Has anyone gone bald?

From medication, Seriously don't want to lose anymore of my once long thick hair. I never noticed it until I changed from supps to enema

Ive been on pentasa for years and didn't notice until I changed to enemas

I've been on Asacol, then Colazal, for the past 15 years.  I started losing my super thick hair over 10 years ago.  I'd say I lost 3/4 of my hair at that time.  My hair is now very thin, but still very long. So it never grows back to the thick hair you once had I'm sorry to say, but it hasn't all fallen out.  Also the hair loss stops at some point and your hair just stays thin.  For me, the hairloss picks back up whenever I have signifcant stress in my life.

I've been tapering off Prednisone (which I've been on for over a year now) and that has really made the hairloss pick up.  It's as bad as it was when it first started falling out except this time I don't have much hair to lose! I'm hoping it stops soon and I won't be going on Prednisone again that's for sure!

Whoops I forgot to say I am now on humira every 2 weeks 80 yr old grand mom

I thinned out considerably from the pred during my last flare. I asked my PCP if it would come back, and she just sort of avoided the question. :(

I used to tease my brothers who inherited my maternal grandfather's hairline, had to stop doing that.

Male, late 20s, was already balding, my rheummy reminded me I'm not allowed to complain about losing my hair b/c I already was. He's lucky I wasn't in a bad mood.

My hair started thinning when I started taking Asacol 10+ years ago. Was it the Asacol or just that I was getting to that age where we start thinning? I don't know, but my brother still has a great thick head of hair and he's 4 years older than me!

My hair was 100% fine and unaffected through all of the meds listed in my signature. It started to thin after surgery, which is a common side effect of general anesthesia (telogen effluvium -- happens to everyone, has nothing to do with IBD or meds). Even so, I've had two major surgeries in the past five months and everyone tells me they can't see a difference in my hair. I can tell and definitely see more hair in the drain after a shower, but I haven't needed to do anything special (like cut my hair, style it differently, etc).

During my first flare (which was very severe) I lost a good amount of hair but all of my hair came back once I got healthy. I was so malnourished that you could even feel my fingernails and see where they slowed their growth and were very thin...I think that hair and nails are made from the same protein (keratin) and b-12 is very important for healthy hair and nails but with UC B-12 can be difficult to absorb because of the inflammation in lower part of the colon. All the meds that we take doesn't help either.

The flare that I am currently in is not that bad and I am staying nourished. Actually my hair feels extremely healthy and soft (like when I was a kid), last year I started using Bumble and Bumble Gentle Shampoo and their SuperRich Conditioner...their stuff is ridiculously priced but my hair is in great shape now.