open letter about our school going peanut free


I know what you're thinking.
I'm a hypochondriac mom.
Or I'm a helicopter mom.
Or I'm a stay at home mom who has too much time on my hands and likes to try and control everything having to do with my children.
Or I'm an attention hog who just wants everyone to focus on me and my child.
Or I'm a food zealot jumping on this "food allergy" bandwagon on a mission against peanuts.
Or I'm just selfish & like to throw my weight around because I can.
I'm probably even making up or exaggerating my child's condition to get my way.
Go ahead, pick your stereotype - I've heard them all.
And none of them are true.
I have five kids, aged 3-11. I don't have time to be a helicopter mom. In fact, I have hardly been involved in any school activities or functions of any kind during the seven years and three children I've already had in school.
I'm not a hypochondriac mom - I've seen my kids have seizures, high fevers with hallucinations, night terrors and sleepwalking, sepsis from skin infections, chicken pox that got infected, failure to thrive, a broken bone, more stitches than I can count, a near drowning and anaphylaxis from allergic reactions several times, to name a few emergencies. 911 has been called to our house exactly twice in eleven years of parenting through all these emergencies. Trust me, I'm not prone to becoming hysterical nor overreacting after this many kids.
And I definitely don't have too much time on my hands.
I'm not an attention hog, either - I don't feel the need to have other people focus on issues that are painful, or personal - especially when those other people are strangers to our family and circumstances.
I'm also not a food zealot because of food allergies - well, not willingly anyway. If you knew me before food allergies, you'd know I raised my kids on mac & cheese from the box, fish sticks, ramen pride noodles, boiled eggs and LOTS and LOTS of peanut butter & jelly sandwiches.
I'm not throwing my weight around because I can, either. In fact, I couldn't - this wasn't my choice and this was forced on me just like it's being forced on you.
And I only wish I were exaggerating my child's condition.
Four years ago I sat in my childrens' Allergist's office with my mouth hanging open.
"NO peanut butter?! As in, like EVER?!" I repeated, astounded and dismayed.
"That's right", He confirmed.
"But what about my other kids, they can still have it, right?"
"It can't be in your home at all, ever." He told me gently.
"What if they eat it outside and come in after?"
"That's really not a good idea either, they will have residue on their hands & clothes & mouths and if they hug or kiss or play with her...it can trigger another reaction.", He explained.
"But, but...what if I wipe them down after they eat it?"
This was the conversation I had where I tried every way I could think of to compromise with what my child's Dr. was telling me. A few days before, my three year old son had given my eleven month old daughter a bite of his peanut butter and jelly sandwich, a common occurrence in our family of no food allergy history whatsoever.
I'd gone downstairs to throw some laundry in and when I came back to the top of the stairs, she was holding onto the gate and making strange noises. It also looked like she'd gotten into some blueberries, because the corners of her mouth were bluish. As I was trying to get the gate open, I noticed the strange noises were her trying to cry and gasp at the same time. I saw her bare stomach sucking in and out and exposing her ribs while she tried to breathe. I scooped her up and noticed hives sprouting right before my eyes, all around her mouth and eyes. Her face was swelling, she was drooling all over both of us and her mouth was still tinged blue at the corners and it wasn't blueberries.
This was her first anaphylactic reaction. I wasn't even sure until we went to the Dr. later and had her tested that it was from the peanut butter in the sandwich. I'd also given her antibiotics for an ear infection about twenty minutes earlier, I was sure (and hoping!) that was the cause. Luckily the Benadryl I had on hand seemed to take effect almost immediately and she recovered quickly.
Our lives changed after that. The Dr. told us the new rules we had to live by which included making her wear a Medic-Alert ID tag at all times, asking people to wash their hands upon entering our home and always keeping an Epi-Pen near or on her person. Despite all of these precautions, she's had three more anaphylactic reactions in her five years. One was in the grocery store, after touching part of the grocery cart and then her face, and one was in a movie theater (even though we covered her seat with a blanket from home). The most recent one was in our home.
Each episode was absolutely terrifying and followed the same pattern. First she gets itchy and breaks out in hives. Then her face begins to swell. Next she says her throat is tickly, then her stomach starts to cramp and she vomits - then she begins to have trouble breathing. I've researched enough to know that the Epi-Pens don't always work, especially in cases where the allergy is very severe. We're told that our daughter's is the rarer and extremely severe kind. I'm terrified the Epi-Pen won't work for my child one day.
So we lived like quarantine patients for a long time.
My five year old daughter has never spent a night at her grandmother's house.
She's never been on a playdate in another home, nor a sleepover.
She's never allowed to step into a neighbor's home for a drink of water while playing outside in the summer. If neighbor kids congregate at our house, we have to ask if they've eaten peanuts or peanut butter recently before she can play with them and they have to wash their hands if they're coming inside.
She doesn't go to friends' birthday parties.
She can't eat bakery cakes or treats.
She can't have chocolate unless it comes from a dedicated, nut-free facility.
She can't play at the mall play areas.
We just tried letting her trick or treat for the first time in her life last year, with gloves on, and then gave the candy away. Every other year she's had to stay in while her brothers go trick-or-treating.
When she joins gymnastics, we ask the studio to go peanut free. They post signs, remove nut foods from their vending machines and have the other students in her class wash their hands before starting the lesson. Her dance studio does the same. When traveling, we notify the airlines and they make our flight a peanut-free one. When we take her places like Disneyland, they work with many food allergy organizations to ensure a safe and fun trip for even life-threatening level peanut allergies. When staying at a hotel, we ask for food allergy rooms and considerations.
We've learned to live with it. We're finding out she can still do normal things and have normal experiences, with planning and care. Sometimes this lulls other people into thinking we don't have to take special steps for her, because they might not realize all the planning and precautions that have gone on behind the scenes.
The biggest hurdle we face in raising her is people who just don't want to get it. Or who don't want to set aside their annoyance at how this inconveniences *them* to try and get it. I've had more people tell me than I can count how their child "won't eat anything else" but peanut butter and this would be an incredible hardship on them and their rights shouldn't be disregarded like this.
When faced with being told that my daughter's life is equal to a favorite convenience food, I just never quite know what to say - I'm astounded. As I mentioned, I have five children - and actually two of them are food allergy sufferers -and the total restrictions these food allergies place on us are nothing short of mindboggling.
