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Teri and Robbin

Well thanks for the kind words and all in all I'm doing fine considering

every time I think chychys getting better something else happens. Her asthma

is doing better but she came home from school today sick again. Her doctor

has her wearing mask at school to protect her but I really dont think the

school uses them.

Another thing Chyanne woke up very stiff this morning and cannot bend her

knee because of the swelling in her knee. So can someone please explain to me

how she can have a sed rate of 7 and still be flaring so badly? I'm truly

confused and any help would be appreciated.

Thanks again,

Charlene (chychys mom)

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Charlene

s sed rate was 3 and her knee and hip was swollen

her knee was 3 times the size of her right knee she also has asthma

even now we have good days and bad days

and it dont just stay in that same hip and knee the other knee swells

her wrists swells hands also her back is also affected

since your child has asthma you know how unpredictable they can be

this is also unpredictable

honey its something we have to deal with on a day to day bases

i thought everything was goin ok great 2 weeks no problems shes out playing

no pain ummm wrong dang just like a cat sneaking up on you she wakes and

its mom i am so stiff and hurting

i remember back years ago when i was awaked with her barely breathein and

gasping for air a severe asthma attack

but i am cautious with her ummm protective YES as with every parent

its my child and when they are sick you protect them more

but i also know to make her do chores and be as normal as possible

shes doing good shes my angel

but charlene a moms job is hard and i can understand how you feel about

the sed rate cause my hubbys dr took his sed rate lolol his was 40

no swelling no pain but melissas sed rate was 3 then 6 and she was hurting

and swelling weird yes

Robbin

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Hi Charlene

I'm sorry to hear that your little one is not doing well right now. The

ups and downs of this disease can be so frustrating!!

Unfortunately, SED rate is not always a good indicator of disease

activity in our kids, if I understand correctly. So a normal SED rate

does not necessarily mean that your child will not have any

inflammation. If I'm wrong, I know someone will set me straight! :)

Wish I could help more.

Liz

chychysworld@... wrote:

>

> Teri and Robbin

>

> Well thanks for the kind words and all in all I'm doing fine considering

> every time I think chychys getting better something else happens. Her asthma

> is doing better but she came home from school today sick again. Her doctor

> has her wearing mask at school to protect her but I really dont think the

> school uses them.

>

> Another thing Chyanne woke up very stiff this morning and cannot bend her

> knee because of the swelling in her knee. So can someone please explain to me

> how she can have a sed rate of 7 and still be flaring so badly? I'm truly

> confused and any help would be appreciated.

>

> Thanks again,

> Charlene (chychys mom)

>

>

> For links to websites with JRA info please visit:

> http://www.geocities.com/Heartland/Village/8414/Links.html

>

> To manage your subscription settings, visit:

> subscribe/

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  • 1 year later...
Guest guest

...where do you live? I have a 2yr boy () with pauci, and have

been trying to get a support group together too...what kind of JRA does

have?

(Mom to Will, Pauci, 2yrs. old)

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Hi ,I live in West Virginia.'s dr. hasn't decided what type of JRA she has.She says it's either poly or systemic.She had allot of high fevers for about 5 months before she started limping.But she never had the rash and such.Are you going to the conference?Her dr. is at Children's Hospital in Washington DC.I'm also trying to come up with a fundraising idea to do in the area to inform to public about jra.Well better go and get something done.Hope to hear from you soon. (mom to 20 months)

Re: hi again

...where do you live? I have a 2yr boy () with pauci, and have been trying to get a support group together too...what kind of JRA does have? (Mom to Will, Pauci, 2yrs. old)

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Guest guest

Sorry to say I've never heard of it.We're in the forgotten part of the state.LOL

Re: hi again

my step dad was born in gary w Virgina you live close by there? Robbin

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Guest guest

Hi ,

I grew up in WV (Huntington and the surrounding area) - what part is the

" forgotten part " We moved around a lot when I was a child and lived in

Wheeling and Moundsville for a few years. Folks back in the Huntington area (at

least our relatives there) would say, " why doesn't the Northern panhandle just

become part of PA - that's where they think they live anyway " - I didn't really

understand what they meant until I was older. (I'm not trying to pry into what

town you live in - but I just wondered what part of the state. - I am thinking

since you take to Childrens in DC that it is somewhere in the mid to

southeastern part of the state.

