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Hi Ann, I was on Remicade from July 07 till May 08, I only stopped it because I

got an infection after each treatment but one, so my new rheumy said let's try

something else, I will be going to Orencia. As far as the treatments go, they

were so easy, I never had one problem. I know three other people who have been

on it for some time and it has been a lifesaver for them. I think you just have

to try until you find the right one. I will only do an infusion biologic

because I like the idea of an RN there if I have a problem (I'm a big chicken).

As far as lymphoma goes, I asked my old rheumy that and his reply was that RA

can cause cancer alone and the risks are small. Remember, it's the quality not

the quantity. in PA

[ ] remicade

i am 56 years old had ra since i was 32.been on all meds. now doc wants me to

go on

remicade.is there any one over 50 on remicade.have you has any side effects.

i read material on this med. it can cause lymphoma,or other cancers.need some

input.i don't post much,but i read all.

your help will be appreciated.thanks

ann

nj

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  • 1 month later...

I would talk to your rheumy. Mtx is normally used along w/ remicade;

but there are other oral medications. When I was getting my remicade

infusions, I took arava instead of mtx. It was a great combination

for me.

>

> I just got back from seeing my GI Doc. She's thinking that even

though my

> Crohn's has been in remission or only causing a little trouble,

that trying

> Remicade would be a good idea. It might knock out both Crohn's and

RA.

>

> She's going to call the Rheum and get his opinion.

>

> It sounds a little scary, but she said most people don't get sick

from it

> and I do get sick from Mtx.

>

> How many of you have had it?

>

> dd

>

>

>

> **************It's only a deal if it's where you want to go. Find

your travel

> deal here.

> (http://information.travel.aol.com/deals?ncid=aoltrv00050000000047)

>

>

>

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In a message dated 8/26/2008 11:01:07 A.M. Central Daylight Time,

megan_hartman@... writes:

>I started Remicade at the beginning of the summer, after 6 months of

Enbrel did nothing for me. It took a few treatments and some

adjusting to the dose, but Remicade is the first thing that has

treated all of my symptoms. I take it along with weekly MTX

injections. >

If it took care of the pain AND the fatigue, I think I would feel like

normal again.

dd

**************It's only a deal if it's where you want to go. Find your travel

deal here.

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DD -

I started Remicade at the beginning of the summer, after 6 months of

Enbrel did nothing for me. It took a few treatments and some

adjusting to the dose, but Remicade is the first thing that has

treated all of my symptoms. I take it along with weekly MTX

injections.

Let us know what your RA doc says!

>

> I just got back from seeing my GI Doc. She's thinking that even

though my

> Crohn's has been in remission or only causing a little trouble,

that trying

> Remicade would be a good idea. It might knock out both Crohn's and

RA.

>

> She's going to call the Rheum and get his opinion.

>

> It sounds a little scary, but she said most people don't get sick

from it

> and I do get sick from Mtx.

>

> How many of you have had it?

>

> dd

>

>

>

> **************It's only a deal if it's where you want to go. Find

your travel

> deal here.

> (http://information.travel.aol.com/deals?ncid=aoltrv00050000000047)

>

>

>

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Good luck DD,

I have not tried Remicade, but have heard great stories from other's.

It does seem scary, but when you start feeling better, it's so worth

it, keep us posted, Tawny

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hi lisa oh my gosh i've been on prednisone for over 33yrs. mtx for9yrs.and last

but least forteo inject. for

5yrs. i'm still in pain,have morning stiffness every single day of my life.

there's more meds but they make

me sick.my throat feels the same way, very dry hard to swallow. sinuses never

had them before but i get it to thepoint i had to b put in the hospital. it sux

but ideal........

god bless,melyndagamez 8/26/08 10:25p.m.central

[ ] Remicade

Hi everyone,

I was diagnosed with RA last Jan, and started mtx. in April.  Actually

I've had the disease for 22 years but it was mild and undiagnosed.  By

last Jan. I was very sick and had already had two hip replacements.

The mtx. did nothing for me so I moved on to Enbrel.  It was better

than nothing but I still was not functioning well and had loads of

pain.  So I finally got Remicade and boy did I feel a difference.  My

throat feels raw and my sinuses are blocked but I'll take it for

pain-free joints.

The bummer is this:  Every site I read seems to indicate that Remicade

will only last for a time.  After a year or two or five, people build

up antibodies to the med.  Is there anyone here who has been on a

therapy longer than five years?

Thanks,

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

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Hi Melynda,

Prednisone worked pretty well for me but of course the docs push us to get off

ASAP. Glad

to hear that you can still take it even if not ideal.

>

> hi lisa oh my gosh i've been on prednisone for over 33yrs. mtx for9yrs.and

last but

least forteo inject. for

> 5yrs. i'm still in pain,have morning stiffness every single day of my life.

there's more

meds but they make

> me sick.my throat feels the same way, very dry hard to swallow. sinuses never

had them

before but i get it to thepoint i had to b put in the hospital. it sux but

ideal........

> god bless,melyndagamez 8/26/08 10:25p.m.central

>

>

>

> [ ] Remicade

>

> Hi everyone,

>

> I was diagnosed with RA last Jan, and started mtx. in April.  Actually

> I've had the disease for 22 years but it was mild and undiagnosed.  By

> last Jan. I was very sick and had already had two hip replacements.

