Support our adoption! http://www.gofundme.com/3kcufg

My little ones are probably sleeping right now in Monrovia, Liberia, which right now is 1044 pm, and still quite warm at 77 degrees with clouds.

Monrovia, Liberia Time

Richardson Family Adoption - Get Them Home!

Please visit our fundraising page for updates, ways you can support us, donation information, contact information, and more at Go Fund Me at http://www.gofundme.com/3kcufg

Thank you for your generosity and your consideration in supporting our adoption.

We are adopting!! - Adoption Fundraiser

 



My husband and I are working towards adopting two beautiful children from Liberia, Africa, a girl age 6 who is 30 pounds wearing size 3 and a boy age 3 who is 20 pounds wearing size 12 months.

They both have cerebral palsy and badly need medical care.
We need your help to get there sooner!!
We are having a fundraiser.
Please consider supporting our adoption and making a donation.

Any amount helps through our website www.academyofthepossible.com

We also ask for your prayers over the next several months for God's provision, grace and blessings.
Liberia is an extremely poor third world country.

We have information on our blog where you can also donate to enter at www.richardsonstudios.blogspot.com where you can also make a donation.

You can make a donation through any of our sites to donate at www.academyofthepossible.com 
www.shop.academyofthepossible.com or our blog www.richardsonstudios.blogspot.com  or http://gofundme.com/3kcufg

At the bottom of our blog are statistics about Liberia. Please help the least, help us adopt these children.

"Defend the cause of the weak and fatherless; maintain the
rights of the poor and oppressed."

Psalm 82 v 3

 

Academy of the Possible Store Now Open at www.shop.academyofthepossible.com

Our store is now open for Academy of the Possible at www.shop.academyofthepossible.com with a new and expanding product line for students, teachers, and homeschoolers.

At www.shop.academyofthepossible.com , products include digital downloadable products including worksheets.

Some of the products that Academy of the Possible has available at www.shop.academyofthepossible.com include worksheets, art, math, Latin, Study Skills, Computer Science, Religion and Catechism, English, Health, Certificates, Book Report Forms etc.

Upcoming products to look for include science, music, eBooks and digital images which can be used for research, essay papers, science papers etc.

Please come shop with us, and check out our products. At Academy of the Possible, we appreciate referrals and repeat customers.

Please share our store site www.shop.academyofthepossible.com with your family and friends. We welcome your feedback. Please feel free to email us your comments and questions at academyofthepossible@gmail.com

Thank you, and God Bless you.
Jennifer Richardson

Updates

Michael got brand new AFO braces that have support across his knees. He is adjusting to them nicely but is not used to being able to stand up so straight. They are patriotic with bright red white and blue USA flags all of them.

Gabriela is getting ready for a trip to UCSF for an evaluation at their Regional Pediatric Multiple Sclerosis Center. The National MS Society and UCSF have been integral at making this happen. After waiting on a waiting list for six months with worsening symptoms to try and see the neurologist, we are thrilled to get Gabriela the help she needs for answers and to feel better.

Joseph has been having "heart pain" for months which we have finally discovered to be severe GERD. He is now taking medications to help that. We are working with Joseph to learn new words and increase his vocabulary.

Joshua is working hard at his school work, although math is a bit of a challenge for him. Although Joshua struggles with communication, Joshua loves to tell stories that interweaves a variety of super heroes which make his stories very interesting to listen to.

Shawna is enjoying playing princess and dolls.

Scott is looking for work again after being laid off again. He is healing well after his new diagnosis of diabetes and has been able to decrease his insulin for a while now.

I myself, Jennifer, manage the care of everyone and look forward to paying off our bills, painting and dreams of having a baby grand piano one day.

For all of our amazing friends who love and care and support us as though we are part of your own family, thank you deeply. You touch our hearts with your kindness and generosity.

To our parents who listen to all our struggles when everyone else tires of hearing the medical challenges we face every day on an ongoing basis, we love you so much.

Our prayer for each of you is that God may bless each of you back a thousand fold. Amen.

Happy Birthday Scott!! I love you!

