causes pain and that it will only get worse to

>the point where it will dislocate completely. He scheduled

>for hip surgery on January 31 (in 8 days, yikes!). He said that

> will be in the hospital for three days and in a 1/2 body cast

>for 6 weeks! I desperately need some input here....anybody had any

>experience with this? I can't imagine how we will deal with

>incontinence issues, etc. in the cast. I asked him about it and he

>said, " you will just have to figure that it will be a dirty cast and

>be obsessive-compulsive about cleaning it! " What, is he kidding? Of

>course, now that we are home, dh and I have 100 questions that we

>wish we had asked the doc... weighs almost 90 pounds without a

>cast. I can't imagine how we will move him from point A to point B,

>much less get him in and out of the car? I wonder if the cast will

>have him sitting up or lying down? won't understand what's

>happening to him...I am so afraid that he will lose what progress he

>has made lately...I am so completely overwhelmed by this..I feel like

>I could just scream! We welcome any and all suggestions as to how we

>can cope with this.

>Terry

>Mom to , almost 14

>

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Hi Margaret...

Thanks for your input. I would love to talk to Maureen. It's not that we

are in a hurry to get this done particularly. We are trying to work around

my husband's work schedule...he started a new job right before Thanksgiving

and they are sending him to some schools back East soon. He will be gone for

weeks at a time so we are trying to schedule the surgery when we know he will

be at home to help. Also, I would like to do the surgery before it gets warm

again...we live in California and I figure that will be even more

miserable during the hot weather in a cast! You are right... is

almost 14 and it's been a long time happening! I think that's one of the

things that bothers me so much.....I have been trying to get someone to look

at the way he walks for such a long time and been getting the brush off. I

am sure that, in the scheme of things, taking into account his other medical

problems, etc., it wasn't much of a priority to the docs. BUT, it would

have been alot easier on him and us if this had been done when he was younger

and smaller! What a mess!

Terry

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Hi Carole,

You know, you just verbalized one of my worst fears! The doctor asked us

yesterday if has been in pain...I told him I don't know because he

doesn't react to pain like you would expect. BUT....I also told him that we

have been medicating the heck out of this kid...he's currently on two

anti-psychotics...and I have to wonder if at least part of the problem has

been pain?!? I could just puke! :( I guess I would be pretty " psychotic "

too if I was in pain and nobody understood!

Thanks for your input. It just makes me that much surer that it's what we

need to do for him. To answer your question, I know that a lot of Down's

kids have really " loose " muscle tone...I always thought that was what they

were talking about with the hip problems. This is a congenital malformation

of the bone and pelvis...the other one is abnormal as well, but not to the

same extreme. I don't think this is necessarily a " Down's " trait...I'll try

to remember to ask the doc. You're right...I'm scared to death!

Terry

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Hi Gail...

Sorry, I guess I got your's and Carole's posts jumbled up....it's been that

kind of day! LOL !!! sigh! Thanks to both of you for your prayers and

support!

Terry

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Thanks for the support, Leah. I really appreciate it. I think I had

told you before that I was worried that " might " need to have

a cast following surgery....I guess I just didn't really consider the

practical ramifications if he did. What a drag! I wouldn't wish

this on anyone, but at the same time I'm hoping that someone has had

some experience with it and some suggestions. I know I can get

bigger diapers...he wears medium now, but that doesn't solve the

problem of inside the cast. isn't potty-trained...just

starting sort of. I don't know if I will be able to " sit " on a

commode chair, for instance, or not. Right now, I sit him on the

toilet and flush...he goes! Take him out of that environment and he

won't understand what I want him to do. I was thinking maybe of

trying something like a Poise pad against his skin and a diaper over

that...thinking that maybe that would absorb the liquid and draw it

into the diaper? Maybe? Of course, pooping is a whole other

problem! Because has bigtime problems in that area, his

stools are soft and not formed....lots of laxatives. I can't even

imagine how to deal with that...I can only hope (and pray) that I can

catch him before he goes....

I need to write up a list of our questions and put in a call to the

doctor with regard to positioning, etc. I know from talking to him

yesterday that he has little or no experience dealing with kids with

developmental challenges and no idea of how this is going to impact

's life. He's thinking from a surgeon's point of view...this

is wrong...fix it and it will be ok! Would that it were so! LOL!

Thanks,

Terry

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We haven't gone through hip surgery, but we did go through knee surgery.

