Back to feed
44
501 10

Has anyone here been using Naglazyme for MPS VI treatment? I've just started and wanted to know if anyone can share their experiences, both positive and negative. What are the most common side effects you've encountered, and how have you managed them? Also, is there any advice for making the weekly infusions easier to handle?

1 min read
last active 2d ago
HOT

Comments (10)

H
harold_carter7d ago

I've been on Naglazyme for about a year now, and it's been a game-changer. The infusions can be tough, but the benefits are worth it. I've had some minor side effects like headaches and joint pain, but my doctor helped me manage them.

B
billy_cook7d ago

Make sure to stay hydrated and take it easy the day of the infusion. It can help with some of the side effects. Also, talk to your doctor about pre-medication to reduce the risk of reactions.

A
amber_sherman7d ago

Sore throat and stuffy nose are my constant companions with Naglazyme. It's not fun, but at least it's better than the alternative.

K
kathleen_gray7d ago

Just got diagnosed and starting Naglazyme next week. Any words of encouragement out there?

C
christian_cox7d ago

I wish I could say Naglazyme has been a magic bullet, but it hasn't been easy. I've had severe infusion reactions a few times. My doctor has adjusted the infusion rate and added pre-medication, which has helped a bit.

R
randy_ramirez7d ago

Has anyone else noticed changes in their hearing or kidney issues? I've been feeling some discomfort in my ears and my doctor is running some tests.

M
matthew_dixon6d ago

I've been on this for a while and honestly, the side effects aren't as bad as you'd think. The toughest part is the weekly trip to the clinic. Just make sure to communicate openly with your medical team.

C
cheryl_vazquez6d ago

I've been lucky so far with not many side effects at all. But the infusions are a pain (pun intended). I always bring a book or my tablet to help pass the time.

F
frank_vargas6d ago

I've heard the infusion reactions can be severe. Anyone have any tips on how to deal with them? I've got my first infusion coming up and I'm a bit nervous.

S
samantha_bailey6d ago

I wish more people knew about MPS VI and the struggles we face. Keep sharing your stories, it helps raise awareness.