I have been noticing more and more over the last couple of years a rather flushed face, I thought it may have been the FA not telling me soon enough that I was actually too hot. However I am now pretty much always flushed much like in rosacea. Has anyone else had similar problems? Ironically the rest of me (particularly hands, feet and legs) get very very cold.
Friderichs Ataxia and Rosacea: I have been... - Ataxia UK
Friderichs Ataxia and Rosacea
Hi annasgonesailing!
My hands and feet can get very cold, also my nose!
On the other hand I can get very hot at times but am
well past the menopause.
I have noticed occasional red scaly patches on my cheeks
on either side of my nose. Prior to diagnosis I convinced
myself this was a symptom of Lupus, the test was negative.
I don't have FA but maybe these symptoms are just common
with Ataxia. xBeryl
Thanks Wobbly bee, I am going to see a Neurologist at the Ataxia clinic in Oxford in May so will put it on my list for them.
Forgot to say I am 29
I get patches of red,dry skin also but I am 54.Could be the menopause.Also go to Oxford.
Hot flushes I was taking amlodipine for high blood pressure stoped them flushes got better I get red blotches on checks too .do you take meds for any thing
Hi I have Friedreichs ataxia and was also diagnosed with rosacea about 18 months ago. I was referred to a dermatologist who prescribed me different creams and what a difference it made! Don't know if the two are related but worth asking?
X
Thanks Cally I believe rosacea can be triggered by flushing too much so it may be F Ataxia related
I suffer with FA a
I have
I found this a most interesting query. Around five years ago I was diagnosed as suffering rosacea. I had never experienced any skin problems prior to this, and was even relatively pimple free. A dermatologist did a good job of ridding me of the facial rash with antibiotics and laser treatment. A year or so later I contacted my doctor due to tthe fact that i was experiencing balance problems, after a brief interval Late Onset SC ataxia was diagnosed, it has now taken a firm grip on me.
I have often wondered whether or not there was a connection between the two conditions. I also find that my face still flares red occasionally. I suspect that the immediate trigger for that may be dietary. However I would be really pleased to receive any further information on this phenomenon so that I may bring it up with my neurologist, a very affable individual who cheerfully views SCA like a freak weather system, of unknown origin and uncertain future.