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Entyvio/ remission

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Ulcerative Colitis
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Theanxiousaries
Regular Member
Joined : May 2021
Posts : 396
Posted 6/3/2022 9:41 PM (GMT -7)
How long did remission take for those on entyvio
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Theanxiousaries
Regular Member
Joined : May 2021
Posts : 396
Posted 6/5/2022 4:53 AM (GMT -7)
Thanks to everyone on entyvio that couldn’t take 2 minutes to answer a question.
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damo123
Veteran Member
Joined : Jul 2007
Posts : 885
Posted 6/5/2022 9:08 AM (GMT -7)
I think that response is a little harsh and undeserved to the other members. You do ask a whole lot of questions on here and in the vast majority of cases members do reply and give you time and consideration.
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GrittyHope
Regular Member
Joined : Mar 2022
Posts : 47
Posted 6/5/2022 10:26 AM (GMT -7)
I think it may be that there aren't as many on Entyvio here? Aries, I'm only three loading doses in myself and feeling okay, but I think the two months of Cortiment (budesonide) went a long way in helping quell my terrible flare.

Are you on Facebook? The Entyvio Warriors group there is very active, and folks often ask this question. From what I can tell, it really varies: some people have good response within 14 weeks, but many others report remission only after six months or a year. Many of the people who've been on it longer strongly advocate trying for a full year before giving up. Some also recommend moving to six weeks or four weeks between infusions, based on blood levels of the drug, but I think different countries have different norms for testing those levels or not.

How are you feeling so far?
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poopydoop
Veteran Member
Joined : Dec 2018
Posts : 1606
Posted 6/5/2022 10:31 AM (GMT -7)
You can use the search function to find similar posts as I'm sure this question has been asked before (I think I even asked it in 2018). There are not many entyvio users active on this forum, plus forum is always quieter at the weekend.
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Theanxiousaries
Regular Member
Joined : May 2021
Posts : 396
Posted 6/5/2022 11:12 PM (GMT -7)

damo123 said...
I think that response is a little harsh and undeserved to the other members. You do ask a whole lot of questions on here and in the vast majority of cases members do reply and give you time and consideration.


I ask a lot of question? Wow. I notice a lot of comments too and you always seem to be on the end of a lot of negativity. Comments like yours are the reason this forum is half of what it used to be.

Post Edited (Theanxiousaries) : 6/6/2022 12:19:38 AM (GMT-6)

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Theanxiousaries
Regular Member
Joined : May 2021
Posts : 396
Posted 6/5/2022 11:23 PM (GMT -7)

poopydoop said...
You can use the search function to find similar posts as I'm sure this question has been asked before (I think I even asked it in 2018). There are not many entyvio users active on this forum, plus forum is always quieter at the weekend.


Thanks poopy doop. I kinda figured it was an old question. Thankyou
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damo123
Veteran Member
Joined : Jul 2007
Posts : 885
Posted 6/6/2022 12:01 AM (GMT -7)
It really is a pity that you have to resort to comments like that TAA. I wish you luck. All help is self-help.
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CCinPA
Veteran Member
Joined : Dec 2014
Posts : 2197
Posted 6/6/2022 3:32 AM (GMT -7)
TAA -- you DO ask a lot of questions. No harm in that at all. Just be patient while waiting for responses. People here are generally willing to help others when they can. Keep in mind that there is a search feature in the forum that can help you find info quickly.

You said you have had 3 infusions -- those would have been your loading doses, correct? Have you noticed improvement even if it's not remission? If so, hang in there and give it more time, but if you haven't had any improvement at all you should probably talk to your doc. Seems like you should be seeing some improvement if Entyvio is going to work for you.

Be careful with adding new supplements right now. You won't know what is working -- the supplement or Entyvio. I know we all get impatient and just want immediate remission. For most, it takes time.
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FlowersGal
Veteran Member
Joined : Feb 2017
Posts : 1404
Posted 6/6/2022 5:53 AM (GMT -7)
I was in complete symptomatic remission by around month 4. But a colonoscopy around that time still showed some microscopic inflammation and disease. The next colonoscopy (not sure how much longer that one was — maybe 6-10 months later?) showed complete remission.

But the point I want to stress is that I didn’t just wake up one day 4 months into my entyvio infusions and be symptom free. Before that there was a lot of improvements! Healing from years of disease or a year-long flare takes a lot of time! Are you starting to see a reduction of symptoms? Fewer BMs, less blood and pain/cramping? If so you can count that as a VERY positive sign!
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Theanxiousaries
Regular Member
Joined : May 2021
Posts : 396
Posted 6/19/2022 3:55 AM (GMT -7)

FlowersGal said...
I was in complete symptomatic remission by around month 4. But a colonoscopy around that time still showed some microscopic inflammation and disease. The next colonoscopy (not sure how much longer that one was — maybe 6-10 months later?) showed complete remission.

