Quote from: Sarah B on March 14, 2024, 07:25:47 PMHi Allie
You mentioned the following in your post above:
You say, "it could be the hormones", so the question remains, why? I've noticed anecdotally that endocrinologists in the states tend to start of hormone therapy on a very low dose.
The question that just crossed my mind is do the 'physicians' maintain a post menopausal estrogen level, for 'us'? I know the body needs hormones, regardless of what type it is given.
When I started I was given a high dose 2 x 2mg (tablet) twice a day, by my then treating doctor, when I saw my endocrinologist at the time, he just monitored my levels (I assume estrogen) and was happy with them. I have always taken the same dosage ever since I first started, which has been 35 years. My doctor who recently took my blood levels said, "your levels are fine", meaning they were 'average' compared to other women.
I'm not a doctor, so my thought is would a higher level of estrogen make a difference in the treatment of migraines? You have mentioned that you have been having botox for a long time, but only 1 year for hormones. Food for everyone's thoughts.
Take care and I wish with all my might that one day you will have a migraine free day.
and Hugs
Sarah B
@imallie
@Northern Star Girl
Hi Sarah -
Well, the reason I heavily qualified my statement is... well, there are LOTS of reasons.
Foremost, especially when it comes to my cluster headaches, it's such a rare condition that there simply isn't enough clinical research on the impact of ANYTHING. It's why, despite the efficacy of Botox on patients like me, insurance will not cover Botox treatments. There simply isn't enough to back it up. It's only by my neurologist framing my progress in terms of incremental improvement in migraine severity does each year get approved.
As for hormones, though, there is plenty of research that shows that Estrogen is, in fact, a "migraine multiplier". It's actually listed as known side-effect for hormone treatment, not just for trans patients, but menopausal women, or any women taking them.
My neurologist, however, still gave me 70/20/10 odds at the outset, even as he advised against proceeding with hormones. 70% it would worsen my issues, 20% it would not impact them at all, and a small (10%) chance it would improve them.
That is why my endo and I decided to begin with microdosing, and were prepared at the first sign of negative impact to pull the plug. And when I started showing continued positive progress, we kept increasing.
But at the same time, Botox is a cumulative procedure. Each quarter's treatment stands on top of the previous quarter's, as it rewrites neurotransmissions of pain in the nerves.
But also at the same time, my neurologist says that at some point in the near future I could hopefully age out of all of this.
So... that is a long way of saying, that is why we say we can't really know what is helping and how much. Each thing might be playing a part, one might be doing all the heavy lifting? Who knows.
I think, however, it is clear that, per my neurologist's percentage scale, I am safely in the non-70% pool. So whether it is helping or not hurting, no one can say. But at this point either one is just fine with me.
I know that's a long explanation, but I promise you, that's the short version.
Love,
Allie