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Our experience with Infectious disease doc's is they take the CDC approach that

it's not lyme, it's old age, or someother ridiculous dodge. Expect an ache or

pain every now or then go home, take aspirin, die, who cares, just leave me

alone. If it is lyme, well then, 28 days of abx will do the trick. If it doesn't

you never had lyme. Hopefully there are some good ones out there, like the one

you're seeing. The ones out here in So. central PA are awful. I had one refuse

to treat me even though I was symptomatic as heck.

Having had symptoms for a few weeks prior to the dx is probably enough for the

doc to treat you til you feel better. 28 days won't likely be enough. I wouldn't

worry too much. It;s not like you had it for years. You might look into

alternatives too to take starting now and continuing past the cut off date of

the abx.

Don't test the kids unless they develop symptoms. Even if they were bitten,

remember not all ticks carry disaese. If they develop a rash and symtoms a LLMD

won't bother with testing. He/she will dx clinically.

Dave

[ ] Thank you!

Thank you everyone for your kind responses. I have to be honest -

I'm scared to death now. I was feeling pretty hopeful but now -

WOW. I printed your posts to give to my doctor so I know what

questions to ask and what information I need. I'll try and find out

if the infectious disease guy that I'm seeing in September is

an " LLMD " . I have another question. I take my kids everywhere I go

and chances are wherever I was when I was bit by the tick my kids

were standing next to me. Should I have them tested also?

Thanks again for all the information.

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  • 7 months later...
Guest guest

Just wanted to thank everyone for all the kind words you sent me. It really

made me feel good. Thank you for that.

Also, thanks for the decorating tips. I'll let you know what we come up with

:)

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  • 3 weeks later...
Guest guest

You are welcome for the replies.

Most of our plagio cases are caused by sleep position....check out

this link for causes of plagio:

http://www.plagiocephaly.org/support/causes.htm

And about none of us in the group had ever heard of " plagio " or flat

heads until after our child had developed it.

You'll be in great hands with the DOCband. Cranial Technologies (maker

of the DOCband) are terrific and experts in treating plagio!! Check

out their webpage for more great plagio info:

http://www.cranialtech.com/

Debbie Abby's mom DOCGrad

MI

> Thanks to everyone who replied to my post. Baby Mo (Moira) will be

> in a DOC band, I believe. That's the booklet they gave me. I've

> never heard of any of this stuff, and I was in medical insurance for

> years! Thankfully, at this time, we have Moira on Medicaid, and

> they cover this. I've been reading that it can get rather

> expensive! Since I have a 2 1/2 year old and a 4 1/2 month old, I

> don't have a lot of time to sit and read, but I'll be looking

> through here and getting as much info as I can when I get the chance.

>

> Does anyone ever tell you what they believe may have caused your

> child's specific problem? I think it's one of two things with

> Moira. She sleeps with us, use to sleep mostly with her head on my

> arm on her right side. I can't imagine that would make her plates

> overlap on the left side, though. The other thing that I wonder

> about is that the Dr. who delivered her used the vacuum to get her

> out, because she was sort of wedged sideways in the birth canal.

> It's sounding like this may have been the culprit. Either the

> vacuum, or her being wedged, or perhaps both. My older daughter

> came out with the vacuum, as well, because she had turned facing the

> side, not that she was wedged sideways (if that makes sense), and

> she hasn't had any problem. With Moira, I was going to a midwife,

> and then at the end of the pregnancy, she was transverse, plus I had

> a low placenta, so the midwife and I both decided it would be best

> if I went to an OB, in case I needed a C-section. She did get into

> the correct position, and I was able to deliver her vaginally in the

> end, but it wasn't a very good experience. She and I have both had

> problems since, and I wonder how gentle the Dr. was with that

> vacuum. We didn't even realize she'd used it until we had watched

> the birth video, that my husband took, about 7 times, then I noticed

> her, at one time, say " vacuum " , and realized what she was doing.

> Didn't bother me, because, like I said, my first had it used on her

> with no problem. But, this was a different state, different Dr.,

> different hospital, and I just wonder....

>

> Any ideas?

>

> Caro (rowwith)...mom of Baby Mo (Moira) in Texas

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I guess it's quite possible this was caused by her sleep position.

Maybe I just don't want to think of it as being my fault, but maybe

it was. My first daughter slept mostly in her bassinet and crib for

the first 6 months, before she ended up in our bed (a long story).

Moira has been in bed with us since night one, and I started

sleeping with her on my arm because we were in a full sized bed,

with my 2 1/2 year old there, as well, because I didn't want to roll

over on her and I didn't want my 2 1/2 year old rolling over on

her. Now we have a king sized bed, much more room, and she sleeps

more just on the bed. She did have a large lump on her head, due to

the vacuum I presume, for several weeks after she was born (my first

daughter's vacuum lump was smaller and went away faster). Then once

it went down, we noticed that the right side of her head was still

bigger or higher up than her left side, and the back of her head is

kind of smushed on the right side (that does look like how she

sleeps, I suppose). Her pediatrician said that it wasn't that the

right side was bigger or higher than the left side, it was the that

the left side was depressed, which lead her to believe it was the

cranio thing. Btw, her dad chose the nickname " Lumpy " for her

because of her vacuum lump! LOL! Anyway, who knows. What's

strange is that normally, I'd be stressing out about this terribly!

Strangely, I'm very peaceful about it, and have no doubt that this

will take care of her problem with no trouble. We've been praying

about this for the past few weeks, since her pediatrician first said

what it might be, and we've had lots of people praying for her, so I

believe that's where my peace is coming from.

Thanks again for everyone's welcome! I look forward to getting to

know you all better!

Caro (rowwith)...Baby Mo's mom

> You are welcome for the replies.

> Most of our plagio cases are caused by sleep position....check out

> this link for causes of plagio:

> http://www.plagiocephaly.org/support/causes.htm

> And about none of us in the group had ever heard of " plagio " or

flat

> heads until after our child had developed it.

> You'll be in great hands with the DOCband. Cranial Technologies

(maker

> of the DOCband) are terrific and experts in treating plagio!!

Check

> out their webpage for more great plagio info:

> http://www.cranialtech.com/

>

> Debbie Abby's mom DOCGrad

> MI

>

> --- In Plagiocephaly , " rowwith " <rowwith@y...>

wrote:

> > Thanks to everyone who replied to my post. Baby Mo (Moira) will

be

> > in a DOC band, I believe. That's the booklet they gave me.

I've

> > never heard of any of this stuff, and I was in medical insurance

for

> > years! Thankfully, at this time, we have Moira on Medicaid, and

> > they cover this. I've been reading that it can get rather

> > expensive! Since I have a 2 1/2 year old and a 4 1/2 month old,

I

> > don't have a lot of time to sit and read, but I'll be looking

> > through here and getting as much info as I can when I get the

chance.

> >

> > Does anyone ever tell you what they believe may have caused your

> > child's specific problem? I think it's one of two things with

> > Moira. She sleeps with us, use to sleep mostly with her head on

my

> > arm on her right side. I can't imagine that would make her

plates

> > overlap on the left side, though. The other thing that I wonder

> > about is that the Dr. who delivered her used the vacuum to get

her

> > out, because she was sort of wedged sideways in the birth

canal.

> > It's sounding like this may have been the culprit. Either the

> > vacuum, or her being wedged, or perhaps both. My older daughter

> > came out with the vacuum, as well, because she had turned facing

the

> > side, not that she was wedged sideways (if that makes sense),

and

> > she hasn't had any problem. With Moira, I was going to a

midwife,

> > and then at the end of the pregnancy, she was transverse, plus I

had

> > a low placenta, so the midwife and I both decided it would be

best

> > if I went to an OB, in case I needed a C-section. She did get

into

> > the correct position, and I was able to deliver her vaginally in

the

> > end, but it wasn't a very good experience. She and I have both

had

> > problems since, and I wonder how gentle the Dr. was with that

> > vacuum. We didn't even realize she'd used it until we had

watched

> > the birth video, that my husband took, about 7 times, then I

noticed

> > her, at one time, say " vacuum " , and realized what she was

doing.

