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Why not use the unsweetened applesauce? It is pretty sweet!

I do not use any artificial sweeteners...why chance it?

Hugs, Donna

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Hi ,

Welcome to the group. I just wanted to say just because you're pregnant you

can still continue kickboxing. I was doing kickboxing, pilates, step aerobics

up to 32 weeks in addition to strength conditioning and yoga.

If I recall correctly, I discontinued traditional sit ups and recline squats at

14 weeks based on recommendations from my OB.

Talk to your OB/midwife and get his/her input.

O

Re: New member

Hello! My name is and I had an Open RNY 09/28/00 in Belvidere,

Illinois. I have lost 130#s and have been pretty stable around 202#s (I'm 5' 9 " )

for the past six months. I am 4wks pregnant, also. I did join a gym four weeks

ago to try to tone up a little and will continue to go there for the excercise;

I'll just forego the kickboxing classes (that really kick my butt) now that I

know I'm pregnant!

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I thought maybe I'd better quit the kickboxing because my heart rate gets over

200 - the skinny little 18-yr-old that teaches the class really gives a good

workout. I was afraid that that was too much for the baby. I do see my OB/GYN

next week to discuss nutrition and I will tell her exactly what I do at the gym

and was going to ask her if I should not let my heart rate get so high. I have

actually always had it get to 180-200 when I want to sweat and get a really good

workout, but I was afraid that was too intense during pregnancy. Any thoughts on

that? I have had excercise instructors tell me that my heart rate is too high at

180-200, but again, mine has been that way for as many years as I can remember,

when I was really heavy and even now after losing over 100#s.

I also love to use the Theraball with a tape at home - do any of you continue to

use an excercise ball? I have to think it's better to do sit-ups and push-ups on

the ball than on the floor but again, I don't want to hurt my baby so would be

interested if any of you have comments about that. I like to use the Theraball

because it helps strenthen my lower back which I have always had problems with.

Again, I'll be speaking to my OB/GYN, but I also like to take into consideration

the info from folks who have BEEN THERE, if you know what I mean. Weight Loss

Surgery is still very new here in Kansas and there are many docs who don't have

a clue.

Up until Monday when I found out I was pregnant, I was taking Celebrex for

terrible lower back pain. Of course I have quit now. I am not certain how I will

make it through nine months if the pain gets as bad as it was when I started

taking Celebrex. I had hoped that losing so much weight would improve my back,

but it has not. Other than back-strengthening excercises, do any of you have any

ideas for me? I'm told I can take Tylenol; my PCP's nurse told me a 'normal'

person could take up to 4,000 mg of Tylenol a day, but they recommended I only

take up to 2,000 mg/day. If I had my druthers I'd not take anything at all, but

again, I have to be able to walk and go to work and if my back starts acting up

again real bad, I'm in trouble.

Sorry for the long posts - I'll try to shorten them up. I'm just so excited to

have others to talk to who are/have been pg since WLS that I have SO many

questions for you all!

---

bkenworthy@...

Re: New member

Hello! My name is and I had an Open RNY 09/28/00 in Belvidere,

Illinois. I have lost 130#s and have been pretty stable around 202#s (I'm 5' 9 " )

for the past six months. I am 4wks pregnant, also. I did join a gym four weeks

ago to try to tone up a little and will continue to go there for the excercise;

I'll just forego the kickboxing classes (that really kick my butt) now that I

know I'm pregnant!

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,

I just wanted to say congrats and welcome!!

Trina

EDD 9/25

> I thought maybe I'd better quit the kickboxing because my heart

rate gets over 200 - the skinny little 18-yr-old that teaches the

class really gives a good workout. I was afraid that that was too

much for the baby. I do see my OB/GYN next week to discuss nutrition

and I will tell her exactly what I do at the gym and was going to ask

her if I should not let my heart rate get so high. I have actually

always had it get to 180-200 when I want to sweat and get a really

good workout, but I was afraid that was too intense during pregnancy.

Any thoughts on that? I have had excercise instructors tell me that

my heart rate is too high at 180-200, but again, mine has been that

way for as many years as I can remember, when I was really heavy and

even now after losing over 100#s.

>

> I also love to use the Theraball with a tape at home - do any of

you continue to use an excercise ball? I have to think it's better to

do sit-ups and push-ups on the ball than on the floor but again, I

don't want to hurt my baby so would be interested if any of you have

comments about that. I like to use the Theraball because it helps

strenthen my lower back which I have always had problems with. Again,

I'll be speaking to my OB/GYN, but I also like to take into

consideration the info from folks who have BEEN THERE, if you know

what I mean. Weight Loss Surgery is still very new here in Kansas and

there are many docs who don't have a clue.

>

> Up until Monday when I found out I was pregnant, I was taking

Celebrex for terrible lower back pain. Of course I have quit now. I

am not certain how I will make it through nine months if the pain

gets as bad as it was when I started taking Celebrex. I had hoped

that losing so much weight would improve my back, but it has not.

Other than back-strengthening excercises, do any of you have any

ideas for me? I'm told I can take Tylenol; my PCP's nurse told me

a 'normal' person could take up to 4,000 mg of Tylenol a day, but

they recommended I only take up to 2,000 mg/day. If I had my druthers

I'd not take anything at all, but again, I have to be able to walk

and go to work and if my back starts acting up again real bad, I'm in

trouble.

>

> Sorry for the long posts - I'll try to shorten them up. I'm just so

excited to have others to talk to who are/have been pg since WLS that

I have SO many questions for you all!

>

> ---

>

> bkenworthy@k...

>

>

> Re: New member

>

>

> Hello! My name is and I had an Open RNY 09/28/00 in

Belvidere, Illinois. I have lost 130#s and have been pretty stable

around 202#s (I'm 5' 9 " ) for the past six months. I am 4wks pregnant,

also. I did join a gym four weeks ago to try to tone up a little and

will continue to go there for the excercise; I'll just forego the

kickboxing classes (that really kick my butt) now that I know I'm

pregnant!

>

>

>

>

>

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You should be quitting any exercise that makes your HR go over 200! IMHO, you

are not conditioned for that particular workout if your HR goes over your target

zone.

I don't know how old you are but your maximum heart rate is about 220 minus your

age so let's say you are 30 years old, your maximum HR would be 190 and you

would want your HR in the target zone (50-75%) of 95-142 beats per minute. Only

if you're advanced would I see 80% (~152) being indicated.

My step aerobics instructor who is certified by practically every fitness

organization out there and who taught the class up to 2 days before her

expected/delivery due date would constantly state that a pregnant woman's (in

good shape and exercised regularly/religiously prior to pregnancy) HR should not

go over 140. When I asked my OB, he agreed.

I can't recall but I think your initial email stated you just started working

out 4 weeks ago, if that's the case, slow down! You're trying to run before

you're crawling. Doing too much too soon, too early is a great way to burn out

on working out. Power walk (either treadmill or street), elliptical,

stationary bike, stair master, swim, prenatal workouts (either yoga, step,

conditioning, etc) is a great way to start off. Start off 10 minutes and build

it up to 20, 30, 45; always remember to warm up and cool down. Keep in mind you

don't want any workout where you have to jump or do traditional abdominals.

You mentioned the fitness ball, that's a great tool for non traditional

abdominals and back exercises besides a tool you can use while you're in labor.

As always, discuss this w/ your OB before setting out to do it.

O

edd 5-25-02 Baby Girl!

Re: New member

I thought maybe I'd better quit the kickboxing because my heart rate gets over

200 - the skinny little 18-yr-old that teaches the class really gives a good

workout. I was afraid that that was too much for the baby. I do see my OB/GYN

next week to discuss nutrition and I will tell her exactly what I do at the gym

and was going to ask her if I should not let my heart rate get so high. I have

actually always had it get to 180-200 when I want to sweat and get a really good

workout, but I was afraid that was too intense during pregnancy. Any thoughts on

that? I have had excercise instructors tell me that my heart rate is too high at

180-200, but again, mine has been that way for as many years as I can remember,

when I was really heavy and even now after losing over 100#s.

