Monday, February 14, 2011

A great day!

On 2-11-2011, as Egypt celebrated, I was quietly celebrating what would become one of my best birthdays ever! Our daughter and her science teacher invited me to the classroom to teach a chemistry song, a former student of mine had written years ago. I hung out for a bit of their lab before heading to a wonderful lunch with the dearest of friends. I mixed a gallon of slime for the school carnival and it was there I received my third amazing present!

Three years ago, the carnival was too much for our youngest. She walked into the gym and was completely overwhelmed by the people, the games, the noise. In panic, she asked to go home. With much encouragement, she played the Plinko game in the farthest corner. Two years ago, after her recent diagnosis of cerebral Lyme disease, she missed carnival altogether when she was downstate for a picc line. Last year, I was downstate for treatment, so it was pure pleasure to watch her completely embrace this year's carnival! She had the confidence to play games with friends, have her face painted, won a goldfish coupon when she tossed a ping pong ball in a bowl, and even mustered the courage to do the cake walk until she won. Only I needed to sit and rest. She continued strong to the end. She was so excited and on the way home declared it, "One of my best days ever!"

I have to say, though I was completely spent and rested much of the weekend, it was truly one of my best birthdays, too!!!

Tuesday, January 11, 2011

Strength, Peace and Grace


Winter is always harder for me. I love it's beauty, but the cold weather brings increased pain and a flare in symptoms. Sleep, medications, cranial-sacral work with acupuncture, a FAR infrared sauna, and a gluten free diet have been my allies in the battle to maintain the ground I've gained.

Our daughters are fighting their own battles. Our 13 year old is wrestling with the pain of arthritis in her spine as we wrestle with how best to help her. Our 8 year old suffered more hearing loss a few weeks ago. Was it the result of drug ototoxicity or a respiratory infection? By waiting a bit to write about this, I can also report that she has regained some hearing. Ototoxicity does not appear to be the factor and she has returned to the drug that was helping her greatly, with careful monitoring. Medication adjustments for both girls brought new herxes and our journey continues.

The chronic Lyme journey brings difficult decisions. Do the benefits of a medication outweigh the risks? Which is more important, sleep or physical therapy; sleep or homework? No book helps you field statements like, "Mommy, I don't understand. When you're not feeling well, I always let you lie down, but when I'm not feeling well, you send me to school," uttered on her first morning back after missing a week of school for a respiratory infection.

My daughter did make it to school that day, after I reminded her how very brave she is.

Sometimes life is messy. It's difficult. We do our best and celebrate the blessings. Wishing you strength, peace and grace as you face life's challenges.

Monday, November 22, 2010

The Power of Caring


Recently, I have found comfort in cranial-sacral massage and acupuncture. As I lie on the table, soft music playing in the background, the experience for me is quite spiritual. I have been sick for so long, I feel as though my body has come to know that as its natural rhythm. During each session, I feel my body is gently wakened to a balanced state. I am reminded of how it should be. I am at peace, my breathing easier and I often sleep deeply after a session. In the few days that follow, I feel a boost in energy. I imagine medications working more effectively. It is not permanent. I schedule two sessions a month.

For those of you who have not experienced acupuncture, the needles are tiny and many pokes are nearly painless. A few are bothersome, but the sensation disappears within minutes as endorphins, the body's natural pain killers, flood the area. Once the needles are in place, I rest. The needles are removed and my session concludes with a cranial-sacral massage; the gentlest massage of the cranial region at the base of the skull and the sacral area of the spine.

Our youngest has experienced three sessions of cranial-sacral massage without acupuncture. Each time, she has fallen into a deep sleep during the session, breathing as easily as I've ever seen her. She feels disoriented when waking, though the time has decreased with each session and it no longer frightens her. Her last session, she ran ahead of me to her appointment, in the door before I. It helps that we place ourselves in the hands of one of the most caring and gentle women I've met when we walk through the door. The visits have been a blessing, but became even more precious when our daughter noticed I was struggling with a headache a few days ago.

