I have been on this drug for 7 years now

I have been on this drug for 7 years now

I've been using Betaseron for 3 months now, having switched from Copaxone. I find the Betaseron injections much easier to take and not at all painful; however, I continue to experience flu-like symptoms for hours following each injection. I've tried Tylenol, Ibuprofen, and aspirin, but I still get the deep aches, chills, headache, sometimes fever. Often my skin even hurts. I hope this stops soon.

I have been on this drug for 7 years now

I've been using Betaseron for 3 months now, having switched from Copaxone. I find the Betaseron injections much easier to take and not at all painful; however, I continue to experience flu-like symptoms for hours following each injection. I've tried Tylenol, Ibuprofen, and aspirin, but I still get the deep aches, chills, headache, sometimes fever. Often my skin even hurts. I hope this stops soon.

I've been on Betaseron for 6 years and have had no new lesions or relapses. I'd like to get off shots but am afraid other medications wouldn't be as effective for me.

I have been on this drug for 7 years now

I've been using Betaseron for 3 months now, having switched from Copaxone. I find the Betaseron injections much easier to take and not at all painful; however, I continue to experience flu-like symptoms for hours following each injection. I've tried Tylenol, Ibuprofen, and aspirin, but I still get the deep aches, chills, headache, sometimes fever. Often my skin even hurts. I hope this stops soon.

I've been on Betaseron for 6 years and have had no new lesions or relapses. I'd like to get off shots but am afraid other medications wouldn't be as effective for me.

Been on 14+ years. Extremely satisfied. Only one new lesion in 14 years of treatment. Just notified by my insurance company they will no longer cover this drug and want me to switch to something else.

I have been on this drug for 7 years now

I've been using Betaseron for 3 months now, having switched from Copaxone. I find the Betaseron injections much easier to take and not at all painful; however, I continue to experience flu-like symptoms for hours following each injection. I've tried Tylenol, Ibuprofen, and aspirin, but I still get the deep aches, chills, headache, sometimes fever. Often my skin even hurts. I hope this stops soon.

I've been on Betaseron for 6 years and have had no new lesions or relapses. I'd like to get off shots but am afraid other medications wouldn't be as effective for me.

Been on 14+ years. Extremely satisfied. Only one new lesion in 14 years of treatment. Just notified by my insurance company they will no longer cover this drug and want me to switch to something else.

Been on Betaseron for nearly 4 years now. Still get chills / aches if I forget to take acetaminophen with it. Also still have redness / inflammation at injection sites for several months afterwards. Have had 2 severe injection site reactions resulting in small open wounds & brusing. I manually inject (the auto-injector clicks loudly & makes me jump) & self-injection gets tiresome / difficult to do after awhile. -----BUT------ I have only had 1 mild relapse in 3.5 years while using Betaseron...I had 3 crippling (while occurring) relapses during the 1 year I used Copaxone. I'm sticking with Betaseron.

I have been on this drug for 7 years now

I've been using Betaseron for 3 months now, having switched from Copaxone. I find the Betaseron injections much easier to take and not at all painful; however, I continue to experience flu-like symptoms for hours following each injection. I've tried Tylenol, Ibuprofen, and aspirin, but I still get the deep aches, chills, headache, sometimes fever. Often my skin even hurts. I hope this stops soon.

I've been on Betaseron for 6 years and have had no new lesions or relapses. I'd like to get off shots but am afraid other medications wouldn't be as effective for me.

Been on 14+ years. Extremely satisfied. Only one new lesion in 14 years of treatment. Just notified by my insurance company they will no longer cover this drug and want me to switch to something else.

Been on Betaseron for nearly 4 years now. Still get chills / aches if I forget to take acetaminophen with it. Also still have redness / inflammation at injection sites for several months afterwards. Have had 2 severe injection site reactions resulting in small open wounds & brusing. I manually inject (the auto-injector clicks loudly & makes me jump) & self-injection gets tiresome / difficult to do after awhile. -----BUT------ I have only had 1 mild relapse in 3.5 years while using Betaseron...I had 3 crippling (while occurring) relapses during the 1 year I used Copaxone. I'm sticking with Betaseron.

flu like symptoms at first but doing very well. been on it for 8 years now. wouldn't trade it for nothing else.

