George Charles Garman 09/09/09 to 01/29/10

January 29, 2010 our world was turned upside down when our 4 month old little boy earned his wings after a battle with Mitochondrial Disease and awoke in the Lords loving arms.

"Life can not be measured by the number of breaths you take, but by the moments that take your breath away."

George's Guardian's of Grace Projects

Stocking project is now in full force collecting donations. We have a list of the items we can use. You can also choose to sponsor a stocking in memory or honor of someone else. We will include a paragraph or two in the cards we place in the stockings to let the recipient know about the person that means so much to you. Our paypal account is posted on this page and ready to take donations. Email us for a list of items needed or with any questions or information you would like included on a sponsored stocking/donation.

Tuesday, October 8, 2013

George's Guardians' of Grace Gift of Giving Project


As many of you know, our family has created stockings in the past to give to the homeless.  We have done this every Christmas since George returned to heaven.  Our annual project is in the works and we have chosen to use bags this year instead of stockings since there are great deals on some of the larger toiletries and they will last the homeless person receiving them much much longer.  Monetary donations are also welcome for those of you who are not local but would still like to give. I am happy to look for the sales and put the donations to great use, making the most of each penny.

For those who want to donate in memory or honor of someone please send us information about that person so we can include it in the cards sent to these people.  These notes have so much meaning to the individuals getting the gifts and helps them to know someone out there cares.  Sharing loved ones with others also helps to let others know how wonderful the person is and if it is in memory, it lets that person live on through such a great project.  Emails with your loved ones information can be sent to:  garman_family@yahoo.com

This has been so successful and  a wonderful way to make something good out of a sad situation.  George's siblings love to do this in his memory each year.  Below you can find a list of items we will need again this year.  We will take travel size items as well as regular sized ones, we even out each bag.  Due to rising amounts of homeless individuals in Camden we may have to actually make close to 150 bags.  Please remember that homelessness does not discriminate so we we need items for men, women, and children.

You can now also follow the projects we do on Facebook. www.facebook.com/georgesguardiansofgrace

Items Needed:
Packs of new socks
Hats
Gloves
Wash Cloths
Tissues
Toothbrushes
Toothpaste
Dental Floss/pics
Shampoo/Conditioner
Deodorant
Soap
Bandaids
Alcohol wipes/antibacterial wipes-individually packed
Q-tips
combs
Box of Cards
Tree ornaments
Wrapping Paper
Ziploc bags
Small children's toys


Tuesday, April 30, 2013

Tenth Avenue North- Worn (with story)

Finally!!!

It has been quite a while since I have posted because google would not let me sign in without tons of drama.  Today I have not been able to sleep so I'm heading into another sleepless night!  I realized that I miss writing here and having this outlet so this was the perfect time to figure it all out.  I did it!!!  Finally!!!

So much has changed in our lives and I'd like to share with those who are still following our story the most recent news. 

We successfully donated 100 bags for George's stocking project to the homeless in Camden, NJ.  It was a moving experience and this year it truly touched Richard's friend Tony who has now become like family.  Both Rich and Tony helped us along with those who did make donations!  It is so hard not to have George during the holidays and this project helps to keep him touching lives and living on through these projects and people.  They truly appreciated it and we have some leftovers for this year's project. 

Michael was granted his wish through the Make a Wish Foundation.  We were blessed to spend a week aboard the Disney Fantasy!  It was such a blessing for our family and definitely a life changing experience. Our trip took us to Mexico and opened the eyes of our children, especially Richard.  All the kids were able to find themselves on this trip and really have some TLC just like Hugh and I did.  It was our first real family vacation since we NEVER go alone.  All of us were challenged not having other family but we kind of learned how to be a little family rather than the larger family we have come to depend on and love.  Our family did make this possible since we did have to cover part of the cost of the trip and were not aware of that.  One thing we knew was they wouldn't let us down and we would surely be able to make this happen for Michael.  Michael LOVED being the center of attention and the "special" child for the week.

We are now in the process of moving back to our house!!!  Yes you read that right, we are going home:o)  In a twist of events, a family member purchased our house and is allowing us to live with them until we are able to purchase it back hopefully again some day.  There is a lot that goes into this but God is good and we are headed back to the place the boys all know as home...it is going to be interesting to see Gabby since she only knows my parents house as home.  She is a smart cookie and I know she will be ok with it all.  None of this would have been possible without our families and we thank all of you who were involved with us being able to live in our home again.

