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Hi

My name is Sharrie, I was just Dx with RA along with several other

medical problems all of which I was told about over this past long

summer. I'm 43 newly married (2nd time)and have to girls aes 17 and

19. We all just moved to Florida (my life dream) a year ago this

month. Since April I have been sick with one thing after another

starting with Mono, then major female problems that I must address(I

had no idea I even had any problems), than herniated discs neck and

low back and while being treated for all these compounding problems

and trying to find why I have been sooo tired and in sooo much pain

in my hips, feet, hands a lab tech mentioned I should check for RA

after watching my RHeum factor go up very quick everytime I went to

the Dr and so I went to a specialist and now this is the latest to

add to my list. Needless to say I have been very depressed and could

use some support.

Thanx for listening(reading) my sob story!!!

We all have one but sometimes it helps to share them

Sharrie

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Welcome Sharrie. Congratulations on your recent marriage. I hope you

have many years of happiness. I just moved to Florida

1 1/2 years ago after dreaming of it for many years also. I hope you

weren't in the path of any of the hurricanes. I'm in Naples and

have been lucky.

Did your joint pain start after the mono?

a

On Oct 4, 2005, at 2:31 PM, sharriedsb7 wrote:

> Hi

>

> My name is Sharrie, I was just Dx with RA along with several other

> medical problems all of which I was told about over this past long

> summer. I'm 43 newly married (2nd time)and have to girls aes 17 and

> 19. We all just moved to Florida (my life dream) a year ago this

> month. Since April I have been sick with one thing after another

> starting with Mono, then major female problems that I must address(I

> had no idea I even had any problems), than herniated discs neck and

> low back and while being treated for all these compounding problems

> and trying to find why I have been sooo tired and in sooo much pain

> in my hips, feet, hands a lab tech mentioned I should check for RA

> after watching my RHeum factor go up very quick everytime I went to

> the Dr and so I went to a specialist and now this is the latest to

> add to my list. Needless to say I have been very depressed and could

> use some support.

> Thanx for listening(reading) my sob story!!!

> We all have one but sometimes it helps to share them

>

> Sharrie

>

>

>

>

>

>

>

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Welcome to the group, Sharrie! Sorry to hear that you've had such a rough

time.

Mononucleosis can cause a rheumatoid factor (RF) test to be positive. I'm

assuming you saw a rheumatologist and that he or she based the diagnosis on

more than the positive RF.

Hope you will be feeling much better very soon.

Not an MD

I'll tell you where to go!

Mayo Clinic in Rochester

http://www.mayoclinic.org/rochester

s Hopkins Medicine

http://www.hopkinsmedicine.org

[ ] Looking for support

> Hi

>

> My name is Sharrie, I was just Dx with RA along with several other

> medical problems all of which I was told about over this past long

> summer. I'm 43 newly married (2nd time)and have to girls aes 17 and

> 19. We all just moved to Florida (my life dream) a year ago this

> month. Since April I have been sick with one thing after another

> starting with Mono, then major female problems that I must address(I

> had no idea I even had any problems), than herniated discs neck and

> low back and while being treated for all these compounding problems

> and trying to find why I have been sooo tired and in sooo much pain

> in my hips, feet, hands a lab tech mentioned I should check for RA

> after watching my RHeum factor go up very quick everytime I went to

> the Dr and so I went to a specialist and now this is the latest to

> add to my list. Needless to say I have been very depressed and could

> use some support.

> Thanx for listening(reading) my sob story!!!

> We all have one but sometimes it helps to share them

>

> Sharrie

>

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Welcome Sharrie!! My name is and I joined this group about a month ago

and it has been a life-changing source of support and comfort. The people in

this group have all gone through things similar to us, and perhaps because of

their suffering, they have developed so much compassion and common sense. I

hope you find as much support as I have. You are not alone. Blessings to you!

sharriedsb7 <sharriedsb7@...> wrote:Hi

My name is Sharrie, I was just Dx with RA along with several other

medical problems all of which I was told about over this past long

summer. I'm 43 newly married (2nd time)and have to girls aes 17 and

19. We all just moved to Florida (my life dream) a year ago this

month. Since April I have been sick with one thing after another

starting with Mono, then major female problems that I must address(I

had no idea I even had any problems), than herniated discs neck and

low back and while being treated for all these compounding problems

and trying to find why I have been sooo tired and in sooo much pain

in my hips, feet, hands a lab tech mentioned I should check for RA

after watching my RHeum factor go up very quick everytime I went to

the Dr and so I went to a specialist and now this is the latest to

add to my list. Needless to say I have been very depressed and could

use some support.

Thanx for listening(reading) my sob story!!!

We all have one but sometimes it helps to share them

Sharrie

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  • 1 year later...

I hate to hear all that you are going thru..

I hope they can give you some help soon if you do have fibro. I know there

are many meds you can try. I also know it is hard being a parent with a

chronic

disease let alone

being a single parent. Hang in there. We are all hear to lend an ear and a

shoulder.

Joy

bp101_brat <bp101_brat@...> wrote:

I was diagnosed with seronegative RA in April 2006. I was

sulfasalazine

and plaquenil. I saw my Rheumy on Jan 2 nd and now she is questioning

Lupus; which my FMD has thought all along. I have seven of the eleven

criteria for the diease. I am so frustrated and in sooo much pain. It

seems that sometimes the doctors poo poo the symptoms as not being as

bad as they are. Since my dx in 4/06 I was also diagnosed with

eplilepsey after a car accident. So now it has affected my heart lung

and CNS....and still wont give the diagnosis offically as RA/Lupus.

Please understand that I dont want Lupus; but I need answers and I am

soo tired of the pain and discomfort I live everyday. I am a single

mommy of two little girls; 4 & 6 yrs old. So I have to be able to get out

of bed in teh morning. If anyone has any ideas to help this really

frustrated single mommy please let me know.

Lots of Thanks,

Joy

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

Visit Joy's Homepage and Reading Room!

http://jhoormann-ivil.tripod.com

Come see My Dog Salsa!

http://www.geocities.com/jhoorm01/Salsa.html

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Hi :

You have come to the right place for support and

information. I have been with this group for four or

five years now, and have learned so much more here

than I ever could have on my own, or even through my

doctors.

I understand your urgency for a diagnosis, a name of

the monster that is causing you so much pain so that

you can fight it better. It sometimes takes a while

to differentiate all of the immune system diseases as

they can share symptoms, and even blood tests are not

100% effective in diagnosis at times. Your physical

symptoms are where the doctors should be focusing -

not everything is found in tests - your body is

speaking for you, and you know yourself better than

anybody.

Until you get the diagnosis, you can always try the

old hot showers/baths way of helping your pain, also

rice socks are great on the joints, but at times ice

is helpful to me as well. You just have to find out

through trail and error. Does your doctor have you on

any medication? You might want to see if he will try

you on a steroid for a short while to see if this

gives you some pain relief. You don't want to take it

for long, but they can be great on the inflammation

and pain.

Please let us know what happens with you - we have all

been where you are now and it's no fun, scary, and

very overwhelming. We are here for you - you are no

longer alone, okay?

Kathe in CA

" Until he extends the circle of his compassion to all living things, man will

not himself find peace. "

— Albert Schweitzer, French Nobel Peace Prize-winning mission doctor and

theologian (1875-1965)

________________________________________________________________________________\

____

Looking for earth-friendly autos?

Browse Top Cars by " Green Rating " at Autos' Green Center.

http://autos./green_center/

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> who doesn't understand what you are

> going through just because " you don't look sick>>>>>

>

My own family doc said that when my rheumy diagnosed me (that he sent me

to) and I told him!

Why did he say that?

Pris

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I totally understand your pain and the frustration at

the limitations that RA can cause us. I live in the

Chicago area and we are known for the bitter cold and

snow/ice. It seems to have been even worse on me since

my surgery on 12/6.

I have started stretching my feet and legs while still

in bed before stepping on the floor. I have found this

to help a bit, especially since during my sleep my

feet and legs become very stiff. I also have found

that it is almost unbearable to start my day on my bad

days but I am learning to press through the pain and

keep moving. By mid-morning my joints seems to be less

painful and I am able to move with less pain.

I go back to work on Tuesday and I am concerned that

my injured foot and RA will make my days tough. I know

that the day will not be the worst part, it seems that

when I get home from work and off my feet that the

pain comes crashing down on me.

I am listening to my body and getting great ideas and

support here. Any ideas of how I can ease my body from

crashing after I finish my work day?

Lastly one of the greatest stress reliefs for me has

been working on crafts. This crafting has been a

blessing in keeping my fingers and hands limber. I

highly encourage crafts as a stress buster and as a

way to ease the RA.

Take care all of you and thanks for all your support!

Patti (Chicago)

" Taking it one day at a time! "

--- bp101_brat <bp101_brat@...> wrote:

> I was diagnosed with seronegative RA in April 2006.