Love you all,
God bless you on your journey,
Jennifer Richardson

Mitochondrial Disease / Organizations and Research

Organizations & Research

Mitochondrial Disease Index Glossary Mitochondrial Disease (cont.) In this Article What is mitochondrial myopathies? Is there any treatment for mitochondrial disease? What is the prognosis for mitochondrial disease? What research is being done for mitochondrial disease? Organizations Mitochondrial Disease Glossary Mitochondrial Disease Index Is there any treatment for mitochondrial disease? Although there is no specific treatment for any of the mitochondrial myopathies, physical therapy may extend the range of movement of muscles and improve dexterity. Vitamin therapies such as riboflavin, coenzyme Q, and carnitine (a specialized amino acid) may provide subjective improvement in fatigue and energy levels in some patients. What is the prognosis for mitochondrial disease? The prognosis for patients with mitochondrial myopathies varies greatly, depending largely on the type of disease and the degree of involvement of various organs. These disorders cause progressive weakness and can lead to death. What research is being done for mitochondrial disease? The NINDS conducts and supports research on mitochondrial myopathies. The goals of this research are to increase scientific understanding of these disorders and to find ways to effectively treat, prevent, or potentially cure them. Select this link to view a list of studies currently seeking patients. Organizations Muscular Dystrophy Association3300 East Sunrise Drive Tucson, AZ 85718-3208 mda@mdausa.org http://www.mda.org Tel: 520-529-2000 800-344-4863 Fax: 520-529-5300 United Mitochondrial Disease Foundation8085 Saltsburg Road Suite 201 Pittsburgh, PA 15239 info@umdf.org http://www.umdf.org Tel: 412-793-8077 Fax: 412-793-6477 National Organization for Rare Disorders (NORD)P.O. Box 1968 (55 Kenosia Avenue) Danbury, CT 06813-1968 orphan@rarediseases.org http://www.rarediseases.org Tel: 203-744-0100 Voice Mail 800-999-NORD (6673) Fax: 203-798-2291 SOURCE: National Institute of Neurological Disorders and Stroke

Copyright 2008-2012. Richardson Studios. All rights reserved.

Calendar

Calendar

Calendar Legend:

Holidays

JanuaryFebruaryMarchAprilMayJuneJulyAugustSeptemberOctoberNovemberDecember 20112012201320142015 Print
Sun	Mon	Tue	Wed	Thu	Fri	Sat
26	27	28	29	1	2	3
4	5	6	7	8	9	10
11	12	13	14	15	16	17
18	19	20	21	22	23	24
25	26	27	28	29	30	31

Legend

Event

4th of July

Halloween

Copyright 2008-2012. Richardson Studios. All rights reserved.

PVL

PVL

PERIVENTRICULAR LEUKOMALACIA
Also known as PVL.

Table of Contents
What is Periventricular Leukomalacia?
Is there any treatment?
What is the prognosis?
What research is being done?

What is Periventricular Leukomalacia?
Periventricular leukomalacia (PVL) is characterized by the death of the white matter of the brain due to softening of the brain tissue. It can affect fetuses or newborns; premature babies are at the greatest risk of the disorder. PVL is caused by a lack of oxygen or blood flow to the periventricular area of the brain, which results in the death or loss of brain tissue. The periventricular area-the area around the spaces in the brain called ventricles-contains nerve fibers that carry messages from the brain to the body's muscles. Although babies with PVL generally have no outward signs or symptoms of the disorder, they are at risk for motor disorders, delayed mental development, coordination problems, and vision and hearing impairments. PVL may be accompanied by a hemorrhage or bleeding in the periventricular-intraventricular area (the area around and inside the ventricles), and can lead to cerebral palsy. The disorder is diagnosed by ultrasound of the head.

Is there any treatment?

There is no specific treatment for PVL. Treatment is symptomatic and supportive. Children with PVL should receive regular medical screenings to determine appropriate interventions.

What is the prognosis?

The prognosis for individuals with PVL depends upon the severity of the brain damage. Some children exhibit fairly mild symptoms, while others have significant deficits and disabilities.

What research is being done?

The NINDS supports and conducts research on brain injuries such as PVL. Much of this research is aimed at finding ways to prevent and treat these disorders.