Trisha has problems with her hips as well but after the knee surgery the hips

seem to have gotten better. Trisha was in Hospital for 3 days, then she was

non=weight bearing for about 4 weeks and then she had wheelchair for another

2-3 weeks. She was in a lot of pain the first couple of days but by the time

she came home the pain has lessened and she only had to take her pain

medicine a few more days after that. The worst part was right after surgery

and the next day, her leg was elavated with ice packs and she would cry if

you even touched it, changing the bandages was hard for her at first but even

that got easier after about the 3rd day. By the 5th day she had learned how

to gain as much sympathy as possible and was eating up the attention. The

rest of the time was a little hard on us, (we had to pick her up and carry

her upstairs etc.) but she seemed to adjust very well and when it came time

for her to give up the wheelchair we actually had to ween her away from it,

because she wasn't letting go of it to easy. She liked sitting in it to

watch t.v. Even now when she sees a wheelchair she thinks she should be able

to ride in it. They had to remove her knee cap then put it back and take the

tendons and muscles and cross over the cap to hold it in place. We've been

told that eventually she will have to have the surgery on the other knee as

well, but so far it hasn't gotten as bad as the right leg did. I don't know

if this helps or not but believe me, they recuperate much faster than we do

as parents. :-)

Carol

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In a message dated 1/23/01 1:40:44 PM Pacific Standard Time,

Csvillars@... writes:

> , they recuperate much faster than we do

> as parents. :-)

>

> I believe that Carol! I have had one heck of a headache since yesterday!

> LOL Thanks for the info. has been through multiple GI surgeries.

> The difference was that, in those, he recuperated at his own pace...I mean

> the only stopping him from doing anything was how bad he wanted to do it.

> This time, he won't be able to move even if he wants to because of the

> cast. Last year he broke his foot and was in a cast for about 4 weeks. It

> wasn't really a " walking cast " but he made it work and after the first

> couple of days, he was hobbling whereever he wanted to go. I'm still

> waiting for the doc to call me so I can find out exactly what to expect

> with regard to the cast. If he can cast him in a " sitting " position, I

> think will do better. At least he will be able to go for walks

> outside in a wheelchair, etc. If he casts him prone, I don't know how we

> will move him around. Figures, the guy will take his time calling me back!

> grrrrr!

>

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He also said that there is a problem

> with his hip. He referred us to an Orthopedic Surgeon in LA. We

saw

> him today and he says that 's femur (leg bone) is malformed

> and so is his pelvic bone that forms his hip joint. He says that

> it " probably " causes pain and that it will only get worse

to

> the point where it will dislocate completely. He scheduled

> for hip surgery on January 31 (in 8 days, yikes!). He said that

> will be in the hospital for three days and in a 1/2 body

cast

> for 6 weeks! I desperately need some input here....anybody had any

> experience with this?

> Terry

> Mom to , almost 14

Hi, Everyone..........Terry.......I think you need to talk to

Maureen. Her daughter, , had hip surgery last spring. I

wouldn't rush into it too quickly until you get all your answers to

what concerns you. is 14.....it's not like this happened

overnight. I will call Maureen and tell her your

problem......perhaps she will get on line.

Joan.....somehow I have been deleted from the digest. Haven't gotten

it for 3 days. Do you take care of that or onelist.com?

Take care, Everyone

Margaret

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if they cast him prone, then ask about a special chair that reclines. Then

he can still go for walks. I don't know what the special chairs are called

but I have seen them.

Carol

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Terry,

I'll be praying for your family untill is out of the hospitlal. I

kindof have the experience of a body cast, I have scholious so for years I

had to sleep in a back brace, to not have rods put in my back. Well It's

kindof the same as a body cast, so if you have any questions please feel

free to ask.

>

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terry,

you might want to call a pediatric hospice or pediatric home health agency.

they for sure would be able to help you out on ideas and strategies since

that is most of their clientale.....or better yet call the nursing director

of the local pediatric ward at a hospital..she or he might offer some

answers...i have found never to ask the surgeons for ideas, they are

clueless...but rather find a person who is directly related to the

situation.....example, ashtons ear....ent was clueless about swimming and

soon...but her special olympics swim coach new what to do and how to protect

her ears.,......again much strength and patience coming your way along with

prayers....take care,leah

>

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Thanks Carole..I just talked to the doc and found out they will cast him

sitting up. I never knew there was such a thing as a wheelchair that

reclines! You guys are such a great resource! :)

Terry

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He also said that there is a problem

> with his hip. He referred us to an Orthopedic Surgeon in LA. We

saw

> him today and he says that 's femur (leg bone) is malformed

> and so is his pelvic bone that forms his hip joint. He says that

> it " probably " causes pain and that it will only get worse

to

> the point where it will dislocate completely. He scheduled

> for hip surgery on January 31 (in 8 days, yikes!). He said that

> will be in the hospital for three days and in a 1/2 body

cast

> for 6 weeks!

