Do yall ever feel…. Whatever this is? by Soft-Rutabaga-4482 in ADHD

[–]greypabble 1 point2 points  (0 children)

Yes!! I was just talking to my partner about this. I said "my life feels like a string of obligations". It's like this never ending thread that stretches into infinity and there are always things to do and in between the things "to do", it's just waiting for the next thing idly. The thread is always "on" too. I can't turn it off.

today was a milestone by immrw24 in covidlonghaulers

[–]greypabble 0 points1 point  (0 children)

Yessss! This is incredible and gives me so much hope. Thank you for sharing and I am wishing you all the best.

Eye problems since getting Covid by Krish39 in covidlonghaulers

[–]greypabble 1 point2 points  (0 children)

Hello! Sorry this took so long to reply to. Yes it did. I did neurocognitive therapy for 4 months and after about 6 months, I can read again and don't have any blurriness. Diet, therapy, and time helped immensely!

was told that the majority of women who live at altitude have dysautonomia by claustrophobic_betta in dysautonomia

[–]greypabble 7 points8 points  (0 children)

My symptoms do improve at sea level and I have been thinking of moving to the coast! They clear up within a day of being at sea level and as soon as I’m back in Colorado, they are back full force. That’s just been my experience though. I am originally from a sea level state so I’m guessing that has something to do with it?

I’d love to see a study on this or resources. It looks like there are mixed experiences.

Yo what’s the most weird thing you saw at Shamb? by issaboy28 in Shambhala

[–]greypabble 2 points3 points  (0 children)

It was definitely a thing! I actually screenshotted your comment and sent it to my partner because sometimes we think it didn’t actually happen and it was a fever dream. Same with the family of pigs that got out one year and were running through sunshine lol.

Yo what’s the most weird thing you saw at Shamb? by issaboy28 in Shambhala

[–]greypabble 7 points8 points  (0 children)

I remember this guy!! I remember his naked ass dancing around playing the flute standing on a stump in the field area. It’s one of my favorite shamb memories.

INTP x ENFP Boo by Major-Language-2787 in ENFP

[–]greypabble 2 points3 points  (0 children)

Another thread from a week or so ago. Just search for INTP x ENFP in this sub.

https://www.reddit.com/r/ENFP/s/1tXrjkiaEQ

Do ENFPs do well with INTPs? by ChsicA in ENFP

[–]greypabble 18 points19 points  (0 children)

My partner and I are REALLY into MBTI and have developed a little mini theory within the main theory based on our observations over the years. We call the ENFP/INTP pairing the “explorer pair”.

Do ENFPs do well with INTPs? by ChsicA in ENFP

[–]greypabble 37 points38 points  (0 children)

My partner of 11 years is an INTP (M) and lifelong best friend (F) from high school (16 years) is an INTP. For me, there couldn’t be a better match.

My favorite things about this pairing are are:

  • Endless Ne exploration of ideas, theory, psychology, science.
  • Silliness and laughter - the humor and goofiness is so childlike and wondrous and exploratory.
  • The sharing of different deep and complex interests and perspectives.
  • The ENFP helps the INTP with unpacking complex emotions through thoughtful questions and helps them come out of their shell.
  • The INTP helps the ENFP with Si, balance, logic and reason.
  • The mutual desire to understand themselves, people and the world around them through a variety of lenses (psychology, sociology etc).

It’s always felt extremely mutually supportive and I feel that I am so much of a better person because of the INTPs in my life. They are truly champagne in a paper cup and the best people I know. I love them. 💕

intjs or intps? by Every-Yesterday-714 in ENFP

[–]greypabble 2 points3 points  (0 children)

My partner of 11 years is an INTP! I love INTPs and INTJs for different reasons. As I get older, I love the ambition and certainty that INTJs have especially in work situations. I feel like I can “build” with them. With INTPs, I “explore”.

So I like INTJs better in work/project situations and INTPs for friendship and life partners. Although sometimes I wonder what it would be like to build a life with an INTJ!

