Since January my health has continued
to decline even with various aggressive treatments, including
chemotherapy. We met again with the neurologist on November 29 and
it seems the disease progression has slowed. He had hoped the
treatments would have made improvement in my current condition, but
was glad the treatments had "kept me out of the ICU and off a
ventilator." I am grateful for that too!
The High Resolution CT of my lungs and abdomen came back normal. No signs of problems except for a "fat liver." That goes along with the rest of my body! The negative CT confirms that my breathing problems are directly related to my Myasthenia Gravis and Small Fiber Neuropathy. So, I will continue with immune system suppression treatments.
At present, the six
months of chemotherapy will probably be extended to one year. I will
keep you posted.
PS: Going for my fourth cytoxan infusion today!
PS: Going for my fourth cytoxan infusion today!
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