Hello,
I have been dealing with chronic fatigue and "spells" for 15 years since I had mono. This year, my "spells" have gotten more frequent and I have many more symtoms and much worse. I always have chronic fatigue, no matter if I'm in a spell or not. But the symptoms I deal with in a spell are bad congitive
dysfunctionBasal ganglia dysfunction
Carpal tunnel syndrome
Causes of sexual dysfunction
Chronic fatigue syndrome
Dysfunctional uterine bleeding (dub)
Ear barotrauma
Erection problems
Female sexual dysfunction
Femoral nerve dysfunction
Orgasmic dysfunction
Sciatica (lose my sense of time, peripheral awareness, short term
memoryMemory loss
Mental status tests). When it gets really bad, I quit driving becuase I pulled out in front of cars
twiceTwice-a-day this year.I deal with mild muscle aches and joint pains that seem to be getting worse, mild tingling in my
headHead and face reconstruction
Head injury
Head lice
Indications of head injury
Radial head injury, blackouts occassionally as I stand up and begin to walk, muscle jerkiness in my arms and
headHead and face reconstruction
Head injury
Head lice
Indications of head injury
Radial head injury that come and go,
tremorsEssential tremor
Familial tremor
Hand tremor
Tremor, slight numbness in my arms and hands, splinter hemmorhages under my fingernails, weight loss. I also have a rash since January that looks like ringworm. I was treated with dyfucan and it had no affect. I use a steroid creme on them and it takes the reddness out but I can tell the rash is still there. They are on my arms, breast and legs. They are flaky and circular. They tend to get larger without the steroid creme. I have tender sores (bumps)on my fingers and palms of my hands that are deep under the skin. They last for several days and then leave a small circle of dry skin. Blood work and lupus panel all ok. Being sent to neurologist. Is that the right Dr. I need to see? Have any suggestions on what may be going on with me? My Dr. is puzzled and says she can tell I am sick but really has no clue. This is very hard on my family as they do not understand how I feel. Thanks!
Chris
I am sorry you are dealing with this, good luck to you.