Original Writings on Various Subjects
by the Mom of all these kids



Subjects:

1. Thoughts on a Loving Family-ideas about the adoption of special needs children.
2. Foster Home Visits-ideas to make transition easier.
3. Inter-racial Issues
4. Ideas to use when your child goes to the Hospital
5. Laughter: An Absolute Necessity=Creative Parenting

Thoughts on a loving family...


It would take a thousand pages to say what I’d like to say about families, but here are a few of my thoughts:

1. All children need a chance to have a family-a mom and/or dad. They have a right to be given the opportunity to succeed, to feel loved, to accept being loved, to give love, to be happy. For some children, their earlier deprivation, neglect or abuse make it extremely difficult to grow into secure adults. Some may not “make it,” but they still have the right to that opportunity. And, parents must continue to offer love, acceptance and be committed, even when the child isn’t open to accept it. It is difficult as a parent to see one’s child make wrong decisions, but the child makes the choice. We can only give them the opportunity.

2. Parents of mentally and/or physically challenged children need to have the strength to not give up. They need to be flexible. They also need to push away feelings of guilt if they do something “wrong.” If services-music, art, sports-seem impossible or too expensive, all parents need to look for creative ways to get those services or look for alternatives.

3. Children who are mentally or physically challenged still have the same wants and desires and dreams as able-bodied children. Our children want to grow up to have an apartment or house, to date, to have a job, play sports, dance, etc. They may have to adapt some of those dreams, but so does everyone.

4. When we think of our child’s disability, we focus on what they can do, not much on what they can’t do. Yet, we are honest; we tell a blind child, “No, you won’t be able to fly a plane alone, but you can travel to faraway lands, climb the tallest of mountains, swim in the warmest sea.” We all have things we can’t do and all have dreams that will never come true.

5. People need to concentrate on what can be done when a child has emotional problems, rather than finding fault. Many teens will have problems developing their independence, some more than others. This is true whether the child is from a large or small, two-parent or single-parent family. It is true for birth children and adopted children. Parents of children who are adopted need to be aware of the possibility of future emotional problems and be open to counseling. This is especially true for children who are adopted at older ages.

6. We look for help when it is needed. This can be by professionals-psychologists, pediatricians, etc.-or from friends. I have several friends from all different kinds of families who offer support, words of wisdom or just a shoulder to cry on.

7. We believe all people continue to grow and learn, even until death. Therefore, we can’t take full credit for an adult-child who is a success. And...we do not need to take blame for one who is not making it. Also, we need to have hope that a wayward son or daughter will make the choice to do right, even if it is years after he or she leaves home. That’s why we must be committed for life. We may not condone a certain lifestyle, but we can love and accept our son or daughter. It’s not easy to let go of our children, but they need to discover they can be independent.

8. We hope each of our children will learn to love and accept being loved, believe they have an important role in life and be able to give to others their time, their love and their service.

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Foster Home Visit Suggestions


Here are some things you might want to try, when visiting a younger child. These ideas can be adapted for older kids, also. We have done these, and feel they help the child to feel more familiar with you before the actual move.

1. send pictures of you and your family. We bought a cloth type, child’s photo book, called Baby’s First Photo Album. It has clear plastic covers for the pictures. The pictures are enclosed in clear plastic covers, in such a way that even if the child sucks on the corners of their book, it won’t ruin the pictures.

2. Send a photo album for the foster family to share with the child. Make it a story book, so the foster family can share names, places, etc. with the child.

3. Send a recording of songs you normally sing to your children. You could even read simple stories, or just talk about things you do as a family.

4. Send some sheets, blankets, etc. so that the child can use them in the foster home, then he/she will be able to bring them to their forever home, and use them the first night home.