Because of this, I've learned that kids will eat what is available to eat, eventually. There are also great alternatives today, like sunbutter (from sunflower seeds) and tahini (from sesame seeds). If my kids truly would not eat anything but one food item and their school suddenly told me that one item was no longer allowed to be brought to school because it could harm or kill another child...and they didn't want anything else...then I guess my children just wouldn't eat until they got home from school, if that was their choice. I doubt they'd choose that option for very long! No kid is going to starve to death without peanut butter. They'd find another option rather than go hungry, trust me on this.
I know people are going to be angry that our school is being made to go peanut free for my daughter. I know there's a lot of confusion and misinformation out there about food allergies. I know everyone knows somebody who says their child is allergic to a food and then sees that child consuming it, only to be told "It's okay once in a while - or in small amounts". This isn't the same thing. This is a true, IgE mediated, multiple test verified anaphylactic allergy. We tested her at eleven months and we tested her again at five, skin and blood tests each time.
The Dr. tells us with a case as severe as hers, there is no chance she will ever outgrow this. It's an incredibly helpless and terrifying feeling to know that my daughter can die from just touching something and then touching her face. Some days I don't even want her to leave the house, ever.
When her Dr. retested her at five and instructed me that her school would have to be peanut free, I was met with resistance. I was told how "inconvenient" the other parents would find it. I had questions fired at me like,
"How can you take her out in public, then?"
"How do you go to the grocery store with her - do you ask them to go peanut free?"
"I heard you went to Disneyland, how can you do that and ask us to go peanut free?"
"Why can't we just put her in an empty classroom to eat her lunch?"
I felt ridiculed, I felt disbelieved and I felt discredited. How anyone can think a quick trip to a grocery store could pose the same risk as being in a school with potentially 400 other students eating peanut butter, for seven hours a day, five days a week is beyond me.
Then, incredibly, the two school officials I was meeting with began discussing how hard it would be on their children not to be able to have peanut butter. They joked that their children would starve to death - they talked to each other and agreed that it would be awful not to be able to have peanut butter, that they wouldn't consider it a normal childhood without peanut butter. I sat there and wondered,
"If my child were in a wheelchair, would they tell me how awful it would be if *their* children couldn't run? Would they tell me how glad they were it wasn't their problem?"
But by the way, we still just want to discriminate against your child with her medical disability by putting her into a secluded room to eat her lunch instead of making the whole school safer.
Our school is supposed to have "nut free classrooms". One of the school's biggest objections to going peanut free for my daughter was that she will spend most of her time in the classroom, and they are already nut free. Just this past St. Patrick's Day, an assembly was held at lunch time, requiring that all students eat their lunches in their classrooms.
I have three children at this school currently and one of them came home to tell me that in his classroom, a child had a peanut butter and jelly sandwich. Another child spoke up and alerted the teacher that he had peanut allergy. The teacher sent the allergic child to the principal's office to eat his lunch, while the peanut butter and jelly sandwich was eaten in the classroom. Had that been my daughter, upon her return to the classroom if there had been any peanut butter residue anywhere and she touched it and then touched her face, she could have had a life-threatening reaction.
This is a perfect example of why the Dr. and the law can mandate that schools go peanut free for children with life-threatening cases of peanut allergy. Rules like special tables, special areas, special times that nuts are restricted are open to interpretation and subject to change based on changing circumstances. I don't know what happened in this case. I don't know if the rules were being flagrantly disregarded, misinterpreted or if this was an exception, but how would you feel if you were told other students could play with loaded guns around your child at your school? Dramatic example, I know - but this is exactly what it feels like to the parent of a child like mine upon hearing that half-measures will be taken.
I try, but I truly don't understand the objections of other parents, the anger and the protests I have seen in the press lately about cases like this. Before my own child was diagnosed and we had to accommodate another food allergy child in our first son's kindergarten class by eliminating not only peanut products but also egg, we were also annoyed. But we never formed protest groups, we never complained to the school or the teacher.
We asked more questions, we talked to his parents, we learned more about it! The bottom line was we didn't want that child to be hurt. And we certainly didn't want to be the ones that hurt him.
I wonder if people who trumpet and rave about their child's right to peanut butter have ever seen their child view anything traumatic in real life. I wonder if they know what their child is going to have to live with, if another student they care about and spend time with falls down and starts choking, vomiting and crying while scratching at their throat as they wet their pants and struggle to breathe.
I know what is going to happen to those children, because I've seen it happen to mine when my daughter has reacted. They are going to panic, they are going to be traumatized, they are going to feel immense guilt -even if they are in no way to blame - and they are not going to get over it for a long time. They are going to become afraid it can happen again, maybe even to them - they may want to avoid things that are connected to the incident, they could have nightmares.
Would you really rather risk traumatizing all those additional children rather than err on the side of caution and just stop sending something you've been told can kill another child, to school?! I have often had the macabre thought that I wish just one of my daughter's reactions could have been caught on video. One viewing and nobody would question what needs to be done for her.
I hope it helps the parents at our school to know that we do feel badly about this. I've dreaded this day since she was diagnosed four years ago. I hoped and hoped she'd outgrow this against the odds and we wouldn't have to deal with this in a school setting.
I spend my time helping other families learn about living with food allergies. I spend my time coming up with safe foods and finding ways to share them with others. I spend my time finding ways to educate others about this issue. I assure you, every step that could have been taken by us not to inconvenience others has been taken. And now we need your help. We can't keep her safe by ourselves anymore. I know you, you're our neighbors, you're our acquaintances, you're our friends, you're on facebook with me, your kids are in activities and on teams with my kids. You're our community.
I see you stand up for your children, I see you advocate for your children, I see you fight against the odds for your children. I see you keep your children safe and healthy. My husband and I have both always worked in the helping professions. We help keep our community safe and healthy both personally and professionally. All we're asking is that we all work together to keep doing this for ALL our children at school.
I'm 100% approachable on the subject of specifics about my daughter's care and condition, please feel free to email or comment if there's anything further I can answer or explain.
My email is MUMMA2WLDTHINGS@MAC.COM.




