06/04/2011 – AppleBee’s Pancake Feed Fundraiser

AppleBee’s Pancake Feed Fundraiser for HLH WARRIOR LIAM SMITH
Time Saturday, June 4 · 8:00am – 11:00am

Location Salmon Creek AppleBees
13006 NE Highway 99
Vancouver, WA

Created By Julia North
More Info – $7per person for Pancake breakfast provided by AppleBee’s.
$5 of every ticket sold is donated to Liam and his family.
To purchase tickets, contact me via email or phone
Julia North 360-518-4270 click on link above to go to my facebook profile to send me a message
Terri Smith 360-518-2637

Posted in Fundraising for Liam | 1 Comment

DAY +6

Kristy’s Twitter Update – Wednesday, May 18, 2011, 10:10 AM

Liams WBC count is still <0.2. platelet count 17 so they will be giving him platelets today. ANC still 0. Day +6 he will get methotrexate 🙁
about 3 hours ago

Liam was up at 4am he threw up and there was blood in it. He just fell back to sleep. We should now more after his labs are back.
about 4 hours ago

Liam threw up again tonight. He had a chest x-ray today it was clear. The Dr. says he is doing very well. She said he gets a A+. 🙂
about 11 hours ago

Liam loved playing in the tub again. Love the smile on his face, brings joy to my heart.

Posted in Liam's BMT updates, Photos | 1 Comment

DAY +5

Kristy said that Liam got sick several times this morning. I haven’t gotten a full update on Liam so I will post more when Kristy give me more info. It is so hard not being with him.

They moved them to a bigger room this morning. No shower but it is bigger, and has a patio off the room. That will be great for Kristy. But Liam should not be out in direct sun light. The doctors said it can sometimes can cause GVH (graft v. host). He will need to be completely covered in sunscreen, even under his clothes. The sun penetrates thru the clothing and can cause skin problems. So the best thing is to avoid it, maybe in the early morning or after sun down.

Kristy’s Twitter Update: May 17, 2011, 10:44 PM
He is still struggling with the pain but still is so sweet. He should start to feel better around day+11, he should also start to graphed around Day +14to +20
about 1 hour ago

Platelet count is at 40 if it drops to 10, he will need a transfusion. ANC (Absolute Neutrophil Count) is still 0. Magnesium level was low so they gave him some.
about 1 hour ago

Today started at 6am Liam got his leg stuck in the crib railing and his leg is now very bruised. Then he threw up and got a bloody nose.
about 1 hour ago

Posted in Liam's BMT updates | 4 Comments

DAY +4

DAY +4 – Liam has mucositis this is causing him alot of pain this morning.

Using suction to remove the mucositis out of his mouth

They had to increase in morphine 3x this morning. Kristy said he is feeling better this afternoon. His ANC was at 0 yesterday. Now we wait.

Liam loved his tub time

He enjoyed his tub last night. Better than last time, for some reason he was very scared. Mommy had to put him in the tub with no water to play a bit before they the added the water. She put a towel on the bottom to sit on. It all worked I watch on Skype he really enjoyed himself. The photo is from Skype, so its not the best quality. More updates later.

 

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DAY +3 ANC 0

Update DAY +3 – ANC 0
Liam Update from Papa (overnight)
[7:31:56 AM]: he went through the night very well. I stayed awake untill 2:30am and no redness and he was still asleep but the nurse said at 4:00am he got red but did not wake up.

Posted in Liam's BMT updates | 1 Comment

DAY +1 ANC 567 +2 ANC 280 – Update on Liam & Hunter

May 13th, 2011 – DAY +1 – Liam’s ANC is 567 on day 1, he had diarrhea last night, seemed to be better this morning. Nurse found blood in his stool, they said it could be from the chemo. Still eating well. Liam skin redness is better today. They increased his pain medication today. It better for him to heal. The doctors said he is right on track for what they expect.

May 13, 2011, 11:55 AM
Hunter is hurting but being very strong Liam did very well with the transfusion. Now we wait and hope for the best. Thank u 4 prayers & support

Papa & Liam - DAY +2

Update: Hunter is doing much better today. Liam is doing ok. He keeps getting red all over. They aren’t sure what the cause is, might be antibiotics or the Methotrexate. He got both within an hour so not sure which one caused it. He just recieved the antibiotics again this morning. So we will have see if he gets red again. He got really flush and his skin was really warm. He looked like a little tomato.

DAY +2 – Saturday, May 14, 2011
Liam’s ANC 280 Today. He still is red. Diarrhea has slowed down. He is still drinking. He is not interested in solids at this point.

Posted in Liam's BMT updates, Photos | 1 Comment

DAY +0 ANC 1092 Liam’s Bone Marrow Transplant is Today, Please say a Prayer

Thursday, May 12, 2011- DAY +0 – Transplant Day 12:03PM

Liam’s ANC is 1092 on Day +0

Today is the day that our Little Warrior will recieve him Life Saving Bone Marrow Transplant. The gift of a second chance for a brighter future. The gift of a brother’s love. Hunter never gave it a second thought to be the donor for his little brother Liam.  He was honored, and felt blessed to be able give his little brother his bone marrow. All three of Liam’s older brothers, Noa, Hunter and Ryder bravely went thru all the needed testing to try and help save their Little Brother Liam. Noa & Hunter fully understood what this all meant for Liam, that he could die with out a Bone Marrow Transplant. Both of them bravely agreed to do whatever was needed to save thier little brother. Liam is so blessed to have had two brothers be a perfect 10/10 match. Hunter and Liam have so many phyiscal triats, looking at baby pictures you could easily be confused on which one it is. It just seemed meant to be that Hunter would be the donor. Noa watched over his brother Hunter everyday making sure he got plenty of rest, and eating healthy foods. All three brother’s played an important roll in helping save their Little Brother’s Life. They are all Hero’s! With so much love for each.

They are all blessed to have each other.

  

Pictures of Liam’s brother Hunter getting ready to go in for his procedure

    

    

    

    

Pictures of Hunter after the procedure below:

    

Hunter seeing Little Liam, before Liam recieves Hunter’s Gift of Life, a second chance…

Such a special moment, the love of Brothers…

    

    

    

 

Grandma Terri says:
got to watch on skype Liam’s transplant going and see Hunter. Noa had his arm around Hunter, helping him walk~they walked over to Liam -Hunter pats his little head and Liam had a big smile for his big brothers! Like he was saying Thank you Hunter and Noa!
Bless them all~ Go Liam!!

 

 

Hunter went back to the Ronald MacDonald house to rest. He slept for several hours. Later that evening he started hurting. He said to me, I didn’t know how much it would hurt. I asked him, knowing that it hurts “would you do it again Hunter?” Without any hesitation he said, Yes Nana I would gladly do it for My Little Liam. 🙂 

Posted in Liam's BMT updates, Photos | 3 Comments

Rascal Flatts song, I Won’t Let Go~dedicated to Kristy,Jared and boys

height=”349″ src=”http://www.youtube.com/embed/N5gBxKEgZqM?rel=0” frameborder=”0″ allowfullscreen></iframe>

Posted in Inspirational Songs | 1 Comment

Jolie’s Poem for Liam

Don’t Be Afraid
You’ve got me standing here, by your side. Everythings gonna be allright.

Cuz, you got me and everybody. Nothings gonna go wrong. If you stay here where you belong. Just don’t be afraid, just don’t be afraid, don’t be afraid, don’t be afraid.

God’s watching you, God’s watching me. God’s watching everybody.
But right now he’s watching over you the most to keep you strong. If you’ve got faith and you’ve got love, then you belong right here.

So, don’t be afraid tonight. We’re gonna keep you here, just stay right here…Don’t leave me. Just don’t be afraid of life. It’s gonna be all right…just stay right here!..

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Pre-eclampsia – Mirror syndrome – Triple oedema – Ballantyne syndrome

New clue to predicting pre-eclampsia

Source: http://www.medicalsearch.com.au/Features/New-clue-to-predicting-pre-eclampsia-9501

“Pre-eclampsia affects an estimated 5000 to10000 women in Australia every year.”
11/05/2012-

An indication of whether a mother will develop pre-eclampsia, the most common and severe pregnancy-related disease, has been identified by a University of Sydney study.

The findings, published in the latest edition of the Journal of Reproductive Immunology could allow the early detection of pre-eclampsia, is currently unable to be diagnosed by symptoms before the disease occurs.

The research also suggests the womb may have a lasting impact on a child’s immune system.

“Pre-eclampsia affects an estimated 5000 to10000 women in Australia every year,” said Professor Ralph Nanan, senior author of the study, from Sydney Medical School Nepean.

