Hannah is a young voice that has a lot to say! Read the previous post to learn about Hannah and Hannah HOPES mission and how you can get involved!
Hannah sporting her AJ'S ALLIES t-shirt...you can have one too....T-shirt proceeds help the orphans in the Philippines! Email tingministries@comcast.net for more information!!!!
CHECK OUT HANNAH HOPES in the post below this message!!!
BE A VOICE FOR THE VOICELESS...Hannah is and you can too!
Proverbs 31: 8 - 9
Sunday, September 9, 2012
Wednesday, September 5, 2012
What one young voice can do - Hannah Hopes ...
When I repeat the phrase over and over...BE A VOICE FOR THE VOICELESS...do you usually think of adults doing something to get the word out about the plight of the orphans around the world? Take a look at what one YOUNG VOICE CAN DO...
Hannah is in the center of the photo collecting stuffed animals for orphans!
Check out the news story on Channel 3 in Michigan and then come back to read the rest of this post (if I were a computer genius I could just post the video here on my blog...but I DO NOT KNOW HOW TO DO THAT...so check out the link and come back and continue reading!!! YOU DO NOT WANT TO MISS THIS and MISS helping out with this amazing project....
Kalamazoo teen helping kids around the world
http://www.wwmt.com/shared/newsroom/top-stories/stories/wwmt_vid_4083.shtml
Hannah is in the center of the photo collecting stuffed animals for orphans!
Check out the news story on Channel 3 in Michigan and then come back to read the rest of this post (if I were a computer genius I could just post the video here on my blog...but I DO NOT KNOW HOW TO DO THAT...so check out the link and come back and continue reading!!! YOU DO NOT WANT TO MISS THIS and MISS helping out with this amazing project....
Kalamazoo teen helping kids around the world
http://www.wwmt.com/shared/newsroom/top-stories/stories/wwmt_vid_4083.shtml
KALAMAZOO, Mich. (NEWSCHANNEL 3) - A West Michigan girl with a big heart isn't even 13 yet, but she's already helped hundreds of kids around the globe.
Hannah Weal lives in Kalamazoo, and says that a couple years ago, she woke up feeling down, and looked to her teddy bear for comfort.
She realized that if it could make her feel better, it could make other kids feel better too, so she set out to do it.
Hannah admires Mother Teresa, so she decided to collect stuffed animals for orphans in Calcutta, India.
She named her project Hannah Hopes.
This year, Hannah is sending love to orphans in Bulgaria and The Philippines.
She's collected around 215 stuffed animals so far, but is hoping for 1,000.
If you would like to donate toys or money to help pay for postage, you can do it through Hope Reformed Church in Kalamazoo.
The phone number there is (269) 349-9788.
Stuffed animal donations are requested to be small rather than large for ease of overseas shipping
Hannah Weal lives in Kalamazoo, and says that a couple years ago, she woke up feeling down, and looked to her teddy bear for comfort.
She realized that if it could make her feel better, it could make other kids feel better too, so she set out to do it.
Hannah admires Mother Teresa, so she decided to collect stuffed animals for orphans in Calcutta, India.
She named her project Hannah Hopes.
This year, Hannah is sending love to orphans in Bulgaria and The Philippines.
She's collected around 215 stuffed animals so far, but is hoping for 1,000.
If you would like to donate toys or money to help pay for postage, you can do it through Hope Reformed Church in Kalamazoo.
The phone number there is (269) 349-9788.
Stuffed animal donations are requested to be small rather than large for ease of overseas shipping
Hannah Hopes and Ting Ministries are teaming up for this project! Hannah is collecting the animals, making the tags, and shipping to our location here in Pennsylvania so that we can then get the special stuffed animals to orphans in Bulgaria and the Philippines! WE might even have the opportunity to share the animals with street children in the Philippines! This is exciting when you view the tags and the love that is put into the tags for each animal. Hannah shares that God is love on the tags. Hannah HOPES that each child that is touched by animal would come to know the LOVE OF JESUS. It is my prayer that each life touched by one of these animals is a life changed by the power of LOVE...by the power of God...by the Power of JESUS Christ and HIS REDEEMING LOVE!
