Kerry's PMDD Diagnosis & Outlook on the Medical System

[@Gaby-fl9bo]

I've been watching your videos and I've found them very helpful. I have been visiting doctors of various specializations and trying out various forms of treatment (birth control, antidepressants, progesterone cream, etc.) for about two years now and haven't had much luck with any proper diagnoses. I wanted to thank you for sharing your opinion on the UK medical system because from what you have said I see many parallels to that of the US. the doctors I have visited are generally uninformed, and don't seem to take any of the information I give to them about my symptoms seriously. Anyways I just wanted to let you know that you aren't the only one that is experiencing disillusion with your medical system. Best of luck to you x

[@johannatheone]

Thanks for sharing this! I suffer from PMDD and i struggle with living a normal life, but it helps so much knowing that im not alone !!!

[@cablekez]

I am so sorry - as this is not on my profile I was never alerted to any comments that were made. I'm so glad that speaking out has helped you in any way :) How are you coping now?

[@gylbgetyourlifeback7439]

Kerry Cable Hi kerry just wondering how you are now? We are a charity in cornwall that support women, girls and their families who are suffering from PMDD whether diagnosed or not. If you would like support please check out our Facebook page Get your life back-Gylb/PMDD/hormones. Best wishes Carrie-ann co-founder/ manager GYLB

[@arielonhealth]

I get frustrated too with the system, I had to find the diagnosis and have suggested all the treatments to my doctors. Some call it that, some don't seem to take it seriously. My therapist and my family sure do, they know PMDD week(s). I get 10 days or so usually. I warn them when it's coming. Then, it happens. I wish you the best.