My LO is 15 months old, and mostly very happy and normal, hitting all her milestones on time, etc. She has recently developed a 'party trick' of opening her mouth widely and sticking her tongue out at us (rude in an older kid, but very cute in a small toddler!). And a few days ago, I noticed that her uvula appears to be distinctly forked (like this).
I've been Googling (which is so often not a good idea) and have seen that this could be a marker of a hidden cleft palate (covered in skin, so not obvious on visual examination), which could affect her speech and hearing, or that there's a small chance it could indicate something called Loeys-Dietz Syndrome which can cause aneurysms. Goes without saying, I'm now a bit freaked out.
I've read that cleft palate often causes feeding problems in infants, and she did indeed suffer from fairly serious feeding problems as a newborn (she was unable to breastfeed and ended up being readmitted to hospital with excessive weight loss as a result of us accepting bad advice from midwives about attempting to EBF -- cue 13 months of me pumping milk to feed her from a bottle). She was examined for tongue tie and no problems were found at that stage, but I understand that it's common for bifid uvula not to be diagnosed until later as it takes a while to show up.
Obviously I will arrange for her to be seen by a doctor about this, but there might be a wait on this due to COVID. So in the meantime... does anyone have any experience with bifid uvula in their own kids, or friends and relatives, and had it turn out to be benign/not a problem?
I'm getting stage one in a few weeks, but still trying to decide the details of scrotoplasty. I think these are the two basic types we have to chose from. I want the most cis-passing as possible. Can I get any input about pros and cons of either? Is it true that with bifid, they're unattached to each other? I havent been able to find many pictures or clear explanations online. And yes, I've talked to my surgeon. I want others opinions.
Sonic have a bifid uvula and I'm really curious as to how rare it is cause the only two answers I've found are 1 in 76 people and 2% of the world and I've never met anyone else in 18 years who has it so I'm really curious
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... keep reading on reddit ā”
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Does anyone know how to solve this cipher?
I believe it's a bifid but I don't know how to approach it, help would be appreciated!
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We went for a regular scan at 27+4 weeks. Everything looked good; Baby was covering his face with his arms as always. Toward the end, when the tech was giving 4D a try, she went a bit quiet and started taking a bunch of pictures of his ribcage. When we were done, she took us over to the doctor's office. The doctor told us that our baby has a suspected bifid rib? Which I guess means one of his ribs has a forked end. She also said that there aren't any other abnormalities to point to anything serious, so it's probably just a funky thing that happened during the formation of his ribs. Baby is also apparently measuring small in his tummy. I am just wondering if anyone else has experienced this. Even though I was told not to worry... I am a worrier.
So I'm trying to learn how different basic hand ciphers work as well as how they can be analyzed and broken. I've looked around on google for a while trying to find how to go about breaking a bifid cipher (or similar ciphers where the coordinates of a letter are used, mixed in some way, and then reassembled into the ciphertext). So far I haven't been able to find much and was wondering what methods are used to try and break one?
I was wondering if there might be a formulaic method for decrypting Bifid ciphers. I've made a program to decrypt them in the way you would using pen and paper but if there was something similar to the way affine ciphers can be decrypted i.e. x=a^ā1 (yāb) % 26 then that would be very helpful in making my code more efficient. I understand it would be vastly different since a Bifid cipher would use a 5x5 grid. Thank you.
Theres a contest I want to win
My 15 month old son was diagnosed with a bifid distal phalanx of the thumb today. This is apparently the rarest kind of thumb duplication with a frequency of occurrence of only 2%. His pediatrician sent him to a plastic surgeon right off the bat and of course he wants to do surgery. My question is, is this really necessary? I have not been given an actual medical reason as to why I should put my son through this procedure other than "he might get made fun of when he's older", which I find ABSOLUTELY ridiculous. With it being so rare, I'm having a hard time finding information on it. I plan to get a second opinion on the matter.
TL;DR my son was born with a rare thumb duplication and doctors want to do surgery because "kids might pick on him".
