ME/CFS
No benefit
Miserable and worn down with ME/CFS, no benefit from NAD+ injections
- Condition
- ME/CFS
- At worst
- Not stated
- Ill for
- Not stated
- Last post
- May 2026
In their words
- Condition: ME/CFS
r/chronicfatigue
In context ↗ - Now: No benefit
as much as I wanted some relief from my conditions, it didn’t.
In context ↗
Read from 1 of their posts and comments; links to the one this page draws on
Summary
A Reddit user with autoimmune problems who was in perimenopause described themselves as miserable and worn down by doctors' gaslighting. They ordered daily subcutaneous NAD+ injections from Amble for about eight months at $225 a month, hoping for relief from their conditions, but felt no benefit and did not reorder at month eight. They remained unwell at the time of writing.
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What they tried
Also tried
Their words about each treatment
- NAD+ injections · No change
Yes, I tried the NAD daily sub q for about 8 months. $225 month from Amble and as much as I wanted some relief from my conditions, it didn’t.
In context ↗