Organizations

National Organization for Rare Disorders (NORD) P.O. Box 1968 (55 Kenosia Avenue) Danbury, CT 06813-1968 orphan@rarediseases.org http://www.rarediseases.org Tel: 203-744-0100 Voice Mail 800-999-NORD (6673) Fax: 203-798-2291

Related NINDS Publications and Information which can be found at NINDS:

• NINDS Cerebral Palsy Information Page
  Cerebral palsy information page compiled by the National Institute of Neurological Disorders and Stroke (NINDS).
• Cerebral Palsy: Hope Through Research
  
  Cerebral palsy information booklet compiled by the National Institute of Neurological Disorders and Stroke (NINDS).

Prepared by:
Office of Communications and Public Liaison
National Institute of Neurological Disorders and Stroke
National Institutes of Health
Bethesda, MD 20892
All NINDS-prepared information is in the public domain and may be freely copied.
Credit to the NINDS or the NIH is appreciated.

Information provided courtesy of NHANES.
NINDS: National Institute of Neurological Disorders and Stroke
NINDS is part of the National Institutes of Health

Copyright 2008-2012. Richardson Studios. All rights reserved.

Microcephaly

Microcephaly

Microcephaly

What is Microcephaly?

Microcephaly is a medical condition in which the circumference of the head is smaller than normal because the brain has not developed properly or has stopped growing. Microcephaly can be present at birth or it may develop in the first few years of life. It is most often caused by genetic abnormalities that interfere with the growth of the cerebral cortex during the early months of fetal development. It is associated with Down’s syndrome, chromosomal syndromes, and neurometabolic syndromes. Babies may also be born with microcephaly if, during pregnancy, their mother abused drugs or alcohol, became infected with a cytomegalovirus, rubella (German measles), or varicella (chicken pox) virus, was exposed to certain toxic chemicals, or had untreated phenylketonuria (PKU). Babies born with microcephaly will have a smaller than normal head that will fail to grow as they progress through infancy. Depending on the severity of the accompanying syndrome, children with microcephaly may have mental retardation, delayed motor functions and speech, facial distortions, dwarfism or short stature, hyperactivity, seizures, difficulties with coordination and balance, and other brain or neurological abnormalities. Some children with microcephaly will have normal intelligence and a head that will grow bigger, but they will track below the normal growth curves for head circumference.

Is there any treatment?

There is no treatment for microcephaly that can return a child’s head to a normal size or shape. Treatment focuses on ways to decrease the impact of the associated deformities and neurological disabilities. Children with microcephaly and developmental delays are usually evaluated by a pediatric neurologist and followed by a medical management team. Early childhood intervention programs that involve physical, speech, and occupational therapists help to maximize abilities and minimize dysfunction. Medications are often used to control seizures, hyperactivity, and neuromuscular symptoms. Genetic counseling may help families understand the risk for microcephaly in subsequent pregnancies

What is the prognosis?

Some children will only have mild disability. Others, especially if they are otherwise growing and developing normally, will have normal intelligence and continue to develop and meet regular age-appropriate milestones.

What research is being done?

The National Institute of Neurological Disorders and Stroke (NINDS) conducts research relating to microcephaly in its laboratories at the National Institutes of Health (NIH) and supports additional research through grants to major medical institutions across the country. A small group of researchers studying a rare neurometabolic syndrome (3-PGDH), which causes microcephaly, have successfully used amino acid replacement therapy to reduce and prevent seizures.

Select this link to view a list of studies currently seeking patients.

Organizations

The Arc of the United States
1010 Wayne Avenue
Suite 650
Silver Spring, MD 20910Info@thearc.orghttp://www.thearc.org
Tel: 301-565-3842
Fax: 301-565-3843 or -5342

Birth Defect Research for Children, Inc.
800 Celebration Avenue
Suite 225
Celebration, FL 34747
betty@birthdefects.org
http://www.birthdefects.org
Tel: 407-566-8304Fax: 407-566-8341

March of Dimes Foundation
1275 Mamaroneck Avenue
White Plains, NY 10605
askus@marchofdimes.com
http://www.marchofdimes.com
Tel: 914-428-7100 888-MODIMES (663-4637)
Fax: 914-428-8203

National Dissemination Center for Children with Disabilities
U.S. Dept. of Education
Office of Special Education Programs
P.O. Box 1492
Washington, DC 20013-1492
nichcy@aed.org
http://www.nichcy.org
Tel: 800-695-0285
Fax: 202-884-8441

Prepared by:
Office of Communications and Public Liaison
National Institute of Neurological Disorders and Stroke
National Institutes of Health
Bethesda, MD 20892

All NINDS-prepared information is in the public domain and may be freely copied. Credit to the NINDS or the NIH is appreciated. Last updated February 13, 2007
National Institute of Neurological Disorders and Stroke

Information provided courtesy of NHANES on Microcephaly.
NINDS: National Institute of Neurological Disorders and Stroke
NINDS is part of the National Institutes of Health

Copyright 2008-2012. Richardson Studios. All rights reserved.

Mother Teresa Quote

" There is no such thing as doing Great Things in this World.
We can only do small things with Great Love." Mother Teresa

Poem: Silent Cries and Hidden Tears

Poem: Silent Cries and Hidden Tears

Tonight a child cries
But no tears come
They cry
Of a heartfelt pain
In deep longing
And of physical pain
Pain from
Lack of food
Lack of love
Lack of shelter
Lack of medicine
Lack of education
These are the
Silent Cries
Cries of a child who
Needs food to nourish them
Needs a home to shelter and cherish them
Needs to feel loved unconditionally
Needs opportunities to grow, heal and learn
But most of all
Needs parents to belong to
And a mom and dad to love them.
These are the Hidden Tears
Tears of a child who
Wants to belong and to be wanted by someone.
These are the Silent Cries and Hidden Tears
Of a Child waiting
Waiting for you to make a difference.

Everytime you donate, you save a life and make a difference forever.

Written by Jennifer Richardson

 

Copyright 2008 to 2012 Jennifer Richardson

Resources and Support / Poem Adoption is a Gift

Resources and Support

" There is no such thing as doing Great Things in this World. We can only do small things with Great Love." Mother Teresa
Our expanding Resources pages are here to provide you with information on the illness, diability, diagnosis, and challenges your child faces. If there is information you would like to see here and don't, please contact us. We will be happy to research it for you and provide information and resources to help you and your child on their journey.

He shall direct your paths !
Trust in the Lord with all your heart, and lean not on your own understanding. In all your ways acknowledge Him, and He shall direct your paths. Do not be wise in your own eyes. Proverbs 3: 5-7

Thank you Lord for being Savior of Our Lives, your unending mercy and love, and for directing our paths.
Jennifer Richardson


Please check out our blog www.richardsonstudios.blogspot.com
In the World, But not Of the World.
Every child has a story, and every child matters !

Poem: Adoption Is A Gift

Adoption is a gift
Of life
Of love
Of faith
Of hope
Of trust,
Of prayer,
And
In the end,
The gift is
Life in the flesh
Love given
Faith received
Hope carried
Trust had
Prayers Answered
in the form of a child.

Written By: Jennifer Richardson

 

For More Information on many different disabilities and illnesses, please see that individual page.

If you cannot find what you are looking for, or would like us to add information on a specific illness or disabilty, please let us know.

Visit our contact us page.

MORE TO COME !

Lupus

Lupus

The Face of Lupus:

 

Other Lupus Resources:

Lupus Foundation of America:
This is a great resource for further information on this disease, and can be found at:
http://www.lupus.org/newsite/index.html

Lupus International:
This organization has regular events to fund research and lupus and can be found at:
http://www.lupusinternational.com/events/race.aspx

Lupus is a puzzle. You never know when or how it might hit you next. Michael has to be strong and fight Lupus everyday. Help us find a cure. Please donate generously. Together we can make a difference in the life of a child. Go to the donations page for further information on how you can get involved.

What are Neurological Sequelae Of Lupus?
Is there any treatment?
What is the prognosis?
What research is being done?
Clinical Trials
Organizations
Additional resources from MEDLINEplus

What are Neurological Sequelae Of Lupus?

Lupus (also called systemic lupus erythematosus) is a disorder of the immune system. Normally, the immune system protects the body against invading infections and cancers. In lupus, the immune system is over-active and produces increased amounts of abnormal antibodies that attack the body's tissues and organs. Lupus can affect many parts of the body, including the joints, skin, kidneys, lungs, heart, nervous system, and blood vessels. The signs and symptoms of lupus differ from person to person; the disease can range from mild to life threatening.

Initial symptoms of lupus may begin with a fever, vascular headaches, epilepsy, or psychoses. A striking feature of lupus is a butterfly shaped rash over the cheeks. In addition to headache, lupus can cause other neurological disorders, such as mild cognitive dysfunction, organic brain syndrome, peripheral neuropathies, sensory neuropathy, psychological problems (including personality changes, paranoia, mania, and schizophrenia), seizures, transverse myelitis, and paralysis and stroke.

