Crow Parenting and lessons Cancer Moms could learn.

1.  They loosely define family. There is always mom and dad and a few hangers-on.  They call them Nanny Crows.  It helps because there are usually two babies a year.  Often the Nanny Crows are young adults from prior years that have not quite left their Mom's basement. 

2. They don't let them out of the nest until they can fly on their own.  When they do let them out, they have two adults with them all the time. 

3. They feed them, they stroke their necks and nuzzel them sometimes and then at some point they also ignore their screeching.  When one parent does not respond, the baby goes to the next parent. When that does not work they follow their parents around and skwack some more.  This goes on all day but in the end the kids start to feed themselves.  They score snacks but they learn and watch and figure things out. 

4. They keep them close for awhile but encourage them to play with other bird friends  Often they even let them play with starlings.  When the babies come out of the nest they are adult size with perfect feathers. The parents and the nanny's are pretty bedragled by this time of year.  The parents keep the babies groomed but when they go play with their friends things get out of control.  You can always tell by a feather or two sticking up.  

5. They pay attention to their kids.  No texting, cell phone calls or television.  They work together as a family to steal food from the Stellar Jays. They spend evenings together and fly away to roost about 30 minutes before sunset.  

I often wonder if the Crows record such observations about us?  They learn from each other, they remember faces, they know when food should appear and demand it regularly if not delivered. They set up their own "homes" and jealously guard them, chasing away the most officious interloper.  Raccoons, cats, dogs, even people are chased and dive bombed.  As a greater group they will even take on a Bald Eagle.  

We have watched, we have been amazed, we have been delighted. Our own little nature show.  They are a part of our lives. A weird but present example of parallel lives. 

Many Mom's mention they feel like they stepped off the path and have a hard time rejoining their former lives.  I think we have to do it the ways the Crows do... a bit at a time.  

We

have been fed and coddled and protected and now we are venturing back into the big world.  The thing we need to remember is we are not alone.  We are being watched protected and will be helped along the way. 

We can do it. 

So here we are.... gliding along, not knowing others are really struggling...

That is a lie.  I know there are horrible battles going on every day, all day and every night. I know kids are dying and mom's are crying and people are getting horrible horrible bad, worse than you can imagine news.

As we head out of this current orbit around the Double Cord Blood Transplant  universe and head to the unknown galaxy of Post DCBT, I try to be a bit like Lot and not looking back at   Sodom and Gomorrah.  I don't want to know what is going on behind me but I know I am turning into a pillar of salt.  I have not found it possible to just walk away.  Or in my case, run like hell. 

It is so hard.  Sitting here tonight, working on my blog, trying to do some editing, figuring out what I need to do to publish and then I hear a ping.  A bell like sound that says I have a private message on Facebook.  I check and it says:  

I thought you would want to know my dear son passed away yesterday. 

I see those words and it is like a kick in the gut.  This is a kid that had 10 months of chemo and a major surgery and was clear and then, it was back just a few months ago and now it is over for him.  20 years old. I can just feel the balloon of hope and prayers collapsing around a devastated family and friends and his best friend that did a campaign for him to go to Europe.  (The hope was to take  both families but from what I can gather, it was just the two boys.   I am sure they had a great time. ) 

So I stop.  I reconnoiter, I check on my kid.  I gather the Momcologist around this devastated mom.  I relieve her of the responsibility of "telling" another human. I start to look for the obituary because I will go to the funeral/service.   I do a quick search and find the child's Facebook and Twitter account.  I heave a heavy sigh. I write a few words and do what I think helps and then I turn away and head back on our road to recovery.  

But I know it is like the Ray Bradbury story about the guy that steps off the designated trail when he goes back in time to hunt dinosaurs.  When he returns the world has changed.  I have stepped on another butterfly and the world will not be the same.  A bit of hope chips away.  

Every time one of these children die, they take a part of the universe with them.  How much they take depends on where they were in the child's life. The moms have a Grand Canyon, Winslow Crater, Pacific Ocean kind of hole in their lives.  The loss is never minor or insignificant.  It is gaping, hard to close and subject to multiple infections and complications. 

So we say goodbye to another child.  A family is decimated, the world looses amazing potential.   His last tweet:

If you do everything right, people won't know you did anything at all.

Gathering and Letting Go

 We are

essentially Hunter/Gathers.  We don't necessarily use those skills for the same reasons anymore.  It has been a long time since I went out and captured something for dinner.  However, I am on the hunt for cool and wonderful and life saving items and concepts and words and interesting things all the time. 