I have been on this drug for 7 years now

I've been using Betaseron for 3 months now, having switched from Copaxone. I find the Betaseron injections much easier to take and not at all painful; however, I continue to experience flu-like symptoms for hours following each injection. I've tried Tylenol, Ibuprofen, and aspirin, but I still get the deep aches, chills, headache, sometimes fever. Often my skin even hurts. I hope this stops soon.

I've been on Betaseron for 6 years and have had no new lesions or relapses. I'd like to get off shots but am afraid other medications wouldn't be as effective for me.

Been on 14+ years. Extremely satisfied. Only one new lesion in 14 years of treatment. Just notified by my insurance company they will no longer cover this drug and want me to switch to something else.

Been on Betaseron for nearly 4 years now. Still get chills / aches if I forget to take acetaminophen with it. Also still have redness / inflammation at injection sites for several months afterwards. Have had 2 severe injection site reactions resulting in small open wounds & brusing. I manually inject (the auto-injector clicks loudly & makes me jump) & self-injection gets tiresome / difficult to do after awhile. -----BUT------ I have only had 1 mild relapse in 3.5 years while using Betaseron...I had 3 crippling (while occurring) relapses during the 1 year I used Copaxone. I'm sticking with Betaseron.

flu like symptoms at first but doing very well. been on it for 8 years now. wouldn't trade it for nothing else.

Betasearon seems to work very well for me. Not many side affects Very little to no pain taking the shot. Just don't stick it in the muscle...

I have been on this drug for 7 years now

I've been using Betaseron for 3 months now, having switched from Copaxone. I find the Betaseron injections much easier to take and not at all painful; however, I continue to experience flu-like symptoms for hours following each injection. I've tried Tylenol, Ibuprofen, and aspirin, but I still get the deep aches, chills, headache, sometimes fever. Often my skin even hurts. I hope this stops soon.

I've been on Betaseron for 6 years and have had no new lesions or relapses. I'd like to get off shots but am afraid other medications wouldn't be as effective for me.

Been on 14+ years. Extremely satisfied. Only one new lesion in 14 years of treatment. Just notified by my insurance company they will no longer cover this drug and want me to switch to something else.

Been on Betaseron for nearly 4 years now. Still get chills / aches if I forget to take acetaminophen with it. Also still have redness / inflammation at injection sites for several months afterwards. Have had 2 severe injection site reactions resulting in small open wounds & brusing. I manually inject (the auto-injector clicks loudly & makes me jump) & self-injection gets tiresome / difficult to do after awhile. -----BUT------ I have only had 1 mild relapse in 3.5 years while using Betaseron...I had 3 crippling (while occurring) relapses during the 1 year I used Copaxone. I'm sticking with Betaseron.

flu like symptoms at first but doing very well. been on it for 8 years now. wouldn't trade it for nothing else.

Betasearon seems to work very well for me. Not many side affects Very little to no pain taking the shot. Just don't stick it in the muscle...

My husband helps me with injections where I can't. He's extremely supportive of me.

I have been on this drug for 7 years now

I've been using Betaseron for 3 months now, having switched from Copaxone. I find the Betaseron injections much easier to take and not at all painful; however, I continue to experience flu-like symptoms for hours following each injection. I've tried Tylenol, Ibuprofen, and aspirin, but I still get the deep aches, chills, headache, sometimes fever. Often my skin even hurts. I hope this stops soon.

I've been on Betaseron for 6 years and have had no new lesions or relapses. I'd like to get off shots but am afraid other medications wouldn't be as effective for me.

Been on 14+ years. Extremely satisfied. Only one new lesion in 14 years of treatment. Just notified by my insurance company they will no longer cover this drug and want me to switch to something else.