> > Didn't bother me, because, like I said, my first had it used on

her

> > with no problem. But, this was a different state, different

Dr.,

> > different hospital, and I just wonder....

> >

> > Any ideas?

> >

> > Caro (rowwith)...mom of Baby Mo (Moira) in Texas

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Guest guest

> I guess it's quite possible this was caused by her sleep position.

> Maybe I just don't want to think of it as being my fault, but maybe

> it was.

Oh Caro!

Heavens NO NO! It's most definitley not your fault any more than the

other tens of thousands of babies with plagio!!! So don't say that,

please.

My daughter's plagio began inutero, we noticed it on weekly

ultrasounds that her head was stuck in the same position, however, we

never worried about a flat head (worried she'd NEVER come out of me,

BUT! hehe). It only worsened after birth because of her sleep position.

Some babies get it, some don't - just like crooked teeth, some get em,

some don't. Absolutely nothign you could do - especially w/o knowing

of it! Can't prevent something you don't know exists, right?!

But I'm so happy to read how at peace you are with this and getting

her a band. She should have a rounder head in no time! I forgot to

mention, Cranial Technology's average treatment time in their band is

4.5 mos., some babies are longer, some less, based on age, severity &

growth spurts. Hard to estimate...but as I mentioned earlier, given

Mo's young age, she'll be hitting many growth spurts over the next

several mos which will round that pretty little head out nicely!

It's also nice to hear how proactive your pediatrician has been with

getting Mo Xrayed and referring her for a band. Many group members

struggle to get their ped. to listen to their concerns.

Please keep us posted :)

Debbie Abby's mom DOCGrad

MI

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Guest guest

Well, you will be in the best possible hands with the DOCband people -

they really know what they are doing!

There are SO many theories as to why plagio develops, but mostly it

seems to happen from inuterio constraint or sleep position. Who knows

who will get it - it's just impossible to say at this point.

Definitely not your fault - that much is for sure!

So keep us posted. At 4 1/2 months Moira (LOVE the name) should get

some great correction with the DOCband!

Marci (Mom to )

Oklahoma

> Thanks to everyone who replied to my post. Baby Mo (Moira) will be

> in a DOC band, I believe. That's the booklet they gave me. I've

> never heard of any of this stuff, and I was in medical insurance

for

> years! Thankfully, at this time, we have Moira on Medicaid, and

> they cover this. I've been reading that it can get rather

> expensive! Since I have a 2 1/2 year old and a 4 1/2 month old, I

> don't have a lot of time to sit and read, but I'll be looking

> through here and getting as much info as I can when I get the

chance.

>

> Does anyone ever tell you what they believe may have caused your

> child's specific problem? I think it's one of two things with

> Moira. She sleeps with us, use to sleep mostly with her head on my

> arm on her right side. I can't imagine that would make her plates

> overlap on the left side, though. The other thing that I wonder

> about is that the Dr. who delivered her used the vacuum to get her

> out, because she was sort of wedged sideways in the birth canal.

> It's sounding like this may have been the culprit. Either the

> vacuum, or her being wedged, or perhaps both. My older daughter

> came out with the vacuum, as well, because she had turned facing

the

> side, not that she was wedged sideways (if that makes sense), and

> she hasn't had any problem. With Moira, I was going to a midwife,

> and then at the end of the pregnancy, she was transverse, plus I

had

> a low placenta, so the midwife and I both decided it would be best

> if I went to an OB, in case I needed a C-section. She did get into

> the correct position, and I was able to deliver her vaginally in

the

> end, but it wasn't a very good experience. She and I have both had

> problems since, and I wonder how gentle the Dr. was with that

> vacuum. We didn't even realize she'd used it until we had watched

> the birth video, that my husband took, about 7 times, then I

noticed

> her, at one time, say " vacuum " , and realized what she was doing.