I love to watch and look and listen and discover.  It is something deeply embedded into my very being. 

One thing I gather are people.  People with interesting and varied lives. I love their stories and histories. I love digging deeply until I find the connection. The thing that makes us the same yet not the same.  For example, last night I had dinner with one friend and found out the server was the aunt of one of Mary-Elizabeth's friends.  I am sure we were at the same Graduation Party.   The threads that connect up are long and mixed up but they are real and are strong. 

We gather people all our lives.  The roll they play varies over the years but if we are lucky there is a continuity of great depth.  They know our stories and we don't have to explain too much. 

I also have hit a point in my life that I am loosing those very friends.  I learned of the deaths of two such people just yesterday.  Both were gone way before was necessary.  Both were in my life at various times and in various ways.  Those ways change but they were still there.  We still had a connection.  

This shedding of friends and family is much more painful then gathering.  I often wondered why Meb was so uncertain about making friends with her Cancer World buddies.  It is way too hard to loose people after 30 years of friendship let alone a couple of years. 

Here is to Alison Beck and Phil Caplan.  Both leaving in their 6th decade.  Way way too soon. 

The cure is such a problem...

She is baking cookies for Camp Sparkle. A summer camp for kids whose families have been effected by cancer.  The kids are going to the zoo today and it is the last day of camp for them.  It has been a quiet week at the Y in the central district, swimming every day, lots of art, lots of time in a gym.  It has been good. 

Today MEB is taking her last dose of Prenisone. Collective breath holding is happening.  She is for all intents and purposes done.  She is finished with this cancer stuff. She is "cured".  

Cured... a weird word. OED explination.

Middle English (as a noun): from Old French curer (verb), cure (noun), both from Latin curare 'take care of', from cura 'care'. The original noun senses were 'care, concern, responsibility', in particular spiritual care (hence sense 3 of the noun). In late Middle English the senses 'medical care' and 'successful medical treatment' arose, and hence 'remedy'.

So, she is cured.  She is doing so so well.  I cann't sing the praises of health enough.  Not everyone has such success.  So many have had little or no luck in the process. So many deaths, so many disappointments.  

Remember our friend Lulu? She fought to get out of the ICU.  That "cure" left her unable to walk or even have full use of her arems.  She was so weak after so much time in bed.  So she is back on her protocol.  First big round of chemo and things are just terrible for her. 

Here is the note her mom posted.

So Lulu Ysarua Martinez will not being going home today...she has not cleared enough chemo out of her so another night at the hospital....the pain is being managed so is the nausea....ortho came up and casted her legs for new braces to wear to walk....they will not be administering vincristeen chemo anymore and will be bringing a new chemo drug on board that is just as effective but it keeps your counts down longer ....has been complaining about side ache and trouble breathing her blood count also dropped so they will be giving her a blood transfusion shortly as well.....will due chest xray to make sure lungs are good.....will update later when I know more.....


She has a fever this morning. I can sense her mom's fear and terror.  Here she goes again.  This is such a hard battle. At some point you just wish there was a way to catch a break!!!!!

So Now What?

So, Mary-E had a discussion with Pearl Anne today.  She explained to her that she was at large and in charge.  She was up for the job and had done a really great job doing her work as the new immune system.  She explained that things were okay and she had been taking care of things just fine.  No need to overreact to every little thing.

  A scarf was not to be feared.  No reason to get all rashy.  A bit of butter on toast was nothing to worry about.  Sushi is really a good thing to be embraced.   No reason to get the gut upset.  There were going to be many battles to be fought in the next few months and years.  She was ready. She has had 2. 5 years to settle in and things are good. 

Now we wait.  Now we wait and see.  The last time the "last" dose was taken there was a party. There was a celebration. There was laughter and relief and joy.  I could barely get out of be this morning.  I have taken to watching "Keeping Up with the Kardashians".  
I have to get a grip.  I have to remember she is 30 months post transplant.  She has gone 30 months without a relapse.  We are half way to the five year mark. The point where most cancers are considered "cured". I should be relieved she has had no signs of any cancer.  

I don't know how to be relieved and happy about this.  Trust that is gone for good was so shattered with the last relapse. 57 months..... 7 years of remission.  I don't know when I will ever believe it is gone for good. 