5. Buy a blanket, and sleep with it a few nights first. Then send it maybe a week before arrival home. That way the child gets to “know” your smells. That sounds quite funny, but a child learns from all their senses. You smell may be a usual soap, shampoo or perfume. You could even ask the foster mom to use your type clothes detergent on the child’s belongings, or send a bottle of your usual perfume, and ask the foster mom to put a few drops on the child’s coat, blanket or sheet.

5. Send some toys that the child can use, and then bring to their new home. Provide easy identification, so it isn’t difficult for the foster family to identify them. Maybe it would be nice to send a game or toy for rest of the foster children in the home. You might even want to have a storage container, to make it easier for the foster mom, even a backpack with the child’s name could be used.

6. Try to remember that the foster family is a very important part of your child’s life. Not only have they loved and cared for your child, you child also has probably begun to bond with them. When they grow, it will be important for them to know that the foster family was there to give them stability as their world was falling apart. So...take lots of pictures, or the foster family, or their home, of the room where the child slept, etc. Give copies to the foster family also.

7. Show respect for the foster family, and try to understand if they may not want contact with you at first or not all. Sometimes, not often though, a foster family might not support the placement. If that is the case, you can still honor them, respecting them and the wonderful job them are doing. Show appreciation for them. Send questions, through the caseworker when needed, asking about the child’s likes and dislikes, ask what their typical day is like with the child, ask for suggestions to make the transition easier, etc. Ask the foster parents what type of lotions, etc. they use on the child. Be sure to ask the caseworker if the foster family wants contact first, and if they want contact after placement. Some will want to continue contact, others will need to move on with their lives and contact would be too painful to them. Each one is unique, and there is no way to know what their reaction will be.

8. Buy a car seat, and send it to the foster family to use. Again, the child would then have their own seat, the one they are familiar with as they travel home with you.

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Inter-racial Issues


Because one of my children is a beautiful child of African American and Hispanic heritage, people often start to talk with us about her and adoption. It really depends on my mood, as to how I will feel about their questions. I’d like to say that each time, I see the questions as very innocent, as a way to spread the word about the joys of adoption. But...to be honest...I don’t always feel that way. Sometimes it’s just a mood I’m in, sometimes it really is the questions being asked. I was shopping with my 2 year old. She was dressed in a cute sun dress, and was saying hi to everyone. I was in a bit of a hurry, trying to find just the right pair of shoes for another daughter. A lady seemed to be wherever we were, and she finally started talking to me about how cute my child was. Soon she was asking all sorts of questions. I tried to be polite, and answer honestly, yet simply, remember I was in a hurry. Finally, a question really got to me. She asked, “Oh is she one of those welfare kids?” That did it! No more politeness, no more friendly smile. I looked her straight in the eye, and said, “My husband is African American.” That shut her up quick. I laugh about it now, remembering her shocked expression...her awkward words tying to cover up her frustration and embarrassment. But...a very important point of this is: if you could not say your spouse was of a minority race, or handicapped, or whatever, you better think twice about adopting a child of color or one with a handicap.

Sometimes I hear people say that they feel they can parent a child of another race, because they will tell the child how unimportant color is, give them a good self-esteem, and basically try to insulate them from discrimination. They will say they understand what it’s like because they used to be teased because they were fat (or short, or shy or whatever). Some say, they could not parent a child of color, because they don’t want to add to the child’s problems. Some say they will just tell the child not to listen to the comments. The problem to me is that the child will probably experience heart breaking pain from another person’s bigoted feelings. That person may be a child or an adult. But, the child will experience this whether they are in your home or in another home, and no matter what color the parents happen to be. It is easy for a white parent to say, “Don’t let that bother you, I love you just the way you are...,” but the Black child will always be Black, they can’t become White just because they are adopted by a white parent. And...the white parent will never, ever truly understand or feel how discrimination feels when it is based on the color on one’s skin.

And...the pain a parent feels is unbelievable when their child is made fun of for any reason. I was walking downtown, carrying my bi-racial child. The day was beautiful, and I wasn’t really paying attention to people around us. I did notice some older teens, sitting along a “decorated” wall. They seemed harmless, but as I walked by one girl said, “Oh yuck, look at the nigger lover.” I was so surprised by her comment, I couldn’t even say a word. What hit me the most was that my child was still young, and didn’t understand what the girl meant...but someday...she will be old enough to hear and feel the meaning. For that I cried within for my precious child. Looking back, I almost wished I would have used the earlier comment... “You bet, I love my African American husband and child. You obviously don’t know what love is.”

These kinds of things happen, but they also happen to people with physical handicaps. It has happened to my daughter, Janice. She was born without eyes, has cleft palate and lip, the tip of her nose is missing, and some fingers were webbed, and some were too short and one was very long. When she was about 1 1/2 years old, we went out to eat at an “All You Can Eat” restaurant. As usual we had to wait in line quite awhile, so little by little we started to talk with others around us. Finally, this man about 45 or 50, looked at Janice, and with pain on his face said, “My God, what happened to her hand? Was it caught in a lawn mower?” Again, silence on my part, trying to think of the right thing to say. Because he was middle aged, I felt I just needed to say something like, “No, she was born that way.” How I wished I could have said “What is your excuse?” Another time, I was waiting in line at the grocery store. (I just realized...maybe that is my problem, waiting in line). Anyway, the cashier said, “Oh the poor little darling, what she involved in a horrible car wreck?” My main pain was in my realization that someday she will totally understand the stupid remarks of supposedly mature adults.

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Hospital Stays

1. Bring a favorite book...for you and one for your child. More is not needed as most hospitals have lots of kids’ books, crayons, computer games, etc.

2. Bring the child’s favorite blanket, stuffed animal, even pajama’s, robe and slippers

3. Bring pictures of the child’s family, friends, pets, etc. Put them around the crib/bed and/or around the room

4. Make a list of phone numbers, addresses, etc. It is so easy to forget even familiar numbers when you are watching your child get an IV, treatment, etc.

5. Check the hospital ahead of time, to see if they have a parent refrigerator, etc. If so, bring your own pop, juices, etc. They will need to be labeled with your name and date, but each hospital has their own suggestions. I often found that in the middle of the night, a pop machine didn’t have the Pepsi that I just had to have, so it was nice to have my own supply. There is also usually a microwave, coffee pot, etc. for parents to use.

6. Have a list of websites you like, passwords, etc. so that you can access your Internet support. Our children’s hospital had a parent resource room, with computers with Internet access, medical books, and someone there to help you find any information you wanted. My son’s floor also had an extra computer that I could use when they weren’t busy with it. I started a file for other parents, under the “favorites” section, with links to medical hospitals, etc. Check ahead of time to learn how to access your email account, etc.

7. Bring lots of film, and take pictures of everything, even the nurse pager thing. My kids love it when I make a photo album of their adventure with surgery. I also save little things, like hospital menu’s, rubber gloves, tubing, etc. and put them in the book.

8. Take a small notebook, and write down everything, especially names of doctors and nurses. In moments of stress it is so easy to forget names, and little details you might want to mention to the doctors. I found that it was so easy to even forget what time it was, or even what day something happened. I would then write down all my questions and put the list on the clip board. I kept a copy for myself. For me, it was important to know all options, plans, therapies, etc. It gave me a slight feeling of empowerment, a feeling that I could do something. Most of the doctors were very willing to answer all my questions. As I became more familiar with technical terms, it required the doctors to really have to stop for a minute or two and think of a way to explain certain things clearly to me., which they did.

9. You might want to get a calling card ahead of time. At our hospital, long distance calls could not be charged to your account, so you had to call collect or use your calling number.