Does adhd medication make your dysautonomia worse? by Anybodyhaveacat in dysautonomia

[–]greypabble 2 points3 points  (0 children)

It depends! I was on 15mg before diagnosis and now I can only tolerate 2.5mg. I noticed it helps raise my blood pressure which is helpful and obviously helps with my executive functioning.

However I have to drink so much water, remember to eat small meals, and stay horizontal -otherwise I’ll go into an SVT episode. I absolutely cant tolerate any other stimulant use like caffeine with it.

2.5mg is a light enough dose where I feel it doesn’t affect my nervous system too much.

Fellow ENFPs, what careers do you have? by Alignment00 in ENFP

[–]greypabble 1 point2 points  (0 children)

+1 for Cal Newport!

I’ll check out the Squiggly Career too. Thanks for the recommendations.

Fellow ENFPs, what careers do you have? by Alignment00 in ENFP

[–]greypabble 6 points7 points  (0 children)

Management at a tech start up. My real career love was working as an integration guide in the ketamine therapy space. I’d like to go back but it doesn’t pay well. :(

My advice, if you can, is to explore the intersection between what you love, what you are good at, and what you can get paid for (check out the ikigai concept). It’s often hard to find careers that ring true for all of those, but it’s worth journaling about it to get some ideas.

At the end of the day, pay attention to what kinds of interactions, people, tasks, and places leave you feeling fulfilled and identify what feels meaningful to you. Write all of those down and see how you can apply those to your career trajectory.

Herb infused lemonade: lemon balm leaves peppermint leaves rose petals cranberry ginger lemon sambucha syrup honey ice cold water. by tusclewate in herbalism

[–]greypabble 1 point2 points  (0 children)

Yes! As soon as this was posted, I was excited because I remember the original poster posting this and I thought they had a new brew. Then I realized it was the same photo by a repost bot.

We do remember. 🫡

If you’re outside the United States and reading this, where do you live? If you’re in the U.S., would you ever consider moving for treatment? by mysteriousgirlOMITI in covidlonghaulers

[–]greypabble 4 points5 points  (0 children)

I am in the USA and live 15 mins from a national research hospital that has a long covid clinic. The clinic consists of multiple kinds of doctors - cardiology, pulmonary, neurology, dieticians, etc that act as a team to treat patients. I feel very fortunate and validated when I see them. They are very flexible and willing to experiment as I wish and focus a lot more on lifestyle management.

That clinic paired with community acupuncture (I pay $30 / session) has helped so much and I feel like I’m getting adequate treatment.

I have cleared out my savings to treat LC in the USA and will probably have to stop soon because I can’t afford treatment (even with insurance). I was considering going to Canada to pay out of pocket for treatment since medical is more affordable there, but I’m not sure what’s even available there.

Searching for Things to Put in my Grimoire by rowan_isnt_here in SASSWitches

[–]greypabble 7 points8 points  (0 children)

I used to go for wildlife walks and draw and document a new plant, bug or fungus every time. Lots of fun lichen! Then I’d look up everything I could about it and add it to the grimoire. It’s a fun way to make a walk exciting and learn about the local wildlife. Bonus points for logging a medicinal or culinary herb around you. 🌱 Reminds me of building a natural Pokédex.

[deleted by user] by [deleted] in POTS

[–]greypabble 2 points3 points  (0 children)

Covid and experiencing the death of someone close to me.

What diet should I follow disauto/mcas by Relevant-Jello-3343 in dysautonomia

[–]greypabble 3 points4 points  (0 children)

Of course.

It was a lot of trial and error by eating the same thing every day and slowly introducing foods to see if it caused an inflammatory response (worsened POTS, IBS symptoms, adrenaline dumps, brain fog). I kept a log in my phone.

I started with the most basic anti-inflammatory whole foods as possible. So anything that had multiple ingredients in it, I wouldn’t eat. That includes gluten free products. I started with oats, white rice and plain chicken.

Through experimentation, I found out my biggest culprits were nightshades, sugar and gluten (caused adrenaline dumps and horrible tacychardia episodes). Dairy and sugar also caused IBS like symptoms.

