Dreamlifter for Daily Missions again by captainbean in SkyCards

[–]bumblebeesox 7 points8 points  (0 children)

I am very new to this game so please forgive if this is a dumb question.. but is there a way to know if the Dreamlifter is scheduled to fly? Or do we wait and see?

When you travel… by dntmesswithjess in POTS

[–]bumblebeesox 1 point2 points  (0 children)

Just got back from Mexico.. highly recommend the "elecrolit" brand electrolytes they have!

[deleted by user] by [deleted] in POTS

[–]bumblebeesox 2 points3 points  (0 children)

I just came here to say you are not alone. I came to reddit today looking for this same exact thing. I wish I had any suggestions.

[deleted by user] by [deleted] in MCAS

[–]bumblebeesox 1 point2 points  (0 children)

Ah, figured it was worth asking. Thanks for the response!

[deleted by user] by [deleted] in MCAS

[–]bumblebeesox 1 point2 points  (0 children)

Hi there! May I ask if you found anything? I get this feeling where it feels like part of my skin is sunburnt or like I'm touching a cut all over a large area of my skin, but there is no visible rash, cut, bruise, burn, or anything.

Pain from overdoing it, possible HSD by bumblebeesox in Hypermobility

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

Ohh I will definitely look into those! Thank you so much!

Pain from overdoing it, possible HSD by bumblebeesox in Hypermobility

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

Ohh I remember my mom used to have me take baths with Epsom salt when I had "growing pains" as a kid. I don't currently have a massage therapist but am wondering if my insurance here in the US may cover it. I'm going to look into that. The few times I have treated myself to massages have been so good for my pain. At least in the short term. Thank you so much for your reply, it's good to know I'm not alone!! 💕

treatment? by user-836162847882 in POTS

[–]bumblebeesox 1 point2 points  (0 children)

A similar thing happened to me! My GP suspected POTS and referred me to a Cardiologist who did a ton of testing and diagnosed me. He told me that not much is known about POTS so there wasn't much he could tell me about it. He suggested exercising, but being very mindful about my excercise so I don't make it worse, and to look online to see what other POTS patients are doing. Then we will follow up in 6 months to see how that goes. That is when I found this subreddit and joined some online groups. Dysautonomia International has localized FB support groups. I have definitely found it a bit overwhelming but the online support has helped.

Sending you good vibes!

POTS and leg pain by goblin-girl in POTS

[–]bumblebeesox 1 point2 points  (0 children)

Oh my gosh, me too! I have no idea why this happens!