The Nuclear Accident in Japan: Impacts on Food



The full impact of the Japanese nuclear crisis remains to be seen, but the health risks posed by radioactive contamination are well documented. In 2006, the National Academies of Science issued a definitive report on radiation exposure that concluded that even low levels of radiation can cause human health problems, including cancer, heart disease, or immune disorders.
The United States imports around 80 percent of its seafood as well as an increasing share of its fruits and vegetables. Unfortunately, the FDA inspects less than two percent of these imports, leaving consumers at risk to a host of food-borne issues, which now includes potential radioactivity.
Take Action Now.
Radioactive emissions from Japan have been detected throughout the United States, from California to Colorado and as far east as Massachusetts. Monitors in the Carolinas have detected the presence of radioactive iodine, the first time this material had been detected there since the Chernobyl accident 25 years ago.
A major avenue for exposure to radioactive contamination comes through food and water. Decades after the Chernobyl accident, the United Kingdom still maintains restrictions on large sectors of the country’s sheep production because radioactive cesium—dispersed through wind and rain—still contaminates grazing lands.
The U.S. imported around 150 million pounds of food from Japan in 2010, a small percentage of what Americans consumed, but not an insignificant amount. Imports from Japan included nearly 600,000 pounds of crab and anchovies and nearly 5 million gallons of bottled water, soft drinks and other non-alcoholic beverages containing water, products that may be potentially higher risk if contamination continues to spread to the ocean and fresh water sources.
American consumers could be at risk through consumption of food products from other countries that experience radioactive fallout from the nuclear accident in Japan as well.

What We Recommend

  • The FDA should immediately ban all food and water imports from Japan, expanding on the FDA’s original step of restricting imports of milk and produce from the region near the accident site.
  • The EPA should increase its monitoring in the United States of air, water, precipitation, and milk for radiation.
  • The data generated by this environmental monitoring should be used by the FDA and the USDA to design sampling programs for soil, water used for irrigation, livestock or crop production, crops including leafy greens, and meat and milk in areas of the United States that are affected by radiation.
  • Congress should provide adequate funding for food inspection, both at home and abroad, instead of attempting to cut both USDA and FDA’s funding, which would weaken their ability to meet their current obligations even without the additional burden posed by this nuclear accident.
  • Congress should rethink our agricultural and trade policies, which encourage importation of an increasing share of our food from countries with weak regulatory regimes. If radiation from Japan ends up affecting these countries’ food systems, regulators there will not have the tools to ensure that food production is safe.

Learn More

from Food & Water Watch

Tandem & Triandem Breastfeeding through Pregnancy.






the way my mind organizes these memories is into two distinct categories: nursing while pregnant during the 1st half of the pregnancies, and nursing during the 2nd half of pregnancies.

pgc #2 (nursing 1 toddler, 8 mos at conception, 16 mos at birth)


fear (can this really cause a miscarriage?)
guilt ( who am i shortchanging more - the baby that needs milk or the fetus that the ob says i am putting at risk?)
thirst !
love/affection for nursling
fierce protectiveness (i'm going to try to do everything i can not to take this (milk) from you.
relief (found LLL!)

~2ND HALF~

burgeoning confidence (this isn't as hard as i've heard!)
gratitude (body is making enough milk for toddler and keeping fetus healthy!)
fear and hope (i hope this pgc doesn't make you wean before you would otherwise)
worry (can't feel letdowns any more and it's becoming painful, is this normal?)
pain (it feels like gravel is passing through my nipples when you nurse !)
triumph and pride (you nursed through the whole pgc and i hung in there despite the cpl wks of discomfort! yay for us!)


pgc #3 (nursing one boy aged 3 and one toddler aged 1)



concern (can i nurse 2 thru a pgc and not be increasing the risk of miscarriage?)
thirst!
gratitude (a reason to sit down and rest when i have to nurse you both)
surprise (i really feel tightening of the uterus and an urge to pee as soon as you start nursing)
fierce devotion ( i won't let the imminence of a new baby change the way i nurture you)
pride ( i don't know very many ppl who've nursed 2 children while pg !)

