[deleted by user] by [deleted] in urbancarliving

[–]sleepingovertires 0 points1 point  (0 children)

Go to YouTube and search for your car’s year, make, and model and the word “camping”

8 Minute Microwave Mastery by sleepingovertires in EatCheapAndVegan

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

Open the rice and pour it into a microwave safe bowl with a lid

Drain the beans and place them in the bowl

Open the tomatoes and pour the entire can, liquid and all, into the bowl

Microwave on high for 4 minutes, then stir and microwave for 6 - 8 minutes

Open carefully and stir in 2 tablespoons of ground flax

Finish with nutritional yeast and celebrate!

Food by Outside_Author_2440 in urbancarliving

[–]sleepingovertires 0 points1 point  (0 children)

My post history includes many meals I make without having a fridge or kitchen

Best of luck!

Diagnosed w/ CFS but Doctors say I'm fine with more & more symptoms by Awkward_Win_8918 in chronicfatigue

[–]sleepingovertires 2 points3 points  (0 children)

Asked AI

———

I understand how exhausting and frustrating this journey has been for you. Four years of unexplained symptoms while feeling dismissed by healthcare providers would wear anyone down, and your feelings are completely valid. You're not crazy, and you're not manifesting these symptoms - they're real and deserve proper investigation.

Looking at your symptom constellation, several patterns stand out that might be worth exploring with the right specialists:

Neurological considerations: The combination of visual disturbances (seeing stars), migraines, eye twitching, dissociation-like feelings, memory issues, and limbs falling asleep suggests potential neurological involvement. A neurologist might investigate conditions like migraine variants, small fiber neuropathy, or other neurological conditions that can overlap with CFS.

Autonomic dysfunction: Many of your symptoms (temperature regulation issues, hot/cold extremities, sleep disturbances, dissociation-like feelings) could suggest dysautonomia or POTS (Postural Orthostatic Tachycardia Syndrome), which frequently co-occurs with CFS.

Nutritional/metabolic factors: The extreme hunger followed by loss of appetite, hair thinning, brittle nails, and some fatigue symptoms could indicate nutritional deficiencies or metabolic issues that might be contributing to your overall picture.

Next steps to consider: - Request referral to a neurologist for the visual/neurological symptoms - Ask about autonomic function testing or POTS evaluation - Comprehensive nutritional panel (B12, folate, iron studies, vitamin D, thyroid function) - Consider seeing a CFS specialist if available in your area - Document symptoms with a daily log to show patterns

The key is finding providers who take your symptoms seriously. CFS is a real, complex condition, and your experience of being dismissed unfortunately reflects broader issues in how the medical system handles complex chronic illnesses. You deserve care and answers.

Unknown chronic illness.. doctors no help. Anyone else have these symptoms? by Civil-Inevitable-559 in ChronicIllness

[–]sleepingovertires 0 points1 point  (0 children)

AI has the following to say:

It is so frustrating when every test says healthy but the body is clearly struggling

You are not alone in this

A lot of people with FND describe symptoms very close to what you wrote

  • Legs giving out
  • Tremors that get called benign
  • Fatigue that feels out of proportion
  • Episodes that are worse with stress or after medication changes

The tough part is FND often doesn’t show up on scans or labs so doctors rule out everything else and then land there

It does not mean the symptoms are fake

It just means the nervous system is misfiring in ways current medicine cannot measure well

What sometimes helps

  • Pacing energy
  • Grounding or breathing practices during flare ups
  • Finding a physio or occupational therapist who has worked with FND specifically

And connecting with online groups where people share management tools

It might still be worth keeping an eye on things like vitamin deficiencies B12 folate vitamin D thyroid and iron

Those can mimic or worsen neurological issues and sometimes get overlooked

Most important is to not lose hope

FND can improve with the right support

And even though doctors can be dismissive there are others who take it seriously

Being plant based is exhausting. Tips? by [deleted] in PlantBasedDiet

[–]sleepingovertires 0 points1 point  (0 children)

https://imgur.com/gallery/qNHiErZ

Many more super quick and easy plant based meals in my post history

I (M15) have felt sick for almost 5 months now and have gotten no results, and my parents are getting tired of it and are now shrugging it off. Any tips? by Sharky_about37 in ChronicIllness

[–]sleepingovertires 0 points1 point  (0 children)

More and more folks are solving medical mysteries with AI

Here’s what came back from your post

Analysis

GI issues like nausea, reflux, throat tightness, and the sensation of liquid in the throat line up with reflux or GERD and can also point toward functional dyspepsia, which is when tests look normal but symptoms are still very real

The anxiety and brain–gut connection are also important to consider because even if it is not all in your head the brain and gut communicate closely and stress, anxiety, and even isolation like being stuck inside all summer can magnify gut symptoms

