Tag Archives: Lovenox

March came in like a lion (in a good way)

Lucy had a very busy day with all the people in and out to check on her.

Dr. Dettis (infectious disease) was by and told her he was better than 90% certain her fevers and leg redness were solely from the clots, but he wants her to be on antibiotics for another day or two. That was reassuring for her to hear.

One of the hospital chaplains stopped by, and then Dr. Thurmes (hematologist) was by to see how she was doing. Unfortunately, her hemoglobin was at 7.1 so she received one unit of blood just before going to IR. He feels the Coumadin and Lovenox are not working and had two other anticoagulants in mind. One is Pradaxa, which is a pill. The other is a once per day injection which she couldn’t remember. We are hoping Pradaxa is a workable solution. Dr. Thurmes had a couple of areas he needed to research first.

Her TPA procedure got delayed because of a couple higher priority cases. She was originally scheduled for 8:30 and finally went down at 12:45. The procedure completed by 1:15. She no longer is on TPA and they can stop doing the neurological tests in another four hours. She should get more sleep tonight and have fewer interruptions.

She did have to have her arm IV access changed. Getting a different one in was very problematic. Her arms have really been poked. Certain drugs cannot be administered into a port, and her antibiotics are all incompatible with heparin.

Julie called tonight and like last night didn’t get much time to talk to Lucy. The arm access IV adventure was just beginning then.

Lucy got to sit on the edge of the bed for over a half hour. She even managed to stand up before getting back into bed. Tomorrow she will get out of bed and go for some short walks.

Getting the TPA catheter removed is a step towards going home. The next two steps are getting her off IV heparin and letting her leg heal a bit more. Getting the heparin level in line will probably be the most difficult given her experiences. We still don’t have a firm release date.

Keep your fingers crossed, and thank you for all the thoughts, prayers, positive energy, and good wishes!

Leave a Comment

Filed under cancer battle, DVT, family, hospital, transfusion

Mondays are supposed to suck, not Fridays

Lucy’s leg started getting worse this morning. She called Minnesota Oncology and they set up an appointment for 2:00 this afternoon.

Her nosebleed started at 1:30 and finally let up around 3:00. The nurse practitioner at Minnesota Oncology helped Lucy with her nosebleed. Anticoagulants are so fun. Dr. Thurmes also contacted her while he was at Fairview Southdale on rounds.

She was admitted to Fairview Southdale as a precaution. Lucy also had some extra blood work drawn along with blood cultures. They need to wait 18 hours after her Lovenox injection before they can start IV heparin. That means she will get awakened at 4:30 am. She just had completed an IV antibiotic because they suspect cellulitis. An ultrasound of the left leg found that the clot in her groin was solidifying. We are hoping she will not need a TPA catheter tomorrow. In the past few hours, she started running a fever, which is at about 102°F right now. The Tylenol will help reduce the fever.

It is frustrating that this clotting problem flared up again. More than likely, she is here until Sunday. We were looking forward to a nice quiet weekend at home and having her leg continue to heal. Now it’s back to a wait and see mode. Keep Lucy in your thoughts and prayers this weekend. It helps us get through these setbacks.

At least I don’t have to play Nurse Ratched with the Lovenox while she’s in the hospital. See, I did manage to find something positive.

Leave a Comment

Filed under cancer battle, DVT, hospital

Down to once per day

We started today with about two inches of snow. That is normally boring news but this has not been a typical winter. The snow was like the mashed potatoes served in the school cafeteria. The snow blower had problems with it because the discharge chute kept plugging. I think the snow lovers might be disappointed with the sloppy stuff, too.

Lucy’s leg puffed back up a bit by almost 2 cm though her pain is about the same. She is really run down today. We had suspected her hemoglobin was dropping and it has. She is at 6.8. Her two-unit transfusion will occur tomorrow at 7:30 am. It will probably take four hours to complete.

