Musings & Events.

Hey Friends!!!

We really need to be better about posting on Seth's blog but let's face it - life is BUSY! I thought Id do a quick event update and also share a few thoughts with you on this glorious Tuesday morning!

First off - Seth is turning 3!!! I cant believe it's been almost three whole years since I witnessed the birth of this beautiful boy - and what I three years it's been! In honor of Seth's big day, we are having a ColdStone fundraiser on June 20th. This will be held at the same shop as it always is, at Val Vista & Baseline in Gilbert.We will post a big announcement & details as the day approaches but for now - mark your calendars!!! 

Okay, next. Ramblings.

Ive been thinking a lot lately about CMV. Being pregnant again with our 6th baby of course brings about thoughts of all the risks and scary things that can happen to a baby in utero - CMV being one of many viruses that can pass through the placenta and one of many many things that can go wrong. 

Ive really noticed over the last few days that there is a lot of fundraising going on for things like autism, cerebral palsy, epilepsy, etc. Millions of dollars have been raised to either research a cure for these ailments or to simply provide help to make life easier and more comfortable for those suffering with these things. That's amazing! It beautiful to see people giving up their own time & money to help the plights of others. The question milling about in my mind is this: What if we could STOP these things from happening? Are we spending all of our time and money trying to fix something that could be prevented entirely?

Each year, at least 30,000 children (1 in 150 in the US) are born with congenital human cytomegalovirus or cCMV. Most babies go home from the hospital with no indication whatsoever that they have been infected with this devastating virus in utero. Most will never show symptoms at all. But maybe they do. Maybe a year and a half down the road, they make it onto the autism spectrum. Maybe at age 2 they develop epilepsy. Maybe they simply have ADD or hearing loss or have severe learning disabilities. CMV is the number one cause of birth defects and physical as well as mental impairments. and yet you would never know your child was infected with CMV in utero unless testing was performed AT BIRTH. Unfortunately, we dont do that here. A simple cheek swab or urine sample would suffice, but because there is no vaccine and no way to prevent CMV, it's deemed pointless to do that kind of research in the US.

The number of known CMV cases each year is huge. It's startling, really. It could be the major cause of autism, CP, epilepsy, hearing & vision impairment, and a host of other things that plague our children - and adults - every day. Yet, most people have no idea what CMV is. We have to raise awareness. We have to get funds flowing in for CMV research. The only way to stop this virus is to find a vaccine. The only way to find a vaccine is to fund research - and that is just NOT happening for CMV.

If I was a famous celebrity with a CMV baby, the whole world would know about it. The whole world would empathize, be on alert, and throwing money at this cause. But Im not. Seth isnt the child of a famous woman, but of a normal girl who happens to be my best friend. He's is still worth it. All of our children are worth the time, effort, and money it will take to raise awareness and - eventually - bring about a preventative vaccine for CMV. 

For lots more information, please visit . Donate if you are able, and spread the word - facebook it, post it on your blog, buy a Stop CMV bracelet and tell everyone you see what it's about. Help us protect the children of our future by stopping this virus in it's tracks.

*Please note: Im not trying to say your child is autistic or has CP or anything else because of CMV exposure in utero, so please dont try to lecture me about MMR vaccines and chemical exposures and oxygen deprivation. I know enough about all of those things. A link between congenital CMV and autism was discovered & noted as early as 1991...why isnt this information out in the public area? This is what Im asking. This is why we need to raise awareness immediately. CMV can directly account for every single disability that is not chromosomal or genetic - which to me, warrants a hell of a lot more research, right now.

Thank you for being a friend to Seth and a supporter of this precious boy & his family! You are all so very loved & appreciated!


Hunger Games

Harkins Chandler Crossroads
202 South and Gilbert
March 23rd at 7:00pm

Please if you are going to see the movie please come and see it for Seth! Tickets are 20 dollars each and will go to help raise money for us to go to San Francisco to the CMV conference in October, video monitor for Seth, therapy needs and toys. Thanks again for helping out our precious little boy!

Please contact me through FB or email if you would like to purchase a ticket. Email address is: