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I think my husband will be diagnosed very soon. He has every symptom in spades. GP still looking
for nutritional deficiency or hormone imbalance; thank good he has not said HE believes its MSA.
I understand that Multiple System Atrophy is very rare. Its not even listed on this site among the
very long of medical conditions.
Is anyone on this site living with MSA or caringi for an MSA patient?
GG
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