Androgen receptors upregulation
Posted: Fri Mar 08, 2019 10:19 pm
Hello,
For almost 10 years I was on dutasteride, for hair loss issues. Because of that my libido was completely destroyed, but I kept my hair for a while. After 8 years hair started to fall again, so I tried to find other drugs... I found Cyproterone (July 2017) and tried without stopping Dutasteride and add estradiol 4mg, and the nightmare begun.
My hair loss increased a lot, itchy scalp started, lost 70% of my hair on the top and around the ears, I had (and still have) pain in the eyes, headaches, pain in the pelvis, bladder and hips. And my libido came back, from time to time (when libido comes back, pain is worse).
My prolactin was a bit high, my doc thought I had prolactinoma, MRI came clean. I stopped Cyproterone, April 2018, testosterone raised up and pain was awful. I was able to convince my therapist to prescribe me Lupron (July 2018). It helped for a while. But the pain came back in a vengeance. I stopped Dutasteride (December 2018).
The pain is becoming unbearable and I don't know what to do anymore. Doctors are clueless. And an idea came to my mind. if all of this was because of my androgen receptors becoming overexpressed. Like men with prostate cancer resistant to anti-androgens. My PSA was very low (September 2018). But because I have pain in the pelvic area + bladder + itchy scalp (and eyes?) ... I think it's related to androgens.
I met 5 endocrinologists and 1 urologist ... they just laughed at me. It was very stressful, because I'm in pain, and I don't know what to do. I must say I have transgender issues, and I cannot accept the idea of giving up and let testosterone coming back. But it's like no matter what I do testosterone is the strongest. My testosterone is in castration ranges (around 20-25 ng/dl, my estrogen is high (200 to 300pg/mL) ... and yet I'm getting more body hair, less scalp hair, more muscles .................................................. ...
I'm really lost at this point. It's like Post Finasteride Syndrome but in the opposite side. Maybe PFS is oversensitive androgen receptors but because of normal testosterone levels androgen receptors just shut down and stop to "accept" testosterone. It's one of my theory, sorry if it doesn't make sense.
So ... What I'm experiencing doesn't seem to be common, but maybe someone can tell me if it happened to someone else, and what the "cure" ? Or, there is no cure ?
My head is hurting like hell right now, same with my eyes, scalp, and pelvic. I did a lot of exams, and saw few specialists. I'm really afraid because I know something bad could happen because of my issue. I'm afraid to stop everything, because the last time was hell and because I really need to be feminine.
If you going to tell me I'm crazy, everything's going on is in my head, please don't. I want ideas, hypothesis, solutions, ...
Thank you for reading.
PS : sorry for my poor english.
For almost 10 years I was on dutasteride, for hair loss issues. Because of that my libido was completely destroyed, but I kept my hair for a while. After 8 years hair started to fall again, so I tried to find other drugs... I found Cyproterone (July 2017) and tried without stopping Dutasteride and add estradiol 4mg, and the nightmare begun.
My hair loss increased a lot, itchy scalp started, lost 70% of my hair on the top and around the ears, I had (and still have) pain in the eyes, headaches, pain in the pelvis, bladder and hips. And my libido came back, from time to time (when libido comes back, pain is worse).
My prolactin was a bit high, my doc thought I had prolactinoma, MRI came clean. I stopped Cyproterone, April 2018, testosterone raised up and pain was awful. I was able to convince my therapist to prescribe me Lupron (July 2018). It helped for a while. But the pain came back in a vengeance. I stopped Dutasteride (December 2018).
The pain is becoming unbearable and I don't know what to do anymore. Doctors are clueless. And an idea came to my mind. if all of this was because of my androgen receptors becoming overexpressed. Like men with prostate cancer resistant to anti-androgens. My PSA was very low (September 2018). But because I have pain in the pelvic area + bladder + itchy scalp (and eyes?) ... I think it's related to androgens.
I met 5 endocrinologists and 1 urologist ... they just laughed at me. It was very stressful, because I'm in pain, and I don't know what to do. I must say I have transgender issues, and I cannot accept the idea of giving up and let testosterone coming back. But it's like no matter what I do testosterone is the strongest. My testosterone is in castration ranges (around 20-25 ng/dl, my estrogen is high (200 to 300pg/mL) ... and yet I'm getting more body hair, less scalp hair, more muscles .................................................. ...
I'm really lost at this point. It's like Post Finasteride Syndrome but in the opposite side. Maybe PFS is oversensitive androgen receptors but because of normal testosterone levels androgen receptors just shut down and stop to "accept" testosterone. It's one of my theory, sorry if it doesn't make sense.
So ... What I'm experiencing doesn't seem to be common, but maybe someone can tell me if it happened to someone else, and what the "cure" ? Or, there is no cure ?
My head is hurting like hell right now, same with my eyes, scalp, and pelvic. I did a lot of exams, and saw few specialists. I'm really afraid because I know something bad could happen because of my issue. I'm afraid to stop everything, because the last time was hell and because I really need to be feminine.
If you going to tell me I'm crazy, everything's going on is in my head, please don't. I want ideas, hypothesis, solutions, ...
Thank you for reading.
PS : sorry for my poor english.