> Didn't bother me, because, like I said, my first had it used on her

> with no problem. But, this was a different state, different Dr.,

> different hospital, and I just wonder....

>

> Any ideas?

>

> Caro (rowwith)...mom of Baby Mo (Moira) in Texas

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  • 2 months later...
Guest guest

well done bert, you and your family will always be in my prayers as will the

rest of the group

love and hugs to all

anita>

> From: " Bertha " <sunshinedotson@...>

> Date: Fri 04/Jul/2003 17:47 GMT

>

> Subject: [ ] Thank you!

>

>

> Hello everyone,

>

> I would like to thank all of you for your kind words, encouragement

> and prayers for my children. I am hanging in there and praying a lot

> too. I accepted everyone's advice and will use it to help me and my

> family get through this rough road. I know if I don't take care of

> me, I am no good to anyone, especially my children. So again, I

> thank you all! Best wishes and LOTS of LOVE to all of you!

>

> HUGS...

> Bert.

>

>

>

>

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  • 1 month later...

Best of luck, Sue.

Hope it all goes well for you all.

Julea :o)

The first step towards success is taken when you refuse to be a captive of

the environment in which you first found yourself.

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How weird, I have no idea why this blank post " came from me " ... I

think I sent someone some ES bath info. If I figure out why it's

here, I won't do it again!

W

> See the attached file for details

>

>

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,

it is very likely that you have a virus on your computer which sent

the letter without your participation. We had not access to Internet

for a day and when we called the provider they told us that the

server was flooded by letters because some new virus gets into your

computer through some port just while you are browsing the Internet,

configures mail server on your computer and starts sending a lot of

letters. Microsoft made some update of the Windows 2000 system to

prevent this, but I do not know if there is antivirus software that

fixes it.

Margaret

> > See the attached file for details

> >

> >

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, It's the virus going around...

[ ] Re: Thank you!

How weird, I have no idea why this blank post " came from me " ... I

think I sent someone some ES bath info. If I figure out why it's

here, I won't do it again!

W

> See the attached file for details

>

>

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> How weird, I have no idea why this blank post " came from me " ... I

> think I sent someone some ES bath info. If I figure out why it's

> here, I won't do it again!

> W

This is the subject header of many of the virus emails I have been

receiving, and even some I have been " sending " , altho it is not me

sending them, it is a spam-bot that found my email address on my site

and sent emails to people purportedly " from me " .

Example subjects:

Re: your details

Re: your application

Re: approved!

Re: wicked screensaver

I receive 1-3 of these emails every minute, which is why I had to

create a new email address. Fortunately I have no addresses in my

address book, and I don't send/receive email to the [i

read web-only], and I have not seen a " spam email from me " show up on

any of my regular message boards, altho sometimes they show up on a

board I rarely use.

I sure hope this problem is fixed soon!

Dana

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  • 1 month later...

Hi Trish,

I just checked out the pics of Carson, he is a doll. I love the hiney

picture. Thanks for sharing.

In order for repositioning to work it must be done 24/7. Will Carson

sleep on his side?

> Wow! Thanks to all you great ladies for all your wonderful and

> informative replies! I spent most of my day yesterday wandering

> around the net educating myself as much as possible.

> I'm pretty sure that Carson does not have torticollis (sp?) He was

> resisting turning his head to the left for a little while, but from

> moving him around in his crib and change table he now has full

> motion (or so I can tell) Also, it looks to me as if he my not have

> true plagiocephaly since his head is moslty flat all the way

across.

> The right side is only slightly flatter (from those few months of

> not realy turning is haed to the left I guess) So, the term that I

> found to describe him is brachycephaly. I'm definitly no doctor, so

> we'll see what the ped. says I guess. There is no way I can get to

> see one before December either.