Terry,

Gosh, what upsetting news. Is this the problem that a lot of downs

kids have, or is this a problem? I have heard our kids are

very prone to having hip problems, but didn't know how bad of

problems they could be. :-( I have no knowledge to share, but I

have prayers and well wishes for you and . I can't imagine

how scared you must be.

Gail

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--- leah

Hi Terry, I don t have any help to offer but wanted to

let you know you and your family are in my prayers.I

also am facing hip surgery for the third time so i

think has very likely been in pain with this

but did not have the means to tell you.I complain all

the time ,take tylenol,and use tubs of bengay , and

walk with a cane . Maybe what was seen as aggression

was just pain and frustration,poor kid.I hope the next

two months go by really fast for all of you .Will you

get nurses aide care when he comes home ?? Carole

leah wrote:

> terry,

> prayers and hugs to you!!! i cant imagine the

> thoughts that are going thru

> your head!!!! i have never experienced this and

> hope i dont have too....but

> i think one of the other list members daughters was

> in body cast, jamie

> maybe???? i am not sure, i think shes a girl...my

> memory is bad..... goes

> along with the gray hair, sagging boobs, and

> wrinkled eyebrows..... :-) i do

> know that when my cousin got hit by a car and was in

> a body cast, they left

> a whole down there and her mom just used big diapers

> and wiped her

> constantly.... goodluck and please know you and

> matthew are in our

> prayers......leah

>

>

> >

> >Reply-To: egroups

> >To: egroups

> >Subject: HELP!

> >Date: Tue, 23 Jan 2001 06:40:53 -0000

> >

> >Hi all....

> >A few months ago I mentioned that we were concerned

> about 's

> >feet...they are flat and he walks on the inside of

> his ankles. Since

> >then, we saw an Orthopedic doc who took some x-rays

> of his feet and

> >his hips. He told us that 's feet " are

> flat " (duh!) and that

> >he will prescribe orthotics. He also said that

> there is a problem

> >with his hip. He referred us to an Orthopedic

> Surgeon in LA. We saw

> >him today and he says that 's femur (leg

> bone) is malformed

> >and so is his pelvic bone that forms his hip joint.

> He says that

> >it " probably " causes pain and that it will

> only get worse to

> >the point where it will dislocate completely. He

> scheduled

> >for hip surgery on January 31 (in 8 days, yikes!).

> He said that

> > will be in the hospital for three days and

> in a 1/2 body cast

> >for 6 weeks! I desperately need some input

> here....anybody had any

> >experience with this? I can't imagine how we will

> deal with

> >incontinence issues, etc. in the cast. I asked him

> about it and he

> >said, " you will just have to figure that it will be

> a dirty cast and

> >be obsessive-compulsive about cleaning it! " What,

> is he kidding? Of

> >course, now that we are home, dh and I have 100

> questions that we

> >wish we had asked the doc... weighs almost

> 90 pounds without a

> >cast. I can't imagine how we will move him from

> point A to point B,

> >much less get him in and out of the car? I wonder

> if the cast will

> >have him sitting up or lying down? won't

> understand what's

> >happening to him...I am so afraid that he will lose

> what progress he

> >has made lately...I am so completely overwhelmed by

> this..I feel like

> >I could just scream! We welcome any and all

> suggestions as to how we

> >can cope with this.

> >Terry

> >Mom to , almost 14

> >

>

>

_________________________________________________________________

> Get your FREE download of MSN Explorer at

> http://explorer.msn.com

>

>

=====

Carole, wife of Rich, mom to and , m-i-l to and ,

grandmom to ,8 ,with d.s.and a.s.d. and 6 with adhd and possible

a.s.d.and Logan 2 year old wild child, and Seth 7months old and better known as

the gerber baby!

In the hour of adversity be not without hope for crystal

rain falls from the black clouds

Persian poem

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I've heard that hip problems do go with Down Syndrome. When we got here, they

did an exam on him (we were becoming dependants again after remarrying). They

also said there's a common defect of the vertebre in the neck. He had to be

cleared on both before they would allow him to participate in PE at school.