Been on Betaseron for nearly 4 years now. Still get chills / aches if I forget to take acetaminophen with it. Also still have redness / inflammation at injection sites for several months afterwards. Have had 2 severe injection site reactions resulting in small open wounds & brusing. I manually inject (the auto-injector clicks loudly & makes me jump) & self-injection gets tiresome / difficult to do after awhile. -----BUT------ I have only had 1 mild relapse in 3.5 years while using Betaseron...I had 3 crippling (while occurring) relapses during the 1 year I used Copaxone. I'm sticking with Betaseron.

flu like symptoms at first but doing very well. been on it for 8 years now. wouldn't trade it for nothing else.

Betasearon seems to work very well for me. Not many side affects Very little to no pain taking the shot. Just don't stick it in the muscle...

My husband helps me with injections where I can't. He's extremely supportive of me.

I hesitated taking medication for my MS symptoms. When the right side of my face went numb and the toes on my feet went numb, I decided it was time. I no longer have new symptoms but the numbness is still an issue.

I have been on this drug for 7 years now

I've been using Betaseron for 3 months now, having switched from Copaxone. I find the Betaseron injections much easier to take and not at all painful; however, I continue to experience flu-like symptoms for hours following each injection. I've tried Tylenol, Ibuprofen, and aspirin, but I still get the deep aches, chills, headache, sometimes fever. Often my skin even hurts. I hope this stops soon.

I've been on Betaseron for 6 years and have had no new lesions or relapses. I'd like to get off shots but am afraid other medications wouldn't be as effective for me.

Been on 14+ years. Extremely satisfied. Only one new lesion in 14 years of treatment. Just notified by my insurance company they will no longer cover this drug and want me to switch to something else.

Been on Betaseron for nearly 4 years now. Still get chills / aches if I forget to take acetaminophen with it. Also still have redness / inflammation at injection sites for several months afterwards. Have had 2 severe injection site reactions resulting in small open wounds & brusing. I manually inject (the auto-injector clicks loudly & makes me jump) & self-injection gets tiresome / difficult to do after awhile. -----BUT------ I have only had 1 mild relapse in 3.5 years while using Betaseron...I had 3 crippling (while occurring) relapses during the 1 year I used Copaxone. I'm sticking with Betaseron.

flu like symptoms at first but doing very well. been on it for 8 years now. wouldn't trade it for nothing else.

Betasearon seems to work very well for me. Not many side affects Very little to no pain taking the shot. Just don't stick it in the muscle...

My husband helps me with injections where I can't. He's extremely supportive of me.

I hesitated taking medication for my MS symptoms. When the right side of my face went numb and the toes on my feet went numb, I decided it was time. I no longer have new symptoms but the numbness is still an issue.

It took me awhile to figure out that the stinging is mostly caused from the tiny air bubbles in the needle, once I figured that out it didn't sting as bad. Also this medication makes me tired all the time, even after getting a good night's sleep. That is one down fall that I don't like.

I have been on this drug for 7 years now

I've been using Betaseron for 3 months now, having switched from Copaxone. I find the Betaseron injections much easier to take and not at all painful; however, I continue to experience flu-like symptoms for hours following each injection. I've tried Tylenol, Ibuprofen, and aspirin, but I still get the deep aches, chills, headache, sometimes fever. Often my skin even hurts. I hope this stops soon.

I've been on Betaseron for 6 years and have had no new lesions or relapses. I'd like to get off shots but am afraid other medications wouldn't be as effective for me.

Been on 14+ years. Extremely satisfied. Only one new lesion in 14 years of treatment. Just notified by my insurance company they will no longer cover this drug and want me to switch to something else.

Been on Betaseron for nearly 4 years now. Still get chills / aches if I forget to take acetaminophen with it. Also still have redness / inflammation at injection sites for several months afterwards. Have had 2 severe injection site reactions resulting in small open wounds & brusing. I manually inject (the auto-injector clicks loudly & makes me jump) & self-injection gets tiresome / difficult to do after awhile. -----BUT------ I have only had 1 mild relapse in 3.5 years while using Betaseron...I had 3 crippling (while occurring) relapses during the 1 year I used Copaxone. I'm sticking with Betaseron.

flu like symptoms at first but doing very well. been on it for 8 years now. wouldn't trade it for nothing else.