Hannah is turning 13 years old! She is being a voice for the voiceless. I am humbled and blessed by this precious young girl and excited to watch what the LORD will do with this very special project and her young life!
I Timothy 4: 12 says "Don’t let anyone look down on you because you are young, but set an example for the believers in speech, in conduct, in love, in faith and in purity."
If you have any desire to help please contact me at tingministries@comcast.net and/or you can donate to the shipping costs on the sidebar. If you would like to donate to the purchase of animals for the orphans you may also do that on the sidebar by the same chip in and designate what you would like the amount to go towards.You can also donate animals to be sent for the orphans. If you live near to the Pennsylvania location you may mail them directly to Ting Ministries. Please email me and I will share with you the shipping address. If you live closer to Kalamazoo, Michigan please call Hannah Hopes (Courtney Weal 269-271-1037)!
Some of Hannah's favorite phrases on her flyer to raise animals for the orphans are below:
-What we can do with little bit of love and God’s help
- We LOVE because God first loved us
-Live with compassion
-God is Love 1 John 4:8
-Have faith that moves mountains
Hannah is one extraordinary child of God that is using her gifts and talents and compassion to give to others! I can not even begin to imagine what the LORD could for the orphans if we as adults took a simple plan and allowed the LORD to make it HIS!
BE A VOICE FOR THE VOICELESS...Hannah is....
Stay tuned for updates on the amount of animals that Hannah HOPES COLLECTS!
Proverbs 31: 8 - 9
Tuesday, August 28, 2012
Kindergarten Taiwan Cerebral Palsy - what do they have in common -
ELLIANNA YA-TING CARPENTER is what they have in common!
Ellianna is now in KINDERGARTEN - TODAY - August 28th 2012
Why is this significant? Why is this more significant than any child beginning their schooling today? Ellianna is a miracle in progress. Ellianna has cerebral palsy. Elliana is adopted from Cathwel Services in Taipei, Taiwan. Ellianna had a diagnosis that was not that hopeful! I write to encourage anyone considering a child with special needs - DON'T let the diagnosis scare you! Look and see what love and nutrition and therapy and hard work and did I say LOVE can do....I write this grieving for the children in Taiwan still waiting! On our Lifeline site www.lifelineadoption.org alone there are 47 precious children waiting for the LOVE that Ellianna feels within her heart!
She was beaming from ear to ear from the time she put on her uniform until the time her big sister came home to see her in her school uniform. We could not get her to take it off. She probably would have slept in it.

Ellianna remembered Sasha wearing the same uniform 5 years ago and to Ellianna wearing that uniform meant she had become somebody! She felt important...she felt worthy...she felt like she was not a child with special issues but one of the chosen...Hmmm...sounds like what we should believe about our selves when we come to know Jesus Christ as our LORD and Savior...we are important...we are worthy...we are chosen...Not because of "what we are or who we are" but because we ARE! The Bible tells us that the LORD created our inmost being....
The children on our Lifeline website www.lifelineadoption.org - the Taiwanese children - the Bulgarian children - all the children - the LORD created them and they are worthy - the children with the special needs - don't look past them - LOOK at what they can become - GOD CAN AND DOES STILL DO MIRACLES!
BE a VOICE FOR THE VOICELESS...do SOMETHING! Ellianna YA-TING would agree...she is worthy! OH MY IS SHE WORTHY! I AM MOVED TO TEARS just looking at her beautiful face, smile and life!
contact me for more information on the Taiwanese children and Bulgarian children and Special children...
stephanie.carpenter@lifelinechild.org
Proverbs 31: 8 - 9
Ellianna is now in KINDERGARTEN - TODAY - August 28th 2012
Why is this significant? Why is this more significant than any child beginning their schooling today? Ellianna is a miracle in progress. Ellianna has cerebral palsy. Elliana is adopted from Cathwel Services in Taipei, Taiwan. Ellianna had a diagnosis that was not that hopeful! I write to encourage anyone considering a child with special needs - DON'T let the diagnosis scare you! Look and see what love and nutrition and therapy and hard work and did I say LOVE can do....I write this grieving for the children in Taiwan still waiting! On our Lifeline site www.lifelineadoption.org alone there are 47 precious children waiting for the LOVE that Ellianna feels within her heart!
