Guys and gals,
I don't know where to put this, so I decided to make a new topic. Several of us are discouraged and/or worried at the moment, so I wanted to share a bit of good news:
Last week I called the CRS at Mayo that examined me a year ago. I also talked with her several weeks ago to get her opinion on the ointment I am using right when I started it after it was prescribed by my local CRS. At any rate, I had not heard back from the Mayo CRS and I told my husband that I didn't think I would hear back from her again. But, she called me last night. Seems that she had been out of town for a meeting. I asked her about Botox at Mayo. She has only been there a year but told me they have been doing it at Mayo for a couple of years and that it was first done in the UK. She said they would have to use an anoscope to check for a fissure before administering the Botox to the patient while asleep. But she said that if a fissure is seen using the anoscope, they stop the exam. I am finishing up my 8th week on the Diliatzem ointment, and she also indicated that I should be able to continue the ointment for another month safely. She said patients can develop sensitivity to the ointment after using it an extended period of time. She will be leaving in another couple of months because she is a fellow in training. I really liked her and hope to know where she goes afterwards.
Also, for those of you on Miralax. I had an appointment with my holistic family doc yesterday. She said that many people on Miralax have trouble regulating the dosage for constipation as the med can cause loose stools, so at least I am not the only one with this predicament. She also thought this support group is a good idea as the AF problem (as we know) is common, but is rarely discussed with others. That is my small bit of good news.
To health,
Cheryl