> I was sulfasalazine

> and plaquenil. I saw my Rheumy on Jan 2 nd and now

> she is questioning

> Lupus; which my FMD has thought all along. I have

> seven of the eleven

> criteria for the diease. I am so frustrated and in

> sooo much pain. It

> seems that sometimes the doctors poo poo the

> symptoms as not being as

> bad as they are. Since my dx in 4/06 I was also

> diagnosed with

> eplilepsey after a car accident. So now it has

> affected my heart lung

> and CNS....and still wont give the diagnosis

> offically as RA/Lupus.

> Please understand that I dont want Lupus; but I need

> answers and I am

> soo tired of the pain and discomfort I live

> everyday. I am a single

> mommy of two little girls; 4 & 6 yrs old. So I have to

> be able to get out

> of bed in teh morning. If anyone has any ideas to

> help this really

> frustrated single mommy please let me know.

> Lots of Thanks,

>

>

>

________________________________________________________________________________\

____

Be a PS3 game guru.

Get your game face on with the latest PS3 news and previews at Games.

http://videogames./platform?platform=120121

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-Kathe~

Thank you for words of kindness and support. You are right it is like

a monster killing me slowly somedays; if not physically then

mentally. It is so hard to get up and face the day and be happy and

cheerful for my beautiful little girls. As I said I am a single mommy

and to be completely honest they are the shining light at the end of

my tunnel. I am very afraid for their futures; I know what I feel

everyday and hope with all my heart they never have to feel even a

minute of the pain I do everyday of my life. I am on Plaquenil for my

RA and prednisone. I am down to 10 mg; but was as high as 80mg daily.

I called the doctor today asking for some pain relief; and they

increased my steriods. I will never get off them at this point!! I do

very warm baths alot. I can only hope that things will get better. I

am walking in May 5K to raise money for Arthritis Foundation. I dont

care if I cry the whole walk; I am finishing the whole walk/run. I am

also part of the Joints in Motion group; training with a trainer for

a marathon......which I will end up walking. I was a long distance

runner for years; but I will finish this race!!! I just hope they can

figure out what is going on with me and help me feel better real

soon!!! Thank you again for all your words of support and kindness!

-- In , Kathe Sabetzadeh <lv2ryd@...> wrote:

>

> Hi :

>

> You have come to the right place for support and

> information. I have been with this group for four or

> five years now, and have learned so much more here

> than I ever could have on my own, or even through my

> doctors.

>

> I understand your urgency for a diagnosis, a name of

> the monster that is causing you so much pain so that

> you can fight it better. It sometimes takes a while

> to differentiate all of the immune system diseases as

> they can share symptoms, and even blood tests are not

> 100% effective in diagnosis at times. Your physical

> symptoms are where the doctors should be focusing -

> not everything is found in tests - your body is

> speaking for you, and you know yourself better than

> anybody.

>

> Until you get the diagnosis, you can always try the

> old hot showers/baths way of helping your pain, also

> rice socks are great on the joints, but at times ice

> is helpful to me as well. You just have to find out

> through trail and error. Does your doctor have you on

> any medication? You might want to see if he will try

> you on a steroid for a short while to see if this

> gives you some pain relief. You don't want to take it

> for long, but they can be great on the inflammation

> and pain.

>

> Please let us know what happens with you - we have all

> been where you are now and it's no fun, scary, and

> very overwhelming. We are here for you - you are no

> longer alone, okay?

> Kathe in CA

>

>

>

>

>

>

>

>

>

> " Until he extends the circle of his compassion to all living

things, man will not himself find peace. "

> — Albert Schweitzer, French Nobel Peace Prize-winning mission

doctor and theologian (1875-1965)

>

>

>

>

>

______________________________________________________________________

______________

> Looking for earth-friendly autos?

> Browse Top Cars by " Green Rating " at Autos' Green Center.

> http://autos./green_center/

>

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Thanks . I too felt 100% better on the Pred.

but finally I was able to wean off of it. There are

days like today when I miss it, but I am praying that

tommorrow will be a better day, aren't we all?, lol.

I had surgery to repair tarsal tunnel. Its similar to

carpal tunnel, but much rarer, its found in a lot of

RA females 40+.

Stay warm and take care.

Patti (Chicago)

" Taking it one day at a time! "

--- bp101_brat <bp101_brat@...> wrote:

>

> Patti~

> Thank you for your reply. What kind of surgery did

> you have??? Im

> sorry that it seems to have gotten worse since your

> surgery. I live

> in Central PA; and we too are known for the cold.

> Although till this

> week it has been in the 50's. So now we hit 20 and

> my joints are

> really bad. My doctor increased the ever popular

> prednisone. I will

> never get off of it; but when my dose is high I feel

> better. Take

> care of you and I hope all goes well with going back

> to work.

