Hi everyone, thank you so much for the love and well wishes yesterday. The upshot is, basically, we’ve been left with more questions than answers. The appointment was supposed to last for 45 minutes but we were in there for two hours just because our case is so complex and unusual. The stumbling block is that Henry has two faulty genes rather than just one and the Consultants aren’t sure they’ll be able to screen out both in our embryos. I’ve had to email over lots more information to the clinic this morning and they are holding a meeting with all their staff to discuss what they can do. We will let you know more as soon as we do x
We’ve just arrived at Guys hospital clinical genetics for our first IVF appointment. We think it’ll just be a consultation, talking through the stages. We have an unusual mix of feelings being nervous, excited and very anxious all at the same time!
But we must say a huge thank you for getting us to this point. Without your kindness, we simply couldn’t have made it this far on our journey. There’s a long way to go. Wish us luck!
Super morning at Rallysport Automotive meeting the team! Henry had such a lovely time looking at the cars and saying hi to everyone. He says he wants a monster truck next Christmas ;). Managed to take a quick (rubbish) picture but better ones to follow! X
Transfusion no.33 ❤. Absolute star, never any fuss, just sits and eats his body weight in junk food for three hours 😂. May have celebrated the blood threshold change a little prematurely yesterday as our local Doc isn’t too keen but we’ll see if Henry can work his charm 😉 x
Huge thanks to Buds for collecting £47 in their Henry collection pot! We should have a lot more collection pots on their way to us so please let us know if you would like one or know anyone who would. Every penny counts 💪 x
Had a little victory today! Community nurse came to take blood this morning, Henry unpacked the box, found the right needles and tried to do it himself! He even took out three test tubes and put them in their holder ready to collect the sample 😂. So well trained already. Anyway, his blood came back very low as I suspected, he’s really been struggling this past week. Called our Addenbrookes consultant to see if we could persuade her to change his thresholds (how low they let his blood drop each month and how much blood they top up) and she’s agreed they will give him a bit more each month and won’t let it drop so low anymore. This sounds like a really trivial thing but it will make so much difference to his quality of life! Won’t be able to do it this month as it would mean giving him too much blood which isn’t safe, but should be on the new plan from next month. Things are looking up 🎉😊 x
Henry’s legs are suffering from the injections.
Update – Been a busy few weeks with Speech and Language, Audiology and a mild panic earlier this week as Henry started to have a bit of a reaction to his pump. Luckily, seems to have resolved but we’ll double check it’s ok with our lovely team on Elective Care when we take him in to hospital next week. Had to bring his transfusion forward as we think his blood has dropped really quickly this month 😔 x
Threw caution to the wind last Saturday and took the boy to the zoo despite terrible weather and the fact that it was the weekend which means crowds and germs. Bit of a reward for having a rough week with the pump and having his molars coming through (a joy to behold for all of us). He had a super time despite getting a bit worn out because he’s getting close to needing blood X
We’ve noticed we’ve got quite a few new followers over the past few weeks so we just wanted so say hi, thank you and tell you a bit more about what we’re doing.
Lots of people ask us about the IVF, so here’s a little update. We need a special type of IVF which is called PGD (preimplantation genetic diagnosis) with PTT (preimplantation tissue typing). This means we’ll go through the usual steps of IVF with some added extras, so that each embryo will be screened for Diamond Blackfan Anameia and also screened to determine their ’tissue type’ (special markers on cells called antigens). If the embryo doesn’t have DBA and is also a matching tissue type for Henry, it could be implanted in the hope of a pregnancy. After Baby Alderson no.2 is born, the umbilical cord would be saved and frozen instead of thrown away, then the stem cells would be taken from the cord and used to give Henry his stem cell transplant. This is all super complicated and takes a long time! It’s also very expensive, each cycle costs approximately £15k.
All of this means a special license has to be granted and there’s only a handful of places in the UK that are able to obtain this, so all of our treatment will be in London. Our first appointment is next month.
I will try and post updates of our IVF journey every day although Henry does keep me busy so bear with me! X