While I muddle through each as best I can , I usually do not speak so much of my physical pain or issues .. my only focus of late is getting where I can be me , and getting my butt to a good doctor .. I have thought that maybe I have had a relapse , I try not to think it , as I have had only one in the past 7 1/2 years ..
But I do believe it is a flare-up of my MS .. not fibro .. as I sit and write this , I must confess that in my heart I know it is ..
There is not much one can do .. when you get inflammed like this all that you can do is rest , hahaha , and realx , hohoho , and pray it only lasts a short time ..
The last flare lasted a bout a year .. it took me six months to get the nerve up to go to a neuro and have an MRI , as my coverage only pays 80% .. and anyone who has had one knows just about how much they cost ..
Wow , that felt good to get off my chest .. and this is the wonders of MS , there literally is nothing I can do .. oh , I could go to a hospital ER , but who would watch my babies ?
Putting them in the hands of strangers , putting myself in that position is a risk in itself .. so I try not to focus on this .. but after I get to telling my bro about my plans , I will talk with my therapist in depth about it ..
Not anything really anyone can do .. no surgery, just an IV or something and I would rather move than do that , at this point ..
I do hope that you all just take deep breathes , pain or no , confusion or not and just breath ... in therapy you can make an "I" statement .. this is mine today ...
Even though I am in pain, and even though I am hurting , I care deeply about myself and love myself and accept myself for who I am" .. and breath .. as I sit and repeat my mantra for the day , each day it may change .. I find it can calm me, soothe me and part of me is happy that I have this place and my "family" here , that I can turn to ..
Peace people, be glad for what you do have today , okay ? me
1LIFE2LIVE



I do hope this doesn't turn out to be a flare...or if it is, that it's short-lived. Please let us know how you are doing.
You are so right about loving and accepting ourselves as we are. Focusing on positive things in our lives can make such a difference. Keep those positive statements flowing!
Hi Adrian,
I am catching up on reading my favourite shareposts. Even though I have read this post originally on the Grind, re-reading this today I felt compelled to write to you today. Sometimes, writings can be just words but yours is written from the heart.
I can sense the worry and also the bravery within you as tell us about your new and re-occurring symptoms......admitting simultaneously to yourself and to us that is may be an MS flare up. I am sorry Adrian that this is happening to you.
Like Karen, I commend your positive mantras as you come to terms with the new symptoms.
I hope you will get to see an MS specialist as soon as possible in Arizona. I understand, from what you have said, that there may not be anything to do but there may be some new developments in the treatment or some new ideas for you to consider to help you cope with your newest symptoms of this flare up.
Thank you for sharing,
DS Deb