~2ND HALF~

pain (oh, there's that gravel in the nipples again - i'd hoped that was a fluke !)
claustrophobic (oh no, here they come to nurse again and i'm so big and uncomfortable i feel like they're smothering me)
restless (are you done yet?)
skin crawly (what happened to the way they nurse ? suddenly they feel like they're all teeth and scrapy cat's tongues !!)
bargaining (if i can make it through just 10 more minutes, they won't wean b/c of the pregnancy)
relief (once you've nursed for a little while and i can hear you gulping, all the discomfort goes away and i am so glad to be breastfeeding you both still)
triumph and terror (neither of you weaned through the whole pregnancy and now i have a third!)

pgc #4 (nursing 4 yr old, 3 yr old and 6 month old)


determination (i've done 2, 3 can't be that much harder, besides the oldest hardly nurses much anymore)
concern (can nursing 3 finally be enough to adversely affect the pregnancy?)
thirsty !
have to pee as soon as they latch on
ever present nausea this pgc increases during nursing
suffocation (are they ever going to get off me ? i can hardly breathe)
hot flashes during nursing
skin crawly
underarms prickling as soon as they latch
panic (why is it so horrible this time, is something wrong w/ my hormones? with my pregnancy?)
exhausted

~2nd half ~

guilt (i hope you guys don't know how much i hate this, this pgc)
cyclical pain (every few wks the gravel-thru-nipples pain is back!)
contractions (constant during nursing this pgc)
gagging (nausea increases enormously during nursing)
resentment (why do none of you ever wean during pgc like the stats say so many do ?)
more guilt (i love you, i want to nurse you as long as you want to nurse, i'm sorry i'm not enjoying it any more)
bargaining (i will give you a sucker if you'll be done nursing for now)
violent fantasies (dear husband, if you tell my children to go ask me for milkies again like my breasts are yours to give out like party favors when you want to bribe or distract them, i am going to wait until you sleep and hurt you slowly and creatively for a long time)
constant worry (surely this time it's going to make the baby come too early, that must be what all these hormonal signs mean)
relief and triumph (i made it again and nobody got hurt or emotionally scarred or weaned!)

pgc #5 (nursing 2 yo and 1 yo)


nervousness (what if it's as bad as the last pgc?)
self-reassurance (it can't be as bad - i'm only nursing 2 again and they are older and on solids so won't need to nurse as much)
thirsty!
tired tired tired
grateful (for the chance to sit down and rest while nursing)
guilty (this pgc is such a surprise, i didn't want to possibly cause you guys to wean, i really hope it doesn't make you wean)
fiercely protective
weepy / emotional

~2ND HALF~

pain (gravel through nipples again but only for a short time mid-pgc, not recurring like last time)
random contractions
smothering (i'm so big and you guys are so big, i feel crushed under all of us)
determined (not much longer and we'll have our family all completed and i'll have no regrets if i can stick it out one last time!)
extreme weepiness
confusion (why am i so weepy when they nurse ?)
more weepiness (why am i so confused i don't even know why i'm crying ?)
profound gratitude (i'm so lucky i've been able to do this so many times, i have to cherish this, it won't last forever)
pride and triumph (made it again, about to be nursing 3 again)


whew! i have to print that out for posterity, it was very intense going back there, i thought about it all day and am so surprised i clearly r/m how very different the experience of bfing was w/ each pgc ! i just wanted to add that no matter what i went through while bfing during pgc, it was all worth it when the older nurslings got their 1st feeding of 'new' milk after the birth. every one of mine almost completely gave up solids for a cpl days when my 'new baby milk' came in and it was sheer heaven to hold them (one at a time on the 'toddler boob') next to the newborn and hear them gulping and sighing in unison w/ eyes rolling back in ecstasy as they stroked the new baby's silky head. if i am lucky enough to be able to prepare for it when my time comes to leave this earth, this is the memory i will conjure up and take with me, it is the very essence of why i work to help women breastfeed.

** update**
I went on to nurse the 3 children above for another 9 months. Then I went on to nurse my last 2 for another 3 1/2 years, until my daughter self-weaned at age 5 1/2.



our 5th child is almost completely self-weaned now, at 5 yrs and 5 months. he is only asking about every 2-3 weeks. we've come full circle and after over 13 years of breastfeeding children without cessation with 11 of those years nursing 2 or 3 at a time, i can look back and say i have never done anything more worthy or rewarding in my life, except perhaps giving birth to them. i will never have to look back with regret and wonder if i'd done it just a bit longer, might they have gotten more benefits? i haven't had to deal with bottle issues, or pacifier issues, or insecurity or object-attachment issues. i am completely convinced it all but eradicated sibling rivalry issues toward new babies coming into the family. i know it saved my last child's life, as there is no formula on the american market that he wasn't allergic to. it wasn't always easy and it wasn't always natural, but it was always the right thing to do. the added bonus of them remembering nursing very clearly is hopefully an increased likelihood that they will grow up to be devout breastfeeding advocates, as well! :-)     Green and Bitchy: the beginning of the end








Skinny Lou Allergy Cookies !



in the last 3.5 years of trying to find foods safe enough to feed my multiple allergy child that are also tasty enough to keep him interested, i've perfected a chocolate chip oatmeal cookie recipe. i've been tweaking and simplifying it multiple times all along. the less ingredients, the better, but i wanted him to have the same ooey gooey, sweet and chewy delectable goodness that my other kids are lucky enough to get with "normal food". he loves them - he will literally eat over a dozen a day if i let him. and since they are bean, applesauce and coconut based, i can let him! :-)

i knew i'd reached and possibly even surpassed my hopes when i started sharing my latest incarnation of this recipe. people who don't even have dietary restrictions or allergy concerns rave about these cookies. it has gotten to the point that every time i make a batch, i know the neighbors will want some, the friends we walk our dog with, the chiropractor, the pediatrician, etc... and i am always making a ton extra for everyone else that loves these.