“It develops in mothers out of the blue, usually in the last three months of pregnancy, causing high blood pressure, kidney and liver damage and severe blood changes. Delivering the baby as soon as possible is the only way to stop it.”

In pre-eclampsia the mother’s immune system appears to attack the foetus.

“Our study looked at the thymus of the foetus, a structure which sits behind the baby’s breastbone and is known as the ‘cradle’ of an important set of white blood cells called thymus-derived lymphocytes or T cells,” said Professor Nanan.

No previous study has looked at the effect of the disease on the fetal organ systems.

“Surprisingly we found the thymus of babies whose mother developed pre-eclampsia was significantly smaller than in babies of healthy pregnant women.”

What further surprised the researchers was that these changes were obvious in mid-pregnancy, long before the mother developed any signs of pre-eclampsia.

“This is a very interesting finding as the thymus plays a central role in shaping the child’s immune system and protecting it against the development of allergies, autoimmune disease and cancers later in life,” Professor Nanan said. .

The group is now conducting a prospective study with over 1200 pregnant women to confirm the findings with the long-term prospect of developing a test for pre-eclampsia. It is also conducting studies which aim to describe the short and long-term effects that early thymus changes have on the child’s immune system and on the development of immune diseases.

The study was conducted by David Eviston, and Ann Quinton and a team of researchers from Sydney Medical School Nepean.

Browse the MedicalSearch directory: Gynaecology & Obstetrics

Source: University of Sydney

________________________________________________________________

Mirror syndrome. A case report.

Abstract

BACKGROUND:

Water retention in a pregnant woman can mirror fetal hydropic changes. This clinical presentation has been named “mirror syndrome.” Awareness of the syndrome is important due to the associated fetal and maternal risks.

CASE:

A 26-year-old woman, gravida 3, para 1011, presented at 31 weeks’ gestation with significant edema and a 7-km weight gain in one week. Sonographic evaluation revealed hydramnios and fetal ascites. Maternal workup was negative for preeclampsia, diabetes, or cardiac or renal dysfunction. A workup for nonimmune hydrops was also negative. Over the next three days there was progression of maternal edema. With diagnosis of mirror syndrome, the decision for delivery was made. Both neonate and mother subsequently did well, with normalization of ascites and edema, respectively.

CONCLUSION:

Our case, along with 19 reviewed in the literature, reiterate the features of mirror syndrome and provide an opportunity to dispel some of the misconceptions in the literature. The condition is frequently mistaken for preeclampsia, although distinguishing characteristics can be identified. Mirror syndrome is a manifestation of extremely severe fetal hydrops. When the specific cause of fetal hydrops cannot be identified and corrected, immediate delivery is necessary in order to avoid fetal death and maternal complications.

________________________________________________________________

Mirror syndrome

From Wikipedia, the free encyclopedia

Mirror syndrome or triple oedema or Ballantyne syndrome is a rare disorder affecting pregnant women. It describes the unusual association of fetal and placental hydrops with maternal preeclampsia.[1]

The name “mirror syndrome” refers to the similarity between maternal oedema and fetal hydrops. It was first described in 1892 by John William Ballantyne

Causes

The etiology may be any of the variety of obstetric problems that range from immunological disorders, including Rh-isoimmunization, to fetal infections, metabolic disorders, and fetal malformations.

Pathogenesis

The etiopathogenetic mechanism of Ballantyne syndrome remains unknown.

Signs and symptoms

Ballantyne syndrome has several characteristics:

  • edema, always a key feature
  • albuminuria of the mother, usually mild
  • preeclampsia, unusual

The fetal symptoms are related to fluid retention, including ascites and polyhydramnios.Fetal hydrops suggests the presence of an important and probably fatal fetal pathology. It can be associated with twin-to-twin transfusion syndrome.

Diagnosis

Although the exact etiopathogenetic mechanism of Ballantyne syndrome remains unknown, several authors have reported raised uric acid levels, anemia, and low hematocrit without hemolysis.

Differential diagnosis

The problem of distinguishing (or not) between Ballantyne syndrome and preeclampsia is reflected in the diversity of terminology used and in the debate that surrounds the subject. It seems much more likely that an etiology of severe fetal hydrops may cause Ballantyne syndrome when the fetal status greatly worsens and that the syndrome is only a manifestation of the extreme severity of the fetus-placental pathology. Platelet count, aspartate transaminase, alanine transaminase, and haptoglobin are usually unaffected and may be used to distinguish mirror syndrome from HELLP syndrome.

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