She was beaming from ear to ear from the time she put on her uniform until the time her big sister came home to see her in her school uniform. We could not get her to take it off. She probably would have slept in it.
Ellianna remembered Sasha wearing the same uniform 5 years ago and to Ellianna wearing that uniform meant she had become somebody! She felt important...she felt worthy...she felt like she was not a child with special issues but one of the chosen...Hmmm...sounds like what we should believe about our selves when we come to know Jesus Christ as our LORD and Savior...we are important...we are worthy...we are chosen...Not because of "what we are or who we are" but because we ARE! The Bible tells us that the LORD created our inmost being....
Psalm 139:13
New International Version (NIV)
13 For you created my inmost being;
you knit me together in my mother’s womb.
you knit me together in my mother’s womb.
The children on our Lifeline website www.lifelineadoption.org - the Taiwanese children - the Bulgarian children - all the children - the LORD created them and they are worthy - the children with the special needs - don't look past them - LOOK at what they can become - GOD CAN AND DOES STILL DO MIRACLES!
BE a VOICE FOR THE VOICELESS...do SOMETHING! Ellianna YA-TING would agree...she is worthy! OH MY IS SHE WORTHY! I AM MOVED TO TEARS just looking at her beautiful face, smile and life!
contact me for more information on the Taiwanese children and Bulgarian children and Special children...
stephanie.carpenter@lifelinechild.org
Proverbs 31: 8 - 9
Thursday, August 23, 2012
An AVI STORY...
It was asked of us..."Why do you want this child when there are so many others that don't have such severe special needs - you could adopt one of those?"
An AVI STORY - Avigayil is the name that we gave our sweet precious adorable much loved and cherished going on 6 years old daughter. Avigayil is the Hebrew for the name Abigail and means "JOY OF THE FATHER" If you would know Avi's WHOLE story this name has even more signficance. We call our Avigayil Avi for short...it fits her perfectly! It fits the petite curly dark haired wonder as perfectly as a name can fit! She is our Avi! She is our treasure from the LORD! The LORD surely blessed our lives when HE gave us Avi!
Avi has spastic quadriplegia and was adopted 16 months ago. Avi will turn 6 years old. Upon picking her up at her orphanage she was at the developmental level of a newborn baby and completely unable to pick up her head, roll over, sit or even focus with her eyes. Avi had spasms in her body that would make her entire body quake and shake. Avi had a urinary catheter for a feeding tube. Avi was unable to be held on your hip like a young child because she had no ability to hold her body,neck or head and had no way of knowing how to be held and carried.
NOW...after 16 months home...
Avi went to the beach for the first time 1 week ago and here is a moment in my life that will forever be etched into my mind and heart! HERE is a small glimpse of heaven through the life of Avi...
We unpack 3 little girls under our beach umbrellas...complete with chairs, food coolers, toys, lots of lotion and LOTS of sand. The girls are all dressed in their adorable little swimsuits. Avi's suit this time was the blue one with the little flowers and the ruffle. She and Lina take turns with who gets which suit...usually decided upon by big sister Ellianna who thinks she knows what each younger sister could possibly want. Actually earlier in the swim season Ellianna even thought it should be her suit because it was the newest one and she promptly left us all know that she would fit into it...she tried and it stretched and it fit but she soon learned that her suits surely did feel better and it was the last time she decided the pretty blue suit with the flowers would be hers to wear. Today it was Avi's suit...So...Avi is all suited up and all lotioned up...and ready for the beach and water. It was to be Avi's first time in the Atlantic Ocean....
I pick up my precious dark haired treasure...complete with a cute little curly pony tail. I scoop her onto my hip and she now sits proudly - OH REALLY SO proudly on my hip...as if to say...I have a MOMMY that adores me and a Daddy that thinks I ROCK this world! She holds up that once limp neck and lifts her little nose in the air. She takes her hand that has cerebral palsy affecting it and curls it around the back of my arm and holds on enjoying the gift of life! She begins to laugh and giggle as she does when riding so proudly on my hip...something she was unable to do less than 1 year ago. I smile at the delight I feel in giving my daughter such a simple joy...little did I know in that split second that it would get even better! Little did I know that a Joy so complete could flood my soul and spirit in a tiny fraction of a moment. Little did I know that I'd glimpse a piece of heaven in the next step.
WE walk towards the water...something she was terrified of less than 1 year ago. She smiles even more broadly and giggles and throws her head back. She seems to sniff the air...she seems to sense the breeze...she seems to notice the waves...she seems to hear the sea gulls...she seems to hear the laughter of other children...she seems to feel the sun warming her body...she seems to breathe the salty air...she seems to hear the waves crashing against the sand castles built just moments ago...she seems to do this all in the blink of an eye.
The smile and joy that began to radiate on her face is worth more than millions of dollars... I caught a glimpse of heaven in that moment...when this child...my daughter...lived life to the fullest in that moment. She was a "normal" child...at the beach...in her mother's arms...proud to be a daughter...worthy to be loved...she knew it and she gave me a piece of heaven that will never leave me...every time I look back to that one radiant joy filled smile I see JESUS...

WHO knows MAYBE she saw HIM walking on the water that moment...telling her how proud HE was of her and how special she is! It was a moment of awe! She took more in with that one moment than we sometimes take in with thousands of moments and with tons of technology!
That is why we would want this child! She is a gift straight from heaven and given to us to love, to cherish! She is our daughter!
This is my AVI story!
Pray for AJ!
Pray for every child that longs to be some one's gift from heaven!
Be a voice for the voiceless!
stephanie.carpenter@lifelinechild.org
An AVI STORY - Avigayil is the name that we gave our sweet precious adorable much loved and cherished going on 6 years old daughter. Avigayil is the Hebrew for the name Abigail and means "JOY OF THE FATHER" If you would know Avi's WHOLE story this name has even more signficance. We call our Avigayil Avi for short...it fits her perfectly! It fits the petite curly dark haired wonder as perfectly as a name can fit! She is our Avi! She is our treasure from the LORD! The LORD surely blessed our lives when HE gave us Avi!
Avi has spastic quadriplegia and was adopted 16 months ago. Avi will turn 6 years old. Upon picking her up at her orphanage she was at the developmental level of a newborn baby and completely unable to pick up her head, roll over, sit or even focus with her eyes. Avi had spasms in her body that would make her entire body quake and shake. Avi had a urinary catheter for a feeding tube. Avi was unable to be held on your hip like a young child because she had no ability to hold her body,neck or head and had no way of knowing how to be held and carried.
NOW...after 16 months home...
Avi went to the beach for the first time 1 week ago and here is a moment in my life that will forever be etched into my mind and heart! HERE is a small glimpse of heaven through the life of Avi...
We unpack 3 little girls under our beach umbrellas...complete with chairs, food coolers, toys, lots of lotion and LOTS of sand. The girls are all dressed in their adorable little swimsuits. Avi's suit this time was the blue one with the little flowers and the ruffle. She and Lina take turns with who gets which suit...usually decided upon by big sister Ellianna who thinks she knows what each younger sister could possibly want. Actually earlier in the swim season Ellianna even thought it should be her suit because it was the newest one and she promptly left us all know that she would fit into it...she tried and it stretched and it fit but she soon learned that her suits surely did feel better and it was the last time she decided the pretty blue suit with the flowers would be hers to wear. Today it was Avi's suit...So...Avi is all suited up and all lotioned up...and ready for the beach and water. It was to be Avi's first time in the Atlantic Ocean....
I pick up my precious dark haired treasure...complete with a cute little curly pony tail. I scoop her onto my hip and she now sits proudly - OH REALLY SO proudly on my hip...as if to say...I have a MOMMY that adores me and a Daddy that thinks I ROCK this world! She holds up that once limp neck and lifts her little nose in the air. She takes her hand that has cerebral palsy affecting it and curls it around the back of my arm and holds on enjoying the gift of life! She begins to laugh and giggle as she does when riding so proudly on my hip...something she was unable to do less than 1 year ago. I smile at the delight I feel in giving my daughter such a simple joy...little did I know in that split second that it would get even better! Little did I know that a Joy so complete could flood my soul and spirit in a tiny fraction of a moment. Little did I know that I'd glimpse a piece of heaven in the next step.
