My neuro and endo diagnosed my tumor way back 2009. I suffered from the symptoms since i am 17 but my parents lacks to give me Medical attention.. I had a regular menstruation back then but when I got married 2005 that was the start of my ganorrhea.. I only had menstruation for twice a year only.. My neuro advice me to take bromocriptine or parlodel as well my endo but it doesn't change anything that's why I asked my endo if there is another way to cure my tumor and advised me to take cabergoline.. From September 2010
That I start taking it my menstrual cycle is normal until I stopped taking it June 2012.. My question is what are the possible effects that may happen to me because I stopped taking medication because of the side effects of this medicines that affects my dailly routine.. I am starting to loose my peripheral vision.. Thanks in advance for your comments..
Please find a pituitary center and a neuro-ENDO to get treatment. You also need to find a neuro-optho to get visual fields.
It does not seem that your endo is treating you properly for your pituitary lesion and it may or may not be a prolactinoma. As a fellow patient, I advise always getting copies of your tests and to get testing on ALL pituitary hormones just in case others are effected. It sounds by your symptoms that you could have other issues.
BTW stopping medication means the tumor grows and that means it could have effected your vision. You should have regular MRIs to monitor as well as regular lab work.
It is hard to say. Pain is not easy (live with it myself). I have used many meds and use acupuncture long term as I don''t like the pills and side effects. I did pain mgmt for a while but did not like how it made me feel with all the pills. I would rather eliminate the source. People react differently. I know one of my docs liked ultram - but you should only do pain meds short term and under supervision.
Before I stopped taking my cabergoline I had my menstruation normal but as I stopped it since August 2012 upto now my menstruation doesn't visit me yet.. Because of loosing hope I am not seeing any of my doctors anymore and also because that I don't have enough money for m treatment ..
Have you contacted the manufacturer for assistance in paying for the scripts? There are sometimes programs to helps. I know my neuro-endo office has information on programs and some medications have even formal programs where they assign you a person.
Your pharmacy or the internet may be able to help you as well.
It is very important that you have followup imaging, particularly with thoughts about stopping the medication. You do not want stop if the tumor is large.
Although the prolactin level can give an idea if the medication is working. There are cases (mix cells) that the tumor respond only partially to dopamine agonist even with the numbers going down.
Any attempt to stop medication should be supervised by your doctors.
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