I'm
A Newson health patient and after some years of monitoring and tweaking and watching and waiting I'm finally at the sweet spot (for now) but I have been classified as a poor absorber.
It's really annoying, but THANK GOODNESS I had the money to go privately to see someone. My GP is on the better informed side but there is only limited scope and time for this to be sorted.
What's wrong with listening to the patient? How they are feeling ie the clinical picture?? They do with other conditions requiring hormones?
I have had my dose slowly increased and monitored over time including blood tests, DEXA scan too. I've tried oestrogel, then Lenzetto, now Everol patches but have higher than the licensed dose. I take Androfemme - which has made me feel so much better.
It shouldn't just be those who can afford it!!
Has the licensed dose changed over the years? When will it be reviewed?
Just because someone is prescribed an amount, doesn't equate to receiving the dose.
I feel that symptoms should be a big part of assessment and management.
For me, I always know when I'm not getting enough because I start getting joint pain along with increasing anxiety and dull headaches. A friend of mine gets irritable, anxious but severe itching and night sweats.
We are individual!!! And being
Treated by the majority of medical professionals like we have something that's being overblown and we are making a meal of it!
I have had an endocrine issue (thyroid) which seems nice and straightforward for doctors to manage - they do very basic blood test and increase or decrease based on results. The GP has NEVER asked how I am or whether I have any symptoms etc they don't have time! It feels like many GP's wish we would just zip it 🤐 so they can just look at blood test results all day and stop whining!
Newson health approach feels more holistic- they take time to ask about other symptoms, use a screening tool and score it ALONGSIDE test results as oestrodiol is notoriously unreliable alone.
Quite honestly, I can't waste 10 plus years of my life while I have no quality of life until someone does proper research or updates guidelines or decides menopause is interesting enough for funding to be found etc etc!
My clinical picture is that I'm a lot better on what I'm taking which has been tailored to my symptoms by a GP with a specialism in menopause under NC - who sees MULTIPLE women weekly so gets a good idea of what's going on as oppose to my GP who Can't be ar$ed and has no time and is scared of doing the wrong thing due to excess pressure and drama so will just do what she's pressured into by certain loud voices on insta and Panorama!