Is there any treatment?

There is no cure for lupus. Treatment is symptomatic. With a combination of medication, rest, exercise, proper nutrition, and stress management, most individuals with lupus can often achieve remission or reduce their symptom levels. Medications used in the treatment of lupus may include aspirin and other nonsteroidal anti-inflammatory medications, antimalarials, corticosteroids, and immunosuppressive drugs.

What is the prognosis?

The prognosis for lupus varies widely depending on the organs involved and the intensity of the inflammatory reaction. The course of lupus is commonly chronic and relapsing, often with long periods of remission. Most individuals with lupus do not develop serious health problems and have a normal lifespan with periodic doctor visits and treatments with various drugs.

What research is being done?

Investigators researching lupus seek to increase scientific understanding of the disorder and to find ways to treat, prevent, and ultimately, cure it. Several components of the National Institutes of Health support research on lupus.

NIH Patient Recruitment for Neurological Sequelae Of Lupus Clinical Trials

• At NIH Clinical Center
• Throughout the U.S. and Worldwide

Organizations

Lupus Alliance of America 3871 Harlem Road Buffalo, NY 14215 info@lupusalliance.org http://www.lupusalliance.org/ Tel: 866-415-8787	Lupus Foundation of America 2000 L Street, N.W. Suite 710 Washington, DC 20036 info@lupus.org http://www.lupus.org/ Tel: 202-349-1155 800-558-0121 Fax: 202-349-1156
American Autoimmune Related Diseases Association 22100 Gratiot Avenue Eastpointe East Detroit, MI 48201-2227 aarda@aarda.org http://www.aarda.org/ Tel: 586-776-3900 800-598-4668 Fax: 586-776-3903	National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) National Institutes of Health, DHHS 31 Center Dr., Rm. 4C02 MSC 2350 Bethesda, MD 20892-2350 NIAMSinfo@mail.nih.gov http://www.niams.nih.gov/ Tel: 301-496-8190 877-22-NIAMS (226-4267)

Prepared by:
Office of Communications and Public Liaison
National Institute of Neurological Disorders and Stroke
National Institutes of Health
Bethesda, MD 20892

Credits Given To: NINDS and NIH

Copyright 2008-2012. Richardson Studios. All rights reserved.

Epilepsy

Please pray for these people with seizures that they may have better control over their seizures and find healing.

Michael

Steve

 

 

Epilepsy is a condition which causes seizures.

Epilepsy affects countless children and adults every day.

 

 

Websites We Recommend:

www.seizuretracker.com

This is a very nice website which is free and gives you the ability to track seizures, and even print seizure logs and reports. Having used this for my son, I have found it extremely helpful in keeping track of his seizures, medication and how he is doing in his seizure management.

Copyright 2008-2012. Richardson Studios. All rights reserved.

Child Sponsorship

Child Sponsorship

Child Sponsorship here in the United States

Consider sponsoring a child?
PLEASE SEE A LIST OF CHILDREN WAITING TO BE SPONSORED AT THE BOTTOM OF THIS PAGE.
There is a child right now who needs your help.

By sponsoring a child, you will help to pay for that child's medical care, surgery, medication, doctor's visit, or medical equipment, school supplies, clothing, food and toys for their development.
You will also help to take some of the burden off their parents who give so much of themselves.
These parents who worry so much about how to make ends meet and how to meet the needs of their little ones.

The Sponsored Child
Each child in our Child Sponsorship program lives within the United States.
The families of these children have extra challenges in providing care their child for a variety of reasons.
These reasons can include unemployment, loss of medical insurance, and life changing illness.
Other reasons may include a child whose medical care is complex, or a life challenge or disability.
Even still, the parents of these children may face extensive bills due to medical care or adoption expense.
Caring for five special children of our own, we understand these daily challenges can sometimes be overwhelming.
The more children we are able to sponsor, the more we can help each of them.

PLEASE READ MORE!