I work in DC - email me @ carneyval@... separately if you might want to get

together sometime when you come in for an appt if you have time to work it in.

I know that appt days aren't the best times for making other plans.

Hope you and are having a good day today!

Val

Rob's Mom (4,systemic)

In a message dated Sun, 16 Jun 2002 2:10:42 PM Eastern Daylight Time,

mommyby3@... writes:

> Sorry to say I've never heard of it.We're in the forgotten part of the

state.LOL

> Re: hi again

>

>

>

> my step dad was born in gary w Virgina

> you live close by there?

> Robbin

>

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Guest guest

Hi ...

sorry its taken me so long to respond.....I can not go the conference, I wish

we could but its just not affordable for us ( my husband is a full time

student getting his masters)....we applied for a scholarship...but did not

get one...maybe next year!

How is ? Any news yet on what type of arthritis?

(Mom to Will, Pauci, 2yrs. old)

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  • 3 months later...

hi penny, i take 20mg of arava a day. i am still in pain, i have not

had an outbreak of p i still have to take pain killers and vioxx but

they just switched me to bextra. i think i need a second opinion i am

not getting much better. i just had a real bad three weeks. almost as

bad when it first hit me. i have been very tired, can hardly get out

of bed and hurt evrywhere. he mentioned remicade so we will see. the

arava has not hurt my liver. i have taken it for about a year. i am

sure i would be worse without it but cant see a big change. i wish

you luck...kyle

> Hi everybody, I'm a mostly-lurker. You may remember me from a few

> months ago, I asked for recommendations for a rheumy in my area. I

live

> in N. Florida. Well, I found one, in Pensacola. I had to wait a

month

> to see him but I expected that. I was pleasantly surprised, he

seemed

> to know all about PA and what he said matched up with what I've

learned

> from this group. It was also VERY nice to be taken seriously! OK,

so

> here's the deal. He said since we won't be able to get our hands on

> Enbrel for a good long while, he wants to start me on Arava. He

said

> Arava can cause liver damage so I'll need to be monitered regularly

to

> watch for that. He also said it lowers the immune system so I'll

need

> to be vigilant about getting antibiotics if I get sick, especially

since

> I'm diabetic this is a big concern for him. I was sorta overwhelmed

> while I was in his office and forgot to read my notes, I remembered

most

> questions but didn't ask all the right stuff about the new

information I

> got. So, is there anybody here that can tell me a little more about

> Arava? How is it taken, and how often? Will it affect the P as

well as

> the PA? How dangerous is it? Has anybody been helped by it? Does

it

> help the pain or will I need to be on something like vioxx at the

same

> time? He says the same thing I've heard here, it's not enough to

treat

> the pain, the joints will be damaged permanently if this isn't

treated

> aggressively. He says one joint in my right hand is already

permanently

> damaged. I asked him about some sort of braces to support my

fingers

> and wrists so I could function more normally. He said to use a brace

> would be a bad idea. It would stop me from moving those joints at

all

> and make permanent damage more likely than if I continue to try and

use

> them. Is this what other rheumys advise? Makes sense, but I sure

would

> get thru the day easier, I think, if I had some strength in my

hands and

> wrists. At the same time, I don't want to cause further damage.

>

> I see him again on October 24th, and I assume I will get the Arava

> then. I appreciate anything you can tell me about this!!!