WE walk towards the water...something she was terrified of less than 1 year ago. She smiles even more broadly and giggles and throws her head back. She seems to sniff the air...she seems to sense the breeze...she seems to notice the waves...she seems to hear the sea gulls...she seems to hear the laughter of other children...she seems to feel the sun warming her body...she seems to breathe the salty air...she seems to hear the waves crashing against the sand castles built just moments ago...she seems to do this all in the blink of an eye.
The smile and joy that began to radiate on her face is worth more than millions of dollars... I caught a glimpse of heaven in that moment...when this child...my daughter...lived life to the fullest in that moment. She was a "normal" child...at the beach...in her mother's arms...proud to be a daughter...worthy to be loved...she knew it and she gave me a piece of heaven that will never leave me...every time I look back to that one radiant joy filled smile I see JESUS...
WHO knows MAYBE she saw HIM walking on the water that moment...telling her how proud HE was of her and how special she is! It was a moment of awe! She took more in with that one moment than we sometimes take in with thousands of moments and with tons of technology!
That is why we would want this child! She is a gift straight from heaven and given to us to love, to cherish! She is our daughter!
This is my AVI story!
Pray for AJ!
Pray for every child that longs to be some one's gift from heaven!
Be a voice for the voiceless!
stephanie.carpenter@lifelinechild.org
Wednesday, August 22, 2012
Children in need of a family - Children with Cerebral Palsy
Beautiful beautiful Avi enjoying a summer day at the beach!!!!!!
Ok...my heart breaks yet again...I see another child lying in a crib with cerebral palsy! Who will want this child? We do ...but we can not adopt any of these precious children at this time...there is a precious little girl in a particular country that we hope and pray to adopt...we have wanted to adopt her since 2010...it is a long story but it is for this precious one that we wait!
The one in this particular country that we want to adopt also has cerebral palsy. All of our daughters you seen in photos on this blog have different types and levels of cerebral palsy/mixed with other special issues.
Please please read and become educated and cry out for these precious children lying in a crib waiting for a Mommy/Daddy to come to pick them up...to hold them...to love them...to help them to learn to move their muscles...to begin to make sounds...to taste food maybe for the first time...to learn to laugh...to learn to hold up their head...to learn to roll over...to learn to sit...to learn to crawl...to learn to walk...to learn to run...to be free and to be loved! OH how my heart aches when I look at these children...I cry...they are desperate...they need someone...but who...BE A VOICE FOR THESE VOICELESS CHILDREN...The children listed in this post have cerebral palsy.
So if you don't want to learn about Cerebral palsy then just skip all the information about what cerebral palsy is and go to the second half of this post and read about the children from Taiwan and Bulgaria that are right now breaking my heart!
Please go to the LIFELINE website and you can see the photos...password is required for Taiwan but email me and I will share the password with you...
To view the Bulgaria children photos just fill out the very short form...your name and email address and you may view the children's photos...that all it takes...then go be a VOICE!!!!
Cerebral
palsy is a broad term that encompasses many different disorders of movement and
posture.
All
children with cerebral palsy have damage to the area of the brain that controls
muscle tone. As a result, they may have increased muscle tone, reduced muscle
tone, or a combination of the two (fluctuating tone). Which parts of their
bodies are affected by the abnormal muscle tone depends upon where the brain
damage occurs.
- Spastic
Cerebral Palsy
(stiff and difficult movement)
With Spastic Cerebral Palsy, the muscles are very stiff, and permanently contracted. Doctors can tell which type of Spastic CP a person has by which limbs are affected. The term PLEGIA, which means paralyzed, or weak, is tacked on the end of each form of Spastic CP. Examples are HemiPLEGIA (one side of the body is affected) and QuadriPLEGIA (all 4 limbs affected). In some people BOTH legs can be affected. They can turn in and cross at the knees. This is called scissoring, and can interfere with their walking ability. Some with Spastic CP may experience hemiparetic tremors. Hemiparetic tremors is uncontrollable shaking, affecting the limbs on only one side of a persons body. Sometimes the tremors are severe, and can affect movement.