When a Child is Welcomed as a Sponsored Child
Each child who is welcomed into our program as a Sponsored Child receives:
a Welcome letter and a Certificate signed by the Owner of Richardson Studios.
What Do I Receive as a SponsorA letter of gratitude signed by the owner of Richardson Studios and the knowledge that every time you send in your sponsor payment that the Lord is smiling at the love you are extending to a child in need.

Our Costs
Every dollar goes to support both the child and administrative costs of continuing our program.
Administrative costs include postage, promotion materials, the cost of this website, and salaries of our team.
The remaining funds go directly toward the sponsored children.

One Time Donation
One time donations in any amount are accepted ($5.00, $10.00, $20.00, $50.00, $100.00, OR MORE).
One time donations are acceptable through the donation button on our blog at www.richardsonstudios.blogspot.com to the right at the top of our posts.

Regular Sponsorships
Weekly is $10.00 ! or Monthly is are $20.00 !

Child Sponsorship is easy!
We have various children right here in the United States who need your help.
Please consider becoming a regular child sponsor.

How To Sponsor a Child
1. Go to www.richardsonstudios.com (if you are not already at our website)
2. Choose whether you would like to be Regular Sponsor, or make a One Time Donation
3. If you choose to be a Regular Sponsor, choose whether you want to donate weekly or monthly.
4.Click on the Child Sponsorship page.
5. Choose which child you would like to sponsor.
6. Click on that child's donation button to sign up.
7. Your account will automatically be billed.
8. You can stop your sponsorship at anytime.
9. To see updates on your child's progress, go to your child's sponsorship section below.
There you will find pictures and information about how your child is doing.

How To Refer a Child Who Needs Sponsorship
If you know of a child you recommend for sponsorship, please email us at academyofthepossible@gmail.com for more information. Be sure to include your email or mailing address, so we can send you the information.
Or, write to us direct at:
Richardson Studios
Attn: Child Sponsorship Referral
6130 Camino Real #50, Riverside CA 92509

Is My Donation Tax Deductible
We cannot provide a tax deductible receipt at this time.
One of our goals as a company is to obtain non-profit status so that we can provide tax deductible receipts to our donors and sponsors.
This is a work in progress. Please check back with us.

Why Don't the Children Have Last Names
In order to protect the privacy of each child and their families, last names are omitted.

Who Are The Sponsored Children
Take a look at the children below.
Each child has unique needs.
Each child's needs will be updated as they change, and as we receive information on them.
Photos of the children are updated as we receive them.

THANK YOU FOR YOUR KINDNESS, LOVE AND GENEROSITY!

Thank you to our Sponsors and Donors who make this possible!

 

 

Our Sponsored Children

 

 

Michael:
Who: Michael is a a delightful 13 year old boy who was adopted from Kazakhstan.

Likes: Michael enjoys video games, and wants to be a musician when he grows up.

Medical Needs: Michael has a variety of complex medical needs including Cerebral Palsy, Auditory Processing Disorder, Short Stature, Cognitive and Developmental Delays, Speech and Language Delays, Thrombocytopenia, Hemolytic Anemia, Evan's Syndrome (a rare autoimmune disorder of the blood), Lupus, Secondary Autism, Periventricular Leukomalacia, Hypoplasia of the Corpus Callosum, and Gastrointestinal Disorder.

Regular Medical Care: medication, lab work and medical tests, and evaluation with multiple specialists.

To Sponsor Michael Weekly Click Here:

To Sponsor Michael Monthly Click Here:

To Unsubscribe from Sponsoring Michael Click Here:

 

 

 

Gabriela:
Who: Gabriela is a charming 11 year old girl who was born in the Ukraine and adopted from a disurpted adoption.

Likes: Gabriela loves animals and to draw. Gabriela wants to be an animal rescuer and artist when she grows up.

Medical Needs: Gabriela has Bipolar Disorder and ADHD.

Regular Medical Care: medication, and on-going follow up with a specialist.

 

Joseph:
Who: Joseph is a wonderful 8 year old boy who was born in Estonia and adopted from a disrupted adoption. Joseph is a ham and loves to be the center of attention.

Likes: Joseph likes everything technical including games, music MP3 players, and computers. Joseph wants to work with computers when he grows up.

