@eviemfitness: The Reality of being a Gym girl with Dysautonomia. I have VVS & POTs and had recently had a week of rest due to lack of sleep & general fatigue. I felt a lot better this morning, so wanted to train uppers with my fiancé and was really looking forward to it. Sadly, this doesn’t always work how I want it to. My blood pressure kept on dropping & I was really flaring with being in that position with my arms above my head. Decided to try seated bicep curls instead, but I was still really struggling with feeling the contraction in the targeted muscles & fighting off the feeling of breathlessness & presyncope. Fiancé suggested I try single arm, to place less stress on my body, but even this was a struggle. This was when I started getting upset because that feeling is still so unnerving and scary. I hate it. The dizziness and nausea, with the ringing, blurred vision and knowing what comes with it, leaves you feeling extremely vulnerable. I am so lucky to have the support system I have & this is so important for those of us with disabilities & chronic illnesses. After we left, I could barely move- my fiance had to practically carry me upstairs and help me get changed. My body had just shut down & I couldn’t stand without passing out, for more than a few seconds. Today has instead turned into a sofa & rest that body day 🩵 so important to listen to your body & whilst I still could’ve kept trying to push it, I know it would’ve resulted in a faint & made me feel both physically & mentally worse. I share these vulnerable moments so that you know you’re not alone & you don’t have to be 🤍 #gymgirl #dysautonomia #dysautonomiaawareness #dysautonomiapots #pots #potssyndrome #posturalorthostatictachycardiasyndrome #vasovagalsyncope #faint #chronicillness #spoonie

Evie | Fitness & Nutrition
Evie | Fitness & Nutrition
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Thursday 17 July 2025 16:01:27 GMT
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river._.is._.tired
River :
What’s the arm thing?
2025-07-19 07:33:03
0
avital.yechiel
Avital Yechiel :
So when you have this flare ups you feel like crying? Cause it happens to me too and i thought it was weird 🙈
2025-07-17 16:54:01
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p1nk.x0x
Pink|✨🎀🎧 :
So much respect to u x
2025-07-26 14:22:22
0
mi_cafecito_con_chisme
La.CaTa:. :
watching this video made my so emotional. The courage in this video. this happens to me sometimes but just figured i need to lose more weight in eat healthier. I'm afraid it's dysautonomia. keep it pushing girl. your strong in beautiful. you got this!
2025-07-23 17:40:20
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madalynolive
maddie olive :
What’s the device u have around ur bicep, I have pots so just wondering if it reads ur BP
2025-07-25 01:15:04
2
lillian_williams
Lillian Williams :
I’m glad that I’m not the only one that still gets scared I feel like I have to hide that I’m scared because I feel I should be used to it since it’s been a year I’ve been diagnosed but it’s comforting to not feel alone about being afraid.
2025-07-17 18:25:59
5
natalie.serene
Natalie :
This is so real 😭 and validating- I feel crazy for wanting to cry every time I feel a faint coming on and then I know it only works me up/stresses me out more- it’s just the worst cycle. Sending spoons 🙏💖
2025-07-24 20:24:14
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lizy7501
lizy✨️ :
Yo también lloro cuando me dan crisis porque no puedo hacer lo que los demás a veces. Te entiendo 😪
2025-08-01 07:33:17
0
lindasmilealot
smilealot58Linda :
Yup , my standing at the cable machine and arms drops my Bp and could be it dropped from my treadmill just doe as it drops a lot…I chk it in the locker room, still at denial stubborn stage…
2025-07-18 04:09:00
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estone1218
emily stone 😇💐🌅💖🫧 :
I have pots and I have just started to exercise again after watching your videos!! you’re doing amazing 🥰🥰🥰
2025-07-17 20:46:23
3
brittany5022
Britt :
It’s soo overwhelming I hate this ! I have pots and can’t do over half the things I used to be able to ! You inspire me to try to do more
2025-07-18 02:51:23
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limehottie31
Kate Joosten :
do you use a heart rate tracker or specific wearable you use to help monitor your flare ups? I have been trying to find a better one than fitbit with a google watch.
2025-07-18 20:18:45
0
kfabe86
kfabe86 :
Do you have a trigger for your vvs? I was just recently diagnosed and have no trigger. It just comes out of nowhere and is so scary!
2025-07-19 03:53:14
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chronicallytiffany
ChronicallyTiffany :
I wanted to give you a hug when I saw you well up with tears. I get it girl. I’m so sorry 💙
2025-07-18 21:43:57
3
elizabeth.d.henderson
Elizabeth Henderson :
Okkk am not the only one that struggles so much with dysautonomia flares with pull-ups ?? Why is this exercise so bad???
2025-07-22 19:45:39
1
cedemccormick
Cede McCormick :
I have POTS and race BMX. I have had to sit on a few races or simply not finish them due to my blood pressure dropping and me nearly fainting while riding. Listening to our bodies is so important. You're doing amazing.
2025-07-19 06:04:18
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siva_thas
Sisi :
He’s so precious with uuuu
2025-07-17 16:22:12
50
grassyassyx
Grace ❤️ :
i’ve had to completely remove any vertical exercises whilst it’s so hot bc i just kept ending up in massive flares and crying
2025-07-17 18:06:40
0
p1nk.x0x
Pink|✨🎀🎧 :
With crohns my reps change allot it’s disheartening
2025-07-26 14:20:55
0
mfajerski
M :
Some days are so hard can’t even go to the gym bc I go alone so that’s amazing that you always keep trying and not give up
2025-07-17 17:43:57
0
diannaxx3
D❤️‍🔥 :
This is so real
2025-07-18 23:22:21
0
coco12345789103
user7072945745138 :
It’s so unnerving and frustrating. That’s great you have support and empathy. It’s difficult to explain what’s happening. I feel like I’m acting dramatic but I literally feel like collapsing
2025-07-17 17:30:52
17
helena.e.j
H :
Girl I can’t even raise my arms above my head with out the room getting dark and almost passing out🥲
2025-07-17 16:43:40
1
em_my2913
Emily Waite :
It’s the most terrifying thing to experience this. So frustrating and eats away at my determination to get things done.. you’re so strong to be able to go to the gym, I’m too afraid to.
2025-07-17 16:56:46
1
kathryn_simon1203
Kathryngotitall :
Mine is different it makes my heart rate sky rocket but it feels so debilitating but when I do have my good days I realize some days I’m just going to have to adjust because my body is different and that’s okay.
2025-07-17 19:59:47
1
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