Feeling very tired and sleepy

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Joined
Oct 31, 2016
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I'm diagnosed with UC/ Crohns. I've been taking Remicade infusions every 8 weeks for over a year now. However I feel extremely tired most of the day. I feel like sleeping a lot of the time and this greatly decreases my productivity.
Does anybody else face this? Can you suggest a good diet to follow that could help with this?
 
Have you had your blood checked? You might need b12 or iron. Ask your doctor
I'm taking both folic acid and iron supplements as well. I start feeling all this at the end of my infusion course (just a week before I need to get one again). Maybe because it's "wearing off" ?
 
Something similar use to happen to me when I was on remicade. A few days before my next infusion i would start feeling bad again.
 
I started feeling real tired and my arthritis would flare in between my infusions. I told me doc and he bumped me from every 8 weeks to every 6. Worth mention to the doc if you haven't already!
 
I started feeling real tired and my arthritis would flare in between my infusions. I told me doc and he bumped me from every 8 weeks to every 6. Worth mention to the doc if you haven't already!
Thank you, I'll speak with my doc about it
 
I had these same symptoms on remicade and was bumped from 8 to 6 weeks before I eventually had to have the j-pouch surgeries. I was tired constantly for a while-it takes a village. These are what I found worked to help give me any kind of energy:
-iron supplements
-Vitamin D
-drip drop (for hydration. it was made by a Mayo Clinic doctor and tastes great. It's a powder that you add to water and is the equivalent of three waters when having 1. You can only get this at walgreens in the pediatric isle.) I add it to coconut water and I am fully hydrated all the time, which gives me so much energy.
 
It's the three-part surgery to completely remove the diseased colon and recreate it out of the small intestine by creating a j-shaped pouch. Only UC patients can have this without a permanent colostomy that Crohn's patients will receive.

If you have any more questions, please let me know!
 
It's the three-part surgery to completely remove the diseased colon and recreate it out of the small intestine by creating a j-shaped pouch. Only UC patients can have this without a permanent colostomy that Crohn's patients will receive.

If you have any more questions, please let me know!
I see. I'm going to have to go read about it now! Thank you
 

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