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Hi-

I'm new to the group and have been lurking for a few weeks. I just

had my first Remicade treatment on Monday(I have RA and fibro)and

haven't been responsive in a consistent way to any of the drugs I've

taken (MTX, plaqunil,(sp) predinisone,(sp) etc)....and I'm wondering

what to expect. I guess I naivelly believed that I would wake up this

morning feeling like my old self. I've been so sad because nothing

feels different yet. My dr. didn't tell me what to expect and I've

done some reading on the web all of which suggest that things will

get better - if I respond to the medicine...but none talk about the

journey towards improvement. So, I quess I wanted to know what the

journey has been like for others on these types of drugs. What can I

expect. (I know everyone is different but I want to get a sense about

the range of possiblities.)

Any information would be helpful.

Thanks!

in IL

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Guest guest

Welcome . I'm not on Remicade so I can't give you any personal

experience. We have many members on it, all with different

experiences. Sometimes it takes a few infusions to feel improvement.

Everyone is different. Hopefully you will respond and feel better

soon.

a

On Wed, 09 Mar 2005 04:15:47 -0000, IndyMochaMom

<kcrawfords@...> wrote:

>

>

> Hi-

>

> I'm new to the group and have been lurking for a few weeks. I just

> had my first Remicade treatment on Monday(I have RA and fibro)and

> haven't been responsive in a consistent way to any of the drugs I've

> taken (MTX, plaqunil,(sp) predinisone,(sp) etc)....and I'm wondering

> what to expect. I guess I naivelly believed that I would wake up this

> morning feeling like my old self. I've been so sad because nothing

> feels different yet. My dr. didn't tell me what to expect and I've

> done some reading on the web all of which suggest that things will

> get better - if I respond to the medicine...but none talk about the

> journey towards improvement. So, I quess I wanted to know what the

> journey has been like for others on these types of drugs. What can I

> expect. (I know everyone is different but I want to get a sense about

> the range of possiblities.)

>

> Any information would be helpful.

>

> Thanks!

>

> in IL

>

>

>

>

>

>

>

>

>

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Guest guest

Welcome . I'm not on Remicade so I can't give you any personal

experience. We have many members on it, all with different

experiences. Sometimes it takes a few infusions to feel improvement.

Everyone is different. Hopefully you will respond and feel better

soon.

a

On Wed, 09 Mar 2005 04:15:47 -0000, IndyMochaMom

<kcrawfords@...> wrote:

>

>

> Hi-

>

> I'm new to the group and have been lurking for a few weeks. I just

> had my first Remicade treatment on Monday(I have RA and fibro)and

> haven't been responsive in a consistent way to any of the drugs I've

> taken (MTX, plaqunil,(sp) predinisone,(sp) etc)....and I'm wondering

> what to expect. I guess I naivelly believed that I would wake up this

> morning feeling like my old self. I've been so sad because nothing

> feels different yet. My dr. didn't tell me what to expect and I've

> done some reading on the web all of which suggest that things will

> get better - if I respond to the medicine...but none talk about the

> journey towards improvement. So, I quess I wanted to know what the

> journey has been like for others on these types of drugs. What can I

> expect. (I know everyone is different but I want to get a sense about

> the range of possiblities.)

>

> Any information would be helpful.

>

> Thanks!