All of us have been doing ok medically.  I have yet again shown positive for the Mitochondrial Defect with significant numbers and also produce a substantial amount of Mitochondria.  We have been working with Dr. Michael Goldenthal at St. Christopher's Hospital in PA.  Unfortunately, he has lost money towards funding the swabs and now has to charge us 200 dollars per swab.  This past time Michael and I were done since we need the black and white paper dx and owe him 400 dollars.  Long story involved with that too.  We will figure it out once we get this move done.There is so much that goes into the move that other things have to be put on hold if possible. All of this is making the days go by so fast.  I really want to work on a fundraiser to help with this diagnosis process since we really need answers and if the doc could find our genetic defect, he would be able to see if we all have it and if George had it for sure.  I'm not sure how long it is going to take before this happens but all of it comes down to money and it kills me.  PLEASE, if you have a way to give towards his research please let me know, we can get anything given allocated towards his research.

We were also able to return to Florida for a trip to Disney with our large family.  My niece who is Gabby's age was fortunate to join us and the girls had so much fun...it is amazing to live through their eyes!  That is what life is all about.  All of us had a great time...it was a challenge at first since it was the same house we went to that George went to with us when he was alive.  God do I miss that little monkey face!!!

Emotionally, I have good and bad days.  I stood in the rain at his grave yesterday with my hand in the dirt where he is buried.  I don't know why I needed to do it but I did.  I probably would have laid there on his grave if it was only his space or it was a place that allowed that but since it is at our church that just isn't possible.  I did sit for the first time on the ground where he was buried to take a picture of myself with his things and grave that I got him for Easter.  Inside I don't understand all of these needs but something just gives me this internal pull that cannot be denyed.  Why do I share this?  I share this for others who think they are crazy or alone when they do things like this.  I know I feel so alone.

Hugh has been his normal self and really working as hard as he can to keep our family going.  He recently hurt his back again and was out on disability for a while. Right now he is still working at Sears but keeping his eyes open for a better option that can support our family better but Sears is safe and there for now.  I just worry about Sears itself tanking and Hugh being without work.  I am still working on my disability paperwork and am on my first appeal but I need that paper saying I have Mito which is gonna cost 400 dollars.  We just keep telling ourselves that God sees the bigger picture or we would be so lost!!!

We are really trying to keep our faith.  There are days when it is all so very hard to do and the pain of this world seems to be overwhelming.  It forever seems like we are needing help and we have yet to understand any of it.  Life for us all has been so tough and people get sick of hearing about it all.  Our family will forever be in need of help and it gets old to people after a while so we always feel like we are juggling things all the time.  Please keep us all in your prayers.  We thank you for coming back and keeping an eye to see if we reposted.  I am planning to start writing again if all things go well.




Sunday, October 21, 2012

Hug Him Once For Me






Today the boys went to grief camp at Comfort Zone. As always, it has brought up so many feelings that I have just tucked away to be able to survive another day without my son here with me. This song is so beautiful and spoke to me. No one knows how much I miss him and wish he was still alive. I would give anything to have him again and so often I look at our family and know he is missing. Every single day of my life my heart breaks a little because he isn't here. I will post later about the wonderful experience camp brought to our family and all the wonderful milestones the boys met and amazed us with!

Saturday, October 13, 2012

Stocking Project


Our Stocking project is now in full force collecting donations.  Below is a list of the items we can use.  You can also choose to sponsor a stocking in memory or honor of someone else.  We will include a paragraph or two in the cards we place in the stockings to let the recipient know about the person that means so much to you.  Our paypal account is posted on this page and ready to take donations.  Email us with any questions or information you would like included on a sponsored stocking/donation.

Packs of new socks
Hats
Gloves
Wash Cloths
Tissues
Toothbrushes
Dental Floss/pics
Shampoo/Conditioner
Deodorant
Soap
Bandaids
Alcohol wipes/antibacterial wipes-individually packed
Q-tips
combs
Box of Cards
Tree ornaments
Wrapping Paper

Any donations are welcome!  We currently are close to the amount of toothpaste needed but always welcome any that you may have since we will hold over items for next years stockings. 

All items are wrapped in Christmas paper and added to handmade stockings.  Our family does this in memory of George and his big brothers and little sister are instrumental in making this happen! 

Thank you in advance for all donations!

Sunday, September 30, 2012

Testimony for Rainbows Program

I was asked to come speak at a church today where our family attended a grief program.  I spent quite a bit of time writing this and wanted to share it.  Miss my little boy every single day, so this of course came from the heart!


