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I understand it’s different for everyone, but I wouldn’t mind hearing a rough ballpark idea or people’s own experiences. I was diagnosed with multiple PEs in March, but I had the symptoms for years before and I am thinking because they were left undiagnosed for so long my symptoms now might last longer. The pain was unbearable at the beginning of treatment but since I have changed to tinzaparin it is a lot better. But twice a month when ovulating and just before my period the pain, my heart rate and my breathing get worse. Is this going to go on for years? Miraculously I have no serious damage to my lungs or heart so I am hoping its not going to be for life.
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