people are always saying to me, "you could sell these!" "you should market these!" "i would pay for these, no problem!"
so i've finally taken their advice and begun selling and shipping my cookies. i mostly do it through my facebook page or email, but will also be opening an etsy store soon, if orders stay at a stable number. i am also very interested in a financial partner that can help me professionally market them.
our pediatrician actually has a contact he thinks might be interested and i am waiting to hear back on that.

in the meantime, i've looked into the laws and rules and decided to start selling them on my own and building a customer base and collecting reviews and feedback! so here is the basic info on the cookies - if anyone wants to place an order, feel free to email me at 'mumma2wldthings@mac.com'. or friend me on FB under the same email addy. i tend to bake on mondays/tuesdays and ship on tues/wed.
basic info on the cookies is:

these cookies are 100%:
vegan
dairy free
egg free
corn free
soy free
gluten free
peanut free
tree nut free
seed free
GMO free

these cookies are made with organic:

gluten free oats
bean-based flour
allergen-free, corn- free chocolate chips
coconut milk
coconut oil
applesauce
sea salt
brown sugar
(also a little organic cane sugar & baking soda).

1st time orders get a 'tester' price of $12/doz.
send me a pic of someone eating the cookies
(or just the cookies if you are camera-shy)
and a review, and you get a 2nd order for $12.
after that, normal price is $14/dozen
(and that includes shipping w/in continental U.S.)

please feel free to email me w/ any questions, i know i'd have to really look into this and know all about cross-contamination precautions and every ingredient before buying for my son!

Toxic Plastics Chemical in Infant Formula


Executive summary


August 8 2007. Laboratory tests of canned infant formula conducted by the Food and Drug Administration (FDA) and a certified commercial laboratory reveal that a plastics chemical called bisphenol A (BPA) leaches from metal can linings into formula. According to a new EWG analyses, the amount of BPA ingested by some bottle-fed infants exceeds the doses that caused serious adverse effects in animal studies.
EWG's analyses of BPA levels in ready-to-eat and concentrated formula, paired with government data on infant formula consumption show:
  • One of every 16 infants fed ready-to-eat canned formula would be exposed to BPA at doses exceeding those that altered testosterone levels, affected neurodevelopment, and caused other permanent harm to male and female reproductive systems.
  • Infants fed concentrated formula mixed with water would also be exposed to potentially unsafe amounts of BPA, in excess of standard government safety margins. While water added to concentrated formula lowers BPA concentrations in the final mixture, our analyses still show that one of every 16 infants fed concentrated formula would be exposed to BPA at doses within a factor of 2 of harmful doses.
  • At the highest BPA levels found in formula, 17 parts per billion (ppb), nearly two-thirds of all infants fed ready-to-eat formula would be exposed above doses that proved harmful in animal tests (Figure 1).
These analyses, coupled with exposure estimates in other studies, demonstrate that bottle-fed infants likely face higher BPA exposures than any other segment of the population, and highlight the urgency of setting standards for this chemical to protect babies who are overexposed through canned liquid formula.

Figure 1. BPA has been found in infant formula at levels ranging up to 17 parts per billion, a concentration at which nearly two-thirds of infants would exceed doses shown to harm test animals.


Source: EWG analysis of BPA exposures based on government and commercial lab tests of BPA in formula, and formula consumption rates and body weights measured in government surveys. This graph reflects procedures described in the methodology section of this report, with the exception that exposure estimates for individual infants created in the exposure model were based on incremental, assumed BPA concentrations in formula, and grouped as a function of BPA concentration for purposes of graphical display. Estimated single-day exposures are compared against BPA dose of 2.4 ug/kg body weight / day linked in lab studies to alterations in testosterone levels and referenced as "toxic dose" in figure above (see Section 3 of this report). Note that results shown above will underpredict infants exposed above even lower doses found harmful in animal studies, including a dose of 2.0 ug/kg/day linked to permanent damage of reproductive system from in-utero exposures.
Failures to protect infants from BPA risks. FDA last assessed the safety of BPA in infant formula in 1996, based on tests of 14 infant formula samples (Bailey 1996). Dozens of peer reviewed studies published since that time reveal adverse effects of BPA at exposures dramatically lower than those known at the time to be harmful, and, significantly lower than exposures for infants drinking BPA-contaminated formula.
Yet despite scientists' dramatically altered understanding of low-dose BPA toxicity, FDA has not tested additional samples of infant formula for BPA, and has failed to reassess the safety of BPA-contaminated infant formula since its original assessment 11 years ago. FDA does not require infant formula manufacturers to test their products for BPA.
Instead, in 2006 the federal government launched a BPA health risk assessment under the National Institutes of Health's (NIH's) Center for the Evaluation of Risks to Human Reproduction (CERHR). From the outset the assessment process has been plagued by concerns over scientific credibility and conflicts of interest:
  • The contractor in charge of the assessment both helped form the panel, which lacks BPA experts, and prepared the initial draft assessment for the panel's review. This contractor was subsequently fired by CERHR over concerns about potential conflicts of interest, but the panel was allowed to continue with its initial membership, working from the draft assessment prepared by the fired contractor.
  • In external review comments submitted to the panel, BPA experts revealed that the CERHR assessment appears to contain nearly 300 errors of fact and interpretation; is biased, inconsistent, incomplete; and clearly fails to meet the most basic scientific standards. [see EWG's full review]
What could have been the first opportunity in a decade to advance public health protections for this problematic chemical instead ended in CERHR issuing a final assessment on August 8, 2007 that fails to support stronger public health safeguards for bottle-fed infants, pregnant women, and other at-risk populations.
BPA has been detected in thousands of people worldwide, including 93 percent of 2,500 people in the United States. More than 100 peer-reviewed studies have found BPA to be toxic at low doses, some similar to those found in people, yet not a single public health agency has updated safety standards to reflect this low-dose toxicity.
This country's toxics law, the Toxic Substances Control Act, fails to require that chemical companies prove thier products are safe before they are sold, even when these chemicals end up in people's bodies, as is the case for BPA. This law was passed in 1976, and 31 years later is the only major public health and environmental statute in this country that has never been updated. This panel certainly has not done their part to help fill the gaps in this broken system of public health protections.
As a result of these policy gaps, BPA is now one of the most widely used industrial chemicals, is found at unsafe levels in people, is allowed in unlimited quantities in a broad range of consumer products including infant formula, and is entirely without safety standards. BPA provides irrefutable proof that our system of public health protections must be strengthened to protect children and others most vulnerable to chemical harm.