Betasearon seems to work very well for me. Not many side affects Very little to no pain taking the shot. Just don't stick it in the muscle...

My husband helps me with injections where I can't. He's extremely supportive of me.

I hesitated taking medication for my MS symptoms. When the right side of my face went numb and the toes on my feet went numb, I decided it was time. I no longer have new symptoms but the numbness is still an issue.

It took me awhile to figure out that the stinging is mostly caused from the tiny air bubbles in the needle, once I figured that out it didn't sting as bad. Also this medication makes me tired all the time, even after getting a good night's sleep. That is one down fall that I don't like.

this has been the only drug for my ms my body has not rejected. i am happy . only issue I have is the stinging as medication is injected.

Went from rrms to spmm while I was on this drug. Worse decision I ever made as I was doing so well. I even received an apology from my Neuro

Went from rrms to spmm while I was on this drug. Worse decision I ever made as I was doing so well. I even received an apology from my Neuro

I have terrible site reactions and knots (scar tissue?) where I have injected for years. My body rejects the syringe at times because of these knots, I am running out of locations to use. Here is a tip to keep bubbles out, after mixing hold the syringe at an angle rather than straight up and down and draw it in slowly.

Went from rrms to spmm while I was on this drug. Worse decision I ever made as I was doing so well. I even received an apology from my Neuro

I have terrible site reactions and knots (scar tissue?) where I have injected for years. My body rejects the syringe at times because of these knots, I am running out of locations to use. Here is a tip to keep bubbles out, after mixing hold the syringe at an angle rather than straight up and down and draw it in slowly.

i found that holding the syringe in for a couple of seconds after injecting medication, my injection site bruises/marks ceased. it is really easy to use, much more so that when i was on avonex (ever see the size of that needle!) but i think it is a normal reaction to hesitate when you're going to stick a needle in yourself. oh, and btw, it had a profound effect on improving my health after a very frightening exacerbation.

Went from rrms to spmm while I was on this drug. Worse decision I ever made as I was doing so well. I even received an apology from my Neuro

I have terrible site reactions and knots (scar tissue?) where I have injected for years. My body rejects the syringe at times because of these knots, I am running out of locations to use. Here is a tip to keep bubbles out, after mixing hold the syringe at an angle rather than straight up and down and draw it in slowly.

i found that holding the syringe in for a couple of seconds after injecting medication, my injection site bruises/marks ceased. it is really easy to use, much more so that when i was on avonex (ever see the size of that needle!) but i think it is a normal reaction to hesitate when you're going to stick a needle in yourself. oh, and btw, it had a profound effect on improving my health after a very frightening exacerbation.

Have some skinsite reactions. Have redness that comes and goes. Depending if hot or cold.

Went from rrms to spmm while I was on this drug. Worse decision I ever made as I was doing so well. I even received an apology from my Neuro

I have terrible site reactions and knots (scar tissue?) where I have injected for years. My body rejects the syringe at times because of these knots, I am running out of locations to use. Here is a tip to keep bubbles out, after mixing hold the syringe at an angle rather than straight up and down and draw it in slowly.

i found that holding the syringe in for a couple of seconds after injecting medication, my injection site bruises/marks ceased. it is really easy to use, much more so that when i was on avonex (ever see the size of that needle!) but i think it is a normal reaction to hesitate when you're going to stick a needle in yourself. oh, and btw, it had a profound effect on improving my health after a very frightening exacerbation.

Have some skinsite reactions. Have redness that comes and goes. Depending if hot or cold.

This has been easy to inject with the provided betaject system and I have learned when and how to massage the injection site when I did not get all the bubbles out. Learning to get all the bubbles out is the trick...they STING when they go in!