>

> Penny

>

> _______________________________________________________________

> Be Unique! Get your personalized email address at www.NamePlanet.com

> <http://www.NamePlanet.com>

>

>

>

>

>

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  • 7 months later...
Guest guest

Judi,

Between a broken ankle, working and helping with your 3 new grandchildren,

it's no wonder you have time to eat! I'm sorry you are in so much pain.

Hopefully now that your cast is not broken, it will calm down.

I don't see how you can possibly watch 3 newborns. I had to give up

watching my grandson and he's only ONE baby. I just can't pick him up.

Finding a babysitter for triplets doesn't sound like an easy task.

I hope she finds someone.

Hope you feel better.

a

> Hello everyone,

>

> I haven't been on line much the last couple of days--helping

> with the babies and working, plus dealing with this @% & ! ankle! They

> put the new cast on Monday, and I'm supposed to be staying off it for

> a full week--that's really no problem, except not moving around as

> much is playing heck with my hips and knees. The pain is still

> pretty intense, and when Dr. Mc (aka Dr. Cute) examined it

> Monday, he said he figures I will be a long time in healing from

> this. I just hope it doesn't cause problms when I go to IU on the

> 12th. I'm going to cheat a bit Sunday for TJ's birthday, as I

> promised I would help him plant his beans and corn in the garden. We

> will have 's in-laws here, however many of them choose to show

> up with whatever attitudes they show up with.

>

> Debs, sorry you are having so much trouble--you are always in my

> prayers, and this HAS to end soon!

>

> a and , sorry I haven't been able to keep up with all the

> interesting things you are sharing with us. Soon, though, I hope,

> when finds some day care. If she doesn't, guess who will be

> watching the babies?

>

> Peace and grace to you all,

> Judi

>

>

>

>

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  • 10 months later...
Guest guest

nne, PLEASE be sure to ask him about Celiac. With you losing

weight, he would be justified in giving you the blood test to screen for

Celiac…good luck.

Debby

[ ] hi again

Miss all of you very much..hope all are doing

well.quick scan and

seems things not too bad for the most part.

Hope Kels doing

better. How is Tony?

Have been on computer very little..still fighting

the joint/muscle

pain..still no def dx as to cause...now getting

lumps/knots/bumpss--

don't know what-- near joints, mostly wrists

elbows-they add to the

fun..come and go. Makes it hard to do

much. Fatigue another

factor. Only good thing have lost a bit of

weight...thingk just too

much trouble to eat somedays.

Seeing gastro fri...see what ideas he has.

Will get back when can. Do take care...think

of you all a lot.

nne

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  • 1 year later...

Barb,

Prednisone not only makes me cranky and crabby but the longer I am on it the

worst it gets. Also high dosages for me (20mg or greater) make me

pyschotic!!! So be careful. I no longer take prednisone. I also had the same

problem with any hormonal type medication....even birth control pills. So I

don't

really have any helpful advice to offer on this one.

Make sure you take your prednisone at the start of your day or it will keep

you awake all nite. Also lots of water helps. I also would take mine with

food. Ihave a very sensitve stomach and it use to make my stomach hurt. I

was the only person that lost weight on prednisone. LOL

Good luck on your MRI. That is cool that they can do only extremities these

days without putting your whole body into the machine.

Toni in Texas

In a message dated 9/6/2005 4:56:30 A.M. Central Daylight Time,

writes:

Tue, 06 Sep 2005 00:10:39 -0000

From: " sassyone3173 " <bdciesinski@...>

Subject: Hi Again

Hi guys. I am not really good at the group thing, i never know what

to

say. One on one I am okay, but in a group I am a " chicken " . This

Thursday I go for an MRI on both elbows, an hour each side! Ouch! My

Rheumatologist asked if i could handle it, I just responded with

" hope

so. " They are using the new extremity MRI where only the joint being

examined is placed in the machine, but holding my elbows that long is

what concerns me. The prednisone they started me on last Tuesday is

making me really moody. Has anyone else experienced that? If so how

did you deal with it? Was there anything you did that helped it? I am

usually a patient person and now I am crabbing at my kids and hubby a

lot. Any imput would help greatly, I am new to this.