But the point I want to stress is that I didn’t just wake up one day 4 months into my entyvio infusions and be symptom free. Before that there was a lot of improvements! Healing from years of disease or a year-long flare takes a lot of time! Are you starting to see a reduction of symptoms? Fewer BMs, less blood and pain/cramping? If so you can count that as a VERY positive sign!


Yes I’m seeing improvements on some days fully formed stools. Other days mucous but usually at the end of a bowel movement. A lot more formed stools but still some burning afterwards. No pain and most days only one bowel movement. My symptoms definitely coincide with my cycle. Days off my hormone cream are the worst I had a calprotectin score of 28 which I’ve never had since being diagnosed. Some days I feel like it working but it’s slow
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CCinPA
Veteran Member
Joined : Dec 2014
Posts : 2197
Posted 6/20/2022 2:01 PM (GMT -7)
It sounds like Entyvio is working!! Congrats! Give it more time before you give up on it. It can be really slow to get to complete remission, but once you get there it will be like you don't even have UC!
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Theanxiousaries
Regular Member
Joined : May 2021
Posts : 396
Posted 6/21/2022 3:44 AM (GMT -7)

GrittyHope said...
I think it may be that there aren't as many on Entyvio here? Aries, I'm only three loading doses in myself and feeling okay, but I think the two months of Cortiment (budesonide) went a long way in helping quell my terrible flare.

Are you on Facebook? The Entyvio Warriors group there is very active, and folks often ask this question. From what I can tell, it really varies: some people have good response within 14 weeks, but many others report remission only after six months or a year. Many of the people who've been on it longer strongly advocate trying for a full year before giving up. Some also recommend moving to six weeks or four weeks between infusions, based on blood levels of the drug, but I think different countries have different norms for testing those levels or not.

How are you feeling so far?


Hi gritty hope. My symptoms are random. I feel like I’m going back into a flare tonight. I’ve had bleeding again though not sure if it’s haemorrhoids. Last calprotectin was 28. I done another one today and I’m expecting it to be back up. I find the results from those more about stool consistency than inflammation. They change rapidly along with symptoms. I want entyvio to work so badly but I can’t help thinking it’s not. I don’t want to go back on steroids. I’m 4 months in and have seen random perfect stools
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GrittyHope
Regular Member
Joined : Mar 2022
Posts : 47
Posted 6/21/2022 11:43 AM (GMT -7)
Hi, Aries. I hope your calprotectin is still low with this test.

My fourth infusion is next week, and so far I'm feeling pretty well. Once in a while I'll go a little extra or feel a little abdominal discomfort, but I keep reminding myself that diet, stress, and sleep cause bowel changes in healthy people, too. I'm trying not to focus too much on the small changes so I don't freak myself out, because I know the stress itself would be counterproductive.

It feels like a real mind game sometimes!

I know all the biologics help some and not others, but I'm really hoping for both of us that this is drug works well with our bodies. Keep us posted!
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Bloom93
Regular Member
Joined : May 2012
Posts : 362
Posted 6/21/2022 7:55 PM (GMT -7)
Hi,
For DD Symptoms quickly improved after the initial entyvio dose.
But lost its benefit close to 1year. She is taking Avsola infusion currently.


Best wishes..
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C_G_K
Veteran Member
Joined : Dec 2006
Posts : 1421
Posted 6/21/2022 7:59 PM (GMT -7)
I was already about 90% of the way to remission when I started, so I was into full remission soon after the first infusion. I assume if you are in a bad flair it could take longer.
I've been on it now for almost 2 years and I am completely symptom free.

Post Edited (C_G_K) : 6/21/2022 10:26:52 PM (GMT-6)

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Sara14
Veteran Member
Joined : Mar 2007
Posts : 7216
Posted 6/23/2022 7:01 AM (GMT -7)
Ask as many questions as you want.

Unfortunately, Entivio didn't do anything to help me. Hope you have better results.
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Theanxiousaries
Regular Member
Joined : May 2021
Posts : 396
Posted 6/25/2022 3:02 AM (GMT -7)

Sara14 said...
Ask as many questions as you want.

Unfortunately, Entivio didn't do anything to help me. Hope you have better results.


Thanks Sara. Can’t believe I was told I ask too many question on a forum designed to help. It’s sad that these kinds of comments are the reason this forum isn’t what it used to be. Sad to see so many knowledgeable members no longer posting. I’ve found entyvio warriors on Facebook. They have been really helpful with my questions. Apparently I’m still in the early stages at 4months so I still have some hope 😊
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