Hi, it's almost 2am so I don't have a lot of time to chat right now, I can chime in with much more detail later, but I felt that I just had to share some information with you tonight. I stumbled across your story a few weeks ago after doing some google searching of my own and have been lurking since. I can relate to alot of what you say. I have a 3 year old daughter and twins.
All 3 of them have issues with low weight (around 5th percentile), my twins have it worse, as their height is also affected (they were born in the 50th percentile for height, and are now in the 10th percentile. My ODD finally walked at 23 months. She attends part time preschool and teacher finds her "intelligent and cooperative", etc.
All 3 of them get horrible open sores on their genitals and buttocks from milk ingestion. My odd also gets rashes from some wheat products. We've been having the runaround for years, nothing conclusive as to what it is, as it tested negative for allergies in my ODD.
My concerns are skyrocketing for the twins, as they are 18 months and girl twins cannot sit up, but she can roll. Boy twin can sit, but cannot get out of that position. I cry every day watching them lie on our floor immobile. They do smile, clap, give "hi-5", etc... I always suspected my twins have the same condition as my ODD, so while it bothered me, I was reassured that my daughter is relatively normal as she walks, goes to school, etc...
My Odd was fully breastfed for one year, twins were unable to latch (even odd took 3 months to latch but i was persistent), with twins I was unable to get them to latch but pumped my milk until my doctor wouldn't renew my domperidone lactating meds anymore at 8 months because of a potential safety issue with the meds... it broke my heart as I was convinced it was the breast milk helping my kids, since the rashes and developmental delays got worse after stopping breastfeeding.
We have been referred to a developmental doctor ,,, like you, doctors just look at me like I'm crazy when I go on about my theories that the rashes and the developmental delays are related and that the key seems to be the breastfeeding... i tell them how it seems my odd is better than my twins since she got more breastmilk, etc.... the docs tell me there is no link between the rahses, the developmental delays or the breast milk. the doctor also sat me down and said that she looked over my odd's file and my twins and says they are 2 different conditions (ie. that they may both have a milk intolerance of some sort, but that otherwise it's a different condition, shes thinking neuromuscular)...
... My general family doctor referred me to a pediatrician in September, whom I finally saw in November and again in December... I am awaiting to see a neurologist and a metabolics doctor... problem is I'm in canada, and I still haven't seen anybody and my twins are getting weaker, my husband and I are losing our minds, I've lost ten pounds from stress in the last month or so ... free health care isn't always great... all we've had done so far is a hearing test! :( ... anyway, we've been debating going to the usa to pay for treatment,
... I am a nurse in a hospital and I teach nursing part time... so I have access to health reserach databases.... and my husband works in computers but took some biology courses in university, so he helps me to search through them... it helps us deal with the powerlessness we feel in this situation... I can't tell you how many hundreds of times in the last 3.5 years I have searched all these symptoms and never came up with anything in the databases.... until now.
What happens to your daughter when she ingests neocate? I went out and bought some hoping it would help our twins as they are getting weaker and losing more weight... well imagine my devastation when it gave them the most nastiest rashses of all the foods ever!!!!! It's supposed to be hypoallergenic!... So I called up neocate Canada and talked to the nutritionist there and said that reactions to neocate are very rare, like she said they had "a few" reports of it in all of the United States, and none in Canada... My odd also got a smaller rash from it (nothing near as bad as the twins, both of them have bleeding sores on their genitals, we were in teh emergency room telling them this but all they did was prescribe hydrocortisone cream ). So I asked her if the other people that called them had any idea what was wrong with their kid. She stated unfortunately they didn't say, but we discussed more about my kid's rashes.. they get a rash from cow's milk, NOT from goat's milk (but it seems to stall their developement), NOT from nutramigen (it's what we're using now since we used it on our odd), and a massive rash from neocate.. they also drink alot of rice milk... we concluded that it could be something in the digestion of amino acids, since neocate is an amino acid based formula... other possibilities we mentioned were problems with sugars, fats or carbs, since we thought it was weird that the goats milk has protein and amino acids and doesn't cause rashes...