>

>

>

>

>

>

>

>

>

>

>

> >

> > > I was diagnosed with seronegative RA in April

> 2006.

> > > I was sulfasalazine

> > > and plaquenil. I saw my Rheumy on Jan 2 nd and

> now

> > > she is questioning

> > > Lupus; which my FMD has thought all along. I

> have

> > > seven of the eleven

> > > criteria for the diease. I am so frustrated and

> in

> > > sooo much pain. It

> > > seems that sometimes the doctors poo poo the

> > > symptoms as not being as

> > > bad as they are. Since my dx in 4/06 I was also

> > > diagnosed with

> > > eplilepsey after a car accident. So now it has

> > > affected my heart lung

> > > and CNS....and still wont give the diagnosis

> > > offically as RA/Lupus.

> > > Please understand that I dont want Lupus; but I

> need

> > > answers and I am

> > > soo tired of the pain and discomfort I live

> > > everyday. I am a single

> > > mommy of two little girls; 4 & 6 yrs old. So I

> have to

> > > be able to get out

> > > of bed in teh morning. If anyone has any ideas

> to

> > > help this really

> > > frustrated single mommy please let me know.

> > > Lots of Thanks,

> > >

> > >

> > >

> >

> >

> >

> >

> >

>

______________________________________________________________________

> ______________

> > Be a PS3 game guru.

> > Get your game face on with the latest PS3 news and

> previews at

> Games.

> >

> http://videogames./platform?platform=120121

> >

>

>

>

________________________________________________________________________________\

____

We won't tell. Get more on shows you hate to love

(and love to hate): TV's Guilty Pleasures list.

http://tv./collections/265

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, Welcome to the family!! You will find all the support you

need here. If you are having a bad day and need to vent, then go

right ahead and vent to us. We are all here for each other. It can

be difficult talking to someone who doesn't know anything about the

disease or talking to someone who doesn't understand what you are

going through just because " you don't look sick " . I've heard that

so many times that I started to think that I was a hypochondriac!!!

Then having to take care of two children on your own!! Geesh,

girl!!! They are at a great age. But, make sure that you take some

time for YOU!! You can't keep going without making a little time

for yourself. We are here for you. Don't be afraid to ask

questions. There are NO stupid questions, so please, don't hold it

all in. It will just eat at you and make your symptoms worse. So,

please ask anything that comes to mind, ok?!? Take care. I look

forward to hearing from you......Hugs and Prayers, marina

--- In , " bp101_brat " <bp101_brat@...>

wrote:

>

> I was diagnosed with seronegative RA in April 2006. I was

sulfasalazine

> and plaquenil. I saw my Rheumy on Jan 2 nd and now she is

questioning

> Lupus; which my FMD has thought all along. I have seven of the

eleven

> criteria for the diease. I am so frustrated and in sooo much pain.

It

> seems that sometimes the doctors poo poo the symptoms as not being

as

> bad as they are. Since my dx in 4/06 I was also diagnosed with

> eplilepsey after a car accident. So now it has affected my heart

lung

> and CNS....and still wont give the diagnosis offically as

RA/Lupus.

> Please understand that I dont want Lupus; but I need answers and I

am

> soo tired of the pain and discomfort I live everyday. I am a

single

> mommy of two little girls; 4 & 6 yrs old. So I have to be able to

get out

> of bed in teh morning. If anyone has any ideas to help this really

> frustrated single mommy please let me know.

> Lots of Thanks,

>

>

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great chatting with you today online melissa! hope we can hook up

again.

Faith

--- In , " bp101_brat " <bp101_brat@...>

wrote:

>

> I was diagnosed with seronegative RA in April 2006. I was

sulfasalazine

> and plaquenil. I saw my Rheumy on Jan 2 nd and now she is

questioning

> Lupus; which my FMD has thought all along. I have seven of the

eleven

> criteria for the diease. I am so frustrated and in sooo much pain.

It

> seems that sometimes the doctors poo poo the symptoms as not being

as

> bad as they are. Since my dx in 4/06 I was also diagnosed with

> eplilepsey after a car accident. So now it has affected my heart

lung

> and CNS....and still wont give the diagnosis offically as

RA/Lupus.

> Please understand that I dont want Lupus; but I need answers and I

am

> soo tired of the pain and discomfort I live everyday. I am a

single

> mommy of two little girls; 4 & 6 yrs old. So I have to be able to

get out

> of bed in teh morning. If anyone has any ideas to help this really

> frustrated single mommy please let me know.

> Lots of Thanks,

>

>

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