Wife to Dewight

Mom to , 10 yrs, DS, PDD-NOS and celiac

and , 19 months and strong-willed

-------------------------------------------------------------

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In a message dated 1/23/01 3:00:03 PM Eastern Standard Time,

smilinggail@... writes:

<< He also said that there is a problem

> with his hip. He referred us to an Orthopedic Surgeon in LA. We

saw

> him today and he says that 's femur (leg bone) is malformed

> and so is his pelvic bone that forms his hip joint. He says that

> it " probably " causes pain and that it will only get worse

to

> the point where it will dislocate completely. He scheduled

> for hip surgery on January 31 (in 8 days, yikes!). He said that

> will be in the hospital for three days and in a 1/2 body

cast

> for 6 weeks! >>

Oh Gosh Terry. I'm sorry. {{{{{{{{{{{{{{{{{{hugs}}}}}}}}}}}}}}}}} I will

be hoping and praying that it all goes well and this is all over soon. You

KNOW we'll all be here to hold your hand-----cyberly, that is!!!!

Donna

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Thanks Donna...it's amazing how quickly the people in this list can become

such an important part of our support system! Everyone's concern, prayers,

and input means so much!!

Terry

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Poor matthew, and poor you, terry, i will pray for you guys, it sounds like

a brain stumper to me all I can add is maybe ask for 6week supply of

sedatives to keep him mellow as can be, and i dont know about the bowels but

for urine, if matthew will leave alone maybe a texas cath, its like a condom

shape cath goes over the penis, but if incontinent of urine this will

collect in bag for you to empty. Its safe, no infection or invasive

procedures for it just slips over on the outside. Also, this will be one of

those casts that can get wet right? I think I would demand it if possible.

shawna.

>

>Reply-To: egroups

>To: egroups

>Subject: HELP!

>Date: Tue, 23 Jan 2001 06:40:53 -0000

>

>Hi all....

>A few months ago I mentioned that we were concerned about 's

>feet...they are flat and he walks on the inside of his ankles. Since

>then, we saw an Orthopedic doc who took some x-rays of his feet and

>his hips. He told us that 's feet " are flat " (duh!) and that

>he will prescribe orthotics. He also said that there is a problem

>with his hip. He referred us to an Orthopedic Surgeon in LA. We saw

>him today and he says that 's femur (leg bone) is malformed

>and so is his pelvic bone that forms his hip joint. He says that

>it " probably " causes pain and that it will only get worse to

>the point where it will dislocate completely. He scheduled

>for hip surgery on January 31 (in 8 days, yikes!). He said that

> will be in the hospital for three days and in a 1/2 body cast

>for 6 weeks! I desperately need some input here....anybody had any

>experience with this? I can't imagine how we will deal with

>incontinence issues, etc. in the cast. I asked him about it and he

>said, " you will just have to figure that it will be a dirty cast and

>be obsessive-compulsive about cleaning it! " What, is he kidding? Of

>course, now that we are home, dh and I have 100 questions that we

>wish we had asked the doc... weighs almost 90 pounds without a

>cast. I can't imagine how we will move him from point A to point B,

>much less get him in and out of the car? I wonder if the cast will

>have him sitting up or lying down? won't understand what's

>happening to him...I am so afraid that he will lose what progress he

>has made lately...I am so completely overwhelmed by this..I feel like

>I could just scream! We welcome any and all suggestions as to how we

>can cope with this.

>Terry

>Mom to , almost 14

>

>

> http://www.onelist.com/community/

>

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I don't know what the special chairs are called

>but I have seen them.

I think those are called " gerichairs " but those are rather big and awkward,

but do roll, recline etc, even have a tray that removes etc for meals or

activities. Maybe you mean something else though? shawna.

>From: Csvillars@...

>Reply-To: egroups

>To: egroups

>Subject: Re: Re: HELP!

>Date: Tue, 23 Jan 2001 17:27:10 EST

>

>if they cast him prone, then ask about a special chair that reclines. Then

>he can still go for walks. >

>Carol

>

>

>

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ya, nathan has hyperxtention in his hip joints too, and gets checked yearly

for Alanta-Axil Instablility --- his neck for sporting activities, so far

his neck has been fine --normal.He sees a rheumatologist for his joints and

possible pain etc, I guess this is common for DS but has had no bone

surgeries or malformations as of yet that ive been told or noticed, prayers

to those that are having trouble with this. shawna.

>From: hsmyangels@...

>Reply-To: egroups

>CC: egroups, egroups

>Subject: Re: Help!