I also love to use the Theraball with a tape at home - do any of you continue

to use an excercise ball? I have to think it's better to do sit-ups and push-ups

on the ball than on the floor but again, I don't want to hurt my baby so would

be interested if any of you have comments about that. I like to use the

Theraball because it helps strenthen my lower back which I have always had

problems with. Again, I'll be speaking to my OB/GYN, but I also like to take

into consideration the info from folks who have BEEN THERE, if you know what I

mean. Weight Loss Surgery is still very new here in Kansas and there are many

docs who don't have a clue.

Up until Monday when I found out I was pregnant, I was taking Celebrex for

terrible lower back pain. Of course I have quit now. I am not certain how I will

make it through nine months if the pain gets as bad as it was when I started

taking Celebrex. I had hoped that losing so much weight would improve my back,

but it has not. Other than back-strengthening excercises, do any of you have any

ideas for me? I'm told I can take Tylenol; my PCP's nurse told me a 'normal'

person could take up to 4,000 mg of Tylenol a day, but they recommended I only

take up to 2,000 mg/day. If I had my druthers I'd not take anything at all, but

again, I have to be able to walk and go to work and if my back starts acting up

again real bad, I'm in trouble.

Sorry for the long posts - I'll try to shorten them up. I'm just so excited to

have others to talk to who are/have been pg since WLS that I have SO many

questions for you all!

---

bkenworthy@...

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Hi Mick ,Edith, Skip and all the other Aussies out there.

Good luck Mick for next wednesday. Enjoy the long weekend and don't

party too much.

All the best

Dasher

> Another Orstralian ....... g'day Edith, I'm in Orange NSW and Dr

Len Walter

> is doing my BHR at the Mater Hospital in Sydney this coming

Wednesday.

> After stopping the Celebrex 10 days ago, I now realise just how

good they

> were. The pain I have been having over the last 2 days has been

quite

> severe and the sooner Wednesday comes the better.

> Hopefully I will be able to offer some help and advice to others

after I

> have been repaired.

>

> Mick.

>

>

> ----- Original Message -----

>

> > Hi,

> >

> > I too am a recent addition to the list and am glad to hear the

reports of

> > Resurfacing working okay.

> > I am hoping that I can have a Resurface done on my left hip in

August. In

> > live in northern Australia and have to travel to Sydney to have

it done as

> I

>

> <<<<<<<<<<<<<<<SNIP>>>>>>>>>>>>>>

>

> > Edith

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Ha ha ..... yeah right .......... I'll try and keep the partying to a

minimum in this wet, cold, foggy part of the world !

Mick. (5 more sleeps!)

----- Original Message -----

> Hi Mick ,Edith, Skip and all the other Aussies out there.

>

> Good luck Mick for next wednesday. Enjoy the long weekend and don't

> party too much.

>

> All the best

> Dasher

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Guest guest

Hi Liz, my name is and I got sick Nov2001 as well..

Welcome to the group.. I hope we can be of some help to you, I know we can show you support... as we have all been were you are.... I did recieve my disability but it was in March of this year.and I applied Jan 2002... just hang in there keep all your information..and have you a lawyer that is willing to help you.. not just take your money....

Good luck to you, and if you need anything questions, about meds, symptoms, etc... this is a very informative group.. we have a couple of doctors, lots of nurses, teachers... so just ask away....

Big Hug,

-- new member

Hi I'M Liz and a new member of this group. I already received a whole

bunch of emails and they were so helpful. I have been Battling this

disease since Nov 2001. My symptoms are getting worse day by day.

I've changed doctors so many times. Many don't understand what I am

going through.I'm on a ton of different drugs and my anti-seizure

meds are starting not to work like they used to. I'm searching for a

neurologist in the New Jersey, North East PA, or manhattan

area.Please send me some suggestions or what doctors I should be

looking for. After the diagnosis of sarcoid, I was Diagnosed with

Fibromyalgia secondary to sarcoid ( no lung involvement yet ) but

many many seizures and loss of consciousness and pain all over on a

daily basis. I haven't been able to work since Nov 2001 and I'm

still fighting disability. Denied twice and now waiting for hearing.

Feel free to write me. I'm taking this one day at a time, being

grateful for each day, whether it's and good day or a bad day.

God bless you all. Praying for healing......LIZ

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Hi Liz and welcome! I wish that I could help you out on finding good

doctors, but I live all the way down in south Florida. But I'm sure you'll

find some useful information on this list. There are a lot of

knowledgeable folks here.

Best wishes,

Neisa

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Guest guest

HI LIZ,

MY NAME IS NICOLE ALSO KNOWN AS CARROTS ON THIS LIST. I AM 20 YEARS OLD

AND GO TO COLLEGE IN TOWSON MARYLAND. I LIVE IN NEW JERSEY AND I NOTICED

THAT U NEEDED A NEURO THERE. I GO TO A WONDERFUL WOMAN NAMED DR RUTH CLARK.

QUINT CAN BE AS MY WITNESS THAT THIS IS ONE OF THE BEST DOCTORS I HAVE

SEEN SINCE I HAVE BEEN SICK. SHE IS VERY THOROUGH, CARING, PATIENT AND

UNDERSTANDING. HERE IS HER NUMBER

SHE IS LOCATED ON CENTRAL AVE IN EAST ORANGE.

CALL AND MAKE AN APPOINTMENT. SHE IS ABSOLOUTELY WONDERFUL LIZ. U CAN

EVEN TELL HER NICOLE JORDAN RECOMENDED YOU.

LET ME KNOW HOW THINGS TURN OUT

NICOLE

>

>Reply-To: Neurosarcoidosis

>To: Neurosarcoidosis

>Subject: new member

>Date: Thu, 31 Jul 2003 22:30:35 -0000

>

>Hi I'M Liz and a new member of this group. I already received a whole

>bunch of emails and they were so helpful. I have been Battling this

>disease since Nov 2001. My symptoms are getting worse day by day.

>I've changed doctors so many times. Many don't understand what I am

>going through.I'm on a ton of different drugs and my anti-seizure

>meds are starting not to work like they used to. I'm searching for a

>neurologist in the New Jersey, North East PA, or manhattan

>area.Please send me some suggestions or what doctors I should be

>looking for. After the diagnosis of sarcoid, I was Diagnosed with

>Fibromyalgia secondary to sarcoid ( no lung involvement yet ) but

>many many seizures and loss of consciousness and pain all over on a

>daily basis. I haven't been able to work since Nov 2001 and I'm

>still fighting disability. Denied twice and now waiting for hearing.

>Feel free to write me. I'm taking this one day at a time, being

>grateful for each day, whether it's and good day or a bad day.

>God bless you all. Praying for healing......LIZ

>

_________________________________________________________________

The new MSN 8: advanced junk mail protection and 2 months FREE*

http://join.msn.com/?page=features/junkmail

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Hi Liz welcome to our loving family. I have to agree with

Dr. is the best.I don't think I would still be

here if I did not have Dr. at the time. and she also

helped me get my disabiliy.Iwill get back to you with the

name of a good eye doc. I have to find his address......Quint

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quint!!!

i have been to dr frohman before!! he is a great doctor. i think i have

seen just about everyone in ny and nj.

carrots

>From: sarcdog@...

>Reply-To: Neurosarcoidosis

>To: Neurosarcoidosis

>Subject: Re: new member

>Date: Sat, 2 Aug 2003 15:47:59 -0400 (EDT)

>

>Liz dear here is the eye doc. Dr. Larry Frohman 90 Bergen st

>suite 6162 Newark, New Jersey. He is good with sarc eye

>problems......Quint

>

_________________________________________________________________

Add photos to your e-mail with MSN 8. Get 2 months FREE*.

http://join.msn.com/?page=features/featuredemail

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quint!!!

i have been to dr frohman before!! he is a great doctor. i think i have

seen just about everyone in ny and nj.

carrots

>From: sarcdog@...

>Reply-To: Neurosarcoidosis

>To: Neurosarcoidosis

>Subject: Re: new member

>Date: Sat, 2 Aug 2003 15:47:59 -0400 (EDT)

>

>Liz dear here is the eye doc. Dr. Larry Frohman 90 Bergen st

>suite 6162 Newark, New Jersey. He is good with sarc eye

>problems......Quint

>

_________________________________________________________________

Add photos to your e-mail with MSN 8. Get 2 months FREE*.

http://join.msn.com/?page=features/featuredemail

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Welcome , This is a great group and YES you will find an abundance of information here. Glad that you have joined us

Ann

new member

Hello to all. i am new to this group however not new to sarcoidosis. I was diagnosed in 1998. At that time it was in my liver and spleen. Now it is in my lungs and kidneys also. I do not have neurosarcoid, but was still interested in joining this group for all the information I could find. Thank you.~~~~ *** ~~~ *** ~~~ *** ~~~~The Neurosarcoidosis CommunityLive Group Chat:-Mondays & Fridays 10pm EST USAhttp://www.elderwyn.com/neurosarcoidosis/chat.phpMessage Archives and Digest Attachment Pictures:-http://groups.yahoo.com/group/Neurosarcoidosis/messagesMembers Database:-Listings of locations, phone numbers, and instant messengers.http://groups.yahoo.com/group/Neurosarcoidosis/database Bookmarks:-Add a website URL you have found useful.http://groups.yahoo.com/group/Neurosarcoidosis/linksPersonal Complaints or problems:-Please email the moderatorsmailto:Neurosarcoidosis-owner Subscription Details:-1) Individual email - means that every email sent to the list you receive.2) Daily Digest - sends you 25 messages in one single email for you to browse. This is an excellent option if you receive alot of email.3) Web only/No mail - means that you can pop into eGroups at your convenience and receive no email.To modify your subscription settings please visit:- http://groups.yahoo.com/group/Neurosarcoidosis/joinTo subscribe email neurosarcoidosis-subscribe To unsubscribe email neurosarcoidosis-unsubscribe The moderators will not be doing it for you!~~~~ *** ~~~ *** ~~~ *** ~~~~Come stand by my side where I am going,Take my hand if I should stumble and fall,It's the strength and love that you share,That gives me what I need most of all.- Hoyt Axton~~~~ *** ~~~ *** ~~~ *** ~~~~

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Hi ,

Welcome to the family. Sure sounds like you have systemic sarc fighting you,

poor thing. :(

You're more then welcome here honey. No vent too long or too short. Just hop

on in anytime!

*hugs*

Love isha

-- new member

Hello to all. i am new to this group however not new to sarcoidosis.

I was diagnosed in 1998. At that time it was in my liver and spleen.

Now it is in my lungs and kidneys also. I do not have neurosarcoid,

but was still interested in joining this group for all the

information I could find. Thank you.

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Hi ,

Welcome to the family. Sure sounds like you have systemic sarc fighting you,

poor thing. :(

You're more then welcome here honey. No vent too long or too short. Just hop

on in anytime!

*hugs*

Love isha

-- new member

Hello to all. i am new to this group however not new to sarcoidosis.

I was diagnosed in 1998. At that time it was in my liver and spleen.

Now it is in my lungs and kidneys also. I do not have neurosarcoid,

but was still interested in joining this group for all the

information I could find. Thank you.

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Hi ,

Welcome to the family. Sure sounds like you have systemic sarc fighting you,

poor thing. :(

You're more then welcome here honey. No vent too long or too short. Just hop

on in anytime!

*hugs*

Love isha

-- new member

Hello to all. i am new to this group however not new to sarcoidosis.

I was diagnosed in 1998. At that time it was in my liver and spleen.

Now it is in my lungs and kidneys also. I do not have neurosarcoid,

but was still interested in joining this group for all the

information I could find. Thank you.

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My name is Candi. I live in Breese, Illinois (deep in the heart of

corn country!!). Not too far from St. Louis, Missouri.

I originally talked to my doctor 16 months ago about the surgery.

It took over a year just to get an appointment for the evaluation.

I did that back in June of this year. The hospital just called me

last week to say my insurance approved me and scheduled me for the

29th of September. Then yesterday I got A call from the Hospital

and someone who was supposed to have surgery this Monday got sick

and they asked if I would be willing to take their place. So day

after tomorrow I will be having my surgery.

Funny thing is I am not nervous. I am doing the RNY/LAP.

But suddenly I felt this need to talk to others who are going

through it. Any southern Illinois people on this list who have had

or are soon to have their surgery?