Medical Needs: Joseph has complex and challenging medical needs which may affect how long he lives and include FAS (Fetal Alcohol Syndrome), Pulmonary Hypertension, Transposition of the Major Vessels Repaired, upcoming open heart surgeries to repair his declining heart over the next 2-3 years, open heart surgery was done for a pacemaker, Cognitive Delays, Speech and Language Delays, Developmental Delays, Learning Disability, Microcephaly, Craniostenosis, and Short Stature. Joseph also wears glasses.

Regular Medical Care: very expensive and multiple medications, lab tests and procedures, mulltiple surgeries and therapies, and on-going follow up with multiple specialists.

 

Joshua:
Who: Joshua is a loving 6 year old boy who was born in Estonia and adopted from a disrupted adoption. Joshua loves to be silly.

Likes: Joshua enjoys dinosaurs, cars and building things. Joshua wants to be an engineer when he grows up.

Medical Needs: Joshua has Fetal Alcohol Effects, and Speech and Language Delays.

Regular Medical Care: speech therapy, and follow up with a specialist.

 

Shawna:
Who: Shawna is a delightful 3 year old girl who was adopted here in the USA. Shawna is a warm and friendly girl.

Likes: Shawna loves real horses and playing dollies and playing animals. Shawna wants to be a blue (as in the color) doctor who helps people when she grows up.

Medical Needs: Overall Shawna is a healthy girl.

Regular Medical Care: follow up with a pediatrician.

 

Thank you again for your generosity, and for making a difference in the life of a child.
We pray the Lord remembers your kind generosity.

LOVE IS....

LOVE IS....

LOVE IS A CHOICE, NOT ALWAYS A FEELING.

LOVE IS HUGGING YOUR CHILD WHEN YOU ARE REALLY MAD AT THEM.

LOVE IS NOT ALWAYS EASY.

LOVE IS SAYING YES WHEN IT IS HARD FOR YOU, AND YOU WANT TO SAY NO BECAUSE NO WOULD BE EASIER.

LOVE IS LEARNING HOW TO BE PATIENT WHEN YOU'D RATHER NOT BE.

LOVE IS LEARNING TO SPEAK CALMLY TO YOUR CHILDREN, WHEN INSIDE YOU'D LIKE TO SCREAM.

LOVE IS SAYING NO BECAUSE IT IS BETTER FOR THEM, WHEN IT WOULD BE EASIER TO SAY YES.

LOVE IS KIND WHEN YOU'D RATHER STICK OUT YOUR TONGUE.

LOVE IS LEARNING HOW TO MEET THE NEEDS OF ALL YOUR CHILDREN, NOT JUST ONE OF THEM.

LOVE IS LEARNING HOW TO BE MORE LIKE CHRIST.

AMEN.




Copyright 2012 Jennifer Richardson

Stories of our Special Children

Stories

These are the stories of our special children. Each of them unique and special. Each of them persevering in their own struggles. Each of them celebrating in their own triumphs.

If you have a story to share, please contact us.
We will be happy to review your story. If it is accepted, we will publish your story on our website.
We request a donation to help cover the administrative costs of the site.

We look forward to hearing from you.

Copyright 2008-2012. Richardson Studios. All rights reserved.

Shawna's Story

Shawna's Story

Thank you Shawna for the beautiful child you are. Your simple presence inspires us to make a difference.

For our youngest Shawna - who brings joy to our every breath. Thank you Shawna for the priviledge of being your parents. Adopting you was the best decision we ever made.

Shawna was born in the United States and adopted independently through a birthmom who had no means to take care of her. We have had her since birth.

Every day Shawna blesses us as she grows and learns. We are delighted to say she is healthy and developmentally on target with a spirit full of energy and joy.

 

Praise the Lord.

Copyright 2008-2012. Richardson Studios. All rights reserved.

Michael's Story

Michael's Story

Thank you Michael for inspiring us to make a difference every day in the lives of other children.

For our oldest Michael - who brings warmth and love to our every moment. Thank you Michael for the priviledge of being your parents. Adopting you changed my life for the better. You were our first. I love you SO much !



This picture of Michael is a week before he got really sick. Forty-four (44) different diseases later, the doctors still don't know entirely why Michael is so sick; and, he has every single one including but not limited to ectodermal dysplasia, systemic lupus, evan's syndrome, growth hormone deficiency, cerebral palsy, and many many others.

 

Michael is a true testimony to the endurance of the human spirit and the reason why adoption is so important.

 

Copyright 2008-2012. Richardson Studios. All rights reserved