As always, I will work through this.  It will be okay. I will be okay. She will be okay.  I just have to adjust my expectations and know that Okay is Okay.  I feel like we have been through a fire storm and and hurricane and then the tornado touched down to clear away the rest.  Just not sure how to recover from this.  Pretty daunting.  

I will sit with this for awhile and count my blessings and watch a few more episodes of bad TV.

Currant Lessons....

5 or 6 pound of these:

juiced makes about 5 cups liquid.

Then you add equal part of sugar.  

Boil for about 20 minutes and you get 

Each of these jars hold about a cup. 

So the process produced about 6 cups of jelly.  

The French are very into Currant Jelly and have a special preserve.  

As of 2012 the House of Dutriez in the town of Bar-le-Duc provides one of the very few hand-made preparations still on the market, la confiture de Groseilles de Bar le Duc (Currant Preserve). The traditionally hand-made product involves épépineurs or épépineuses (seed extractors) de-seeding the currants with goose quills to flick out the tiny seeds without disturbing the flesh of the small fruit. Sometimes sweetened jellies, consisting of mashed and sieved currants of a significantly lower cost and quality, appear on the market under the same name.


Mine was made by steaming the currants, letting the juice gather in the reservoir.  Sugar added and boiling in a French Jelly Pan stirred with Ms. Ferguson's Mother's Jam spoon. 

 Not a single goose quill was used to de-seed the berries.  I clearly disturbed the skins.  My berries were mashed and abused and oh my. 

Life is all about compromise. Nothing is perfect. Sometimes it has to be okay to have  a mashed and sieved life.

So Currently I am trying to learn from my Currants and simply carry on. 

She is down to One Last Sirulimus

Next week at this time the "Girls" or more specifically, Pearl Anne will be flying solo. She will be in charge of keeping all that invades from MEB's body. 

Protocol:  Immunosupressants - 180 days post transplant.

Mary-Elizabeth 31 months or about 900 days. 

She is almost done with this step, 24 months, three different kinds of suppressants  she is almost done with them.  I am currently not totally freaked out about it.  

I think we are all so tried of this it is hard not to just be ready to be DONE

I am feeling like the time as come to end this blog after 10 years.   Maybe I am done and leaving this writing forum will help me be DONE.  I won't quit writing, I will just do so in another place, another title, another forum.  

Maybe it is time to move on in the way one can  It is a tentative moving on, not really but sort of.  Hanging out in a different place in Cancer World.   As we all know, we don't ever get to really leave.  Now it is about managing the long term side effects. Kidneys, lungs, brain, menopause, thyroid, cataracts.  (These are not just stuff that might show up, these are guaranteed to be a concern. )  

So this morning, I will just drink my coffee.  Water a bit. Watch some plants grow.  Read my book a bit.  I will enjoy this moment, this instant. This bit of Seattle Sunshine.

 

Not

Why Mom's just don't get over the death of their cancer kids...

I am sure not everyone experiences motherhood the same way.  I know the instant I realized I was pregnant, I had a bond.  I was attached.  Of course she was sort of attached to me but I was attached.  It was like nothing I had ever experienced. My life changed in a way I didn't  understand.

I often hear about Mom's that had to "bond" with their child.  I wonder how that happens but I know even in those situations, the bond is there.  After we are clearly and permanently attached, then we have to become unattached so the kids can grow and mature and find their own lives. 

While the leaving the nest part is gradual, there are times the process is like lighting.  7th and 8th grade is one of the big pulling away times.  A time they are finding out who they are and how they fit with all of their friends.  It is a time many mom's mourn the loss of their babies but it is part of the process.  Little by little we let loose, they grow bolder, they develop out of family friendships.  It creates a place in their lives, creates a crease in the bond that allows a clean break to be made in a painless but significant way.

The entire process is mess up if at any time they enter Cancer World. Instead of a child gently pulling away, the Mother/Child bond intensifies exponentially.  All of a sudden not only are you caring for your child in an intense 24 hour a day, seven days a week way, your child is sick. You are on an adrenaline rush that lasts for several years.  No breaking away, no time to think, constant, intense caregiving.  It makes the bond so so much tighter.  Just imagine a strand of thread as the normal bond and a 10 inch cable made out of spider web as the bond created after Diagnosis. The cable eventually becomes the size of a 1000 year old Red Wood Tree. If they get better, the bond is always strong.

So here is the situation.  Child born, bond created. Child grows, child moves away in the natural course of things.  Child gets Cancer child moves back, no breaks not natural cut off, bond becomes super natural in order for the child to survive.  

But what happens if child dies?

Nothing is gradual. Nothing is normal. Nothing prepares anyone for the death.  It is like amputation without anesthesia.  And when it is done, the final most abhorant break in the bond occurs, Mom's are supposed to just go on. They are to be strong and brave and act like nothing happened.

Like many in Cancer World, we have seen the fall-out of the amputations.  I still hear from Guliany's mom in Turkey.  I hear from Shannon, and Kate and Kristi.  I see posts from Nyla's mom and Mario's moms.  I see the gut wrenching screams and pain and suffering of these Moms.  Jackie and Sheri and  Elizabeth or countless more.  Mom's that did all they could to keep their children with them.  Keep the bond going. Keep the connection.  

I don't perceive there is a difference in whether or not the child died suddenly or it was a long process.   They see other children with exactly the same flavor of cancer, same treatment and some kids do fine.  Some make it out alive.  They scream..... in pain about the unfairness of their child's death.  We need to let them scream and not make them feel like they are failures for not "moving on".

There is no way to figure it out.  Just don't ever assume that because the child died a year ago, two months ago or 40 years ago it is okay to ask how the mom or dad got over it.   The hole might have been walled off and there might be appearance of Normal but those parents could still use a hug. A hungry listening ear and understanding. 

So much potential. So much loss. So sad for everyone. 

If you ever doubted.....

Children are resilient.  Lulu is up, talking and here is the most recent post from her mom.  It really really does say it all. 

does anyone in the royalton are have a large pet carrier i could borrow...OREO is allowed to visit lulu but his FAT BUTT just broke ours beyond repair......

And by the way... I wish pets were allow to visit at Seattle Children's...

This crisis has passed.  The universe is good.

Back on the road to a cure.... again. 

The "Strength" Cancer Mom's Exhibit Is not What You Think it Is...

Stay Strong

Hang in there

You have an amazing attitude

Your such an inspiration

You can do it, you have done it before

Hold on it will be okay

You're so strong....

Your a trooper...

I read these statements over and over again.  

I don't know about other Cancer Mom's but it is all a farce.  There is nothing amazing about being a Cancer Mom.  We are not trying to show the world of an example of how much we can handle. We are not trying to get be a trooper.  We are doing what you see us do because we HAVE NO CHOICE!

We are doing this because we got the call.  The "we regret to inform you" call. The call that slammed our lives into another universe.  No chance to pack. No chance to organize. No chance to say good-bye to our lives.  One second life was just fine and the next we were on the other side of the universe having been pulled into the Black Hole of Cancer World. 

We are amazing. Some of us are positive. Some of us are just out there, screaming about what it is like to have a child with cancer.  Some of us retreat to some dark, sad, scary place and never emerge again. 

 I have to write.  I cannot keep all the anger, fear and frustration inside or I would just implode and become one of those really bad headlines. 

Nice Quiet Mom Explodes at the ..... fill in the blank.

Today there was some good news, someone is waiting for news, someone is remembering good news that has gone sour.  Everyone is scrambling to make them feel better while all knowing how fast it can all go very very wrong. 

These mom's are strong, they are able to hold on, they are the most amazing troopers you could ever know.  But their strength is a different kind of strength.  They are not lifting a million pounds or taking some force and changing the world, they are simply standing in front of the leaking dam and holding it together.  
They are using all of their strength of will to keep the dam from completely collapsing.  Some days there are more leaks then anyone can clog. Some days a nap is possible. The thing is they know they can never, ever, ever stop from holding back the dam.  

They looked away once before and took a little vacation or went to a play or went out to dinner or learned how to speak French. They did something fun and the dam collapsed.  

These are special people with a strength and deep core of power only few every have a chance to use.    But they are all looking for the same result.  A chance to have their child "return to normal".    

Here's to Normal.

Fireworks for Lulu

Lulu Ysarua Martinez is off ventilator talking to me (mom)and breathing on her own will post later


What a happy bit of news before the 4th of July.  Little does Lulu know but the fireworks are for her.....

So how do we define it....

Prayer, chanting,  putting good energy into the universe, wishing, meditation, it is all the same. It might have a different name or method but it in the end it is the same thing. It is those moments when we speak to the otherness surrounding us.  Lots of people say they are non-believers but I have heard them curse and God is usually in the mix. 