>Date: 23 Jan 2001 21:04:00 -0800

>

>I've heard that hip problems do go with Down Syndrome. When we got here,

>they did an exam on him (we were becoming dependants again after

>remarrying). They also said there's a common defect of the vertebre in the

>neck. He had to be cleared on both before they would allow him to

>participate in PE at school.

>

>

>

>Wife to Dewight

>Mom to , 10 yrs, DS, PDD-NOS and celiac

>and , 19 months and strong-willed

>

>

>-------------------------------------------------------------

>Sign up for ICQmail at http://www.icq.com/icqmail/signup.html

>

> http://www.onelist.com/community/

>

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Terry,

I don't know a lot about your situration. Although I did have otherpedic

shoes put on me so I could walk, but that was when I was younger. I do know

a autistic child that had(has) foot order and something wrong with his feet.

I don't know what it was, but the parents and teacher's would spray some

stuff on his feet.

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  • 7 years later...
Guest guest

HI everyone! I've sent a couple of post out already on what I'm about

to talk about (thanks Margret & for your input). My son Logan

is five and has Down Syndrome and Autism and has been diagnosed. He

also at birth had an imperforate anus and a thethered spinal cord

which both thur surgeries have been corrected. He has a hole in his

heart which is an asd that they feel hopefully will close on it's

own. Logan is fully mobile and really has no problem getting around

except for walking up and down stairs. But he can crawl up them on

his own or walk up them with assistance and he sits on his bottom to

come down. He has sensory issues which he hasn't been formally

diagnosed with but they are there. He hand flaps, chews on

everything, will only eat baby food, can't feed himself, only drinks

from a bottle, spins, grinds his teeth, makes clicking and throat

noises, watches the reflection of the tv more then the tv itself,

fingers are always in the mouth and just always stemming. He doesn't

play with toys and throws everything. The hardest part is trying to

get Logan to do things. He's nonverbal and he doesn't always

understand when you say something to him. He loves to make noises and

sounds though. He doesn't like school except for gym, computer and tv

time. Anything else he fights you on kicking, crying and screaming.

He hates to get a haircut and his nails cut and a couple of us have

to hold him to get the job done. He so hard to know what he'll like.

For example we took him to an animal farm and I thought he would love

it. He loves petting our neighbors dog but as soon as we got there he

freaked out and we had to leave. We've gone back a couple times but

we get the same result. I've sinced realized our neighbors dog is the

only dog he likes. We've learned that thur going for walks. He

doesn't like things forced onto him so getting him to try new things

is rough. He also because of his imperforate anus goes to the

bathroom around every half hour and is not potty trained. At home

here Logan is very happy and so loving. He loves to kiss and cuddle

and laugh. His favorites are playing ball and watching his movies

with you. ABA doesn't seem to work for Logan but the floortime

approach does. The reason why I'm telling you all this is because I

need some advice. Logan will be starting school in the fall and we

just went through all of our evaluations at our home. The school

Psychologist at the end of his evaluation said I see the Downs but I

don't see the Autism. He thinks Logan is going through the terrible

two's because Logan would not work with him. He also thought Logan

was way to social to have Autism because he sat on his lap. The other

evaluations went the same way. Logan would not let them touch him to

much. Yesterday we had our MFE meeting and they want to give him the

disability of Mutiple Disabilities and not Autism. My fear with that

is they won't treat the Autism. It was horrible they all went around

the room and voted should Logan have the label Autism or Mutiple

diabilities? We were out voted 8 to 2. There were two people from the

Autism school that Logan was attending and the special Education

director asked them if they think Logan he has Autism and they said

he has Autism tendencies. We refused to sign anything and are going

to fight this. What I fear next is we haven't even talked about where

he'll go to school and the team is going to take a vote on that at

our next meeting. I already know the school isn't going to want him

and they're going to pick our local MMRD school. We toured it and ALL

the kids in Logan's class if he went there are in wheelchairs. He

would be the only one that can walk in the classroom he's in.

Everytime I've toured the school all the kids are just sitting around

and watching tv. I don't know if it's the times that I've gone but

I'm scared for him to go there! Can anyone help and give me advice on

what to do? The school is telling me that they are not saying he

doesn't have Autism (even though the school Psycologist told me and

the two people from his Autism school said they don't see it) he just

has so many issues that Mutiple disabilities is the best fit for

Logan! Does anyone have Autism as their disability determination or

do you have Multiple disabilities? Am I making to big of a deal about

the label they want to give him? I'm sorry this post is so long but I

wanted everyone to understand what Logan is like. Please if anyone

could help! I just don't know if we have the right to disagree with

their determination and if the law is on our side? Thanks so much!

Lori

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