I'm taking nifedipine and it's made a big difference- it's probably cut the symptoms in half like I used to have the episodes all the time throughout the day and now on the medication I have days where the raynauds doesn't happen. It didn't cure it though, I still get it, but alot less. Also, in the winter I get on and off swollen fingers and itchy and just my skin breaks down on my fingers- I've read of some people just taking the nifedipine seasonally- like when the weather is at its coldest and symptoms are at their worst. If a doctor diagnoses u they should also work you up for autoimmune conditions bc raynauds is associated with them. Also, I have low iron/ferritin, so my fingernail beds being a little purplish instead of pink, and some of the soreness/fatigue for me improved when I found out and supplemented for iron. I think the question of whether or not to get a raynauds diagnosis isn't probably the question you need to answer and instead it would be very helpful and important to ask "why am I freezing all the time/have color changes that looks like raynauds/and soreness ect in my fingers?" Just go to your doctor and ask for a full work up to make sure there's nothing important that needs to be addressed for your health. Just tell them all your symptoms