>

> in IL

>

>

>

>

>

>

>

>

>

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Guest guest

Hi, !! Welcome to the group! I was on Remicade for about 10

months before I was switched to Enbrel. Well, what can I tell

you...hmm. For one thing, make sure you take either Zyrtec,

Benadryl or what ever your rheumy may have told you as well as some

Tylenol. They want you to have this in your system to help decrease

the side effects. Personally, I did not take the allergy meds

because I was getting enough protection from the prednisone, but

follow what ever you were told to do. It is given over about 2

hours by infusion. They will check your vital signs periodically

during the infusion to make sure your temp, blood pressure, and

heart rate are ok. If you start to feel anything, let the nurse

know. I would occasionally feel flushed (like a hot flash) and a

little light headed. I always to a book and my gameboy to kill

time. They had a TV in there, but I always went late morning so

they always watched Dr. Phil--I went through a lot of books and got

really good at the gameboy!! Anyway, you may want to have someone

drive you in the first time, and if you live far away, for all your

infusions. Reason being, most people I have talked to, myself

included, gets very tired afterwards. For me it usually kicked in

with in an hour. I would go home and just sleep most of the day

away. I tried to go to work once after an infusion and chose not to

do that ever again!! One other tip, you may want to eat a little

something before the infusion as well. It does help. If you have

any specific questions, feel free to email me...Take care...Marina

--- In , " IndyMochaMom " <kcrawfords@s...>

wrote:

>

>

> Hi-

>

> I'm new to the group and have been lurking for a few weeks. I just

> had my first Remicade treatment on Monday(I have RA and fibro)and

> haven't been responsive in a consistent way to any of the drugs

I've

> taken (MTX, plaqunil,(sp) predinisone,(sp) etc)....and I'm

wondering

> what to expect. I guess I naivelly believed that I would wake up

this

> morning feeling like my old self. I've been so sad because nothing

> feels different yet. My dr. didn't tell me what to expect and I've

> done some reading on the web all of which suggest that things will

> get better - if I respond to the medicine...but none talk about

the

> journey towards improvement. So, I quess I wanted to know what the

> journey has been like for others on these types of drugs. What can

I

> expect. (I know everyone is different but I want to get a sense

about

> the range of possiblities.)

>

> Any information would be helpful.

>

> Thanks!

>

> in IL

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Share on other sites

Guest guest

Hi, !! Welcome to the group! I was on Remicade for about 10

months before I was switched to Enbrel. Well, what can I tell

you...hmm. For one thing, make sure you take either Zyrtec,

Benadryl or what ever your rheumy may have told you as well as some

Tylenol. They want you to have this in your system to help decrease

the side effects. Personally, I did not take the allergy meds

because I was getting enough protection from the prednisone, but

follow what ever you were told to do. It is given over about 2

hours by infusion. They will check your vital signs periodically

during the infusion to make sure your temp, blood pressure, and

heart rate are ok. If you start to feel anything, let the nurse

know. I would occasionally feel flushed (like a hot flash) and a

little light headed. I always to a book and my gameboy to kill

time. They had a TV in there, but I always went late morning so

they always watched Dr. Phil--I went through a lot of books and got

really good at the gameboy!! Anyway, you may want to have someone

drive you in the first time, and if you live far away, for all your

infusions. Reason being, most people I have talked to, myself

included, gets very tired afterwards. For me it usually kicked in

with in an hour. I would go home and just sleep most of the day

away. I tried to go to work once after an infusion and chose not to

do that ever again!! One other tip, you may want to eat a little

something before the infusion as well. It does help. If you have

any specific questions, feel free to email me...Take care...Marina

>

>

> Hi-

>

> I'm new to the group and have been lurking for a few weeks. I just

> had my first Remicade treatment on Monday(I have RA and fibro)and

> haven't been responsive in a consistent way to any of the drugs

I've

> taken (MTX, plaqunil,(sp) predinisone,(sp) etc)....and I'm

wondering

> what to expect. I guess I naivelly believed that I would wake up

this

> morning feeling like my old self. I've been so sad because nothing

> feels different yet. My dr. didn't tell me what to expect and I've

> done some reading on the web all of which suggest that things will

> get better - if I respond to the medicine...but none talk about

the

> journey towards improvement. So, I quess I wanted to know what the

> journey has been like for others on these types of drugs. What can

I

> expect. (I know everyone is different but I want to get a sense

about

> the range of possiblities.)

>

> Any information would be helpful.

>

> Thanks!

>

> in IL

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