The rainbow has taken on so many different meanings over the course of time, but none greater than that of God’s promise after the storms that wiped out the Earth.  For someone facing a significant loss in their life, they often find themselves looking to God for help and guidance in their time of their personal storms.  We consider all significant losses, like a death for they are the death of the dreams you had for your life and that of your loved ones.  I believe everyone here can identify with loss on some level. 

Our family has been no stranger to loss.  My husband Hugh found himself jobless when the market tanked and the shipping industry he worked in no longer needed as many works as Imports to our country drastically decreased.  The job he lost was finally the good paying job we had been praying Hugh would acquire after difficult struggles with medical issues and finances.  Our family had been taken aback when a few years prior, our son Joshua was diagnosed with Mitochondrial Disease, a life threatening metabolic disease.  Medical care was scarce to come by and required many out of state trips to meet basic needs.  We had to become educated and I became Joshua’s doctor. It came no surprise when our son Michael was diagnosed with the disease a year after his birth.  I could no longer work and Hugh was working two full time jobs to just pay medical costs and basic living costs before he landed this dream job.  There have been so many moments we felt as if we were just able to keep our heads above water.

Not once in all of those trials did we lose our faith but rather found ourselves clinging to our faith when there were no answers. We always believe that God will provide.  Hugh was devastated after his layoff when job after job interview proved to not turn up anything promising. He was our provider and knew so much rested on his shoulders.  Shortly after his layoff, I was needed to care for both of my elderly grandparents who were ailing and returned home to God Oct 29th and Nov 29th of 2008.  Following their deaths, Hugh’s father was diagnosed with cancer and returned to heaven Nov 15th 2009. We were both instrumental in his end of life care.  We were not walking alone in these losses, our children were right there with us feeling the ups and downs associated with it all.  We came to realize that often times children are the forgotten ones in moments like these…we discount their feelings and often times can’t see past our own pain and upset.

Thrown in that mix, we were blessed to find out we would be welcoming another addition to our family. Hugh and I were elated to find that God had yet again entrusted us with one of the most precious gifts he can give, even if we faced harsh criticism by many around us.  George Charles Garman was welcomed into our family September 09, 2009, yes 09/09/09.  I would always tease saying he just wanted to be the one who’s birthday we would finally remember being the 4th boy in our family.  From the very beginning I had a very special bond with George. Deep inside, I knew he was only going to be with our family for a short time, even though I prayed that feeling was wrong.  George showed symptoms of the same disease his two big brothers battle and I knew he was my sickest little guy.  I took him to doctor after doctor trying to get them to help me but he would never do anything odd in front of doctors.  By that point all of our doctors familiar with the disease, were no longer in practice or taking patients and we were on our own.

January 29th, in his sleep, George was called home.  Hugh woke to find him unresponsive in his bed.  I will never forget that scream as I ran upstairs and Hugh thrust George into my arms looking at me, hoping I could save our son.  Despite all my efforts and that of the officers, EMT’s, and hospital staff, George did not return to be part of our family here on Earth.  We stood watching the hospital staff work on his lifeless body.  In the back of my mind all that I could think of was “God, please let this cup pass from me, but thy will be done” I knew deep in my heart what God’s will was for my little monkey from the moment I first held that blue eyed blond haired wonder in my arms for the very first time and it was to change lives but not necessarily through his life but rather his eternal life.  The moment Hugh handed George to me that awful cold January morning; I knew my baby was gone.  I had to still try everything to save him but through the chaos, an internal calm came over me as I told the hospital staff to stop working on him.  George would never have been that happy smiling baby and it would only be my own selfishness to want him to stay.  I wanted the best for my son from the moment I knew he would be mine to watch over, and I knew then that the best thing for him was heaven, even though I knew my arms would forever ache until I was reunited with him again someday.

The first person we asked to be called was a minister, followed by our family.  The very last thing George wore was a baptismal outfit because we knew we were turning him back over to God.  Never once has our faith waivered, even though we would like to know what God is thinking sometimes.  We have our good days and bad but both Hugh and I were not concerned for ourselves or even George; it was for our children that were left behind.  Richard was 11, Joshua was 4, and Michael was 2 and Joshy and Mikie witnessed all the chaos of that morning. Along with other family members, we spent hours poring over the internet praying for God to help us find somewhere our children could get the help we knew we were not capable of giving them.  Trying to find help for them was virtually impossible, add in that you wanted a faith based program or therapist along with our financial problems and the only program listed was the Rainbow’s program.