Sincerely,

Barb ( Sassyone3173)

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Barb,

Prednisone not only makes me cranky and crabby but the longer I am on it the

worst it gets. Also high dosages for me (20mg or greater) make me

pyschotic!!! So be careful. I no longer take prednisone. I also had the same

problem with any hormonal type medication....even birth control pills. So I

don't

really have any helpful advice to offer on this one.

Make sure you take your prednisone at the start of your day or it will keep

you awake all nite. Also lots of water helps. I also would take mine with

food. Ihave a very sensitve stomach and it use to make my stomach hurt. I

was the only person that lost weight on prednisone. LOL

Good luck on your MRI. That is cool that they can do only extremities these

days without putting your whole body into the machine.

Toni in Texas

In a message dated 9/6/2005 4:56:30 A.M. Central Daylight Time,

writes:

Tue, 06 Sep 2005 00:10:39 -0000

From: " sassyone3173 " <bdciesinski@...>

Subject: Hi Again

Hi guys. I am not really good at the group thing, i never know what

to

say. One on one I am okay, but in a group I am a " chicken " . This

Thursday I go for an MRI on both elbows, an hour each side! Ouch! My

Rheumatologist asked if i could handle it, I just responded with

" hope

so. " They are using the new extremity MRI where only the joint being

examined is placed in the machine, but holding my elbows that long is

what concerns me. The prednisone they started me on last Tuesday is

making me really moody. Has anyone else experienced that? If so how

did you deal with it? Was there anything you did that helped it? I am

usually a patient person and now I am crabbing at my kids and hubby a

lot. Any imput would help greatly, I am new to this.

Sincerely,

Barb ( Sassyone3173)

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--Toni,

Thanks for the advice about the prednisone. It is really frustrating

because I am such a calm easy going person and these past couple of

days the pain and I imagine the prednisone has made me a crazy person!

I heard that the prednisone keeps you awake, so taking it in the

morning is what I do. I have enough trouble sleeping without

prednisone keeping me awake!! You know what is funny? A lot of people

say that their appetite increases on this stuff, I found that I have

no appetite. I have to make myself eat or I would go all day and

night not eating at all. Guess I wont have to worry about getting

over weight on this med. Thanks for the luck, could use it! I hope

being on the prednisone is a totally temporary thing or I will be

trying to sneak emails to you all from the nut hatch! LOL

Barb

- In , aclavern33@a... wrote:

>

> Barb,

> Prednisone not only makes me cranky and crabby but the longer I am

on it the

> worst it gets. Also high dosages for me (20mg or greater) make me

> pyschotic!!! So be careful. I no longer take prednisone. I also

had the same

> problem with any hormonal type medication....even birth control

pills. So I don't

> really have any helpful advice to offer on this one.

>

> Make sure you take your prednisone at the start of your day or it

will keep

> you awake all nite. Also lots of water helps. I also would take

mine with

> food. Ihave a very sensitve stomach and it use to make my stomach

hurt. I

> was the only person that lost weight on prednisone. LOL

>

> Good luck on your MRI. That is cool that they can do only

extremities these

> days without putting your whole body into the machine.

>

> Toni in Texas

>

> In a message dated 9/6/2005 4:56:30 A.M. Central Daylight Time,

> writes:

>

> Tue, 06 Sep 2005 00:10:39 -0000

> From: " sassyone3173 " <bdciesinski@h...>

> Subject: Hi Again

>

> Hi guys. I am not really good at the group thing, i never know what

> to

> say. One on one I am okay, but in a group I am a " chicken " . This

> Thursday I go for an MRI on both elbows, an hour each side! Ouch!

