I am in desperate need of info regarding
SLECentral sleep apnea
Developmental reading disorder
Drowsiness
Insomnia concerns
Irregular sleep
Irregular sleep-wake syndrome
Islets of langerhans
Isolated sleep paralysis
Lupus - resources
Measles
Measles on the back and its involvement (or
> affect on) with the
autonomicAutonomic nerves
Autonomic neuropathy nervous system.
I feel like I am not getting proper medical treatment and am ready to check into
a hospital because I have been house-bound for 4 months, have been ordered not to drive
by the docs, not to walk more than 2 houses from my own, and IF I am able to go out
I have been ordered to stay in a wheelchair!
I have had
SLECentral sleep apnea
Developmental reading disorder
Drowsiness
Insomnia concerns
Irregular sleep
Irregular sleep-wake syndrome
Islets of langerhans
Isolated sleep paralysis
Lupus - resources
Measles
Measles on the back for 8+ years and recently was Dx'd. With steroids my symptoms have improved
> greatly except one
majorMajor tears
Major-gesic problem remains: I get horrible
convulsionsConvulsions
Convulsions - first aid - series
> that last 10-30 minutes (in 3 min. increments). One rheumatologist calls them
> seizures even though I don't lose consciousness (another is convinced their violoent
muscle
spasmsCoronary artery spasm
Croup
Eyelid twitch
Facial tics
Hand or foot spasms
Urge incontinence
Vascular spasm). However, each episode is preceeded by an elevated resting heart rate (140+),
an abundance of adrenaline, and then these violent full-body convulsions.
I also seem to be suffering from Transiet Ischemic Attacks ~ for me what happens is
I will be going along just fine and all of a sudden I "lose my muscles." Most of the
time I hit the floor, other times I grab hold of something. But it generally has the
same result, which is if I keep trying to physically move I become psuedoparalyzed, i.e.,
I FEEL like I cannot move. I try desperately to move, but it feels like my muscles are
fully maxed (like as if you're lifing too much weight).
>
> My rheumatologist is testing me for Neurocardiogenic Syncope, but I can't help but
wonder if this is getting off the beaten path. Any input?
Incidently, you may find it helpful to know that my anticoagulant test
> was boarderline, and my head MRI & CT scan, EEG, EKG,
> ECHO were all "normal." I have been exercising regularly for 21 of my 33
> years, I'm trim and otherwise "healthy."
Thank you!!
Dear Tee,
Your symptoms are a bit confusing. The neurologic signs in patients with SLE can include seizures, TIA's and strokes. These symptoms are often attributed to thrombosis (blockage) of small vessels and tiny hemorrhages in the head. Another mechanism could be the result of emboli from inflammation of the heart valves or low platlets. The lesions produced in the brain from a stroke should be seen on MRI scan. The seizures are secondary to the strokes. A generalized seizure that causes shaking of all 4 arm/legs usually causes an alteration in consciousness. TIAs are "mini strokes" produced by the above mechanism, however, the symptoms resolve in less that 24 hrs. There are not any MRI changes that occur following one of these spells. The symptoms you are descibing "feel like I cannot move" etc. are a bit unusual for a TIA. It does not sound as if you are having any symptoms that might be attributable to syncope other than "collapsing". Occasionly, we do see patients (with similar symptoms to yours) that have an underlying phychiatric explanation for the symptoms. The spells may occur "subconsciously". This is just one additional possibility. Drop attacks ( a type of seizure) can alos cause sudden loss of muscle tone. Perhaps a second EEG may be helpful. I hope this helps. Good Luck.