Resources

Lab tests of canned food — BPA contamination in more than half of 97 name-brand canned foods: http://www.ewg.org/reports/bisphenola
EWG comments to CERHR summarizing nearly 300 errors of fact and interpretation in BPA assessment identified by BPA experts: http://www.ewg.org/node/22333

product review/rave!



i have been struggling to get and keep my allergy guy, elijah (3) at baseline since last june, when we lost our tenuous hold on it after several viruses invaded our home and he suddenly became allergic to nearly everything left in our very restricted diet. once the illnesses and consequent testing and re-testing for false positives were over, we had lost most beans, lentils and sesame (in addition to our forbidden top 8 plus corn) but were otherwise able to get back to "our normal"/restricted diet.

i just haven't been able to quite get him all the way back to baseline, no matter what i try. we lost shampoos, conditioners and soaps for him shortly after last june - his scalp began peeling and then cracking and bleeding even with only weekly washings. we now anoint his head with raw virgin coconut oil and use a fine tooth comb to section and comb it throughout. then i put a little knit cap on overnight, rinse it in a hot shower the next day and he's great! no more cradle cap at all. we have to do it 2-3 times weekly. we also discovered 'kiss your face' brand aloe and olive oil soap and use that only on the parts that really need it - just water for the rest.

still, on a scale of 1-10, with 10 being the worst, he's remained flared up and broken out at a out a 3/4 until recently. i'm still not sure if it's a coincidence or not, but a facebook friend (thank you again, lynette!) posted about hazelwood jewelry and its purported ability to absorb excess acids in the system that can lead to things like eczema, rashes, reflux, etc...

i've embraced heartily the philosophy of, "if it can't hurt...why not try it?"
so i did!

i have to say, the next day, he was down to a 1 on the breakout scale. i ended up putting 2 of them on him at once. he's been at a ZERO ever since!! the company i ordered from was fabulous - a tiny piece of wood broke off the first necklace and i sent them an email with pictures of it. they promptly sent me a replacement at no extra charge. i got it from www.hazelaid.com and plan to keep one on him indefinitely.

i'm usually a total skeptic about these things but it's really the only new thing i've done in the last 6 months - this is not a child you can introduce new things to as far as diet and personal care products. i'd love to hear it if other people have had other experiences or if you decide to try it as well
-leave a comment and let me know how it went!

candy in schools rant


below is a response i posted on my fb profile about an article i reshared on gluten issues. it's just after valentine's day and i've been grappling with my every-holiday frustration about the schools providing my kids with candy for the occasion. as well as ice cream with candy toppings this year. @@. i got the expected dissention on my profile and told i need to lighten up about the issue, but i just can't. i'm trying to examine why.

all i can come up with is: if you've ever done weight watchers or any other type of intensive diet, you might understand a little. your world narrows down and you get tunnel vision about food. you obsess over it, you think about it constantly, you have to train your mind to be brainwashed into accepting the new restrictions. it's insanely hard, which is why everyone i know who lost weight on atkins & south beach has now gained it back and then some. you have to go through your anger, your grieving, your relapsing, your seeing through eyes that decide everyone else has the same issue you do, but don't know it (you know, like recovered alcoholics that are sure everyone else is an alcoholic, too!), and finally to acceptance and resigned self-denial. well, i don't know if most fad diets last 3 years, but part of what happens when you have to do it this long is some level of intolerance.

i feel very intolerant of someone else feeding my kids crap i know is harmful. when i've had to be this rigid for this long, it's pretty hard to make my mind flexible again around the concessions i've already made.

i have had to go on the most extreme elimination diet of just about anyone i've ever heard of - starting 3 yrs ago. we now have to completely eliminate:

dairy, corn, egg, soy, wheat (gluten 99% - b/c i don't have to worry about cross-contamination) seafood, shellfish, peanuts and tree nuts, most beans, lentils and sesame.

and i consider us lucky, b/c there was a time last summer when we had to go down to nothing but rice and a few fruits for over a week, when 'lou became allergic to everything on the limited menu we had been eating!

so, imagine the mindset it takes to maintain living this way for this long. if you got all emotional about giving up your favorite foods for atkins or weight watchers or south beach, imagine what i went through. there's no days off for me, no reward days, not even any cheating, ever. i tried that the 1st few wks and watched what it did to my son and the guilt was hideous.