She also has to change her injection schedule before the next labs. We were targeting her injection for around 6:00 pm. This would avoid conflicts with work schedules, dinner, and TV. Now she is to get her injection at 11:00 tomorrow and work towards 10:00 by Monday’s lab appointment. The lab appointment also moved to 4:30. Of course, she’s going to be at Fairview Southdale IV Therapy at 11:00 tomorrow.

One thing we are happy about is she is down to daily Lovenox injections rather than twice daily. We also enjoyed Julie’s stew tonight. OK, enjoyed is an understatement; devoured is more like it.

Here’s hoping we have a dull and boring day tomorrow.

Leave a Comment

Filed under cancer battle, DVT, family, weather

Tomorrow will be a better day

Lucy couldn’t visit her dad today. Her thigh was too painful. This happened the last time she had a clot in her left leg. The good news is her calf diameter was almost a full centimeter smaller and the erythema is almost gone. Her right calf diameter also was 0.8 cm smaller.

It is astonishing at how painful a blood clot is. Her clots are maybe the diameter of a single piece of couscous. At times, she rates the pain as worse than her post-surgical pain. I’m hoping her leg pain is better tomorrow.

I visited her dad today. On my way there, I saw three bald eagles soaring over Highway 100 at Minnehaha Creek. He’s in pretty good spirits and enjoyed having company. Suzy and Steve also came by. Lucy’s family has treated me so well through the years and I enjoy being with them. I’m very lucky because I know too many people who have issues with their in-laws.

Her first Lovenox injection went well today and her second one was OK. I am either getting the hang of it or she’s learning to lie really well (just kidding!). I picked up one of her favorites from Qdoba on my way home tonight. That helped brighten up her day.

Lucy’s next blood testing will be on Tuesday. She was originally scheduled for one test on Monday and another test on Tuesday, but the two blood tests are combined now. We can’t wait for Tuesday because that is when her Lovenox cuts back to one injection per day. It appears she will be receiving injections for at least 30 more days. I do hope that she eventually goes back on Coumadin.

Leave a Comment

Filed under cancer battle, DVT, family

Laissez les bons temps rouler!

One sees the French phrase in the title plastered all over New Orleans before Mardi Gras and it supposedly translates to “Let the good times roll”. Well, maybe not today. Lucy woke up with stomach problems this morning and was running a mild fever spike because of her blood clots. Her mood wasn’t very cheery and she was completely wiped out. Alimta is usually well tolerated, but it still can cause a bit of stomach distress and wipe out. That’s why she has to take the oral steroid dexamethasone twice a day for the day before, the day of, and the day after chemo. The past few months have seen her face a number of challenges and it takes its toll. My guess is today’s stomach problems were a direct result of her breakfast choices. She hadn’t eaten Lucky Charms in several months. The whole grains sometimes cause a bit more fermentation in the gut when one is not used to eating them. She started feeling better later this afternoon.

Her first shot Lovenox shot went better than yesterday’s. We’re probably figuring out the right timing and rhythm. The humorous thing about the Lovenox self-injection guide is the phrase “think love handles”. Lucy doesn’t have any. Heck, I’ve dropped 54 pounds in the past year and barely have any remaining.

We hope Lucy will be feeling up to visiting her dad tomorrow. Her left leg circumference was almost a full centimeter smaller than yesterday’s measurement. Her discomfort is now mostly from both ankles and is probably joint pain rather than tissue pain. The painkillers are still effective and she is using fewer of them.

I think I am suffering from chemo brain by proxy. I forgot to mention Lucy had a coworker stop by Thursday morning with some homemade soups. Her coworkers have been so wonderful and supportive! They have made meals and sent cards and flowers. It’s nice to know there are some good companies left.

While on the subject of chemo brain, I managed to mangle the “Comfortably Numb” lyric yesterday. Sorry about that! How I managed to turn “just a little pin prick” into “you’ll feel a little pin prick” is beyond me. I’d like to say “Damn you, autocorrect” but I wasn’t posting from an iPhone. I have an Android phone and I can’t find an autocorrect equivalent, perhaps thankfully.

For those of you that are able, we hope you enjoyed a walk today. We hope Lucy is walking normally soon.

Leave a Comment

Filed under cancer battle, DVT