i do eat like a toddler. and i’m not ashamed. 🤪
it’s easy, and YES i eat my vegetables too. this isn’t all that i eat, and i love to cook!! but i find myself gravitating toward outrageously simple food…
any theories? 🤔
i think it’s because of my POTS and slow GI motility, it’s just for my gut easier to break this stuff down. 🍔
Love and Light Wellness
Contact information, map and directions, contact form, opening hours, services, ratings, photos, videos and announcements from Love and Light Wellness, Coach, .
Riley Goodrich NBC-HWC, M.Ed, RYT
Nationally Board-Certified Health and Wellness Coach, health educator, and patient advocate specializing in hEDS/POTS/MCAS, nervous system health, and the diagnostic journey from confusion to care plan!
so many things to consider when treating my hEDS/POTS/MCAS, and it was so overwhelming at first to figure out what to do. 😵💫
here’s the most important things i’ve tried so far that have actually helped me!! ⭐️
the good news? 90% of my treatment is really just lifestyle change. and as a nationally-board certified health and wellness coach, i work with folks who have hEDS/POTS/MCAS everyday alongside their providers to figure out what works best for them!! 🥳
comment “bendy” or check out my website in my linktree for more information and a link to book a free consultation!!
💻 loveandlightwellnessvt.com
hEDS/POTS/MCAS is so misunderstood!!! 🥲
labs almost always come back “normal” (surprise, there is no lab for hEDS), and the recommendations most providers make are vague at best…
why should i eat more salt? how much? what does it do for POTS? 🧂
what does getting a hEDS diagnosis do for me? 🤔
i know i look healthy, but i don’t feel healthy. is it all in my head…? 😟
you’re not crazy. it’s not in your head. and there is a way out. 💛
as a nationally board-certified health and wellness coach who works exclusively with folks who live with hEDS/POTS/MCAS or think they might, these are all questions i get everyday. and i go IN DEPTH about how our bodies work. because if you don’t know the WHY, we definitely can’t do the HOW. ✅
getting a correct diagnosis changes the playbook for your care!! it is VITAL!! i’ve seen it myself because i’ve lived it.
check out my website for more information and a link to book a free consultation!! ⭐️
💻loveandlightwellnessvt.com
30/05/2026
COMMENT SUMMER FOR A LINK! ⭐️
https://calendly.com/loveandlightwellnessvt/hypermobility-huddle-a-zebra-support-space
The past few weeks, I’ve been flooded with questions about dealing with the summer heat and traveling with chronic conditions. I am so happy that you all have such exciting adventures planned! ☀️
And I hear you when you say you’re worried about the plane ride, long drive, or not being in your safe space. 🚘😳
I’ve got you. 💛
Mark your calendars — our next virtual Hypermobility Huddle is Sunday, June 14, and we’re diving into a topic so many of you have asked about: traveling and dealing with the summer heat with hEDS, POTS, and MCAS. 🥵🧊
We’ll talk pacing strategies, packing essentials, navigating flares away from home, communicating needs with travel companions, and how to make trips feel possible without the post-travel crash being the whole story. Bring your questions, your wins, and your “what would you do here?” scenarios. ⭐
The group is trauma-informed and accessibility-minded, facilitated by a National Board Certified Health & Wellness Coach (NBC-HWC) and experienced yoga and meditation teacher who lives in a hypermobile body herself. 〰️
Whether you’re newly diagnosed or have been navigating this for years, you are warmly welcome here. 🦓
All sessions are recorded, and if you can’t make it, I always send out the video to all who registered! 🎥✅
If cost is a barrier, please reach out. I want this gathering to be as accessible for everyone as possible, and that includes making it affordable based on your situation. 😊
“why does everyone have POTS all of a sudden?”
girl. we just had a pandemic. 🦠
there is an abundance of cited research that connects long-covid and POTS. there are also connections between POTS and other conditions like hypermobility disorders, hEDS, and Lyme. ⛓️💥
📣 POTS IS REAL! AND WE AREN’T FAKING IT!! 📣
i’m convinced that since POTS primarily affects women, it just isn’t “worth looking into” for most providers because it presents like anxiety. 🥲
if you want help getting your POTS properly diagnosed and treated, i’ve got you. ⭐️
as a nationally board-certified health and wellness coach (NBC-HWC) who works with folks daily on the diagnostic process for hEDS/POTS/MCAS, this is my bread and butter. 🍞🧈
check out my website for more info and a link to a free consultation!!
💻loveandlightwellnessvt.com
25/05/2026
taking time off is so important, especially when you live in a body that needs more slowness to thrive. 🐌⭐️
during my week off i…
⭐️ graduated with my M.Ed!!! 🎓
⭐️ went camping for the first time this season 🏕️
⭐️ attended an amazing community gathering hosted by 🌷
⭐️ applied to speak at a naturopathic education conference, thank you for your recommendation !! 🙌🏻
⭐️ paid attention to my pace points using my visible band .health (check out my linktree for $20 off yours!!!) 💛
⭐️ read two books from the throne of glass series (and now i’m hooked on dorian…) 📚
⭐️ ate a beautiful, gluten and dairy- free, earl gray blueberry cake from my amazing bestie tal’s bakery 🎂
⭐️ took so many sunset walks and ate so many cremees!! 🌅🍦
⭐️ tried out my new wheelchair downtown, and winnie did so good! ♿️🐶
i missed seeing my clients this week, and am so excited to hear all of their updates!!! 💞
what do you look forward to doing on your time off this summer?! ☀️🍉
chronic illness teaches us that self-care is not an option. 🙂↔️
health is inherently political. when disabled folks use the accommodations and aids they need, it is not only self-care but a rejection of the message that we need to be in a different body to be okay. 💛
be exactly who you are, in exactly the body you’re in. ⭐️
hEDS rarely acts alone. 🥴
i myself have 5 diagnoses, and many of my clients present with at least one other condition alongside hEDS. 💛
this is why screening for comorbidities is so important during the diagnostic process!! many of the most debilitating symptoms for folks aren’t from hEDS, but actually from its comorbidities. ✅
want support with all of this? the diagnostic process is TOUGH! and as a nationally board-certified health and wellness coach with a bunch of clinical experience in this field, i’ve got you. ⭐️
check out my website for more info and a link to book a free consultation! 😊
💻 loveandlightwellnessvt.com
MCAS is one of those conditions that gets missed BIG TIME in both primary care and speciality clinics…. 👩🏼⚕️🩺
📣 never medical advice! 😊 📣
so many folks have system-wide symptoms like migraines, flushing, acid reflux, weight fluctuation, and insomnia, but none of their physicians are putting together the missing piece: mast cells. 🔬
the diagnostic criteria is up for debate right now in the MCAS research scene, but symptom improvement with antihistamines is a big piece of it. ✅
want support with the diagnostic process for conditions like MCAS, POTS, and hEDS? i’ve got you - and i’ve done this before myself. as a nationally board-certified health and wellness coach who works with folks who are dealing with complex chronic illness, this is my jam. 😛
check out my website for more info and a link to book a free consultation!! ⭐️
💻 loveandlightwellnessvt.com
go outside today - even just a minute or two. 🌳
your body and your nervous system will thank you for it. ⭐️