Candi

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welcome candi & here's a high five for grabbing monday's surg date.

i had my wls 16 months ago, & it's truly a brand new life. ask any

specific ?s, we're a captive audience.

lori h.

> My name is Candi. I live in Breese, Illinois (deep in the heart

of

> corn country!!). Not too far from St. Louis, Missouri.

>

> I originally talked to my doctor 16 months ago about the surgery.

> It took over a year just to get an appointment for the

evaluation.

> I did that back in June of this year. The hospital just called me

> last week to say my insurance approved me and scheduled me for the

> 29th of September. Then yesterday I got A call from the Hospital

> and someone who was supposed to have surgery this Monday got sick

> and they asked if I would be willing to take their place. So day

> after tomorrow I will be having my surgery.

>

> Funny thing is I am not nervous. I am doing the RNY/LAP.

>

> But suddenly I felt this need to talk to others who are going

> through it. Any southern Illinois people on this list who have

had

> or are soon to have their surgery?

>

> Candi

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<kitamaiden@y...> wrote:

> Congratulations Candi on getting approved and then to have surgery

moved up. At least you won't have to be nervous for to long this

way.

Thanks!!!

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Grimmlah1@a... wrote:

I had the lap RNY on 8/25/03 and it was without

> any complications and I am doing fine and you will too.

Wow 8/25!!! How are you feeling? Are you doing things around the

house again?

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" " <Leeds@e...> wrote:

> Where is Breese exactly? I used to live in ville if you know

> where that is. I loved it there.

We are not all that far from ville. My daughter goes to

school at SIUE. It's about 45 minutes. We are farther south. We

are about 30 minutes south of AIR Force Base if you know where

that is.

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Hi Brock.........welcome to the group....I started out with sarc in the

lungs and now it is in other places.....was diagnosed in 1997 after a two

year battle with many Doctors trying to find out what was wrong with

me......:-) You will find many knowledgeable people here on the list

and many are eager to share and help........so just ask........and again,

welcome!

Hugs,

Darlene

Moderator

Hello Everyone,

> My name is Brock and i am new to this support group. I have been

> dealing and battling medical problems for two years. I have sarc

> in the lungs and in my pituitary gland. I look forward to talking

> with people.

>

> Brock

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Hey, Brock! Welcome to our family. We're more than 200 strong, all over the world. Sorry you had to get the sarc monster in order to meet us. Rose from Indiana

New Member

Hello Everyone,

My name is Brock and i am new to this support group. I have been dealing and battling medical problems for two years. I have sarc in the lungs and in my pituitary gland. I look forward to talking with people.

Brock~~~~ *** ~~~ *** ~~~ *** ~~~~The Neurosarcoidosis CommunityLive Group Chat:-Mondays & Fridays 10pm EST USAhttp://www.elderwyn.com/neurosarcoidosis/chat.phpMessage Archives and Digest Attachment Pictures:-http://groups.yahoo.com/group/Neurosarcoidosis/messagesMembers Database:-Listings of locations, phone numbers, and instant messengers.http://groups.yahoo.com/group/Neurosarcoidosis/database Bookmarks:-Add a website URL you have found useful.http://groups.yahoo.com/group/Neurosarcoidosis/linksPersonal Complaints or problems:-Please email the moderatorsmailto:Neurosarcoidosis-owner Subscription Details:-1) Individual email - means that every email sent to the list you receive.2) Daily Digest - sends you 25 messages in one single email for you to browse. This is an excellent option if you receive alot of email.3) Web only/No mail - means that you can pop into eGroups at your convenience and receive no email.To modify your subscription settings please visit:- http://groups.yahoo.com/group/Neurosarcoidosis/joinTo subscribe email neurosarcoidosis-subscribe To unsubscribe email neurosarcoidosis-unsubscribe The moderators will not be doing it for you!~~~~ *** ~~~ *** ~~~ *** ~~~~Come stand by my side where I am going,Take my hand if I should stumble and fall,It's the strength and love that you share,That gives me what I need most of all.- Hoyt Axton~~~~ *** ~~~ *** ~~~ *** ~~~~

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