Face Pain Right Side - Not Sinuses

I have had MS since 2006, however, just diagnosed in 2018. Mobility, vision impaired, chronic pain in face which resemble sinuses. So for the month of May until now which is June 18, the pain has had me to urgent care/ER twice a week in tears. The pain has been so horrible cannot even compare to childbirth. I have had my blood pressure shoot from 287 over 115 as if I am about to have a stroke.

Prednisone and migraine medication have been my only comfort

Finally, was given Prednisone and medication for migraines, which has been the only comfort. Nevertheless, each time I go to ER/Urgent Care and explain I have PMS, I can on Ocevous treatments still the doctors question my explanation of the pain.

No one understands

I am often confused because I do not have MS to a science on what will be the next pain crash, but what I know it is this MS and how often we ALL might suffer with some of the same and then there are those things that are all brand new and no one understands what I am saying. I get the feeling that they believe I am making it up, does anyone else ever feel like that?

I am allergic to anything that has narcotic so I am not asking for medication, I just need the pain to go away. It is safe when you have 5 good days out of a month and I still laugh and smile because of my illness.

By providing your email address, you are agreeing to our privacy policy. We never sell or share your email address.

More on this topic

This article represents the opinions, thoughts, and experiences of the author; none of this content has been paid for by any advertiser. The MultipleSclerosis.net team does not recommend or endorse any products or treatments discussed herein. Learn more about how we maintain editorial integrity here.

Join the conversation

or create an account to comment.