My

> Rheumatologist asked if i could handle it, I just responded with

> " hope

> so. " They are using the new extremity MRI where only the joint

being

> examined is placed in the machine, but holding my elbows that long

is

> what concerns me. The prednisone they started me on last Tuesday

is

> making me really moody. Has anyone else experienced that? If so

how

> did you deal with it? Was there anything you did that helped it? I

am

> usually a patient person and now I am crabbing at my kids and

hubby a

> lot. Any imput would help greatly, I am new to this.

>

> Sincerely,

>

> Barb ( Sassyone3173)

>

>

>

>

>

>

>

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--Toni,

Thanks for the advice about the prednisone. It is really frustrating

because I am such a calm easy going person and these past couple of

days the pain and I imagine the prednisone has made me a crazy person!

I heard that the prednisone keeps you awake, so taking it in the

morning is what I do. I have enough trouble sleeping without

prednisone keeping me awake!! You know what is funny? A lot of people

say that their appetite increases on this stuff, I found that I have

no appetite. I have to make myself eat or I would go all day and

night not eating at all. Guess I wont have to worry about getting

over weight on this med. Thanks for the luck, could use it! I hope

being on the prednisone is a totally temporary thing or I will be

trying to sneak emails to you all from the nut hatch! LOL

Barb

- In , aclavern33@a... wrote:

>

> Barb,

> Prednisone not only makes me cranky and crabby but the longer I am

on it the

> worst it gets. Also high dosages for me (20mg or greater) make me

> pyschotic!!! So be careful. I no longer take prednisone. I also

had the same

> problem with any hormonal type medication....even birth control

pills. So I don't

> really have any helpful advice to offer on this one.

>

> Make sure you take your prednisone at the start of your day or it

will keep

> you awake all nite. Also lots of water helps. I also would take

mine with

> food. Ihave a very sensitve stomach and it use to make my stomach

hurt. I

> was the only person that lost weight on prednisone. LOL

>

> Good luck on your MRI. That is cool that they can do only

extremities these

> days without putting your whole body into the machine.

>

> Toni in Texas

>

> In a message dated 9/6/2005 4:56:30 A.M. Central Daylight Time,

> writes:

>

> Tue, 06 Sep 2005 00:10:39 -0000

> From: " sassyone3173 " <bdciesinski@h...>

> Subject: Hi Again

>

> Hi guys. I am not really good at the group thing, i never know what

> to

> say. One on one I am okay, but in a group I am a " chicken " . This

> Thursday I go for an MRI on both elbows, an hour each side! Ouch!

My

> Rheumatologist asked if i could handle it, I just responded with

> " hope

> so. " They are using the new extremity MRI where only the joint

being

> examined is placed in the machine, but holding my elbows that long

is

> what concerns me. The prednisone they started me on last Tuesday

is

> making me really moody. Has anyone else experienced that? If so

how

> did you deal with it? Was there anything you did that helped it? I

am

> usually a patient person and now I am crabbing at my kids and

hubby a

> lot. Any imput would help greatly, I am new to this.

>

> Sincerely,

>

> Barb ( Sassyone3173)

>

>

>

>

>

>

>

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Hi Barb,

We are your RA family, and soon you will feel so comfortable with the

group, it just takes time. We all go through the same thing, and we

stand strong to help each other. I hope the MRI goes alright

tomorrow. I know this is so hard, two hours:( Maybe they can give you

breaks, I hope so. The prednisone made me really moody, and I felt so

out of control. I didn't like it at all, and I got off it. A short

term taper isnt' too bad, but the long term, it would not be my

choice. It does help a lot of people with the pain and swelling, but

that is about it. The side effects just keeps me away from it. I

noticed that Jerry lost about 80lbs after going off it. His

face looked so awful when he was on it, and what a change, he looks

so great now. Keep us posted how things go, and will keep you in my

prayers, Tawny

--- In , " sassyone3173 " <bdciesinski@h...>

wrote:

> Hi guys. I am not really good at the group thing, i never know what

> to

> say. One on one I am okay, but in a group I am a " chicken " . This

> Thursday I go for an MRI on both elbows, an hour each side! Ouch!

My

> Rheumatologist asked if i could handle it, I just responded with

> " hope

> so. " They are using the new extremity MRI where only the joint

being

> examined is placed in the machine, but holding my elbows that long

is

> what concerns me. The prednisone they started me on last Tuesday is

> making me really moody. Has anyone else experienced that? If so how

> did you deal with it? Was there anything you did that helped it? I

am

> usually a patient person and now I am crabbing at my kids and hubby

a

> lot. Any imput would help greatly, I am new to this.

>

> Sincerely,

>

> Barb ( Sassyone3173)

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Hi Barb,

We are your RA family, and soon you will feel so comfortable with the

group, it just takes time. We all go through the same thing, and we

stand strong to help each other. I hope the MRI goes alright

tomorrow. I know this is so hard, two hours:( Maybe they can give you

breaks, I hope so. The prednisone made me really moody, and I felt so

out of control. I didn't like it at all, and I got off it. A short

term taper isnt' too bad, but the long term, it would not be my

choice. It does help a lot of people with the pain and swelling, but

that is about it. The side effects just keeps me away from it. I

noticed that Jerry lost about 80lbs after going off it. His

face looked so awful when he was on it, and what a change, he looks

so great now. Keep us posted how things go, and will keep you in my

prayers, Tawny

> Hi guys. I am not really good at the group thing, i never know what

> to

> say. One on one I am okay, but in a group I am a " chicken " . This

> Thursday I go for an MRI on both elbows, an hour each side! Ouch!

My

> Rheumatologist asked if i could handle it, I just responded with

> " hope

> so. " They are using the new extremity MRI where only the joint

being

> examined is placed in the machine, but holding my elbows that long

is

> what concerns me. The prednisone they started me on last Tuesday is

> making me really moody. Has anyone else experienced that? If so how

> did you deal with it? Was there anything you did that helped it? I

am

> usually a patient person and now I am crabbing at my kids and hubby

a

> lot. Any imput would help greatly, I am new to this.

>

> Sincerely,

>

> Barb ( Sassyone3173)

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  • 2 months later...

Cosima,

Dr. Kolb is terrific. The only question I have is how

long it will take you to get in.

The implanting surgeon is usually the worst choice. .

.. They are reluctant to admit mistakes and are more

likely to try to cover them up.

Dr. Kolb's website is www.plastikos.com. Her

pre-explant protocol can help you begin feeling better

even before explant.

I don't know her personally, but she's very popular

with the women here who have been to her.

Hugs and prayers,

Rogene

--- Cosima <cosimaf@...> wrote:

> I was wondering if any of you here are familiar with

> Dr. Kolb in

> Atlanta.Has anyone here been to her or had

> explantation surgery done

> by her.I've just about decided that I can't wait the

> 2 1/2-3 months

> to see my original plastic surgeon and I don't trust

> that he would do

> a total capsulectomy. He's more into the business of

> putting them in

> but I/m sure he's also taken them out too. My chest

> is really feeling

> uncomfortable and achey right now. My breasts feel

> sore and the skin

> on them and my nipples have become sensitive.They

> don't look red or

> anything that would seem to indicate infection or

> inflammation but

> they feel inflamed.so I'm thinking that I might

> could get in to see

> Dr. Kolb sooner.Atlanta is only an hour and ahalf

> further than from

> me that ville, Fla. where my surgeon is.The

> only thing is that

> since I'm already an established patient with my

> surgeon his fees

> might be lower for both the consult($50 I was quoted

> on phone)and the

> surgery. I'm not able to work right now and don't

> have health

> insurance and neither does my husband. I did read on

> her website

> about payment arrangements but will the consult with

> her cost a lot?

