Haemochromatosis and Parkinson's Disease

[nh_user_60793]

Six years later, I find that I now have Parkinson’s Disease. Now knowing the signs, I have had it for years but it is now so arduous to walk and stand. It sounds strange but the symptoms of HH morphed into symptoms of Parkinson’s. The fatigue, bone and muscle pain, thermo disregulation, gut pain, hormone imbalance, etc. etc. are all part of Parkinson’s too. But HH has got nothing on Parkinson’s. I would rather just still have the HH. I still have vx every three months. Just putting it out there. I wonder if there any others have developed Parkinson’s.