10. Bring your own pillow and blanket. I hated the pillows they had for parents. Also, be sure to bring your own soap, shampoo, and such. Towels and washrags are usually provided for parents’ use. And, remember a robe. Most parents went ahead and slept in their own pajama’s, but none of us felt comfortable walking around in the middle of the night without our robes. There were nights when I just couldn’t sleep, but I sure made up for the loss of sleep when we went home. The first morning home after “Marc’s” brain surgery, he and I both slept until 11:00, and it was a very sunny day!!

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Laughter: An Absolute Necessity=Creative Parenting


One must have a good sense of humor in order to survive parenting a child, especially a child with special needs. One must focus on the things that are most important, but sometimes it's too easy to concentrate on so many negative things, that the joy of parents is no where in your house...and no where even in your city. Here are some things that have happened to us, that could have been seen as "serious" but to us are now funny. By the way, at the time I would usually try not to let the child hear the laughter in my heart, ha, ha.

1. Whenever my kids are quiet for more than a few minutes, I know that trouble is soon to come. I was on the compter, doing just what I'm doing right now, editing my website. The sun was shining, early in the day when the air is just starting to warm up, and...it was too quiet. I couldn't hear their laughter, I couldn't hear their "work." So, as any mother will do, I headed outside to look for them. I quickly saw their newest "game." They actually looked kind of cute: huge cowboy boots on their feet. And...they had taken out 2 dozen eggs, and had a great time smashing the eggs with the cowboy boots, on indoor/outdoor carpeting!! The looks on their faces...they knew they had done something wrong, and were very worried about being caught. It took a lot of strength on my part not to smile. But, I did not want them to continue with the game in days to come. So, I put on my serious mommy look, and sadly said, "Oh no, now we have no more eggs for egg salad sandwichs. We'll just have to have plain old peanut butter sandwichs." Tears whelled up in their eyes, and they started to cry, "Oh no, no more egg sandwichs." Well, it worked, we haven't had stomped eggs for months. By the way, I would usually have had them clean up the mess, but have you ever tried to clean up raw eggs on a carpet? It's amazing, but if you rub with a wet washcloth, as I did, foam even appears. A sharp serving spoon was the best, in case it ever happens to you. Another Example (especially regarding chldren born drug affected):

Roger is 2, and has quite a temper, typical of kids this age who feel they know everything, and that they deserve everything (even if they just now noticed that their sister has a toy car, one that they wouldn't play with an hour ago). His temper tantrums are much more than that, though. He will grab whatever is around him and hit to get what he wants. He has no patience, and will not, under any circumstances, give up. He will then throw himself to the floor, and scream and kick. It is so much more intense than any child we have ever parented, and yes loved. It can be quite frustrating, as any parent knows. What I realized, rather quickly, is that threats, yelling, or spanking would only esculate his out of control behavior.

By accident, I found two things that actually worked with him. One, instead of turning up the volumn of my voice, I spoke very, very softly. It was quite funny the first few times, because all he could see was my mouth moving. I was very antimated, but not an angry expression. He had to quietly yell, and that was pretty hard. He would start to yell again, but I kept talking softly, so he finally stopped. I was giving him an alternative, rather than just telling him no," or "Don't do this." The second thing I learned was that sign language has a lot of power. I don't know many signs, but the "stop" sign worked wonders. I just kept signing, "stop" over a couple of times, at first using words also, but then verbal words weren't needed. It was as if the emotions of speaking interferred with his obedience.

Now, I usually get down on his level, gently, but firmly hold his shoulders, talk softly, and always offer something else he can or should be doing. Now I realize that he's getting older and probably just going beyond the tantrum stage, but I feel my gentleness helped him to learn to be more in control. I also feel that a child having a tantrum feels a loss on control which is quite scarey to him/her. When a parent reacts with yelling, spanking, etc. that just makes the child feel less in control, and more fearful. They learn that "if mom yells, then it must be okay if I yell."



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Poems by Mom

  • "Wall of Feelings," is a poem I wrote.

  • God Can Turn Tears to Joy is a story I wrote about the murder of my best friend, right at the front door of her home. This happened 4 years ago.

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