midodrine

I have midodrine pills (5mg), but do not want to take it orally anymore. I want to make what this paper is proposing: https://jamanetwork.com/journals/jamadermatology/fullarticle/2290938 "Midodrine, 0.2%, in a moisturizing skin cream (Vanicream) was compounded at the Mayo Clinic pharmacy and...

Vascular dysregulation has been one of my most pressing Long covid symtoms. The worst part about it is the blood pooling in my feet. In the beginning I could sit up to work without issues. Around one year into the illness, I had one episode where I believe I overexerted myself, mainly my legs...

I started taking midodrine yesterday. I'm after input from people who have ME and POTS and take midodrine. When you take it you're not meant to lie down for 4 hours. Now for me that's quite a long time to not lie down/put my feet up. Does taking midodrine at the right dose take away the need...

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4951503/ (open access)

My 23-year old daughter was diagnosed with neuropathic POTS. She tried Florinef, at 1/4 of the smallest dose, and she took it in the mornings, but she had terrible insomnia from it. It also took about 2 weeks for those side effects to fully go away. Her doctor recently prescribed midodrine...

I've been prescribed midrodine for NMH and started off at 2.5mg plus sodium tablets, 3 times a day. That dose had no effect on my BP or symptoms after ten days so yesterday I was told to increase the midrodine to 5mg, 3 times a day. It didn't do much for my BP but it did seem to improve my...

I couldn't find a thread on this particular aspect of Midodrine and really wanted to get some feedback. I was started on Midodrine by my new cardiologist in the hospital, first at 2.5 mg 2x/day and now at 5 mg 2x/day. The goal was to raise my BP (which is in the 80's/50's without Midodrine)...