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Looking for answers to what to expect next. My husband was diagnosed

with sarcoidosis in 1990 when a tumor was removed from salivary gland.

He had no symptoms until in 1998 he developed hydrocephalus (water on

the brain) which led to shunt being inserted and discovering sarcoid

lesions in the bain. Since this time, he has various neurological

issues -- leg tremors, unsteady gait, hands shake, confusion, muscle

and joint weakness, etc. He also has developed severe sleep apnea,

bradycardia (resulted in pacemaker implant) bilateral hearing loss,

vision impairment due to keratoconus, diabetes, hypertension and poor

performing pituitary gland (male hormone replacement and thyroid

medication). Fell and developed a blood clot in leg but doctors are

reluctant to treat with thinner due to medical risks. Recently legs

and feet were severely swollen so doctor prescribed water pills and

increased airflow volume on CPAC. Also on nebulizer 5 times a day

using Albuterol and Pulmocort. Legs continue to swell are extremely

hard and red. Hate going to the doctor because it only seems that

another medication gets prescribed on top of long list already being

taken. Wanted to discuss with doctors possibility of decreasing some

of the meds. Have any of you experienced these symptoms and what

actions have you taken?

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