Abigail Helen Martin

Abigail Helen Martin MY ONLY REAL PAGE. All others are fake & unfortunately i cant do anything about it 🫠
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The woman who made my childhood colorful 💛🦋💐 I love you mama 🫂
05/10/2026

The woman who made my childhood colorful 💛🦋💐 I love you mama 🫂

A morning in our backyard ✨🌷🌲🐛🦋🌾
05/03/2026

A morning in our backyard ✨🌷🌲🐛🦋🌾

The surf trip of my dreams 🌞🌊🐠🌵✨💛📷 -I’ve been taking this camera everywhere for the last 2 years and it has quickly beco...
04/17/2026

The surf trip of my dreams 🌞🌊🐠🌵✨💛📷
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I’ve been taking this camera everywhere for the last 2 years and it has quickly become my favorite camera I’ve ever used🤞🏻 Nicaragua was such a perfect trip, & going back through all the photos makes me feel like I get to re live it all over again :,)
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To get the film/warm/grainy look I use the simulation “portra 400 Warm” from Fuji Weekly!!

04/08/2026

Surf trips> any other trip ☀️🌊💛

For the girls who just wanna lay by the river 🦋✨☀️🌈💛
03/31/2026

For the girls who just wanna lay by the river 🦋✨☀️🌈💛

03/20/2026

Expensive but WORTH IT✨
These are the Clarika Cotton Wide Leg pants! When I saw the price tag I immediately was like “absolutely not” BUT- these would’ve saved me so much hassle & money in the past trying to find a pant that I love & actually fits me!
Taking them climbing next week so time will tell how they hold up!

03/19/2026

Oh how I love being a woman ✨🎀
5 years ago I was diagnosed with PCOS from a doctor that, in hindsight, did not do enough testing to formally diagnose me. Since then I’ve tried really hard to balance my hormones by decreasing inflammation via diet & exercise. But a lot of my symptoms kept getting worse, and no longer fully correlated with PCOS. For the last month I’ve done a lot of tests (blood panel, topical ultrasound, pelvic ultrasound, pap) and found a doctor who actually LISTENS to me, and doesn’t just tell me to take ibuprofen and tough it out.
She told me in infact (likely) dont have PCOS (it could just be in remission), and that endometriosis is likely the culprit.
The average time it takes women to get diagnosed with Endo is 9-12 YEARS. Partially because of the difficulty of diagnosis, and partially because of doctors not believing women when they say they’re in pain.
I’ve been turned away from so many doctors saying “periods are just painful, take some Tylenol”, or just immediately prescribing birth control.
It took me 10 years to actually find out what’s going on in my body, and I wish I would’ve known it wasn’t my fault.
I hope I can somewhat spread awareness and encourage women to ADVOCATE for yourself!! If a doctor isn’t listening to you- find someone who will, or demand the testing anyways.
I’m hoping to get the surgery in the next 1 1/2 years and find some relief. If you’ve gone through a similar experience I’d love to hear your story❤️

03/05/2026

Well worth the hype I must say 😮‍💨

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Portland, OR

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