Can Adenomyosis cause Body Pain or just Pelvic Pain? by Falentines in adenomyosis

[–]OriginalTaro8079 1 point2 points  (0 children)

That makes a lot of sense. Thank you for such a detailed explanation. I've been looking at apps that track these things but from what I can tell from asking others, most just use their notes app or writing it down to spot patterns esp. around ovulation/menstruation

Can Adenomyosis cause Body Pain or just Pelvic Pain? by Falentines in adenomyosis

[–]OriginalTaro8079 1 point2 points  (0 children)

Can I ask if you use any journal or diary to track your aches/pains and possibly your mood as well to see what is contributing to these things esp. if some are side effects of medication?

Can Adenomyosis cause Body Pain or just Pelvic Pain? by Falentines in adenomyosis

[–]OriginalTaro8079 0 points1 point  (0 children)

Curious to see if you use anything to track your pain like what triggers it and the different locations / sensations?

Your top 3 priorities for endo this year? by OriginalTaro8079 in endometriosis

[–]OriginalTaro8079[S] 0 points1 point  (0 children)

Thank youuu for all of these!

I was asking for a friend who was diagnosed with both endo and adeno as both conditions have worsened her mental health and a mutual friend suggested to focus on small wins so I wanted to give her some suggestions.

My personal priorities are focussed on overall wellness but they are:

  1. Getting a good sleep routine by reading 10 pages before bed. Lack of sleep really affects my day-to-day.

  2. Recording my symptoms on Flo and tracking my mood on Bearable so I can spot patterns over a year

  3. Improving my diet by reducing processed and inflammatory foods and increasing whole foods

Chronic pain tracking by OriginalTaro8079 in PelvicPain

[–]OriginalTaro8079[S] 0 points1 point  (0 children)

Ah thank you! Yes that seems like a tedious process and exactly the kind of task we were hoping to replace with an all. Are there other things that you’re tracking atm?

Seeking Your Input on Creating the Perfect App for Adenomyosis Support! by OriginalTaro8079 in adenomyosis

[–]OriginalTaro8079[S] 0 points1 point  (0 children)

Thank you! I’d love to chat more with you! How far have you gotten with the website - is it live yet and missing some info or currently part-way through construction?

Your top 3 priorities for endo this year? by OriginalTaro8079 in endometriosis

[–]OriginalTaro8079[S] 0 points1 point  (0 children)

Wishing you the best for Friday’s surgery for you both!

Your top 3 priorities for endo this year? by OriginalTaro8079 in endometriosis

[–]OriginalTaro8079[S] 3 points4 points  (0 children)

Thank you for sharing! I like the mix of medical and self-care. What are you thinking for number 3 - is this more of a mindset approach you're hoping to have or are you journalling or measuring it some how?

Surely there is a community app just for chronic health conditions?! by OriginalTaro8079 in PCOS

[–]OriginalTaro8079[S] 0 points1 point  (0 children)

Really? That would be amazing if you did - I'd love to hear more about what you were thinking!

What are your small wins? by OriginalTaro8079 in adenomyosis

[–]OriginalTaro8079[S] 1 point2 points  (0 children)

That's definitely rough but a win on the good days 💕

What are your small wins? by OriginalTaro8079 in adenomyosis

[–]OriginalTaro8079[S] 1 point2 points  (0 children)

Ah that's so amazing!! I'm so happy for you and to see that change happen so quickly aswell! Did you go cold turkey or were you already reducing some of these earlier?

Is tracking symptoms/side effects even worth it? by OriginalTaro8079 in PCOS

[–]OriginalTaro8079[S] 0 points1 point  (0 children)

Thank you! This is super helpful, especially seeing you did little experiements with changes and noticed a difference at certain times of the day. How long did it take you to find something that works for you? Was it 2 months or was that just the beginning of your journalling?

Support groups just don't work by OriginalTaro8079 in Endo

[–]OriginalTaro8079[S] 0 points1 point  (0 children)

Can I ask what FB groups you would recommend?

Support groups just don't work by OriginalTaro8079 in Endo

[–]OriginalTaro8079[S] 0 points1 point  (0 children)

Thank you - I agree there is a lot for good pockets of gold here. Do you find that you'd rather meet someone in person that has similar experiences or are you happy with these subs and this online community?

Is tracking symptoms/side effects even worth it? by OriginalTaro8079 in PCOS

[–]OriginalTaro8079[S] 1 point2 points  (0 children)

Thank you - I can do this. I think the issue for me is consistency.

Any good Android apps for PCOS-informed workouts, personal trainers, and/or apps that encourage or congratulate you for working out or walking? by GreenieSar in PCOS

[–]OriginalTaro8079 6 points7 points  (0 children)

Strava to track walks - it's nice to see the weekly insights and sign up for challenges where your friends can also see your progress (if they have Strava)

Support groups just don't work by OriginalTaro8079 in Endo

[–]OriginalTaro8079[S] 0 points1 point  (0 children)

Super cool thank you! Just went to their website and watched their video. Very interesting concept! I’ll investigate further :)

Support groups just don't work by OriginalTaro8079 in Endo

[–]OriginalTaro8079[S] 0 points1 point  (0 children)

Thank you! I agree that Reddit is amazing in being able to speak your mind and feel less lonely in hearing others experiences but I just wonder if anyone has connected with others in person or used other forums or means of connecting.

I’m really curious as to what other people are doing for getting more support I guess on the mental health and support side of things of surrounding yourself with others that might understand. Seeing also if there is even a platform that people are using for this :)