By the time we found the listing I had given up on finding help that was so desperately needed and my mom actually made the first call.  Brother Sim was the person to return her phone call.  My mother thrust the phone at me; I rolled my eyes at her figuring it was another dead end.  As when I called all the other places, he told me that the program wasn’t running because of lack of interest but that he would hold onto our information and get back to me if they were able to come up with enough people the following summer.  I was at a loss as to help my children when they would just break down crying in sheer pain over the loss of their brother and the deep aching they felt that I could not ease no matter how hard I tried.  So many nights I cried myself to sleep not only for my pain but for that of my children and how I could not help them.  Often times I could never even formally pray and would just cry out in pain to God asking him to help me…”Please God, I can’t do this alone!”  Finally that phone call came and God answered all of my prayers!

Hugh and I were excited to be able to attend this program as a family but the kids were reluctant at first.  I knew if we could get them to the first meeting, it would all work out in the end.  The second week, we didn’t have to even tell them when it was time to go, they were telling us when it was time.  We found ourselves looking forward to, and also needing the camaraderie of others who knew loss.  Each of us had a different type of story and loss, be it divorce or death, but we were all able to respect one another in such a way that we found God was with us at these meetings.  You could feel his very presence during the moments we laughed and cried, through the kind words of another, passing of tissues, a much needed embrace, or just having someone to listen without judgment.

In our day to day lives, neither our children nor we adults found this sort of love and compassion like we did when attending a Rainbows session.  The facilitators, all not only gave of their time but they gave of themselves.  They showed us that there are people who care and understand.  Compassion and God’s love were what so many were seeking and only found here through the Rainbows program.  The skills we learned transferred to daily life on so many levels and everyone who attended walked away changed for the better and knowing God’s love like never before.    These walking works of God,  gave not only us the gift of themselves and God’s love, but they gave our children things we could only ask God to do.  All of the children, along with us adults were so sad to see the program come to an end in August…if we could have done it every single week I think we all would have and there were families who drove an hour or more to attend a meeting ever week. 

By your church allowing this program to take place, you have come to change the lives of many people who will also go out in the world and change the lives of others…there will be such an outpouring of God’s love to the world by those who allowed our Lord to call them to do his ministry through this program.  Thank you just is not enough to express the gratitude of all the families who were blessed to attend now hold in their hearts.  The last night we all gathered just summed up the road we had traveled as a newly found family that had started out as strangers.  There was laughter, tears, embraces of facilitators, children, and parents alike, but most of all there was this amazing feeling that filled the room as we all crammed in for a final prayer.  There was not a person who left this program not wishing it was not ending and praying for it to continue in years to come.

Our family still knows loss every single day; September 3rd the home we brought all of our children from the hospital to went up for sheriff sale.  In all of this we have to trust in God’s bigger plan but this program helped our whole family come to terms with this obstacle, unlike before when we faced another loss in our life, this time we were able to place it in God’s hands. We don’t always know why things happen when they are happening, but applying many of the tools learned from the Rainbows program, we are able to fully trust in God and know he has not abandoned us in our hour of need but is instead using these moments to glorify His name.

Hugh’s loss of his job did ultimately lead to the loss of our home but it gave him all of my pregnancy and the 4.5 months that George was with us,  to get to really know George as a little person. We were able to show George unconditional love, and there is no price that can be placed on that.  Our home is always where we are, not a physical place, and God’s greatest gift to us was time with George; his gift to George was that he never had to know the pain of this world.  Even through all of this, God has also blessed our family with our own personal rainbow, Gabrielle Grace.  She is what, in the child loss realm, is known as a rainbow baby; a child that survives after a miscarriage or the death of a child.  Every day God shows us mercy and grace through the people he has put in our lives.  Our family is slowly learning how to live without George, but we know with God as our foundation, we will stay strong through it all.

One of the biggest things I learned from this program was that, it is how we adults allow our children to view personal tragedies and our reactions to them. God uses us to help these precious souls, process obstacles that have caused them to know the trails of this life early on.  Many of you probably don’t know, but the adult part of the program is called Prism.  In order to create a rainbow you need the sun, God’s grace and love, and a prism, the rain or personal tragedy, to form a Rainbow.  “The soul would have no rainbow if the eyes had no tears.” Our children are now able to go into the world and show they are a rainbow. God is using them to show his grace in the face of tragedy.  We need to accept and learn to process our own grief pertaining to our loss in order to allow these children to be just that…God’s walking Rainbows.