"Mom, would you like a caring massage?"

She gently took my head in her hands. My heart melted. Last night her older sister was hurting. Her solution? Another caring massage, remembering each soothing detail as she administered comfort. Her sister went off to bed with a smile on her face. We all did.

This Thanksgiving, our family is grateful for the gift of caring shared by so many who have touched our lives. When it comes to Lyme disease, it often takes courage to care, and to those who have the courage to make a difference in the lives of others, we are especially grateful! Wishing you and your family a blessed holiday!



Sunday, October 3, 2010

A Vacation

The idea came as we were returning home from another round of appointments. Some of our symptoms were weighing heavily on my mind, but with each passing mile, I was calmed by the golds, oranges, pinks and reds that paint the roadsides in a northern Michigan fall. Grammy and friends had enjoyed a color tour earlier in the week. Were we up to a similar trip?

For the past eight years, our road trips have been reserved for appointments. As a casualty of our seemingly endless medical sagas, I realized our daughters had never been to Tahquamenon Falls, a few hours north. The girls are pros at travel and I bounced the idea off my husband because he would need to help with driving. Falling leaves prompted our decision and he spent extra time on homework yesterday, making the idea reality. This morning we headed north. Even our Border Collie was excited at the prospect of a sunny day spent together.

The girls' enthusiasm when crossing the Mackinaw bridge bubbled over, making us both smile. We stretched our legs at the Cut River Bridge, and our youngest exclaimed, "I've never gone across a bridge where it wasn't to go to an appointment! Today, it is like a real vacation because I can just have fun!"

Bless her heart. Miles passed as we sang songs from GLEE, soothing a few rocky moments.

Today we took a vacation. A vacation from school, demands of home, and Lyme. We thrilled in the gorgeous colors of fall and the wonders of the Upper Peninsula. For my husband, it brought back fond memories of a biological sampling trip years ago. For me, memories of trips to Michigan Tech. For our daughters, our mini vacation provided the wonder of possibility. Special memories were created for all of us!

It felt so good to capture a bit of the magic of living, the joy reflected in our faces. What a blessing to have traveled this far in our healing so we could enjoy today! Never has the importance of living in the moment been more clear to me. Wishing you a wonderful magical fall and sending you our very best!

Thursday, September 30, 2010

A Birthday

Thirteen years ago today, I woke to contractions. I was 34.5 weeks pregnant and scheduled for a hospital visit and pre-registration later that morning. We met my ob-gyn at her office beforehand. I still remember her words, "What do you think?"

"I think we're going to have a baby, today."

My son had been born 9 weeks prematurely. Doctors tried to stop the contractions without success. This doctor was hopeful my contractions would stop. She sent us to pre-registration at the hospital, asking them to check me again at the end of the visit.

We were given a quick tour by a very nervous receptionist. My water broke at the end of the visit and we were quickly moved into the room we had just toured. I was going to have another preemie.

There were several complications during the birth, the most dangerous being the umbilical chord was wrapped around our daughter's neck not once, but twice. Each contraction would be bring a slowing heartbeat. Enter high doses of Pitocin and I dilated from 3 cm to 10 cm in 20 minutes, avoiding a C-section by minutes. Our daughter arrived, weighing just 4 pounds 4 ounces, tiny and blue. Yet, like Kate DiCamillo's tiny mouse, Despereaux, she was "born with eyes open." My husband and I will never forget when she turned her tiny head to look directly at him the first time she heard his voice outside of the womb. The bond formed at that moment was a bond that will last a lifetime.

She was unable to maintain her own body temperature and her heart rate was of concern. She was rushed to the neonatal intensive care unit, her home for her first week. Doctors discovered a reflux that affected both breathing and heart rate and she would go home with a monitor that weighed nearly as much as she. It would be her guardian for the first year of her life.