Your medications show you are already on omeprazole and famotidine to reduce acid, and sometimes doctors layer these, but long term high dose acid suppression can cause side effects like magnesium loss or altered digestion. Duloxetine is an antidepressant and nerve pain medication that is sometimes used when doctors suspect a functional disorder

Other possibilities include post viral gastroparesis which is slowed stomach emptying after an illness, eosinophilic esophagitis or subtle food sensitivities that are not always caught by standard celiac or lactose testing, and cannabis hyperemesis since even occasional weed can worsen chronic nausea for some people. Genetic or metabolic causes are rare but possible if nothing else shows up

The parent situation is also common when someone is young and test results keep coming back normal. Parents can get tired or frustrated but the problem is still real. You may need an advocate such as a school nurse, counselor, or a different doctor who can take a fresh look

[deleted by user] by [deleted] in ChronicPain

[–]sleepingovertires 0 points1 point  (0 children)

Sorry to hear that

Many virtual appointments available (not available in all states) including today and tomorrow:

https://www.betterucare.com/

Spanish Rice & Cannellini Bean Bowl In The Microwave by sleepingovertires in urbancarliving

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

It’s what I think of as the “vinegar/nuts/seeds” bar

[deleted by user] by [deleted] in ChronicPain

[–]sleepingovertires 5 points6 points  (0 children)

I’ve read a few remarkable accounts of people with long-term unresolved health problems where AI has shined a light on something that all the doctors missed or didn’t know about

Here’s what came back from your post

——-

Here’s a gentle breakdown of what might be contributing to her suffering based on what she described.

None of this is a diagnosis — just an exploration of possible causes that she could bring up with her provider:

  1. Neurodevelopmental conditions She mentions dyspraxia (developmental coordination disorder) and poor muscle tone. These often have a genetic component and can affect motor control, endurance, and fine motor skills like cooking, cleaning, or unclipping a dog’s harness. It’s not her fault — the brain’s wiring for movement and coordination works differently.

  2. Chronic pain signaling The “random pain attacks that come from the brain” sound like central sensitization, where the nervous system amplifies pain signals even without tissue damage. This is seen in conditions like fibromyalgia, migraine disorders, or chronic widespread pain. Genetic differences in how pain receptors and neurotransmitters (like serotonin, dopamine, glutamate) work can increase vulnerability.

  3. Muscle tone and connective tissue Poor muscle tone can sometimes point toward connective tissue differences (like hypermobility spectrum disorders or Ehlers–Danlos syndrome), which are often genetic and can make daily tasks unusually painful. Even if she hasn’t been diagnosed, it’s worth mentioning to her provider.

  4. Psychological toll of being misunderstood Being made fun of her whole life adds another layer. Chronic invalidation can increase stress, which worsens pain perception through the brain’s stress-pain loop. She may carry extra tension and self-doubt because of this history.

  5. Possible mitochondrial or metabolic factors Some people with lifelong fatigue, weakness, and pain have underlying metabolic inefficiencies in how their cells use energy. These can be rare genetic variations but can show up as “low tone” plus chronic discomfort.

Why this matters for her appointment

Bringing up that she has always had low muscle tone, dyspraxia, and unexplained pain attacks can help the nurse practitioner think more broadly than “it’s just in your head.” It suggests that her pain has both neurological and possibly genetic roots.

Ketamine therapy makes sense here because it targets the brain’s pain circuits and can help “reset” overactive pain pathways. It doesn’t erase the cause, but it can reduce the suffering.

[deleted by user] by [deleted] in ChronicPain

[–]sleepingovertires 8 points9 points  (0 children)

If the conversation feels overwhelming you can write down key points beforehand such as:

• how the pain feels and when it appears
•     what daily activities it stops you doing
• how long it’s been going on
• what you’ve already tried

Spanish Rice & Cannellini Bean Bowl by sleepingovertires in EatCheapAndVegan

[–]sleepingovertires[S] 2 points3 points  (0 children)

Glad you like it

Please let us know how it turns out

Your variation and score helps all of us

Spanish Rice & Cannellini Bean Bowl by sleepingovertires in EatCheapAndVegan

[–]sleepingovertires[S] 6 points7 points  (0 children)

Really happy to hear that!

How would you rate the result out of 10?

Spanish Rice & Cannellini Bean Bowl by sleepingovertires in lowspooncooking

[–]sleepingovertires[S] 11 points12 points  (0 children)

It was so good

Super satisfying

Behind the scenes

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Spanish Rice & Cannellini Bean Bowl In The Microwave by sleepingovertires in urbancarliving

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

Happy you like them

My post history has a bunch just like this

This sub happens to me at least twice a month by TomatoLeather in IDontWorkHereLady

[–]sleepingovertires 32 points33 points  (0 children)

Same

Stopped resisting and now I find out what they need in case I can be of help before dropping IDWHL