Monday, September 24, 2012

Takes Me Back

Missing you so much...had a hard day today...on the way to taking Joshua to the doctors, an ambulance drove by with is lights and sirens on.  Just hearing them brought me back to the morning you left...it hurts so bad today.  I was fine only to find myself with tears running down my face and trying to keep it together at the doctors office.  That siren just kept blaring in my mind and the events of that morning just came flooding back yet again.

No one will ever really know what that does to me.  Daddy yelled the other day and it was just like that morning when he screamed for me after he found you.  My god this is nothing anyone should have to bare in their lives.  You weren't suppose to die.  I wasn't suppose to live my life like this.  Every day I try to do what people want me to do and live life as best I can but living without you is like having to live without air.  I'm told to look at the brighter side of things and be happy for the things I do have and I really want to but it doesn't work that way and being told that only makes all of it so much worse.  I'll have my moments and should just be allowed them...God will get me through it even if it is during some moments by just helping me to breath and put one step in front of another. 

Tonight I went to get Josh a milkshake since he has strep throat and the guy at the window told me how I have beautiful blue eyes.  I thanked him but could not think past how this boy had no idea what these eyes have seen and how they have really lost the happiness that used to be there.  Never again will they shine with joy like it used to be, true joy without pain.   You had those same blue eyes that God blessed me with and all I kept thinking was how beautiful they were and how much I missed seeing them.  I see them in pictures but they are not the same...I miss seeing that love and connection that we had with one another that no one else did or knew.  It was funny because I remember having you in my belly wondering if you would have mine or daddy's eyes.  All those moments are gone. 

I think with all the other things and having to drive past the house all the time now since the RV is parked in the driveway, I just die all over again. We used to park in the driveway so it didn't matter what way we came down the road but now it does.   I'd be lying if I said when I got in the van or coming home, I don't try to find another way to not have to go past our old house where I felt your presence...it's like you are in arms reach but just ripped way each time I drive past.  Today I looked at your garden and just cried...it was so overgrown and resembled nothing like it used to when we took care of it and tended it. 

I had to leave so much behind but that is one of the hardest...especially the boulders that no one would go get for me.  After we found out Gabby was going to be part of our family, we bought one for each of us to put in your garden.  I asked over and over again for daddy and poppy to get them but they told me they couldn't.  We got them back there but no one could bring them back...just another sad thing that breaks my  heart when I think of it.  In the end I was really the only person they mattered to and there was a lot of meaning behind them to me.  I know you knew...I'd sit on one next to your plaque and talk to you or just spend quiet time there trying to just make it through another day.

It seems just as I have it together something happens and I am back ten steps just praying that God will get me through because I know I can't do it.  Never do I feel more alone than the moments where I miss you the most.  I don't know how they say that it gets easier because for me it has just gotten harder.  I'm not sure if all the other stuff like loosing our house and generally crappy life circumstances adds to it but I keep waiting for a time when it doesn't have to be so hard and we don't have so many challenges.  I know you are with me in my heart but it is nothing like when I had you in my arms...they feel so empty when I miss you. I know that heaven is great and I am so glad you are there but I want you here and I'd be lying if I said anything different.  Besides your daddy, you are the love of my life...just in a different way...our connection was so unique and I was the center of your world...you left this world knowing your mothers love...something that was never changed because you never got to grow up.  I know you understand even if no one else does.  If only I could hug and kiss you right now!!!  For now I will just go as tears run down my face and yet again I pray to God to help me through all of this.

Video Tributes/Celebration of Life Footage


Here is a link to a video tribute that was made by Richard's dad in memory of George. Get out your tissues!


http://www.facebook.com/#!/video/video.php?v=1360981185308&ref=mf



We Finally have footage from the service up and running:



http://www.facebook.com/?ref=home#!/video/video.php?v=1368692138077&ref=mf



http://www.facebook.com/?ref=home#!/video/video.php?v=1368733099101



http://www.facebook.com/?ref=home#!/video/video.php?v=1368770540037



http://www.facebook.com/video/video.php?v=1368789060500



It is in 4 sections running about 17 mins each. If you were unable to attend, you can now see what you missed. We were so blessed to have everyone there with us in person and in spirit!









Me With My Prince Charming In Front of the Castle

Me With My Prince Charming In Front of the Castle