u/FoolofaTookie93

I was diagnosed with raynauds back in January. All of my blood tests looked normal with rheumatology so it was said that I have primary. I have been having a lot of other health issues that lead me to believe I may have secondary and my PCP thinks so as well, we talked about me maybe getting a second opinion and I have been keeping record of all my symptoms. Has anyone been diagnosed with secondary raynauds even though all of your blood tests came back normal?

Hello! I am currently going through a lot of testing to find out if I have POTS, my doctor is leaning towards most likely yes but is wanting to rule out anything else. She recommended documenting any symptoms I notice. Does anyone have any recommendations on how best to do this? So far I have been taking pictures of my heartrate/blood pressure and jotting down how I felt and things like that. I'd really appreciate tips on how to get a good photo of blood pooling in my fingertips lol. In person I can really see how red my fingertips are but I have a lot of red undertones throughout my hands so it's hard to get it to show up in photos. For a long time I thought a lot of the symptoms I was having were from my anemia. What are some not so common symptoms some people are having? For example, my nose gets stuffy almost everytime I eat.