Went from rrms to spmm while I was on this drug. Worse decision I ever made as I was doing so well. I even received an apology from my Neuro

I have terrible site reactions and knots (scar tissue?) where I have injected for years. My body rejects the syringe at times because of these knots, I am running out of locations to use. Here is a tip to keep bubbles out, after mixing hold the syringe at an angle rather than straight up and down and draw it in slowly.

i found that holding the syringe in for a couple of seconds after injecting medication, my injection site bruises/marks ceased. it is really easy to use, much more so that when i was on avonex (ever see the size of that needle!) but i think it is a normal reaction to hesitate when you're going to stick a needle in yourself. oh, and btw, it had a profound effect on improving my health after a very frightening exacerbation.

Have some skinsite reactions. Have redness that comes and goes. Depending if hot or cold.

This has been easy to inject with the provided betaject system and I have learned when and how to massage the injection site when I did not get all the bubbles out. Learning to get all the bubbles out is the trick...they STING when they go in!

I've been using this Betaseron medication twice since 1999. For a short period of time I switched to another, but came right back to the Betaseron. I had only one relapse,and that was in 2009.

Went from rrms to spmm while I was on this drug. Worse decision I ever made as I was doing so well. I even received an apology from my Neuro

I have terrible site reactions and knots (scar tissue?) where I have injected for years. My body rejects the syringe at times because of these knots, I am running out of locations to use. Here is a tip to keep bubbles out, after mixing hold the syringe at an angle rather than straight up and down and draw it in slowly.

i found that holding the syringe in for a couple of seconds after injecting medication, my injection site bruises/marks ceased. it is really easy to use, much more so that when i was on avonex (ever see the size of that needle!) but i think it is a normal reaction to hesitate when you're going to stick a needle in yourself. oh, and btw, it had a profound effect on improving my health after a very frightening exacerbation.

Have some skinsite reactions. Have redness that comes and goes. Depending if hot or cold.

This has been easy to inject with the provided betaject system and I have learned when and how to massage the injection site when I did not get all the bubbles out. Learning to get all the bubbles out is the trick...they STING when they go in!

I've been using this Betaseron medication twice since 1999. For a short period of time I switched to another, but came right back to the Betaseron. I had only one relapse,and that was in 2009.

I have been on Betaseron for 16 years. At different times I have had problems with injection site reactions and flu-like symptoms but overall I have remained extremely healthy which I attribute to being on the medication. I feel very fortunate.

Went from rrms to spmm while I was on this drug. Worse decision I ever made as I was doing so well. I even received an apology from my Neuro

I have terrible site reactions and knots (scar tissue?) where I have injected for years. My body rejects the syringe at times because of these knots, I am running out of locations to use. Here is a tip to keep bubbles out, after mixing hold the syringe at an angle rather than straight up and down and draw it in slowly.

i found that holding the syringe in for a couple of seconds after injecting medication, my injection site bruises/marks ceased. it is really easy to use, much more so that when i was on avonex (ever see the size of that needle!) but i think it is a normal reaction to hesitate when you're going to stick a needle in yourself. oh, and btw, it had a profound effect on improving my health after a very frightening exacerbation.

Have some skinsite reactions. Have redness that comes and goes. Depending if hot or cold.

This has been easy to inject with the provided betaject system and I have learned when and how to massage the injection site when I did not get all the bubbles out. Learning to get all the bubbles out is the trick...they STING when they go in!

I've been using this Betaseron medication twice since 1999. For a short period of time I switched to another, but came right back to the Betaseron. I had only one relapse,and that was in 2009.

I have been on Betaseron for 16 years. At different times I have had problems with injection site reactions and flu-like symptoms but overall I have remained extremely healthy which I attribute to being on the medication. I feel very fortunate.

I was allergic to copaxone, tried rebif and was sick with every shot and my liver enzymes started climbing, so my doctor switched me to betaseron. I have to mix it so it takes more time to prepare but my liver enzymes, after 6 months on it, are back to normal, and I have only had two times when I was sick. Normally I just have a mild headache that tylenol takes care of. My MRI was good with no new lesions, so my doctor and I are both happy.