› Forums › General Melanoma Community › Interferon treatment #1
- This topic has 22 replies, 9 voices, and was last updated 13 years, 2 months ago by Donna M..
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- September 20, 2011 at 1:08 pm
well, no nausea, but I have chills, headache and very much fatigue. I wanted to know if everyone who has interferon has to be stuck with a new iv everyday? I am afraid I will run out of good veins.
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well, no nausea, but I have chills, headache and very much fatigue. I wanted to know if everyone who has interferon has to be stuck with a new iv everyday? I am afraid I will run out of good veins.
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- Replies
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- September 20, 2011 at 1:15 pm
I just completed 11 months of interferon. That first month I had a port put in so I would not have to get a new IV everyday. I highly recommend this. Some others had a pick line done. There is more potential for infection that way though. Good luck to you on your treatments.
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- September 20, 2011 at 1:15 pm
I just completed 11 months of interferon. That first month I had a port put in so I would not have to get a new IV everyday. I highly recommend this. Some others had a pick line done. There is more potential for infection that way though. Good luck to you on your treatments.
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- September 20, 2011 at 2:13 pm
Will keep my fingers crossed for you that your side effects become milder as time goes on as mine did. I only had the fever and chills for one night.
I opted to have a PICC line placed rather than get a new IV everyday. They can also draw blood from it for those twice a week blood tests, so there are no "sticks" at all. You might want to look into that. It was a very simple procedure to have it placed, the only downside is that you can't get it wet. If you do decide to do the PICC line, check out the protector that I use to keep it dry. You can find it at drycorp.com.
Feel better!
Donna M.
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- September 20, 2011 at 2:13 pm
Will keep my fingers crossed for you that your side effects become milder as time goes on as mine did. I only had the fever and chills for one night.
I opted to have a PICC line placed rather than get a new IV everyday. They can also draw blood from it for those twice a week blood tests, so there are no "sticks" at all. You might want to look into that. It was a very simple procedure to have it placed, the only downside is that you can't get it wet. If you do decide to do the PICC line, check out the protector that I use to keep it dry. You can find it at drycorp.com.
Feel better!
Donna M.
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- September 20, 2011 at 2:26 pm
I'm 9 months into Interferon. I had a pic line inserted every Monday and Removed after Fridays dose was completed. Good Luck, I hope everything goes well for you.
scot
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- September 20, 2011 at 2:58 pm
Vicki,
I had a fresh stick every day, except ….I did my infusion during the holidays, so a couple of times I had to have a picc line inserted, then get my infusion at the hospital, since the clinic was closed. I'll tell you that my skin is so sensitive that the picc line drove me nuts. I hated it. I know others who've had a port inserted, and maybe that is better, but I was happy to just have a fresh stick. plus.. in the 8 yrs since then, I've had many many IV's and blood draws and never run out of veins. AND…since my left arm is a 'no stick' arm, all of these things have happend on my right arm.
Drink a lot of water and it will help them get into those veins. You'll need to be drinking a lot anyway with the interferon, which dries out your whole system
Good luck! hope this month goes by quickly for you.
dian in spokane
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- September 20, 2011 at 2:58 pm
Vicki,
I had a fresh stick every day, except ….I did my infusion during the holidays, so a couple of times I had to have a picc line inserted, then get my infusion at the hospital, since the clinic was closed. I'll tell you that my skin is so sensitive that the picc line drove me nuts. I hated it. I know others who've had a port inserted, and maybe that is better, but I was happy to just have a fresh stick. plus.. in the 8 yrs since then, I've had many many IV's and blood draws and never run out of veins. AND…since my left arm is a 'no stick' arm, all of these things have happend on my right arm.
Drink a lot of water and it will help them get into those veins. You'll need to be drinking a lot anyway with the interferon, which dries out your whole system
Good luck! hope this month goes by quickly for you.
dian in spokane
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- September 20, 2011 at 9:29 pm
I had high dose interfon treatments everyday for 30 days. I had a port put it and it was worth it. No pain or issues with the port, but made the treatments very easy. Sorry about the chills and nausea – I experienced those too. Once I saw the pattern, I would come home from treatment and get a little done around the house while I felt OK, then take a hot bath to deal with the chills and rest for the afternoon watching TV – only time in my life I was able to watch Oprah every day as was usually at work! Take care – I know you may experience a lot of side effects, but you can do it!
Patricia, stage IIIA
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- September 20, 2011 at 9:29 pm
I had high dose interfon treatments everyday for 30 days. I had a port put it and it was worth it. No pain or issues with the port, but made the treatments very easy. Sorry about the chills and nausea – I experienced those too. Once I saw the pattern, I would come home from treatment and get a little done around the house while I felt OK, then take a hot bath to deal with the chills and rest for the afternoon watching TV – only time in my life I was able to watch Oprah every day as was usually at work! Take care – I know you may experience a lot of side effects, but you can do it!
Patricia, stage IIIA
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- September 20, 2011 at 11:52 pm
Hang in there…the first nights are the roughest. I opted to get a fresh line every day. It was just easier for me, but you need to do what is best for you. Make sure you drink lots of water and sleep as much as possible. Best of luck with the rest of your treatments!
Tricia
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- September 20, 2011 at 11:52 pm
Hang in there…the first nights are the roughest. I opted to get a fresh line every day. It was just easier for me, but you need to do what is best for you. Make sure you drink lots of water and sleep as much as possible. Best of luck with the rest of your treatments!
Tricia
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- September 21, 2011 at 6:18 pm
I am about 30 days our form the daily infusions. I had a port placed for my infusions. The chemo center may allow your to keep your IV in place for up to 3 days depending on their policy, you may want to ask if this is an option at your facility.
Best wishes your way,
Allen
Stage III
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- September 21, 2011 at 6:18 pm
I am about 30 days our form the daily infusions. I had a port placed for my infusions. The chemo center may allow your to keep your IV in place for up to 3 days depending on their policy, you may want to ask if this is an option at your facility.
Best wishes your way,
Allen
Stage III
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- September 21, 2011 at 9:55 pm
For my husband they put a new port in weekly. They put it in on monday and took it out on friday. He had pretty much the same symptoms as you. DUring the HD, he ended up working just 5 hour days but went back to a normal work schedule once the LD started.
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- September 21, 2011 at 9:55 pm
For my husband they put a new port in weekly. They put it in on monday and took it out on friday. He had pretty much the same symptoms as you. DUring the HD, he ended up working just 5 hour days but went back to a normal work schedule once the LD started.
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- September 21, 2011 at 11:16 pm
Just to further clarify my experience, my PICC line was placed on August 22 and has been there ever since. There is no need to remove it, only change the dressing weekly (unless it gets wet).
Hope you're doing well through these first few days of treatment. =)
Donna M.
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- September 21, 2011 at 11:16 pm
Just to further clarify my experience, my PICC line was placed on August 22 and has been there ever since. There is no need to remove it, only change the dressing weekly (unless it gets wet).
Hope you're doing well through these first few days of treatment. =)
Donna M.
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