We have recently been assigned a dietician at the hospital while waiting further testing... so when we explained her the story and what the neocate rep. said, her first reaction when we told her about the rash was to ask us if we were sure we haven't changed diaper brands (same cloth diapers since twins' birth.... I had been through all this before, ruined a batch of cloth diapers by bleaching them when my odd started similar rashes when she weaned off breast and went on cows milk at one year old). ... she phoned me back later and mentioned that some people have an illness where they pee out their proteins instead of absorbing them which could cause weight loss, developmental delay, etc... She then said she would call the metabolics specialist office to see "where we are on the waiting list"... I can't take this waiting anymore, I'm going insane.
... so armed with that information, I began a vigorous search through databases... having the words metabolic... protein.... really helped to at least start to narrow my search.... I read through the descriptions of hundreds of different diseases, having to google so many words to find out their meaning (I am a nurse, but nonetheless this sure is very technical stuff as us nurses tend to deal more with the bedside aspects, but I could still get the basic principles behind what I was reading)...
Then I stumbled upon : LYSINURIC PROTEIN INTOLERANCE (LPI) . I began to shake as I read about this illness... my husband was in the washroom at the time but I ran in with the laptop to show it to him... he was skeptical at first (as we've gotten our hopes up so many times in the last 3.5 years of searching), but after reading more and more articles about this we believe our kids may have this (or an illness in this family of illnesses), as it explains so much about them...
I have copied and pasted some information about this illness, I wonder if this is something your doctors have checked your daughters for : If you'd like to PM me your contact info. I can send you some articles to further read if you'd like :
Below I pasted for you the intro of an article that summarizes this illness : It's so rare that is why nobody knows about it!!! Have your docs tested your daughter's lysine levels? This is a disease of lysine transport (it's an amino acid... hence why my kids react to the amino acid based formula... when you can't transport lysine, you end up peeing it out .. hence why the lysine levels are high in the urine tests despite being low in blood... In the urine, ornithine, and arginine would also be elevated as they are all part of the broken metabolic process... one of the key features of this disease is that symptoms are noted after stopping breastfeeding!!!!!!!!!!!!!!!!!!!!!!!!
Here is the info from the article :
Lysinuric protein intolerance (LPI) is an inherited aminoaciduria caused by defective cationic amino acid transport at the basolateral membrane of epithelial cells in intestine and kidney.
LPI is caused by mutations in the SLC7A7 gene, which encodes the yþLAT-1 protein, the catalytic light chain subunit of a complex belonging to the
heterodimeric amino acid transporter family.
LPI was initially described in Finland, but has worldwide distribution.
Typically, symptoms begin after weaning with refusal of feeding, vomiting, and consequent failure to thrive.
Hepatosplenomegaly, hematological anomalies, neurological involvement, including hyperammonemic coma are recurrent clinical features.
Two major complications, pulmonary alveolar proteinosis and renal disease are
increasingly observed in LPI patients. There is extreme variability in the clinical presentation even within individual families, frequently leading to misdiagnosis or delayed diagnosis. T
his condition is diagnosed by urine amino acids, showing markedly elevated excretion of lysine and other dibasic amino acids despite low plasma levels of lysine, ornithine, and arginine. The biochemical diagnosis can be uncertain, requiring confirmation by DNA testing.
So far, approximately 50 different mutations have been identified in the SLC7A7 gene in a group of 142 patients from 110 independent families. No genotype?phenotype correlation could be established.
Therapy requires a low protein diet, low-dose citrulline supplementation, nitrogen-scavenging compounds to prevent hyperammonemia,
lysine, and carnitine supplements. Supportive therapy is available for most complications with bronchoalveolar lavage being necessary for alveolar proteinosis.
I happened to already have an appointment for my twins regular vaccinations tomorrow, they have the flu and are not getting the vaccines, but I will be showing this to my doc in the hopes he can contact the children's hospital and get us seen !!!!
... also, low lysine foods (which are in turn high in arginine) will cause problems in people with lysinuric protein intolerance... ie, my odd also reacts to soy milk, mini wheats cereal... those foods are high in arginine!!!... hence why it's not an actual allergy... it's a disorder of amino acid transport....
Ok, I apologize for the lenght of my post, I hope it can be of assistance to you, keep us posted... thanks for reading my extremely lengthy post (writing this all out and sharing it basically feels like therapy for me at this point as our family has been stressed for so long) :(
good luck and prayers to you...