Initially, I posted my situation in early October at which time I stated that I have
MalignantCancer
Gestational trophoblastic disease
Lymphoma, malignant - ct scan
Malignant melanoma
Malignant otitis externa
Melanoma of the eye
Multiple myeloma
Skin cancer, malignant melanoma Hyperthermia (diag. via biopsy, 1999) and that I was scheduled to see a neuromuscular doc for severe/pervasive muscle cramping/stiffness throughout my body (but primarily in upper back and lower legs)...at that time you replied w/ the following thoughts:
centralCentral sleep apnea
Central-vite core disease, myotonic
dystrophyBecker's muscular dystrophy
Duchenne muscular dystrophy
Muscular dystrophy
Muscular dystrophy - resources
Pseudohypoparathyroidism, and proximal myotonic
myopathyCardiomyopathy
Dilated cardiomyopathy
Hypertrophic cardiomyopathy
Muscular dystrophy
Peripartum cardiomyopathy
Restrictive cardiomyopathy. Since my initial posting I've had an EMG w/ results that stated "EMG showed SASD's in all muscles tested." WHAT IS/ARE SASD's? Note: I've since learned (over past several weeks) that my mother, 2 sisters, 1 brother, and a cousin have some similar symptoms.
My
primaryPrimary amyloidosis
Primary biliary cirrhosis
Primary hyperparathyroidism
Primary insomnia
Primary lymphoma of the brain question is this: It seems as though many of the
myopathiesCardiomyopathy
Dilated cardiomyopathy
Hypertrophic cardiomyopathy
Muscular dystrophy
Peripartum cardiomyopathy
Restrictive cardiomyopathy w/ symptoms similar to mine (e.g., Muscle stiffness, Muscle twitching, Muscle cramping, Increased Sweating, Delayed muscle relaxation, Pharyngeal Dysphagia, Poor/fitful sleep, Migraines, and Fatigue) are diagnosed earlier in life, whereas I'm 38 and have only started having problems in the past 3-5 years. More specifically, I've only started to develop these symptoms since my 1999 surgery, during which I had an MH reaction during a surgical procedure. I'd sure appreciate any additional thoughts. P.s., I have a follow up appointment for a muscle biopsy in 6 months. Sincerely, Steve
* Cramps and stiffness
--Distal > proximal
--with pharyngeal involvement
* Hyperhidrosis
* Fasciculation
* Myokymia/Neuromyotonia
* Fatigue
Although Isaac's syndrome is rare, your symptoms seem to match (especially the excessive sweating). You should have labs done for CK (elevated in 50%), K+ antibodies. There is no cure for Isaac's syndrome. Its course is varied and symptoms fluctuate. They are exacerbated by exercise. Treatment is symptomatic, involving anti-seizure and immunosuppressive treatments.
Ask your Neuro about this.