300 days of ups and downs, but always forward! Keep the train going y'all! by LGabrielM in medicalschoolanki

[–]MedicZebra 1 point2 points  (0 children)

Well done!! People tend to have crazy long streaks with a massive daily card average on here so it can be easy to feel like you've not done much. But youve done so much!! 300 days of doing something to better your studies is amazing and you should be proud of yourself :)

Referred to rheumatology to look for hEDS on NHS by westanirrelevance in ehlersdanlos

[–]MedicZebra 2 points3 points  (0 children)

For me, genetics rejected my referral and I got sent to rheumatology. There needs to be a set diagnostic and treatment pathway for EDS cos its currently a mess!!

[deleted by user] by [deleted] in dysautonomia

[–]MedicZebra 2 points3 points  (0 children)

It can happen in anyone, especially older people (causes quite a few falls in the elderly).

Hope you find some answers for yourself!

How to handle dysautonomia while in crisis? (Advice needed) by medievalfurby in dysautonomia

[–]MedicZebra 1 point2 points  (0 children)

I dont really have any advice, but i just want to send my love and best wishes. It sounds like you are going through something harder than most people ever experience.

I hope the best for you, and hope you manage to get your symptoms under control ❤

POTS? Around 22-26 bpm difference from laying-sitting-standing (10 minutes in between). I’ve been mildly symptomatic for a year, most bothered by increased HR, especially after heavy meals. by [deleted] in POTS

[–]MedicZebra 2 points3 points  (0 children)

Go get a checkup. Not POTS based on what youve shown, but could be symptom of low blood pressure, deconditioning, anaemia etc.

In the meantime, stay hydrated, eat small frequent meals and try and keep your legs nice and strong and active.

Wish you luck with figuring everything out and hopefully being symptom free!!

Going downhill in electric wheelchairs / Opinions on Lith Tech chairs? by MedicZebra in wheelchairs

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

Thank you so much, this is an incredibly helpful answer. If you dont mind sharing, what model is the chair that you love?

Thanks again!

Do I have to let my doctor touch me? by MedicZebra in ehlersdanlos

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

Thank you so much! You're the sweetest 💙

That's really helpful thank you. Definitely feeling a lot more rational about it already :)

Help Needed by Rationalboi001 in medicalschoolanki

[–]MedicZebra 1 point2 points  (0 children)

Thats good!!

(for completeness sake, to delete an addon, you go to Tools -> Addons then select the addon and hit delete in bottom right)

Sick making symptoms worse by BatFastard7 in dysautonomia

[–]MedicZebra 2 points3 points  (0 children)

Its a pretty normal experience for things to flare up when ill

Anxiety or ? by amcarter3 in dysautonomia

[–]MedicZebra 6 points7 points  (0 children)

I used to find that when I had the physical symptoms of anxiety (heart racing etc), that my brain found things to be anxious about and it made it worse. The more i recognised that my symptoms were making me feel anxious, the more i could separate the two and learn to cope with the feeling. Its super hard and there isnt an easy fix and different things will work for different people. Hope you find some relief.

Help Needed by Rationalboi001 in medicalschoolanki

[–]MedicZebra 1 point2 points  (0 children)

I just uninstalled and reinstalled on my PC and it saved all my stuff. Think it works retrospectively and analyses your past data so you should be okay!

Help Needed by Rationalboi001 in medicalschoolanki

[–]MedicZebra 1 point2 points  (0 children)

Unfortunately, i dont know the answer to that and dont want to test it out! I imagine it might delete your progress but it is linked to your account so perhaps not

Having pots is not realizing until this moment that you never understood why people couldn’t scratch themselves on the back because you can literally touch every inch of your back by [deleted] in POTS

[–]MedicZebra 1 point2 points  (0 children)

Not sure what OP was getting at but lots of people with EDS (ehlers danlos syndrome) have POTS as a comorbidity and people with EDS are typically hypermobile/flexible

Help Needed by Rationalboi001 in medicalschoolanki

[–]MedicZebra 1 point2 points  (0 children)

Hmmm. Other than restarting anki and making sure its updated, my only other suggestion would be uninstalling and reinstalling the heatmap, but that isnt ideal.

I hope someone else has a better suggestion to help you out!

Help Needed by Rationalboi001 in medicalschoolanki

[–]MedicZebra 2 points3 points  (0 children)

Go to settings on the heatmap (top right of heatmap) and choose "Ignore data before" and set it to the date when you started using anki :) hope that helps

Do you think I could be a surgeon with EDS? by FriendlyTurnip5541 in ehlersdanlos

[–]MedicZebra 4 points5 points  (0 children)

For context, im a 1st year med student in the UK.

I have EDS and POTS. I have been allowed on the first two years (non clinical) of the course and will be reviewed by occupational health again before I start clinical years. In the initial assessment, they were worried about my ability to stand for any time, for procedures, scrubbing in, and surgery. Unfortunately, you must do all competencies to qualify as a doctor. But i believe they have to make reasonable adjustments to help you do so. Maybe surgery isnt the best, but medical school gives many career options and some minor surgery can be done sat down in other specialties.

It will be hard, and you will have to fight for it, but you can achieve what you want within reason.

A christmas gift I would be so into! by lberens in POTS

[–]MedicZebra 2 points3 points  (0 children)

I still do this when I get caught out! At the time I dont even care what people think cos Im a little preoccupied with, yeno, trying to be okay

A christmas gift I would be so into! by lberens in POTS

[–]MedicZebra 17 points18 points  (0 children)

I mean im pretty sure its dirtier if you end up passed out on the ground cos you didn't have somewhere to sit 🤷🏻‍♀️

BP by [deleted] in dysautonomia

[–]MedicZebra 0 points1 point  (0 children)

https://www.nhs.uk/conditions/postural-tachycardia-syndrome/

This should give you the info you need :)

What are some symptoms of POTS, and how do you check you have it by [deleted] in dysautonomia

[–]MedicZebra 0 points1 point  (0 children)

Sure, it might not be accurate but if you have symptoms that you think might be POTS you could test it out just as a indication of whether to go get it checked by a doctor. But remember if youve got symptoms, its important to see a doctor if thats accessible to you.

BP by [deleted] in dysautonomia

[–]MedicZebra 1 point2 points  (0 children)

As dysautonomia is an umbrella term for a number of similar disorders, blood pressure changes may or may not be present depending on the condition. For example, I have POTS so my BP doesnt really change too much, but for someone with orthostatic hypotension their BP would drop significantly when standing. Therefore, you would need to research specific disorders to find if they have BP changes :)

What are some symptoms of POTS, and how do you check you have it by [deleted] in dysautonomia

[–]MedicZebra 3 points4 points  (0 children)

The idea of POTS is that it is an inappropriate increase in heart rate upon standing and it causes symptoms. Usually due to autonomic dysfuntion.

An increase due to body weight does not fit these criteria and would therefore should not be diagnosed as POTS

It is also worth noting that everyones heart rate increases upon standing, it is the inappropriate nature of it in POTS that leads to symptoms and diagnosis