> The mtx. did nothing for me so I moved on to Enbrel.  It was better

> than nothing but I still was not functioning well and had loads of

> pain.  So I finally got Remicade and boy did I feel a difference.  My

> throat feels raw and my sinuses are blocked but I'll take it for

> pain-free joints.

>

> The bummer is this:  Every site I read seems to indicate that Remicade

> will only last for a time.  After a year or two or five, people build

> up antibodies to the med.  Is there anyone here who has been on a

> therapy longer than five years?

>

> Thanks,

>

>

>

>

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

>

>

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  • 1 month later...

dd and group;

I am so happy your Remicade has been approved.. I waited about 2

months before they approved my humirra.. I began to worry... I

just took my third shot this evening.. It's like a rush for a junky

haaaaaaaaaaaaa. No I don't get a rush but just a figure of speech..

gentle hugs

Clora

> I got a call today that Remicade has been approved. My first

infusion is

> October 14th. I also got the blood work back from my RA doc. He

didn't seem to

> excited about giving me Remicade when he did it. It was

recommended by my GI

> doc and PC.

>

> But he wrote a note on the blood work and said my inflammation

level is high

>

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Hi dd,

Glad your approved for Remicade, and your getting it soon! I've heard

it does help with Crohn's too. I pray it will work well for you, and

able to stay on it for awhile.

They should keep a watch on your lab work. It sounds like you have some

super docs. Let us know how it works for you, Tawny

>

> I got a call today that Remicade has been approved. My first infusion

is

> October 14th. I also got the blood work back from my RA doc. He didn't

seem to

> excited about giving me Remicade when he did it. It was recommended by

my GI

> doc and PC.

>

> But he wrote a note on the blood work and said my inflammation level

is high

> again and it is a good thing I am starting Remicade. CRP was 7.6 and

high

> should be .9. Liver is still ok. Hemoglobin is back in normal range.

>

> I'm anxious to see if the Remicade will alleviate some Crohn's

symptoms and

> take away fatigue. That would be a miracle.

>

> btw, I'm O positive and have never had the drug you are talking about.

>

> dd

>

>

>

> **************New MapQuest Local shows what's happening at your

destination.

> Dining, Movies, Events, News & more. Try it out!

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>

>

>

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  • 2 weeks later...

I had my first infusion today. It didn't take as long as I thought it would

-- I still had to watch the end of the movie they gave me.

I'm really tired tonight and don't know if it's related or not. At one

point, I got a weird taste in my mouth -- no other problems.

The only bad thing was the music the nurse was playing. I usually like

classical music, but this was more like new age. The stuff that is supposed to

calm you down? I find it so annoying it cranks me up. She gave me earphones for

my movie to drown it out and that helped. I had forgotten my library book and

that would never have worked.

Next time I will stop by Red Box and get a current movie that I really would

like to see and I will bring the kind of headphones you use for shooting in

case I want to read. I will also ask for the chair away from the music if

it's available.

Will let you know if my symptoms get better -- so far no change.

dd

**************New MapQuest Local shows what's happening at your destination.

Dining, Movies, Events, News & more. Try it out

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dd,

I hope anything negative will stary far away from you. Get some good

rest tonight.

Shirley

>

> I had my first infusion today. It didn't take as long as I thought

it would

> -- I still had to watch the end of the movie they gave me.

>

> I'm really tired tonight and don't know if it's related or not. At

one

> point, I got a weird taste in my mouth -- no other problems.

>

> The only bad thing was the music the nurse was playing. I usually

like

> classical music, but this was more like new age. The stuff that is

supposed to

> calm you down? I find it so annoying it cranks me up. She gave me

earphones for

> my movie to drown it out and that helped. I had forgotten my

library book and

> that would never have worked.

>

> Next time I will stop by Red Box and get a current movie that I

really would

> like to see and I will bring the kind of headphones you use for

shooting in

> case I want to read. I will also ask for the chair away from the

music if

> it's available.

>

> Will let you know if my symptoms get better -- so far no change.

>

> dd

> **************New MapQuest Local shows what's happening at your

destination.

> Dining, Movies, Events, News & more. Try it out

> (http://local.mapquest.com/?ncid=emlcntnew00000002)

>

>

>

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  • 2 weeks later...

DD,

Question...

Should you take your Remicade and MTX on the same day? Isn't that too much

on one day? I know it's different for everyone, just curious. I take my

Enbrel on Monday, and MTX on Thursday.

Heidi in Mass.

In a message dated 10/26/2008 9:05:22 P.M. Eastern Daylight Time,

dgd301@... writes:

I'm supposed to get my 2nd Remicade infusion tomorrow. I've had a runny nose

this week, so will tell the nurse about it and see what she says.

I also take my Mtx tomorrow. It still makes me feel icky for a couple of

days. I wonder about injections, but haven't brought it up yet.

So far the Remicade has improved my intestinal problems, but my main problem

from RA right now is fatigue and it hasn't helped that so much.

Now that I'm down to 5 mg of Prednisone, my heart is not beating as fast as

it was, so I'm gradually getting better.

dd

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