Typical of today's subhuman care in the US.
So we started talking about my irregular bleeding which has started again. And she looks up my chart and she's like, two years ago we saw what we "thought" was a uterine fibroid. But I can't guarantee you it's not cancer. (Basically it's an unidentified f-ing object) But it's probably just a fibroid and the bleeding is cause it got bigger.
So, I'm sitting there like, you let me go for TWO years and never once said you weren't sure it was a uterine fibroid. And never told me to get it checked out further. That's just classic.
IMO, it's hormonal cause I just switched doses on the thyroid med again and I've been going through massive stress with the crazy relatives. Plus the soy that got into my diet. Soy makes me bleed. And too much dairy lately, too. But what she said did bug me!
The rest of the visit was just the same as usual. They always comment on my blood pressure and I always have to explain that it's totally normal for a POTS patient.
The insurance company refuses to pay for the real Levoxl, the pharmacy wanted me to pay twenty bucks a month for the real thing, so I said no, give me generic junk again. So I guess I'll just suffer with the bad side effects forever. I can't afford more money a month.
She had no answers for me on my Lyme arthritis or anything else really. Just keep on taking what I'm taking, bloodwork in two months, and see you again in January.
And I left feeling like I'm not really getting much care.
So we started talking about my irregular bleeding which has started again. And she looks up my chart and she's like, two years ago we saw what we "thought" was a uterine fibroid. But I can't guarantee you it's not cancer. (Basically it's an unidentified f-ing object) But it's probably just a fibroid and the bleeding is cause it got bigger.
So, I'm sitting there like, you let me go for TWO years and never once said you weren't sure it was a uterine fibroid. And never told me to get it checked out further. That's just classic.
IMO, it's hormonal cause I just switched doses on the thyroid med again and I've been going through massive stress with the crazy relatives. Plus the soy that got into my diet. Soy makes me bleed. And too much dairy lately, too. But what she said did bug me!
The rest of the visit was just the same as usual. They always comment on my blood pressure and I always have to explain that it's totally normal for a POTS patient.
The insurance company refuses to pay for the real Levoxl, the pharmacy wanted me to pay twenty bucks a month for the real thing, so I said no, give me generic junk again. So I guess I'll just suffer with the bad side effects forever. I can't afford more money a month.
She had no answers for me on my Lyme arthritis or anything else really. Just keep on taking what I'm taking, bloodwork in two months, and see you again in January.
And I left feeling like I'm not really getting much care.