> I'm trying not to put him on his back at all right now (except to

> sleep), but it is so hard since he LOVES to lay under his toys and

> kick and swat at them! Well, I guess for now that will be my plan

of

> action. I have posted a couple of pictures of him in a new folder

> called Carson H. and am waiting for my batteries to re-charg in my

> camera so I can take a few more! lol

>

> Thanks again,

> Trish

> Barrie, Onatrio

> Ben - 2 1/2

> Carson - 5 months

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Trish, Carson's head looks like a classic case of Brachy to me. He

is such a cutie!!! Thanks for sharing and let us know how things are

going with you.

Dustie

> Wow! Thanks to all you great ladies for all your wonderful and

> informative replies! I spent most of my day yesterday wandering

> around the net educating myself as much as possible.

> I'm pretty sure that Carson does not have torticollis (sp?) He was

> resisting turning his head to the left for a little while, but from

> moving him around in his crib and change table he now has full

> motion (or so I can tell) Also, it looks to me as if he my not have

> true plagiocephaly since his head is moslty flat all the way

across.

> The right side is only slightly flatter (from those few months of

> not realy turning is haed to the left I guess) So, the term that I

> found to describe him is brachycephaly. I'm definitly no doctor, so

> we'll see what the ped. says I guess. There is no way I can get to

> see one before December either.

> I'm trying not to put him on his back at all right now (except to

> sleep), but it is so hard since he LOVES to lay under his toys and

> kick and swat at them! Well, I guess for now that will be my plan

of

> action. I have posted a couple of pictures of him in a new folder

> called Carson H. and am waiting for my batteries to re-charg in my

> camera so I can take a few more! lol

>

> Thanks again,

> Trish

> Barrie, Onatrio

> Ben - 2 1/2

> Carson - 5 months

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Hi Trish - Carson is a doll! I am glad that you educated yourself on

this that is exactly what I did when I found out about it too. I

learned so much more on the net than I did from any DR. My sone also

had slight flatening on the right side but the whole back was pretty

flat as well and we are seeing great correction. Good Luck!

Donna and Xavier DOCband 7/25 and 10/8

> Wow! Thanks to all you great ladies for all your wonderful and

> informative replies! I spent most of my day yesterday wandering

> around the net educating myself as much as possible.

> I'm pretty sure that Carson does not have torticollis (sp?) He was

> resisting turning his head to the left for a little while, but from

> moving him around in his crib and change table he now has full

> motion (or so I can tell) Also, it looks to me as if he my not have

> true plagiocephaly since his head is moslty flat all the way

across.

> The right side is only slightly flatter (from those few months of

> not realy turning is haed to the left I guess) So, the term that I

> found to describe him is brachycephaly. I'm definitly no doctor, so

> we'll see what the ped. says I guess. There is no way I can get to

> see one before December either.

> I'm trying not to put him on his back at all right now (except to

> sleep), but it is so hard since he LOVES to lay under his toys and

> kick and swat at them! Well, I guess for now that will be my plan

of

> action. I have posted a couple of pictures of him in a new folder

> called Carson H. and am waiting for my batteries to re-charg in my

> camera so I can take a few more! lol

>

> Thanks again,

> Trish

> Barrie, Onatrio

> Ben - 2 1/2

> Carson - 5 months

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Trish,

I have a 6 month old daughter, Jordyn, who has brachy. Carson's

head looks a lot like hers - flat across the back and higher on top.

She also doesn't have tort, so the flatness is pretty much uniform

across the back of her head. You can see a picture of the top view

in her folder that shows the flatness. I think that I already took

out the side view picture.

Good luck and let us know how it goes with repo. :)

& Jordyn (DOCband 10/13)

Dallas

> Wow! Thanks to all you great ladies for all your wonderful and

> informative replies! I spent most of my day yesterday wandering

> around the net educating myself as much as possible.

> I'm pretty sure that Carson does not have torticollis (sp?) He was

> resisting turning his head to the left for a little while, but from

> moving him around in his crib and change table he now has full

> motion (or so I can tell) Also, it looks to me as if he my not have

> true plagiocephaly since his head is moslty flat all the way

across.

