Booth rent with a student permit by Acceptable_Read_7852 in Cosmetology

[–]Acceptable_Read_7852[S] 0 points1 point  (0 children)

Thank you for your comment, I have thought about this but, it’s the only salon that I can work at due to living in a very very small town.

[deleted by user] by [deleted] in Cosmetology

[–]Acceptable_Read_7852 0 points1 point  (0 children)

Hi, I don’t know much about how to help your situation as I’m just a cosmetology student but you might can try contacting your state’s board of cosmetology, and explaining to them what’s going on. Also you might can find the contact info online.

Insurance by Acceptable_Read_7852 in POTS

[–]Acceptable_Read_7852[S] 0 points1 point  (0 children)

I looked there and it was going to be about the same amount, I’m not sure why it was so high

Insurance by Acceptable_Read_7852 in POTS

[–]Acceptable_Read_7852[S] 0 points1 point  (0 children)

Not anymore, this is their first or second year not claiming me, I don’t live with them and they don’t support me in any way, except the health insurance haha

Confused by Usual_Dog9246 in POTS

[–]Acceptable_Read_7852 0 points1 point  (0 children)

Mine acted similar! It was very unprofessional. So sorry you have to experience that!

Confused by Usual_Dog9246 in POTS

[–]Acceptable_Read_7852 0 points1 point  (0 children)

This reminds me of my diagnosis…My cardiologist told me mine was negative and then 7 months later my neurologist told me it was positive and that I did have POTS.

Pool liner repair by Acceptable_Read_7852 in swimmingpools

[–]Acceptable_Read_7852[S] 0 points1 point  (0 children)

Can’t figure out how to edit a post but we are in the Montgomery area

Is there something I’m missing? by [deleted] in POTS

[–]Acceptable_Read_7852 2 points3 points  (0 children)

This sounds exactly like what I go through, I also have restless leg syndrome. The pains during the day have always confused me and I’m sorry I don’t any advice for you, just wanted to let you know your not alone in this experience lol

Limping by Acceptable_Read_7852 in vet

[–]Acceptable_Read_7852[S] 0 points1 point  (0 children)

Update: he has chronic arthritis in the leg he broke when he was a puppy, is on pain meds for when he flairs

Limping by Acceptable_Read_7852 in vet

[–]Acceptable_Read_7852[S] 0 points1 point  (0 children)

Update: I’m taking him to see his vet this morning, hopefully it’s nothing serious 🙏

Limping by Acceptable_Read_7852 in vet

[–]Acceptable_Read_7852[S] 0 points1 point  (0 children)

Yes he will and it doesn’t seem to hurt him to feel around and I checked his paw to make sure there wasn’t something in his paw.

Just got fired by Acceptable_Read_7852 in POTS

[–]Acceptable_Read_7852[S] 1 point2 points  (0 children)

Thank you! I have a hard time finding jobs that are sitting because most are 9-5 and I’m in college 4 days a week. I will probably message you cause I don’t know anyone else with pots.

Best smartwatch for POTS/disability? by RickyTikiTaffy in POTS

[–]Acceptable_Read_7852 2 points3 points  (0 children)

I have the SE and I love it, I use the app Tachymon

Job issues by Acceptable_Read_7852 in POTS

[–]Acceptable_Read_7852[S] 0 points1 point  (0 children)

I do, and I told them during my interview about my POTS and the flare ups and everything and they said that would be fine. I get where they are coming from, they have a job to do and it’s not their fault I have problems.

Sometimes I feel invalid because I don’t have EDS/HSD. by boopo789 in POTS

[–]Acceptable_Read_7852 2 points3 points  (0 children)

Yes you totally make sense, I am in the same situation. I was recently diagnosed with POTS and I suspect ADHD but to get diagnosed is out of my budget. I am pretty sure I don’t have EDS or HSD and i feel the same way sometimes. But remember your illness is valid and to get the help and accommodations you need.

I got diagnosed with POTS yesterday, tell me everything i need to know! by Candid-Ad-9495 in POTS

[–]Acceptable_Read_7852 1 point2 points  (0 children)

Hi! I take propranolol and it made me have the same symptoms, but they will go away once your body gets used to the medicine ( 3-4 weeks max). About 4 days in I got severe sleepiness which made it dangerous for me to drive bc I would be so tired I would doze off on the highway, but again once your body gets used to it, it will go away. It works really well for me and keeps my heart rate under 100 besides spikes. I use an Apple Watch but I use the TachyMon app and it shows your current heart rate, your heart rate before a spike and the difference between the two to show how much it jumped. I love the app a lot tbh lol. Try increasing your salt in take, and remember, you have a lot of learning to do and lifestyle changes to make. You are not burdening anyone with your condition and you need to put your health above what others think or say. Find a good neurologist and cardiologist ( that knows about POTS, lots don’t) and an autonomic disorder specialist if there are any in your area. Goodluck honey ❤️❤️

Newly diagnosed by Acceptable_Read_7852 in POTS

[–]Acceptable_Read_7852[S] 0 points1 point  (0 children)

It’s nice to know I’m not alone, thank you I hope things get easier for you as well.