i have to spend a huge chunk of my free time learning about foods today. trying to understand why 2 of my kids could die from eating foods that should nourish them. finding other families with kids like this so i can learn about and from them, too. and oddly enough, as a lactation counselor who mostly gets clients through word-of-mouth, i seem to be attracting mainly new moms that have just been told their babies are allergic to one, several or many foods the mom eats. so you could say my whole world is pretty much about these issues for the past 3 yrs or so. so this could either make me a real radical...or a lay expert, depending on if you want to learn anything about (or agree with) what i'm saying.

one thing it doesn't make me is someone who can afford to lighten up about it.

with my oldest three children (11, 9.5 and 6 now) -they can eat almost anything they want w/ no ill effects (except dairy - they all get sinus and ear problems from it). even before food allergies, i never allowed any of my children to have straight cow's milk, ever - nor did i ever drink it myself - except before i was too young to have a choice. they've never had soda or juices or much candy at all. i definitely bought into the "they're not fat, so we can do fast food" philosophy and absolutely hated cooking and fed them from boxes and cans and thought it was pretty normal and even healthy!!
( "there's tomatoes in spaghettios!! tomatoes are very healthy"!!)

it's been hardest on them to convert to this restricted diet and all the home cooked meals. they remember the addictive trash food more than the younger kids. i've made a compromise with them. they have to eat as we do at home. but for school, i still use more traditional foods in their lunches. i buy the trader joe's or annie's organics spaghettios now and then. i make wraps with "normal" tortillas as well as spinach or tomato ones. but *i* choose when, how much and why.

just like i imagine spankers who got up in arms about the schools paddling their kids back in the day, so do i feel about the schools giving my kids candy and junk food. it upsets the balance i'd already decided i could live with. and truly, our school is pretty excessive about it as far as i can tell when comparing with other parents. and I'M the parent and they're MY kids - nobody else gets all the rights i have to make these decisions for my kids. i think the problem is that most other people don't even realize that standard food is pretty much like poison for families that have to live as we do.

anyway! rather than absolutely forbid my kids to ever experience the temptations out there, i do see they need to learn moderation (my definition of moderation might differ from most people's, i know - LOL!) and learn how to navigate social pressures about food choices for themselves. i'm trying to find ways to help them make better decisions when on their own rather than push my doctrine onto them further.

for example, knowing the school party was going to be another sit-in-the-classrooms-and- gorge-yourself-on-candy event, i told all 3 of my sons that if they politely declined any and all candy and donated what they received from friends back to the teacher, i would reward them with a $5 bill and immediate trip to spend it after school. only my oldest took the incentive, but the wails of protest from the other 2 told me i might have more takers for the next party!

it was a valuable lesson for my oldest and it was interesting to hear his perception of resisting the junk food. there were no other activities available in the classroom, everyone was eating candy and ice cream. he sat at his desk and read his ebook. his teacher came up to him several times and asked if he was feeling all right and urged him to go get some of the treats. they had all been ill recently, so i understand her concern over how he was feeling.

i am so proud that he resisted her urgings toward the junk food. jake is a real people pleaser. it's very important to him to be well thought of and have adults happy with him. he felt he was somehow disappointing, worrying or inconveniencing his teacher by not doing as the other children were. but he politely stood firm and didn't eat any of it and i rewarded him immediately after school, as promised.

i don't blame the teacher here or think in any way she was trying to harm my son - i honestly think she wanted to give the kids a treat and a fun day and everyone knows kids love candy and ice cream best. she's just being nice. and honestly, it's the room moms who organize and bring the treats in - the teacher just goes along with their choices. if i really want to change things, i know i need to become a room mom and lobby to bring in healthy treats or take the emphasis off food as a means of celebrating and do crafts or games or ask that they exchange things like silly bandz instead of candy or something.

but guess what? i don't want to be a room mom. i don't even particularly want to be much of an involved school mom. i don't want to fight the norm and upset everyone and ask for all these changes. my plate is already more than full w/ the educating and advocating i do elsewhere in my life. my kids are top students, completely independent, well-adjusted, socially responsible little people (thank you, APing!) and i don't need nor want to hover. my free time is used helping a much more needy and fragile demographic - new babies that need their moms to breastfeed them and learn how to eat, without eating things their babies are allergic to. i need my kids to learn how to make good decisions for themselves now that they're old enough to. i haven't succeeded as a parent if i have to go to school and remove every obstacle for them. besides, i'm going to have to whether i like it or not when my allergy children start school, so i really need to make sure the other 3 can make good decisions on their own.

this doesn't mean i won't rant and rave about it when i hear how much temptation and pressure their school puts on them toward unhealthy foods, though!! with the diabesity epidemic our kids are dealing with today, i'm shocked every time i hear another candy-filled holiday party is scheduled or another pizza party for meeting some goal during the week is coming up. i can't believe other parents aren't protesting it.

so, there's the background on the facebook rant and here's the rant. i think it's worth preserving for days when i feel like i just can't do this anymore...and if it helps someone else along the way, even better. if it offends you or makes you defensive and you just don't think any of it will ever apply to you or your family - ignore it. but know i can't let it go or shut up about it, i'm stuck living this way with children who are harmed by what has happened to food today...and i spend my time helping other babies being harmed by it and i need to speak up or spontaneously combust sometimes, it's just how i'm built. if you can still be my friend despite our differences of opinion on such incendiary matters, we have a resilient friendship indeed & i will try to return the favor. :-)