- Athetoid
Cerebral Palsy
(involuntary and
uncontrolled movement)
The second type, Athetoid or Dyskinetic CP affects 10-20% of people who have CP. People with Athetoid Cerebral Palsy will have uncontrolled, slow, writhing movements. These movements will often affect the hands, feet, arms, or legs. Sometimes the muscles in a persons face or tongue will be affected, causing drooling. These movements a person with Athetoid CP has, will often increase during stressful times, and will most likely disappear while sleeping. Also, people with this particular type of CP may have problems coordinating muscle movements that are needed for speech. This is called dysarthria.
- Ataxic
Cerebral Palsy
(disturbed sense of balance and depth
perception)
The third type, Ataxic CP only affects 5-10% of people who have CP. This type of CP is very rare, and affects balance and coordination. A person with Ataxic CP may walk unsteady and have a wide step. They could place their feet far apart, and may have difficulty with quick or exact movements, like buttoning a shirt, or writing. Also, they could have "intention tremors." This type of tremor will start with a voluntary movement, for example, reaching a book. This may cause trembling in the body part that is being used. The tremor will get worse as the person gets near that object…in this case, the book.
Mixed Cerebral
PalsyThere may be a combination of
these types of cerebral palsy for any one person. The last type is mixed types. The most common type of mixed types is a mix of Spastic CP and Athetoid CP. But, other combinations are very much possible(stiff and difficult movement)
With Spastic Cerebral Palsy, the muscles are very stiff, and permanently contracted. Doctors can tell which type of Spastic CP a person has by which limbs are affected. The term PLEGIA, which means paralyzed, or weak, is tacked on the end of each form of Spastic CP. Examples are HemiPLEGIA (one side of the body is affected) and QuadriPLEGIA (all 4 limbs affected). In some people BOTH legs can be affected. They can turn in and cross at the knees. This is called scissoring, and can interfere with their walking ability. Some with Spastic CP may experience hemiparetic tremors. Hemiparetic tremors is uncontrollable shaking, affecting the limbs on only one side of a persons body. Sometimes the tremors are severe, and can affect movement.
(involuntary and uncontrolled movement)
The second type, Athetoid or Dyskinetic CP affects 10-20% of people who have CP. People with Athetoid Cerebral Palsy will have uncontrolled, slow, writhing movements. These movements will often affect the hands, feet, arms, or legs. Sometimes the muscles in a persons face or tongue will be affected, causing drooling. These movements a person with Athetoid CP has, will often increase during stressful times, and will most likely disappear while sleeping. Also, people with this particular type of CP may have problems coordinating muscle movements that are needed for speech. This is called dysarthria.
(disturbed sense of balance and depth perception)
The third type, Ataxic CP only affects 5-10% of people who have CP. This type of CP is very rare, and affects balance and coordination. A person with Ataxic CP may walk unsteady and have a wide step. They could place their feet far apart, and may have difficulty with quick or exact movements, like buttoning a shirt, or writing. Also, they could have "intention tremors." This type of tremor will start with a voluntary movement, for example, reaching a book. This may cause trembling in the body part that is being used. The tremor will get worse as the person gets near that object…in this case, the book.
Severity LevelCerebral palsy is often classified by severity level as mild, moderate, severe, or no CP. These are broad generalizations that lack a specific set of criteria. Even when doctors agree on the level of severity, the classification provides little specific information, especially when compared to the GMFCS. Still, this method is common and offers a simple method of communicating the scope of impairment, which can be useful when accuracy is not necessary.
- Mild - Mild cerebral palsy means a child can move without assistance; his or her daily activities are not limited.
- Moderate - Moderate cerebral palsy means a child will need braces, medications, and adaptive technology to accomplish daily activities.
- Severe - Severe cerebral palsy means a child will require a wheelchair and will have significant challenges in accomplishing daily activities.
- No CP -No CP means the child has cerebral palsy signs, but the impairment was acquired after completion of brain development and is therefore classified under the incident that caused the cerebral palsy, such as traumatic brain injury or encephalopathy
- Topographical classification describes body parts affected. The words are a combination of phrases combined for one single meaning. When used with Motor Function classification, it provides a description of how and where a child is affected by cerebral palsy. This is useful in ascertaining treatment protocol.
Two terms are at the heart of this classification method.
- Paresis means weakened
- Plegia/Plegic means paralyzed
- Monoplegia/monoparesis means only one limb is affected. It is believed this may be a form of hemiplegia/hemiparesis where one limb is significantly impaired.
- Diplegia/diparesis usually indicates the legs are affected more than the arms; primarily affects the lower body.
- Hemiplegia/hemiparesis indicates the arm and leg on one side of the body is affected.
- Paraplegia/paraparesis means the lower half of the body, including both legs, are affected.
- Triplegia/triparesis indicates three limbs are affected. This could be both arms and a leg, or both legs and an arm. Or, it could refer to one upper and one lower extremity and the face.
- Double hemiplegia/double hemiparesis indicates all four limbs are involved, but one side of the body is more affected than the other.
- Tetraplegia/tetraparesis indicates that all four limbs are involved, but three limbs are more affected than the fourth.
- Quadriplegia/quadriparesis means that all four limbs are involved.
- Pentaplegia/pentaparesis means all four limbs are involved, with neck and head paralysis often accompanied by eating and breathing complications
The brain injury that causes cerebral palsy affects motor function, the ability to control the body in a desired matter. Two main groupings include spastic and non-spastic. Each has multiple variations and it is possible to have a mixture of both types.
- Spastic cerebral palsy is characterized by increased muscle tone.
- Non-spastic cerebral palsy will exhibit decreased or fluctuating muscle tone.
Muscle Tone
Many motor function terms describe cerebral palsy’s effect on muscle tone and how muscles work together. Proper muscle tone when bending an arm requires the bicep to contract and the triceps to relax. When muscle tone is impaired, muscles do not work together and can even work in opposition to one another.Two terms used to describe muscle tone are:
- Hypertonia/Hypertonic — increased muscle tone, often resulting in very stiff limbs. Hypertonia is associated with spastic cerebral palsy
- Hypotonia/Hypotonic — decreased muscle tone, often resulting in loose, floppy limbs. Hypotonia is associated with non-spastic cerebral palsy
GMFCS Classification Levels (Gross Motor Function Classification System)
- GMFCS Level I- walks without limitations.
- GMFCS Level II- walks with limitations. Limitations include walking long distances and balancing, but not as able as Level I to run or jump; may require use of mobility devices when first learning to walk, usually prior to age 4; and may rely on wheeled mobility equipment when outside of home for traveling long distances.
- GMFCS Level III- walks with adaptive equipment assistance. Requires hand-held mobility assistance to walk indoors, while utilizing wheeled mobility outdoors, in the community and at school; can sit on own or with limited external support; and has some independence in standing transfers.
- GMFCS Level IV- self-mobility with use of powered mobility assistance. Usually supported when sitting; self-mobility is limited; and likely to be transported in manual wheelchair or powered mobility.
- GMFCS Level V- severe head and trunk control limitations. Requires extensive use of assisted technology and physical assistance; and transported in a manual wheelchair, unless self-mobility can be achieved by learning to operate a powered wheelchair
Taiwan:
Carter
Male, Age 4 1/2
Diagnosis of cerebral palsy
Diagnosis of cerebral palsy
Many photos and documents available!
This precious 3 year old named Carter left the orphanage in Taiwan to be placed in a long term care facility! He has a diagnosis of cerebral palsy. He is
an adorable little boy that just needs his family to love him and care for him.
Please contact me as soon as possible if you would like to see his files, photos
and videos. Lifeline will continue to advocate for a family for him even since his
transfer to this facility.
Daniel
Male, Age 4 1/2
Cerebral Palsy, Epilepsy, Anemia, Developmental delay – MR
Many photos and files available!
