@mhonley: Let’s go over the results of my genetic test from @sequencing 🧬 #genetic #genetictesting #pots #potssyndrome #posturalorthostatictachycardiasyndrome

Mhonley
Mhonley
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Monday 29 December 2025 21:15:33 GMT
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laurakmr1
Laura :
40%+ if the population has the MTHFR gene.
2025-12-30 07:46:25
40
46537867767789k
Stephanie :
Btw this isn't reliable or very accurate results for genetic testing. Please go to your doctor.
2026-01-31 22:19:36
1
ttvangelbabyy
✨✨Angelbabyy ✨✨ :
I have POTS, Hypermobile EDS, Endometriosis and 4 autoimmune diseases 🥹 how much does this test cost?
2026-02-02 09:23:21
0
alilove2run
Ali Williams :
Why would it say you might have mthfr? Why would it say you did or didn’t
2026-02-01 06:24:24
1
neonglitch106
Kayla :
If you have a hard time breathing it could be more than asthma. Look into alpha-1 gene mutations. I am a carrier and they’re monitoring my lungs 😭
2025-12-29 23:25:36
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curatedbybrittny
Curated By Brittny :
I wanna get this done, but I hear such mixed reviews on sequencing.
2026-02-03 03:00:36
1
aliciag1234567
Alicia_2022 :
I just had genetic testing at Johns Hopkins. If anyone’s interested, they take self refer as
2026-01-01 04:00:22
4
qu33n_b333
Jessica Hart :
Do you have any idea of any insurance companies will cover this test?
2026-01-01 03:06:40
1
chronically.roxii
Roxann Fredette :
I have the double MTHFR mutation
2025-12-30 15:13:28
4
clumsy_bunny56
Bunny :
I want to do this test because I have underlight chronic conditions that still need solving, and I know nothing about my genetics .
2026-01-30 18:26:18
1
cediez256
cediez256 :
with you having raynauds and the nitric oxide being flagged look into endothelial dysfunction. this is when the lining of the vessels dont produce enough nitric oxide leading to vessels spasms. it is linked to dysautonomia and things like raynauds
2025-12-30 08:50:52
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molly_mo357
MO⛓️Y ⚜️ :
Do you mind me asking how much this cost? Super interesting in doing this! Thank you for sharing
2025-12-29 21:40:22
2
atravelingblingbar
Amy’s Traveling Bling Bar :
So did sequencing also, but where did you see the heart attack in there?
2026-01-01 09:45:56
1
kamilynn4
Kami :
Can you do the test while pregnant or will that change things? If not how long after should I wait?
2026-01-02 14:42:53
1
awarner4
Awarner :
I had mine done but sure can’t figure it out.
2025-12-31 17:35:39
1
jeepmomma93
jeepmomma93 Potslife :
I want to do this but nervous
2026-01-29 17:22:04
1
mariblesi
Mari Blesi :
How much did this cost?!
2026-01-30 04:18:51
2
1219rrc
Remington + Ruger :
What package did you use that showed pots? Thank you!
2025-12-30 04:55:02
4
agutheragu
Agu 🏥♾ :
My geneticist sent me for a whole genome evaluation for 3500 and it came out all normal which is good I guess 😅
2025-12-30 20:48:20
2
victoriarawrz
Victoria | Empoware :
Where did you go to get these tests/results?
2025-12-30 04:09:28
1
sahm.brook
Chronically ill Mama :
FYP. Fellow potsie here.
2026-01-28 23:55:07
2
daisymay8008
Daisymae8008 :
does genetic testing show illnesses you have or may have or is it just percentages of risk? I am considering having one done but it will be out of pocket for me.
2025-12-30 12:08:51
0
queenoverwatch
queenoverwatch :
I’m going to look into this. TY!
2025-12-29 22:46:25
2
chelleandcookies
Chelle Doesn't Share Cookies :
do you feel anxious, physically restless and uncomfortable if they give you normal saline in the hospital instead of lactated ringers? POTS usually comes from a brain injury, although there is at least one type of genetic POTS. So you can totally have both a sensitivity to salt due to genetics while still having POTS from a brain injury. I have POTS acquired from a head injury and normal saline gives me a reaction. I need about 3x the amount of salt normal people need, but i don't feel so great if I get any more than that.
2025-12-30 08:43:55
2
courtneyfinley28
Courtney Finley :
I have MTHFR & MTRR & COMP. And my sister has Hirschsprungs disease. And I have all the gene mutations as well and they tell you that typically you get diagnosed as a baby, but my sister didn’t. and she has horrible issues she had been in and out of the hospital, her whole life, but she didn’t get diagnosed until she was almost 30. You need to look more into your mutations. You probably just read your little doctors document. There’s a lot more in there. It’s kind of interesting to learn about it.
2025-12-30 18:09:01
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