> I don't get any more college loan money until

> February and that is

> basically what we live on in addition to my husbands

> jobs. frankly,

> I'm not sure how I'm making through grad school as

> awful as I feel

> most of the time.I just want these things out of my

> body before

> things either get worse or I end up in a crisis. I

> did email Dr. Kolb

> but I'm thinking about going ahead and calling her

> office tomorrow

> but maybe she might be too busy to actually talk to

> me on the phone

> and I'll just have to make an appointment.Please let

> me know if any

> of you have talked to/seen her.

>

>

>

>

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I'm glad you found Dr. Kolb - I didn't use her, I chose Dr. Feng

instead because she was closer in location than Dr. Kolb, and I felt

she was equally impressive, but Dr. Kolb has explanted many of the

women on this site, and I'm sure you'll be getting alot of feedback

on her. When I called Dr. Kolb while investigating explantation,

she responded to my e-mail on a weekend and then called me during

that same weekend, and spoke to me in great length. How many

doctors do that?

Sis

>

> I was wondering if any of you here are familiar with Dr. Kolb in

> Atlanta.Has anyone here been to her or had explantation surgery

done

> by her.I've just about decided that I can't wait the 2 1/2-3

months

> to see my original plastic surgeon and I don't trust that he would

do

> a total capsulectomy. He's more into the business of putting them

in

> but I/m sure he's also taken them out too. My chest is really

feeling

> uncomfortable and achey right now. My breasts feel sore and the

skin

> on them and my nipples have become sensitive.They don't look red

or

> anything that would seem to indicate infection or inflammation but

> they feel inflamed.so I'm thinking that I might could get in to

see

> Dr. Kolb sooner.Atlanta is only an hour and ahalf further than

from

> me that ville, Fla. where my surgeon is.The only thing is

that

> since I'm already an established patient with my surgeon his fees

> might be lower for both the consult($50 I was quoted on phone)and

the

> surgery. I'm not able to work right now and don't have health

> insurance and neither does my husband. I did read on her website

> about payment arrangements but will the consult with her cost a

lot?

> I don't get any more college loan money until February and that is

> basically what we live on in addition to my husbands jobs.

frankly,

> I'm not sure how I'm making through grad school as awful as I feel

> most of the time.I just want these things out of my body before

> things either get worse or I end up in a crisis. I did email Dr.

Kolb

> but I'm thinking about going ahead and calling her office tomorrow

> but maybe she might be too busy to actually talk to me on the

phone

> and I'll just have to make an appointment.Please let me know if

any

> of you have talked to/seen her.

>

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I live in South Florida, and I went to Dr. Kolb. I had my explant in April,

2004.

Dr. Kolb will find time to talk with you on the phone. She is an excellent

surgeon, and very

concerned about implant issues... She takes the time required to do the job

right.

> >

> > I was wondering if any of you here are familiar with Dr. Kolb in

> > Atlanta.Has anyone here been to her or had explantation surgery

> done

> > by her.I've just about decided that I can't wait the 2 1/2-3

> months

> > to see my original plastic surgeon and I don't trust that he would

> do

> > a total capsulectomy. He's more into the business of putting them

> in

> > but I/m sure he's also taken them out too. My chest is really

> feeling

> > uncomfortable and achey right now. My breasts feel sore and the

> skin

> > on them and my nipples have become sensitive.They don't look red

> or

> > anything that would seem to indicate infection or inflammation but

> > they feel inflamed.so I'm thinking that I might could get in to

> see

> > Dr. Kolb sooner.Atlanta is only an hour and ahalf further than

> from

> > me that ville, Fla. where my surgeon is.The only thing is

> that

> > since I'm already an established patient with my surgeon his fees

> > might be lower for both the consult($50 I was quoted on phone)and

> the

> > surgery. I'm not able to work right now and don't have health

> > insurance and neither does my husband. I did read on her website

> > about payment arrangements but will the consult with her cost a

> lot?