> The right side is only slightly flatter (from those few months of

> not realy turning is haed to the left I guess) So, the term that I

> found to describe him is brachycephaly. I'm definitly no doctor, so

> we'll see what the ped. says I guess. There is no way I can get to

> see one before December either.

> I'm trying not to put him on his back at all right now (except to

> sleep), but it is so hard since he LOVES to lay under his toys and

> kick and swat at them! Well, I guess for now that will be my plan

of

> action. I have posted a couple of pictures of him in a new folder

> called Carson H. and am waiting for my batteries to re-charg in my

> camera so I can take a few more! lol

>

> Thanks again,

> Trish

> Barrie, Onatrio

> Ben - 2 1/2

> Carson - 5 months

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  • 2 weeks later...

<To whoever made the brilliant suggestion of adding cocoa to eggnog,

thank you a billion times over. I am trying to wean my kids off cold

cereal and they won't drink the fruit smoothies I make. I made an

eggnog today with raw goat milk kefir, cream, eggs, maple syrup,

vanilla and cocoa powder and it was devoured by both girls! I just told

them it was chocolate milk, which, technically, it was. :) I had some

myself and it was so super tasty. Thank you!!>

If we don't stop talking about eggnog I am going to have to leave work soon

and go home and make my own! :)

_________________________________________________________________

Frustrated with dial-up? Get high-speed for as low as $26.95.

https://broadband.msn.com (Prices may vary by service area.)

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  • 2 months later...

THANK YOU!

You all have raised $1212.00 so far! Thank you! Because of you, we're all that

much closer to reaching the $6k mark.

Less than 20 hours to go and, along with helping fund some much-needed projects,

you have the opportunity to snag some bargain merchandise. T-shirts as low as

$3.00, etc. (I can tell you from experience that's a quarter less than the

shirts I buy at Goodwill and those have already been worn.) You can click on the

'online store' option at http://www.nationalautismassociation.org/index.php

ALL donations will go to these two projects:

Projects:

NAA Crisis Fund:

Sometimes tragedies happen within the ASD Community. A family may lose their

home, their employment, etc. The crisis fund will provide families in urgent

need with financial support whether it be for emergency shelter or covering

medical/funeral expenses should the unthinkable happen.

SafeMinds VSD Research Project

See below for more details, and once again, thank you...

Lori McIlwain

National Autism Association

Phone: 877-NAA-AUTISM

Email: Lori@...

http://nationalautismassociation.org/

Don't Miss the 24-hour NAA Fire Sale starting tomorrow morning (Thursday) at 8

am!

Prices on autism-themed merchandise will be marked down 50% to 70%. Items

include, T-shirts, Awareness Ribbon Lapel Pins, Key Chains, License Plate

Frames, Slogan Buttons, Hats, Tote Bags, Syringe Pens and more!

Some items will sell for as low as $.50 for 24 hours only! Buy for your kids,

your family, or yourself. Imagine the awareness you'll raise in your community

while helping to raise funds for research and family programs.

ALL proceeds will go to the projects listed below. The National Autism

Association is a nonprofit, not-for-salary organization. Prices will be marked

back up starting at 8:00 AM January 16th.

Please forward this onto family and friends. With everyone's help, we all can

get so much accomplished in 2004.

Projects:

NAA Crisis Fund:

Sometimes tragedies happen within the ASD Community. A family may lose their

home, their employment, etc. The crisis fund will provide families in urgent

need with financial support whether it be for emergency shelter or covering

medical/funeral expenses should the unthinkable happen.

SafeMinds VSD Research Project

Thank you!

The NAA Team

www.nationalautismassociation.org

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  • 6 months later...
Guest guest

Randy,

I was sorry to see you felt like there was little support here.

Guess I shoulda said something earlier. Just lately have been doing

more reading and not much posting. Have just had so much going on

that my time on line is short. The people here, all of them, are

never far from my thoughts. I do keep up with the postings, and

always send up a prayer for those having rough times.

Glad you got through the MRI - dang shame they did not get the

sedative right - I share your " love " of the whole MRI experience.

Will be thinking of you tomorrow and hoping for positive results.

nne

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