The reason for my premature births remained a mystery. I did not drink or smoke. I ate well and exercised. I was not severely under or overweight. I was told that if we chose to have a third child, it would be a preemie. The doctor was right. Nearly five years later, our youngest entered the world, at almost the same age as her sister, weighing just 2.5 pounds. It would be many more years before we would learn the reason for the premature births. I was fighting a chronic bacterial infection. I had Lyme disease.

It has been well documented in scientific literature that the Lyme bacteria, Borrelia burgdorferi, can cause miscarriages, premature births and still births. Transplacental transmission has also been documented and we are convinced both of our daughters have been fighting this disease since birth. I would love to see Lyme tests for mothers and infants after unexplained premature births, though I wish we had a better test, knowing that the current test would potentially miss many.

On this day, we celebrate our daughter, a beautiful young woman, who brings so much joy to those who know her. We give heartfelt thanks to the fabulous doctor who saved her life at birth and to the fabulous doctor who has given her a new lease on life as she continues to fight Lyme and its co-infections. We are blessed beyond words.

Saturday, June 19, 2010

A Bit of Mourning

Tonight I can't sleep. It is warm and humid and Borrelia do not like heat. Our youngest has awakened several times, anxious and in pain. Though she's finally sleeping, I've given up for the moment and here you find me. At the computer at 4am. Perhaps I'll sleep better in a bit.

Each time I sit down to the computer, I face the evidence my life has changed. In high school, I was blessed with an English teacher who taught me to write well. With Lyme, what once took minutes can take hours. I read and reread because of multiple errors; errors I never made before.

My girls want to learn to play piano. Our teacher encourages parents to take lessons first so they can help their child during the week at home. This week I took my second piano lesson and teared up. I don't know how to explain it other than the piano acted as a magnifying glass to the weaknesses that have developed in my body. The muscles in my hands and arms were screaming their fatigue. I felt there was a wrestling match taking place between my brain and the rest of my body. The piano teacher was patient and kind as I tried to explain my emotions. I learned if I look at my hands as I play, my brain has an easier time communicating with the rest of my body. I sense piano could become a form of physical therapy in my healing. It also raises the question should I look at myself as I walk? I may try this in a safe place in our home as my legs occasionally have a mind of their own.

To face Lyme, it often takes superhuman strength, both physically and emotionally. Perhaps tonight I needed to mourn for a bit the person I used to be, as I feel the need for sleep returning. Sweet dreams and bless you for sharing this journey.

Sunday, May 9, 2010

Happy Mother's Day

It is Mother's Day and I woke to wonderful gifts from my daughters, a book and a beautiful mobile of ribbon, Shrink Art, beads and fabric flower petals. The gift of creativity is very much intact. My best gift is the progress we've made in our fights against Lyme.

Lyme disease is tough. The fatigue, joint pain, headaches, cognitive and neurological challenges wear you down. For a mother with Lyme, the challenge can be especially emotional if you're not able to do all you would like. From reading to playing, cleaning to cooking dinner, all have taken a hit at one time or another; most daily. And for those of us who have passed this disease unknowingly to our children in utero, it can be especially heart wrenching as we watch our children face the challenges of this disease on their own. From their tenuous beginnings as preemies, to their own daily physical, cognitive and emotional challenges, it breaks our hearts. I know. Both of our daughters have been fighting this disease since before they were born. It is all they've ever known.

A doctor once said, "We would never wish something like this on a child, but kids that endure grow to be pretty special adults."

We have seen this in our daughters' perseverance, compassion and zest for life. Just last week, our youngest strapped on her roller blades and helmet, grabbed a bag of dog treats and our Border Collie's harness, tossed a treat down the hall and held on for the ride of her life! As we rescued the dog, we applauded her tenacity, her love of life.

And so today, we celebrate all of the amazing women who have touched our lives and the lives of our children. Our inspirations each and every day! Wishing you much love and joy this Mother's Day!