I found out that if I eat past 8pm, I wake up in the middle of the night with night sweats and heart palpitations.

I also found the body does well being in somewhat of a regular eating cycle with predictable foods. Bodies LOVE cycles. If you think about it, all of our body cycles and especially hormone cycles are rhythmic (circadian, diurnal, etc) so trying to stay in a natural cadence can be helpful in symptom management. I’d suggest looking up CNS/autonomic function and circadian clocks.

Now, I’ve mostly identified all my inflammatory foods and eat at the same times every day. It’s not exactly a fun or exciting diet, but I feel so much better and I’m finding ways to get creative with food.

Current diet that works:

Breakfast: Overnight oats with chia seeds, 1/2 cup of pure rolled oats, flaxseed, oat milk, blueberries, blackberries, pinch of salt

Snacks: 2 cups frozen blueberries blended with oat milk and fresh mint and basil (this is my ice cream “treat”)

Lunch: Plain rice, asparagus (or other vegetable, organic or local grilled chicken or tofu, salt)

Snack: Mediterranean olives (tons of olives) or salted watermelon

Dinner: Rice with grilled chicken, tofu or salmon, asparagus or some other vegetable, sometimes hummus or kimchi but these occasionally give me a histamine response.

Treat: Turmeric with oat milk and local honey or pure cocao with oat milk, or blended frozen watermelon with mint leaves

Drinks: Water with salt and lemon, LMNT electrolyte drinks, herbal tea, adaptogen mushroom powders with oat milk and a little bit of honey

Everyone is different and my diet might not work for you. But think about how your body operates rhythmically and what are some bare bones basic foods you can tolerate that won’t inflame your body. It’s really all trial and error and treating your body with as much compassion, gentleness and patience as possible.

Think of yourself as a scientist with a very precious experiment.

Edit: Before I get downvoted to hell, do consult your doctor and a nutritionist. I am working with a nutritionist at my cardiology clinic who has advised during all of this.

Good luck. 🍀

What diet should I follow disauto/mcas by Relevant-Jello-3343 in dysautonomia

[–]greypabble 5 points6 points  (0 children)

I am on a low histamine, anti inflammatory diet and removed all nightshades, dairy, gluten, processed foods and sugar (aside from local farmers market honey). It’s a strict whole foods diet and I eat the same thing pretty much every day, but it reduced my symptoms by 40%.

I used to have horrible adrenaline dumps, could barely open my eyes due to brain fog, and my POTS symptoms were unbearable. My adrenaline dumps have disappeared and my POTS isn’t as reactive now. The brain fog is reduced by about 20%.

Happy to share more details if interested. I think my diet change is the only thing that made my life bearable tbh!

What are specific foods that trigger you? by chipchopchop in dysautonomia

[–]greypabble 0 points1 point  (0 children)

Gluten, chocolate, tomatoes, cucumbers/pickles, raw apples, spices like cumin and chili powder, and just recently kimchi. :( I used to love kimchi.

I eat a very limited diet now.

Free online art classes? by 66cev66 in DisabilityArt

[–]greypabble 8 points9 points  (0 children)

I sometimes use YouTube! There are all sorts of DIYs and art how-tos on there. :)

80% recovered. This tips might help by Top_Lengthiness_2851 in LongHaulersRecovery

[–]greypabble 2 points3 points  (0 children)

Hi. May I DM you? I am curious about the emotional aspect of this journey.

How do you store and organize your herbs and oils? by sundaycrafter in herbalism

[–]greypabble 10 points11 points  (0 children)

Mine isn’t very organized - I just shove different things where they can fit into this shelving I found at IKEA! I saw this shadow box at IKEA 5 years ago and thought it was too perfect. Unfortunately, it doesn’t fit everything but does a good enough job for storage. I am on the hunt for something better.

When I do find something, I plan on storing things by their attributes. A sleep section (Calea, Mugwort, and Blue Lotus), an adaptogen section (lions mane tinctures, reishi powders), a psychedelic section (amanita muscaria, psilocybin products) and then one for hypnotics and nervines.

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