The Fog Thickens

The fog has become increasingly difficult to navigate. During this phase I have been in lately with the pain being ever present I find the fog has gotten more intense. I did not know what the Fibro Fog really was for me until recently. But now I see it clearly.

For me there is nothing more disturbing than to have someone tell you that you had a conversation with them, but yet you do not remember it at all.  It has been happening mostly during stretches where my pain is intense and I am unable to control it. I find this strangely comforting however, because I can assign it to my fibromyalgia and not alzheimers, (I hope!)

The “I Hope” part is the most alarming of all. I have no way of knowing for certain that it isn’t Alzheimer’s only that the Fibro Fog is also a significant symptom discussed by Doctors as happening to those of us who have fibromyalgia. So it is to that I cling. In the meantime I think it best not to spend a lot of time worrying about something that I cannot control at this point. I will however, be searching for any suggestions on ways to control or limit “the fog”.

Peace and Blessings

About C. Matusky

Owner of retail online store selling items for gifts and to help folks like myself who have chronic pain conditions.
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