> > I don't get any more college loan money until February and that is

> > basically what we live on in addition to my husbands jobs.

> frankly,

> > I'm not sure how I'm making through grad school as awful as I feel

> > most of the time.I just want these things out of my body before

> > things either get worse or I end up in a crisis. I did email Dr.

> Kolb

> > but I'm thinking about going ahead and calling her office tomorrow

> > but maybe she might be too busy to actually talk to me on the

> phone

> > and I'll just have to make an appointment.Please let me know if

> any

> > of you have talked to/seen her.

> >

>

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thanks to all of you for your feedback and support. I plan on calling

Dr. Kolb's office tomorrow to make an appointment and hope they let

me talk to her as well as I seem to becoming pretty ill real fast

over the last few days. I feel like I have the flu but I don't have a

fever like I usually do when I have the flu but in every other way I

feel just like the flu except my chest/breasts are hurting a lot-

feels like a lot of pressure in the middle of my chest and it makes

it hard to breathe.But yet there's no redness or anything I can see.

I hope and pray that she can see me before the pain becomes

unbearable or something worse happens.

--- In , " Molly Bloom " <mollyb54@b...>

wrote:

>

> I live in South Florida, and I went to Dr. Kolb. I had my explant

in April, 2004.

> Dr. Kolb will find time to talk with you on the phone. She is an

excellent surgeon, and very

> concerned about implant issues... She takes the time required to

do the job right.

>

> --- In , " auntsisnj " <auntsisnj@l...>

wrote:

> >

> > I'm glad you found Dr. Kolb - I didn't use her, I chose Dr. Feng

> > instead because she was closer in location than Dr. Kolb, and I

felt

> > she was equally impressive, but Dr. Kolb has explanted many of

the

> > women on this site, and I'm sure you'll be getting alot of

feedback

> > on her. When I called Dr. Kolb while investigating explantation,

> > she responded to my e-mail on a weekend and then called me during

> > that same weekend, and spoke to me in great length. How many

> > doctors do that?

> >

> > Sis

> >

> >

> > --- In , " Cosima " <cosimaf@b...>

wrote:

> > >

> > > I was wondering if any of you here are familiar with Dr. Kolb

in

> > > Atlanta.Has anyone here been to her or had explantation surgery

> > done

> > > by her.I've just about decided that I can't wait the 2 1/2-3

> > months

> > > to see my original plastic surgeon and I don't trust that he

would

> > do

> > > a total capsulectomy. He's more into the business of putting

them

> > in

> > > but I/m sure he's also taken them out too. My chest is really

> > feeling

> > > uncomfortable and achey right now. My breasts feel sore and the

> > skin

> > > on them and my nipples have become sensitive.They don't look

red

> > or

> > > anything that would seem to indicate infection or inflammation

but

> > > they feel inflamed.so I'm thinking that I might could get in to

> > see

> > > Dr. Kolb sooner.Atlanta is only an hour and ahalf further than

> > from

> > > me that ville, Fla. where my surgeon is.The only thing

is

> > that

> > > since I'm already an established patient with my surgeon his

fees

> > > might be lower for both the consult($50 I was quoted on phone)

and

> > the

> > > surgery. I'm not able to work right now and don't have health

> > > insurance and neither does my husband. I did read on her

website

> > > about payment arrangements but will the consult with her cost a

> > lot?

> > > I don't get any more college loan money until February and that

is

> > > basically what we live on in addition to my husbands jobs.

> > frankly,

> > > I'm not sure how I'm making through grad school as awful as I

feel

> > > most of the time.I just want these things out of my body before

> > > things either get worse or I end up in a crisis. I did email

Dr.

> > Kolb

> > > but I'm thinking about going ahead and calling her office

tomorrow

> > > but maybe she might be too busy to actually talk to me on the

> > phone

> > > and I'll just have to make an appointment.Please let me know if

> > any

> > > of you have talked to/seen her.

> > >

> >

>

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