“I experienced pain in joints for years, but I always thought my days as a runner was the reason. My heart fluttering started 3 months before my diagnosis.
I continue to experience joint pain and I am scheduled for an MRI of my liver and heart so I feel very nervous about those results.”
Read more from Shellshocked in the full post.
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“I experienced pain in joints for years, but I always thought my days as a runner was the reason. My heart fluttering started 3 months before my diagnosis.
I continue to experience joint pain and I am scheduled for an MRI of my liver and heart so I feel very nervous about those results.”
Read more from Shellshocked in the full post.
Continue reading
“I experienced pain in joints for years, but I always thought my days as a runner was the reason. My heart fluttering started 3 months before my diagnosis.
I continue to experience joint pain and I am scheduled for an MRI of my liver and heart so I feel very nervous about those results.”
Read more from Shellshocked in the full post.
Continue reading
“I experienced pain in joints for years, but I always thought my days as a runner was the reason. My heart fluttering started 3 months before my diagnosis.
I continue to experience joint pain and I am scheduled for an MRI of my liver and heart so I feel very nervous about those results.”
Read more from Shellshocked in the full post.
Continue reading
“I experienced pain in joints for years, but I always thought my days as a runner was the reason. My heart fluttering started 3 months before my diagnosis.
I continue to experience joint pain and I am scheduled for an MRI of my liver and heart so I feel very nervous about those results.”
Read more from Shellshocked in the full post.
Continue reading
“I experienced pain in joints for years, but I always thought my days as a runner was the reason. My heart fluttering started 3 months before my diagnosis.
I continue to experience joint pain and I am scheduled for an MRI of my liver and heart so I feel very nervous about those results.”
Read more from Shellshocked in the full post.
Continue reading
“I experienced pain in joints for years, but I always thought my days as a runner was the reason. My heart fluttering started 3 months before my diagnosis.
I continue to experience joint pain and I am scheduled for an MRI of my liver and heart so I feel very nervous about those results.”
Read more from Shellshocked in the full post.
Continue reading
“When the covid-19 lockdown first started in March, one of the early suggestions going around in nutritional circles was to up your intake of vitamin C and Zinc especially the liposomal vitamin C, highly absorbable. So I did that starting in the beginning of April…by the mid to end of April I had become increasingly jaundiced and exhausted all the time and I could not keep food down, so my doctor ran tests and found it.
I was Triple National gold medalist in competitive swimming and I’m looking forward to feeling like being much more active very soon.”
Read more from Spacey and dive into the full story by clicking on the post.
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“I have a prior rare blood platelet disorder that had required life sustaining transfusions that combined with other treatments activated the HFE gene mutations. I have no issues yet but iron must be reduced. I was tested as my brother was diagnosed last year. Unfortunately due to the stabilized rare platelet disorder, I am not a candidate for standard phlebotomy treatment and had an adverse reaction to Deferasirox an oral chelator, and now will require subcutaneous Deferoxamine chelation.”
Read more from Ang by clicking on the post.
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Diagnosed with hereditary hemochromatosis around 12 or 13 years old.
“I still get very tired, and I experience a lot of anxiety and heart flutters. My biggest symptom now is hair loss.
I am a 20 year old Auckland girl who loves working, exercising and having a good laugh!”
Read more about Iron Lady’s story by clicking on the post.
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