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it is a slap in the face, isn't it? i r/m when i 1st started learning about all this stuff...i absolutely did not want to hear it and didn't really b/l it, either. i would get so overwhelmed i couldn't even absorb the facts. i'd push it all away and decide it was radical, biased, hyped up BS -just scare tactics. i'd cheat "just a little" on the diet restrictions and watch my son get sicker.

i know it pisses ppl off and annoys them, makes them defensive and makes them roll their eyes or think i'm some crunchy radical treehugger when i go off on my tangents about foods and the school feeding my kids junk... but how can i unlearn what i've learned? how can i unexperience what i've experienced?

how can i not be territorial and possessive about what someone gets to feed my kids when i know what i know? it's one thing for ME to decide to take exactly so much risk in letting the non-allergic ones have 5 or 6 pizza and ice cream days a yr...i can prepare for it, monitor it, and make myself okay w/ it b/c it's in such moderation. but to think of someone else like the school doing it...w/ no moderation, little monitoring, at the drop of a hat w/ no notice or permission from me...just drives me crazy.

as a parent today, i've learned that i have to worry about melamine in the food supply, GMO's, now plastic particles in chinese rice (!!) besides the allergens that are an every meal concern...there's no way a teacher can check labels and ingredients for all that for 25-30 kids.

w/ the rising rate of food allergies and strange new GM foods being made today, i simply don't think anybody should be feeding kids except their parents or caregivers, for liability reasons, if nothing else!

what if jovie had had her 1st anaphylactic reaction at school during a holiday party instead of home? what if it happened when she was way out on the playground, behind the trees? how long until some kid *does* have their 1st reaction at school? is the teacher going to come to the hospital and stay there w/ my kids until they're recovered? is the school going to help pay for dental care for cavities back when they had a party nearly every day for student bdays? help my kid lose weight when they get fat from pizza parties every friday and then some? no? then guess what? if you're not going to address the issues harmful food is going to cause for my kid - and it's going to be MY problem if you unknowingly feed them melamine chocolate or something - then YOU shouldn't be feeding them!

we just don't know what's in the food today, let alone how ppl are reacting to it - it should be up to me what my kids eat and how often i'm willing to let them get the crap. i don't need the schools or anyone else stacking the deck towards more potential harm for them.

ppl want to pretend it's just about too much fat and preservatives in our foods and decide that moderation is okay -"my kid doesn't have a weight problem, we can do mcdonald's a cpl times a wk" but it's not about trans fats and preservatives anymore. the food we eat today is almost unrecognizable as the food we ate when we were kids and nobody has any idea what it's really doing to our kids. the saddest part is ppl really don't want to know. which is why our food industry gets away w/ feeding us slop other countries won't even take from us for their animals.
wake up and smell the GMO's, peeps - we're one sick nation.

reallergic peanut allergy update


jovie had her retesting done on jan 18th. it confirmed severe (level 3) peanut allergy.

so, just like that, we are back at square one and i am left confused and wondering how she could have truly been over the allergy and is now right back where she was. her allergist says he has only read of such cases, but it does happen. i wish i'd never given her any peanut and just left well enough alone when he told me she was no longer allergic. at least now she'd be walking around w/ a little bit of a buffer for accidental exposures. i mean, if it took 3 or 4 instances of directly and intentionally eating almost a tablespoon of peanut butter, she could have had quite a few tiny accidental exposures before she would be immediately anaphylactic again. now i've used up that buffer b/c i gave that much to her every single week.

and if she overcame it with 4 years of total elimination of peanuts once, can i expect that with 4 more years of avoidance, she might outgrow it again? her dr. says no, that it is a lifelong allergy now...but can he really know for sure? i'm not looking for my child to someday be able to eat peanut butter on a regular basis, i just want that buffer back - so she isn't always one crumb away from choking to death from her airway closing up. i'd give anything just for a little buffer again.

one good thing to come of it, however, is that her dr. discussed the case with his fellow allergists in their practice and mentioned my recommendation that all severe allergy cases should have TWO food challenges in their office before being declared "cured" of their allergy, since the 1st exposure would count as the (new) sensitizing exposure in a child that had outgrown an allergy to the offending food. the next exposure would really be the telltale one. had we been in a controlled environment and looking for it, the dr. would have caught jovie's 1st reaction at her 2nd exposure to peanuts. we were very lucky, her most recent (anaphylactic) reaction could have been much worse or even fatal.

i didn't think the dr. would take my suggestion seriously as it is evidently so rare for any person to become re-allergic like this - so soon and so seriously - but her allergist told me they have changed their policy at their practice to adopt my suggestion and it's already in practice! i LOVE a dr. who is open to learning from his patients!! it makes me feel like we are truly in the same boat and working as a team - we are all learning as we go along and open to listening to each other's viewpoints.

the next step is meeting with her school about going peanut free, which i am hoping will go smoothly as our high school already is and it seems pretty inevitable anyway. so far the 504 coordinator has been nothing but helpful and concerned, so i am encouraged.

i am still left pondering why my children always seem to be the ones that never fit in w/ the way things usually work. if there's a rare side effect, it happens to them. if there's a "variation of normal", it's them. if there's a "one in a ten/hundred/thousand/ten thousand" chance, it happens to my kids. at times it's made me really insecure, self-conscious, be called a 'munchausen-by-proxy mama' or even ignore or downplay my children's symptoms b/c i don't quite believe it myself or want to be "that mom" who always has the weird issues.

but i'm beginning to formulate a theory about what might be behind it all and am putting my thoughts together for another post all about it - stay tuned! :-)

60 Minutes Report : Phthalates: Are They Safe?