Colleague - PCOS


(Scott Telfer) #1

Just wanted to share this experience here as very few people would understand outside this forum. A colleague of mine has displayed arthritic signs for over a year now. She is a young female (under 25) extremely tall, beautful and has a fabulous figure, we happened to be chatting about health (I normally veer away from this topic at all costs as I’m over the confrontation and explaining myself to people who’s business it is not) and she mentioned she was diagnosed with PCOS (quite a share), putting this together with the knowledge of her arthritis I couldn’t help but blurt out of frustration ‘what’s your diet like?’.

She responded ‘oh it’s not that, I eat better than anyone else in here; lots of fruit, low fat, bread, mostly vegetarian…’

My heart just sank, I bit back from going into a tirade and simply said ‘maybe you could look at other women who’ve experienced this and some different approaches?’ as I HATE it when other people are pass remarkable on my diet and lifestyle or feel it’s ok to pass comment on your health.

I’m not really looking for advice, just needed a place to rant. This poor girl’s issues must be so aggravated by her diet and so much could be solved with a different approach, but it’s certainly not my place to say it. Very frustrating.


(Miss E) #2

Hey Scott, I’m also in Perth, also have PCOS. I’m three weeks into keto, would be happy to talk to her about my experiences. I’m sure the lovely folk here can provide some science for the links between PCOS and keto, or at the very least gluten free.


(Scott Telfer) #3

Hi Eva, I’m going to see if this topic comes up again and if it feels appropriate I’m going to direct her this way. Thank you so much for your kind offer. Much appreciated :slight_smile: Cheers


(Melanie Armistead) #4

I’m happy to chat to her too - I’m south of Perth (Wellard).

Let her know that Arthritis WA run coffee catchups - I go to the Cockburn evening one (4th Wednesday of each month @ Cockburn Dome 7-9pm)

I’ve put my arthritis into remission after 20 years. CRP on Humira and Methotrexate was 22, 14 months medication-free and it’s now 4.


(Miss E) #5

Honestly, I wouldn’t even wait till it comes up again. I would say something along the lines of “I don’t have a uterus and I don’t want to tell you what to do to help yours feel better but I just wanted to give you this link, I have seen several posts about this WOE relieving symptoms and in some cases reversing the condition all together. No pressure, it’s there if you want to check it out and I’m here if you have any questions”.

Obviously the uterus part is optional :stuck_out_tongue: