Nice having many of my doctors in one place: endocrinologist, rheumatologist, medical oncologist. It is chronic disease alley. The pain clinic is also there. Haven’t been to that one yet. Lucky for us, the nurses and assistants are very helpful people. The place is always decorated for the current season or holiday. Coffee and tea are served as well as juices and graham crackers. There is never more than a few minutes wait. It is a welcoming, reassuring place. We even have our own lab. Never more than one person ahead of you.
Other areas of the hospital should follow their example. I don’t dread my appointments.
Dr L is an expert in her field. She is conservative, thoughtful and considerate. Her visits are never rushed. I am 100% confident in her choices for me.
I had not seen her(had talked to her on the phone) since my RAI (Radioactive iodine) treatment. The pill that had been presented to me in its 20# lead container was impressive and got my son’s attention that day. Being radioactive was fun only in that my meals were delivered to me. I read, watched movies and chilled. The next week I had a full body scan(doesn’t include knees down for some reason).
The complication came suddenly with severely inflamed salivary glands, throat, total mouth and tongue. Quite painful! Impossible to eat. Dr L ordered prednisone and soon my whole head and neck was feeling better. This is a common complication. Avoid it if you can. Drinking a lot of water is really the only help.
My Dr L’s appointment started as 20 minutes but ended up an hour. I have new cancer. The RAI might have helped it but in all likelihood it will still be there for the next ultrasound. Another surgery would be the next step. The suspicious lymph gland may not be receptive to the RAI, may be gone, may be something else. A biopsy might be next with possible external beam radiation. I’m still hypothyroid so more levothyroxin for now with a possible change to medication with T3 as well asT4.
Might just as well feel like a hero in your own movie.