Hi ladies, hope everyone is keeping well?
How are you all managing with the delays in being able to see consultants and receive medication etc? I had an appt (telephone, unable to do face-to-face in my area) and was told I would need to begin Zoladex due to severity of Endo and pain management, this was over a month ago and the consultant has still not even written the letter to be sent to my GP. On top of that my GP surgery only has one nurse and her appt waiting time is 9 weeks which I cannot book in advance without the said letter!
I am in a really bad way managing my Endo at the moment both physically and mentally, and this just seems to be the icing on the cake.
I have sought advice from the hospitals PALS service, but does anyone have any further advice or tips to be taken seriously or be heard at the moment?
I always feel like women with Endometriosis have such a disadvantage when it comes to diagnosis and treatment, and now it seems my full time job (on top of my actual full time job) is to chase consultants and receive proper care.
To make matters worse my consultant even said my case is really severe and it was a priority for me to start Zoladex!
Sorry for the rant.
x