Has anyone had an issue with your cheeks always being pink? I have noticed that mine are constantly blushed. I am not sure if this has anything to do with PD (I am very newly diagnosed) I could really use some feedback . Thank you for being there for each other.
Blushed cheeks: Has anyone had an issue... - Cure Parkinson's
Blushed cheeks
When describing her trauma Miss Andrews turned a deep red. Her mind was going somewhere it did not want to go, panic issued. That is me dealing with anxiety. See her neck, they tried to cover the blush with makeup.
That poor girl! I wake up with rosy cheeks so it’s not from stress or anxiety. Although I do get very red during those moments. Thank you for responding.
I try not to get anxious ,but sometimes its hard.I take antidepressants and they help.
Might be worth looking up 'Rosacea'.
Thank you M_rosew I will look into Rosacea.
Just don't spend too much on a cure, I took years to get my rosacea under control.
😊
Mine have been lately, but only after I started taking all the vitamins and supplements everybody suggested. I had a total hysterectomy very early, so no hormone influence there.
Thank you for mentioning that because I to am taking vitamins and supplements and had a partial hysterectomy at forty, I am now 61 so I don’t think that hormones are affecting me either.Maybe it’s all connected.
MIne started about a month ago when I added the magnesium and B12 to my vitamin and supplement regimen, it has to be one of the two. I've never had a hot flash in my life and I skipped menopause, my ovaries left with the hysterectomy. Some doctors like to blame every ailment female patients have on menopause, and it isn't fair. I see your name is shakinginnc, I live just north of Charlotte, and I'm still trying to find a good neurologist. Somebody told me about one in Chapel Hill, but that's pretty far for me to go, although I might need to.
I have been taking vitamin B12 daily for about four years , I also had B12 shots prior to that for a deficiency so maybe that’s what is causing it. I live in Chocowinity (eastern NC) and go to a Neurologist in Greenville, She has a private practice, she is a bit of a nut case but has done so much more for me than my last Neurologist ever did. I hope you find one that you are comfortable with who can help you.
What sort of things has she done for you? My last three neurologists weren't much help.
She tested me for neuropathy which she found that I have. I had tons of blood work ups (they check everything) she sent me for an MRI and found damage in my neck. She sent me to PT for my neck and for gate training.
My old Neurologist didn’t do squat and told me that it was just essential tremors which run in my family, and I did have but developed into PD.He told me that “it might be an embarrassment but I’ll live with it ,other people have bigger issues than you. I am going to refer you for a psych work up” That was the last time I went to him!!!
Gee, sounds exactly like the last neurologist I went to, I'd think it was the same guy if I knew you didn't live so far away. What I love about this website is that people actually give you ideas about what you can do to alleviate symptoms and make life more tolerable. My feet cramped up so bad I couldn't even walk when getting up a few months ago, my toes would curl up underneath, now I don't have that problem because I've been taking the magnesium, and that's just one issue I've been able to fix, there are many more. What is gate training?
Gate training helps you to walk better, I take very short steps and use a cane because I don’t feel very steady. PT work with you to take bigger steps they put a belt around your waist and hang on to it to give you support. It helped for awhile but I am back to taking small steps again😳