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hi there, almost passed you by....lol. Hope this site helps, I know

it's helped me. I don't post very often, but read a lot. Good luck.

Laurie

> I was just Diagnosed with autoimmune hep last month after doing

test since Aug. They only found out i had it as i went to emergency

room for another matter. had biop last month and thats what the doc

said i had. was worried alot as i have never heard of this. I am on

prednisone right now and waiting on more blood work to be done. so

hope this is a nice place to talk about this.

>

>

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

>

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Welcome what kept you so long before you found use? It is really nice to meat you I was dx AIH on 1998. If you feel the need to ask questions or just to vent feel free you have come to the right place. Jeanette UK AIHdx 1998 Cirrhosis dx 2001

PS what is your name? what medication are you on?. homeatrl <homeatrl@...> wrote: hi there, almost passed you by....lol. Hope this site helps, I know it's helped me. I don't post very often, but read a lot. Good luck. Laurie> I was just Diagnosed with autoimmune hep last month after doing test since Aug. They only found out i had it as i went to emergency room for another matter. had biop last month and thats what the doc said i had. was worried alot as i have never heard of this. I am on prednisone right now and waiting on more blood work to be done. so hope this is a nice place to talk about this. > > > --------------------------------->

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  • 4 months later...
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Hi Toni,

Glad you found us. We definitely know what you are going through. I am 35,

divorced, and a mother of a 6-year old. I was diagnosed with RA 2 years ago

and have found great comfort in this group. If you have any questions, all

you have to do is ask and there is always someone in this group that either

knows the answer or can help you find it. The support that I have found here

has saved my sanity. Welcome.

Love and Hugs

Stacey in PA

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Hi Toni...welcome! My name is Tess...soon to be 51, single, mom of 4,

grandma to 2.

I was first diagnosed with " sero-negative lupus " and " mixed connective

tissue disease " in 1980 at the age of 29. 4 years ago the rheummy

decided I had Rheumatoid Arthritis, Psoriatic arthritis and

fibromyalgia. I have my good days & bad days, but have done better

since starting Remicade treatments last winter. I also take

methotrexate injections.

There are so many sweet, courageous people here, and answers to most

questions you will have. I'm glad you've found us...I hope you feel

better everyday.

In Hope...

Tess

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Hi Toni. My name's Carol, and I live in Florida. I'm 36 and was diagnosed

with RA last February. We're still trying to get my RA under control.

Presently I'm on Methotrexate and Plaquenil, among other things.

There are a lot of caring people in this group, as well as great information

on RA. This group has really helped me to cope with the changes RA has

brought to my life.

We're glad to have you!

Hugs,

Carol

[ ] Hi I am a new member

Hi My name is Toni I am a 32 year old female that has Rheumatiod

Arthritis and I am looking to make some new friends that also know

what it is like to suffer from this. I hope to hear from someone

soon.

Thank You

Toni

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Hi Toni,

My name is Gail and I'm in my early 50's...have suffered with RA for 12

years.

You have come to the right place for support and love and comfort. It's like we

all understand where each is coming from....and we understand each others pain.

Feel free to vent your aches and frustrations...there are some very sweet and

knowledgeable women on the list. Hope you can find some comfort here. I Have.

Gail

[ ] Hi I am a new member

Hi My name is Toni I am a 32 year old female that has Rheumatiod

Arthritis and I am looking to make some new friends that also know

what it is like to suffer from this. I hope to hear from someone

soon.

Thank You

Toni

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Hi Toni:

Welcome - I am 48 and have been diagnosed with RA for

three years now. Currently I am on Methotrexate,

Arava, and Bextra, as well as other medications for

chronic asthma and allergies. Waiting for that

elusive Embrel! I am maintaining for the most part

pretty well, have good days and bad days like we all

do, but consider myself fortunate to still be able to

be as active as I am. Some activities and things have

had to be given up because of the RA but I am still

able to ride my horse fairly often so I am very lucky.

My husband and my two kids are very supportive of me

and help out when needed although I hate asking them

for help and admitting I cannot do something that I

used to have no problem with. Even if you don't post

very often just reading the posts of others in the

group has been very helpful to me. You will learn a

lot from people in this group, very knowledgeable and

supportive souls here, and I am happy you have found

your way to us.

Kathe in CA

__________________________________________________

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Hi Toni--your reading about my situation with Joe and all the support I am

getting -- there is no better place for you to be then here in the comfort

and thoughts of these folks! Seems weird that sometimes you get more

support from cyber friends then family support. My hubby Joe is 33 and has

RA and OA. His main meds are Enbrel--which he LOVES! He is still on

Metho--cant seem to come lower then the 8 pills a week. Celebrex, Folic

Acid, Calcium, Magnesium, Allegra for allergys, Univas for High BP.....I

think thats it. Ask away -- this is a great group of friends!

and Joe in PA

[ ] Hi I am a new member

> Hi My name is Toni I am a 32 year old female that has Rheumatiod

> Arthritis and I am looking to make some new friends that also know

> what it is like to suffer from this. I hope to hear from someone

> soon.

>

> Thank You

> Toni

>

>

>

>

>

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Guest guest

Hello Toni, I will be 52 the 22nd of this month and have had RA for

15 years, I am presently on Methotrexate injections, folic acid and

Lodine XL. They have tried me on Remicade, gold shots, Arava,

Enbrel, Kineret, Plaquinel and Sulfazaladine, none of which did any

good, but many of the people on this site have had success with many

of these, so thats good. Methotrexate has worked the best for me and

makes it so I am able to move around with less pain. My

Rhuematologist told me last week that we are doing as much as we can

until they come out with more meds to try and my sed rate is down

more than last blood work.

I have two children boy (30) and girl (29), and 6 grandchildren, 5

girls and 1 boy. They are my life. I also have a husband (Fred)of

31 years that keeps me going.

I am having trouble with my right wrist, carpel tunnel I think,will

know Tuesday after the nerve conduction test. I am lucky because I

have had very little damage from the RA.

Since joining this group I have learned more than I have the whole 15

years about this disease. Hope you enjoy your membership and it is

nice to talk to people who can understand your pain.

in WA

Can you tell us more about yourself so we can get to know you better?

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Hi this is Toni again thank you all for your welcoming letters I really

appericated all of them I was diagnosed about 5 years ago and so far the only

thing that has been helping me is Celabrex. My doctor last Tuesday started me on

Azulfidine which I think I am unable to take as it makes me feel as though I am

drunk and causes me to be very light headed and vomit I am waiting to her from

her still to find out what is going on. On top of having Ra I also suffer with

depression and panic attacks. I can no longer do so much that I use to do that

it makes me mad. I am also married and have been married for 13 years now and we

have no children but we do have alot of neices and nephews which is great !!!

Anyway thanks again so much for making me feel welcome I hope to learn more from

all of you and to make some long lasting friendships.. Toni

staceycrwfrd@... wrote:

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

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