05/08/2026
IV therapy isn’t risk free
First off, I’m incredibly thankful for the access of tools that are truly supportive for some people. Right now, I am one of those people!
However, the more I am in these settings, the more concerned I am for the average consumer. As IV therapy becomes more popular and accessible, we need to remain advocates for own care and be given enough information to make informed decisions.
Red Flags
-Most people getting the same bag
-Everyone at a facility being “prescribed” an IV.
-Patients having a false sense of security when they finally feel listened to, maybe have some “in depth labs done” and feels safe when the person in scrubs hooks up their IV.
-Medical professionals selling supplements
-Medical professionals making unsubstantiated claims on treatment options that have very little clinical data
-“Water soluble” being used to imply “risk free”
Just a few of some real potential risks with IV therapy
-Infection
-electrolyte, mineral and or vitamin imbalances
-kidney stress
-vein damage
-medication and condition interactions
As someone currently undergoing weekly IV therapy for POTS and malabsorption, I can tell you it’s been a wonderful tool in my care and management of symptoms. I can also tell you I have to advocate for what I need every single time to make sure that I’m getting the correct care. I have watched many a time as person after person next to me adds things to their bags they don’t need, asks questions and are met with unsubstantiated claims, or are told flat out incorrect information that puts them at ease.
I’m all for access. And I know how hard it can be to fight for good care. I also believe we all deserve the right to make an informed medical choice. Get your IVs if that’s what you and your medical team decide. But know the risks, know your labs, learn what you need and what you don’t, and never take off your self advocacy hat!
Im not a doctor and this isn’t medical advice. Question everyone, including myself.