Thanks Mer,
I’m so sorry that you are having such a rough time. I hope you get some relief soon. I'm glad to see you are maintaining a sense of humor. I think about you and others on this forum all the time. I think Harvey gets a little jealous of the amount of time I spend checking in. But I can never forget the relief I felt when I first stumbled on this forum. I had no idea how many people were suffering the effects of ESLD. The support I found here proved invaluable. I want to give back as much as I can.
The additional tests you mentioned were performed on Harvey after he was hospitalized at Florida Hospital. It further confirms for me that Shand’s was blowing smoke. We met two other patients that had similar experiences with Shand’s and ended up getting their transplant at Florida Hospital. It’s a crying shame.
Thank God for the Internet. When Harvey was first diagnosed with PSC, few people had access to the Internet. I went to the public library and only found one reference to this disease. It was in a large medical reference book and it was only one paragraph long. It wasn’t encouraging at all.
The knowledge I gathered from the Internet has helped me actively participate in Harvey’s care and engage those responsible for his medical care. It’s given me the confidence to advocate for him.
I gotta get ready for work. Take care of yourself and your husband. Keep the faith. You are in my prayers as always.
Love,
Penny