I had two options on the date….Nov 3rd and Nov 23rd. I decided to go with the earlier date for a couple of reasons.
1. Why shouldn’t I get this surgery over with as soon as possible? If I waited until the 23rd that would be the absolute last day I could have the surgery without having to get another Lupron shot. Just in case we get a freak snow storm in late November, I am NOT going to pay another $1000 for a shot.
2. The sooner I have it, the more Lupron I have left in my body (even though I think that it is supposed to be a time release-type shot over the three months). The more medication I have left in my body= less bleeding during the surgery.
3. Thanksgiving will be three weeks after the surgery which means I should have no problems walking around, hanging out with CP’s family, etc.
4. The surgery will now be a full five weeks and a day before CP and I leave for the Bahamas for a quick December vacation. I’m hoping to get cleared for some scuba diving!
5. The earlier in the month I had the surgery, the greater the possibility my mom could fly out and help CP out.
6. Last but certainly not least, the sooner I have the surgery, the sooner my uterus can heal and the sooner CP and I can start the first IUI treatment!
I recently found out my genetic test results. No cystic fibrosis or other genetic problems with me (YAY!). The only thing that I do have is something a bit weird…. Pseudocholinesterase Deficiency (huh?). From the website:
Pseudocholinesterase deficiency is a condition in which a person's body is abnormally slow at breaking down a certain class of drugs used for surgical anesthesia. Known as choline esters, the most commonly used of these drugs is called succinylcholine (suxamethonium). This drug is used by doctors to induce muscle relaxation and temporary paralysis, often for the purpose of inserting a breathing tube. After receiving a normal dose of succinylcholine, people with pseudocholinesterase deficiency will experience a longer than normal period of breathing paralysis. Typically medical teams who administer these drugs would be equipped to handle such an event.
People who are carriers of pseudocholinesterase deficiency - that is, people who have one copy of the gene with a mutation and one normal copy - show a slightly prolonged period of breathing paralysis after receiving choline ester drugs. This period lasts longer than 5 minutes but less than an hour. For people with two mutated copies of the gene, this episode lasts more than an hour and can last as long as three hours.
Less than 1 in 1000 people have pseudocholinesterase deficiency. It is more common among the some Alaskan Eskimos, where it may affect as many as 10%. In the Persian Jewish community, 1 in 10 individuals is a carrier of the mutation. Among white Americans, the mutation is thought to affect 1 in 3,000.
Who knew? I have never heard of this and as far as I know, I am only a carrier. This is only a big deal if CP also has this mutation….so we will have to talk to my doctor to find out if it is worth CP getting tested for this mutation too.
