Because of the episode this morning, the ultrasound tech was unable to do the scan of Lucas's heart again to see it the PDA treatment worked. The next biggest hurdle for us is getting this heart valve closed. Until it is, Lucas will continue to have issues like this morning because his heart is not pumping blood and oxygen the way its supposed to. This may mean Lucas will have to have surgery which means he'll be transferred to Children's Hospital. It increases the risk we'll lose him too. The doctor is looking at his options to remove Lucas's umbilical cord IV and insert a ***PICC line because it lasts longer and is more suited for the efforts of giving Lucas medicine
We are gathering hope in the success stories of other micropremies, but are reminded daily to be prepared to lose our son. Going home without him today was hard but not nearly as hard as being home alone with an empty crib knowing it may never have my baby in it.
The bright news today is that the new medication I started last night has brought my blood pressure down well and I'm maintaining below 150's/90's. I'm moving slowly, but my furry babies were as excited as I've ever seen them to have me home. I've got plenty of chocolate to make me feel better and most of my fish lived through me being away though Brandon forgot to feed them most days. Thank you for follow our story and I hope you have a blessed night!
~Kristen
P.S. Prayers and best wishes to Aunt Alisa and her family for her surgery and recovery today.
*** Definition: Percutaneously inserted central catheters (PICC lines), are long, thin, plastic tubes that travel from a vein in an arm or leg into one of the large veins near the heart. In premature infants, they are used to deliver fluids or medications.
A PICC line is similar to a peripheral IV, but is longer and lasts longer. Premature infants have fragile veins, and peripheral IVs usually last only 1 to 3 days. A PICC line, though more difficult to insert, can be used for 1 to 2 weeks or more. PICC insertions are less invasive, have decreased complication risk associated with them, and remain for a much longer duration than other central or periphery access devices.
Stay strong.. there is a lot of us praying for you and Lucas you are a very special lady GO LUCAS!!!
ReplyDeleteKristen, I have tried not to post anything because I dont want my experiences to make you scared or nervous. I work in Labor and Delivery and I also float over to our Nicu and work there sometimes. I am not a nurse but a CNA and I have about 18 years experience in what I do. I dont know everything but I do know alot about micropremies and their development issues and sucesses. We almost always have at least 1-2 micropremies the age of Lucas in our unit. They all have alot of issues but usually end up going home with mom. Its not rare that they die but its more rare than them going home. Its great that he has done so well for the last 5 days. As you have been told its going to be a rollercoaster of ups and downs for him. Thats completely normal. They have made so much improvements in the technology lately in what they can do for these babies. My family is thinking of you daily and I check here often to see if there is any changes in him. Stay strong. This will be one of the scariest times for you. We love you.
ReplyDeleteAngel
still praying! You & Brandon & Lucas are in our thoughts constantly...you two are such strong & awesome parents for your little guy already!
ReplyDelete-Jackie D
Praying for you and your baby Kristen. Stay strong coz he needs a lot of support and love. Take care
ReplyDeleteSrijana