On January 13th, Chuck gave us a scare. His heart rate was up to 212 and not going down. He was not overdoing it as he was relaxing on the couch when this happened. So we took him to the Emergency Room and the doctor said that he had what they call PSVT which is short for paroxysmal supraventricular tachycardia. http://www.medicinenet.com/paroxysmal_supraventricular_tachycardia_psvt/article.htm is a website that explains more information about what it is and what the symptoms are and how it is treated. Chuck’s doctor prescribed a beta blocker for him to take. He did a followup appointment and everything seemed like it was okay but then he seemed to get more symptoms afterwards that we thought could be side effects from the beta blockers he was taking. It turned out not to be side effects however.
On January 24th, we made another trip to the Emergency Room. He was having a hard time breathing without pain. He also had heart palpitations and a heart rate of 220 when he got to the ER. So they ran tests on him and thought at first that maybe he had pneumonia but then determined after a CT scan that he has a blood clot in his lower right lung. So they have been doing blood tests and giving him blood thinners and meds to ease the pain. They admitted him to the hospital that night and have been monitoring him closely. He is in an ICU room but not because he needed to be in ICU, simply because the hospital was full and they did not have a room for him except for ICU.
After he was admitted to the hospital that night and I had the kids all tucked into bed, I took time to look up blood clots in the lungs and what came up was “pulmonary embolism”, which after reading was really scary. I almost wished I hadn’t taken the time to look it up. What I read seemed to fit all the symptoms Chuck has had so it really put things into perspective for me but it sure scared me too. But when I mentioned this to Chuck, he seemed to think that according to the doctor, this wasn’t what he has but it would seem to me that the doctor may not want to use that term when discussing his illness and treatment with him. I am hoping to learn more from the doctor soon. At any rate, this is something that sure makes you NOT take life for granted. It makes you realize what your family and loved ones really mean to you.
Today Chuck told me that they did an ultrasound of his heart. He said it was neat seeing the colors and how the heart works.
He also said that the care he has been receiving here at the Glendive Medical Center has been really wonderful. We are hoping he will be home in another day or so.
Any prayers you want to send his way would be greatly appreciated. I know I sure have been saying my share of prayers lately, with his health the way it is and no income for us right now either. Things have not been so great for us in the first month of 2009. But we are hopeful things will improve. We are trying to stay positive through all this.