Quote from: Ryuichi13 on June 28, 2017, 07:12:33 AM
Since developing (genetic) High Blood pressure, I feel the same way about it as I do the pills I take, that its just another thing I do to stay healthy. I try to take all my meds around the same time every night, so that helps. Since I'm on the gel, I found a app by the same company that helps me track it, which also helps.
I too haven't missed a dose in 8 months.
Just think, if you don't take your shot, then all the problems you had prior to it may return, the body dyshoria, shark week, (possibly) even some facial feminization. Its worth it to keep taking the shot.
Good luck with your insurance, I know the insurance situation here in the US i getting stupid with the new administration.
Can your endo list your T/the gel as "hormone replacement?" Mine does, and it seems to have made it easier.
Ryuichi
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Thank you for the suggestion!
I've tried reminding myself of all of the changes that aren't permanent, and I do get upset at the thought of losing those changes, but at the same time it hasn't worked in pushing me through the bad depression days. When I'm that bad, it's like a "one shot won't change anything" more than it is an "I'm done with T." Because ultimately at 3 years on T, one shot every once in a while really is meaningless in terms of changes or reverting. I'm trying to find a way to counter that thinking that's strong enough for the depression. It's why I miss only 1 or 2 at a time because when I get to 3, I am able to recognise the higher risk of changes starting to revert and take the shot again. So reminding myself of those things will ultimately work, it just hasn't worked as early as I would like it to.
My doctor has been able to get the hormone testing covered that way (thank the lord) but unfortunately the company is extremely hyperfocused on testosterone. It's easier to get estrogen, but with testosterone though they only cover "men with diagnosed low T" and "women with inoperable breast cancer." I don't have breast cancer so that wouldn't work, and since I can't change my gender in my state right now, they won't cover a diagnosis like "man with low T" either because I am not a man to them. They have left no room for interpretation or vague reasons.
It is technically illegal now for them to be doing this, but I do not have the resources to fight it. The employer who the insurance is through constantly voices that equality is important and, because this is a core value for them, when we brought this exclusion to their attention, they were upset and had no idea the exclusion was there. My hope is that the employer will fight the battle for us, or at least for future employees. I have no doubt that eventually I can switch to the topicals, but when that is, I still have no idea. It could be a few months or it could be when I graduate and get my own job with a company that has inclusive plans.
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