CuttingEdgeScience said:
drswole said:
CuttingEdgeScience said:
I plan to move over to Tirz from Reta, since I keep coming across accounts from other people praising it as better for inflammation. Living with POTS, MCAS/MC, and similar issues, I've been stunned by how many foods I previously had to give up are now tolerable, yet I have a hunch that Tirz might bring about deeper shifts at the source of inflammation.
Does anyone know whether the dosing is different for the two? Once side effects kicked in at a higher titration, I ended up staying at 1.5 mg of Reta. Reta has cut down food noise a lot for me, but my weight hasn't moved much (I'm only slightly above the "normal" range, though I used to be lower before getting sick.)
Any input or observations would be welcome!
my guess is that tirz gets called "better" for inflammation simply because far more people are on it (it's prescribable and so on) compared to reta. possibly it's more about the situation than tirz actually being superior.
another possibility: does the glucagon activity of Reta get in the way a bit?
though honestly, every GLP-1 that hits the GIP receptor for inflammation brings down systemic inflammation.
for me, the sweet spot came from slowly titrating up to 4mg a week; after roughly a month at that dose i could eat properly while still getting the benefits i was after (lipids)
could adding TA1 or TB500 help with inflammation?
It makes sense that Tirz has a much larger user base - here, I've come across several accounts from people with mast cell conditions who made the switch away from Reta. My own view is that for those of us already dealing with some form of POTS or Dysautonomia, the heart rate effects that come with Glucagon activation are a drawback. On top of that, I have ADHD, so anhedonia as a side effect might be one more thing to weigh in the balance.
At 2 mg of Reta I was already experiencing side effects, so I stepped back down, and my increases had been fairly gradual throughout. What's strange is that even low doses clearly affected my appetite, yet I wondered whether inflammation might be preventing the weight from coming off. I hoped to get up to 2.5 mg, but that didn't work out. Over a few weeks I went down to 1.5 mg, then to 1 mg. As I went, I felt better - my mood and other sensory problems appeared to diminish.
So yesterday I took my first 1 mg dose of Tirz. Something definitely felt different, and for now I'll say I can see what people have been describing. Breathing seems slightly easier. My pain is reduced, even though I didn't fall asleep until 4 AM, and today I received two new lots of IVIg for my infusion with almost no side effects, which is pretty uncommon.
My food noise hasn't really changed, but it's only been a day, and I'm likely still winding down from the 1.5 mg doses I was on before. Food tolerance remains fine, and if anything my GI system is calmer. Only time will show how this experiment turns out - I wanted to see the difference for myself before recommending anything either way to other friends in the chronic illness group.