Cerebral Palsy, Epilepsy, Anemia, Developmental delay – MR
Many photos and files available!
Wesley
Male, Age 5 1/2
Wesley has been diagnosed with Bilateral hearing impairment, Epilepsy – takes medication, Cerebral palsy, and Global Developmental delay due to abuse. Despite all this little guy is going through, he smiles or verbalizes to interact with people, shares the food or toy in his hand, pulls other children to present his intention of interacting with them, enjoys exploring his surroundings, is developing the concept of “object permanence”, and is able to uncover hidden objects. It is reported that Wesley is also able to stand with support, walk with support, and uses pincer grasp to transfers object from hand to hand.
BULGARIA:
Wesley has been diagnosed with Bilateral hearing impairment, Epilepsy – takes medication, Cerebral palsy, and Global Developmental delay due to abuse. Despite all this little guy is going through, he smiles or verbalizes to interact with people, shares the food or toy in his hand, pulls other children to present his intention of interacting with them, enjoys exploring his surroundings, is developing the concept of “object permanence”, and is able to uncover hidden objects. It is reported that Wesley is also able to stand with support, walk with support, and uses pincer grasp to transfers object from hand to hand.
BULGARIA:
Brittany
age: 6
Special Need: Hypoxic ischemic encephalopathy with subsequent multiple organ dysfunction; Infantile cerebral palsy; Microcephalus; Symptomatic epilepsy; Hypotrophy; Severe developmental delay
Special Need: Hypoxic ischemic encephalopathy with subsequent multiple organ dysfunction; Infantile cerebral palsy; Microcephalus; Symptomatic epilepsy; Hypotrophy; Severe developmental delay
Chris
age: 2
Special Need: AD-type holoprosencephaly; Severe non-communicating external hydrocephalus; Congenital anomaly of the central nervous system; Prosencephaly; Microcephalus
Special Need: AD-type holoprosencephaly; Severe non-communicating external hydrocephalus; Congenital anomaly of the central nervous system; Prosencephaly; Microcephalus
Eli
Age: 8
Special Need: Infantile Cerebral Palsy
Special Need: Infantile Cerebral Palsy
Gia
age: 10
Special Need: congenital malphormations, Microcephaly, arachnoid cyst in the posterior cranial fossa, Retardation in the psychomotor and physical development.
Special Need: congenital malphormations, Microcephaly, arachnoid cyst in the posterior cranial fossa, Retardation in the psychomotor and physical development.
Isaac
age: 1.5
Special Needs: Hypoxic ischemic encephalopathy; Infantile cerebral palsy; External and internal hydrocephalus; Developmentally delayed
Special Needs: Hypoxic ischemic encephalopathy; Infantile cerebral palsy; External and internal hydrocephalus; Developmentally delayed
Kent
age: 8
Special Need: Child cerebral paralysis; Inguinal hernia on the right.
Special Need: Child cerebral paralysis; Inguinal hernia on the right.
Robby
age: 8
Special Need: Microcephalia, Retardation in the normal psychomotor development, feeding tube
Special Need: Microcephalia, Retardation in the normal psychomotor development, feeding tube
Thomas
age: 10
Special Needs: Infantile cerebral palsy; Corrected ectopic testis; Severe malnutrition; Developementally delayed
Special Needs: Infantile cerebral palsy; Corrected ectopic testis; Severe malnutrition; Developementally delayed
Timmy
age: 9
Special Need: Domestic violence – severe sull-brain trauma by the father that led to brain swelling, encephalopathy and “awake coma”; Severe lagging behind in the physical and neuro-psychical development; Marasmus
Special Need: Domestic violence – severe sull-brain trauma by the father that led to brain swelling, encephalopathy and “awake coma”; Severe lagging behind in the physical and neuro-psychical development; Marasmus
Zeke
age: 11
Special Need: Infantile cerebral palsy; Anomaly of the brain parenchyma; Scoliosis
Special Need: Infantile cerebral palsy; Anomaly of the brain parenchyma; Scoliosis
Get the word out...these kids need a family...don't you want to be blessed by a kid like ME!!!!!!!
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