I think it is just our nature to want to make sense of the world.  At some point I know I thought I had some control over how the world would turn, or at least the little bit I inhabit.  I can plant the right flowers, cook the right food or go to the right restaurant. I can save for college for my child and for retirement.  I can work hard and help people while making money.  I can take a few pictures and capture a few memories. I can plan for fun events and try to be strong when unfun things happen.  I can grasp things within my reach and keep the world calm and productive.

Ha.... Oh boy... was I so so wrong. Evidently the first time my child suffered with cancer was not enough.  I had to be taught that lesson again.  Nothing. Absolutely Nothing is in my control.  Well... the way I react and respond is in my control but other than that it is a free-for-all.  

Plan and execute the glorious front flower pot.  Watch it struggle and sag and fail. Reasons, many.  Should I have known that slugs and snails love, I mean, love the little petunias... Nothing eats Petunias.  Wrong, those are just sort of petunias.  They have been genetically modified into slug food.  In stead of glorious massive beautifulness. I have this is it. So.... what to do now. 

This is something simple. Something I know how to do.  I have a green thumb.  Hey look at this basket..

So, do I swear at the universe, mope because I have lost my green thumb or go try something really different...

We shall see, because in the end it is not up to us.  We have no control. 

Hyper Pin Point Focus....

We get so focused...So focused on the goal that sometimes we don't see the big picture. 

 The big picture is there all the time but being in cancer world deletes your ability to see that picture.  You have one set of goals.  It starts out big... Cure Cancer. Cure and defeat Leukemia, AML or ALL or , Brain Tumor, Sarcoma...Wilms, the list is endless.  Cure, Cure, Cure.

Only later do we face the reality of what the cure means.  80% of the time it means life.  Survivorship, a future, a way to return to normal.  I told someone a long time ago I was not giving a dime to anyone that wanted to cure Cancer, only to those that wanted to figure out how it happens and make it stop. 

I sit here this week and look at the fall out from being in Cancer World twice and now it is damage control.  Sort of like the bombs dropped on Nagasaki and Hiroshima.  They stopped World War II but then what.  At what cost to those sitting around innocently having a morning cup of tea?

Mary-Elizabeth and all of our children have been subjected to a nuclear blast. Many cells and organs and future cells and eggs took one for the cause.  Her thyroid died, her eggs are (ready to be served on) toast, she is guaranteed cataracts and skin cancer and a whole list of possible other cancers.  

Don't get me wrong, I would make every single decision the same except I would have pushed for egg harvesting when she was about 17 or 18.  I didn't think about it then and now it is too late. 

We are so singularly focused on a date, a place, an event, a result.  Please let my child's body be ready for more Chemo. Please let my child's body be able to 4 days of twice a day total body radiation and high dose chemo so that she will be completely helpless against any sort of bug!  Please let them do some more scans or run a scope down into her stomach and take a biopsy.  Please let them operate and remove huge parts of her bones and replace them with some foreign metal in a new experimental surgery.  Please, we will take anything, just let her live...

If we ever stood back and took a look at what was really happening and thought about it, I don't know what would be the result.   I guess our brains know we can't handle too much.  So we are able to chop up the ongoing crisis in little bits and pieces to be handled one step at a time.  Today we do the biopsy or the scan or the chemo... Tomorrow we evaluate and keep going until we hit CURE.  We will take the dead thyroid, the deeply upset kidneys, the brain die-off the massive infection that will not heal, the relapse, the 14 days in ICU, the emotional storm of anxiety and depression and all the rest.    

We are focused on a Cure.  Nothing more, nothing less. 

    

Lulu

Lulu s DOING good...Ventilator DOWN To 30 percent lungs still have goo but she is doing majority of work. ..her pancreas is enlarged and her number is high so checking her for pancreantitis fever is down and so is blood pressure...if she continues to do good they are talking about taking her off ventilator next week....our prayers are heard and being answered...thank you... thank you...thank you all for your love and support.our girl is amazing and strong and healing...from the icu ‪#‎lulustrong‬


Thus reports her mom..... Long road to recover

from this blip on the way to a transplant. 

I will continue to follow this family and continue to update. Seems things are good for now.  While it seems to be "if it's not one thing it is another" but then anyone that knows anyone in Cancer World knows that is the case. 

The think about Childhood Cancer is the resilience of the children and their bodies.  They have "new" parts and over the years the doctors have learned they push much harder and have good success. 

I remember when Meb had a conversation with a Breast Cancer survivor.  The woman asked Meb about her port.  She shared with Meb that she had had 6 rounds of chemo therapy.   My lovely daughter commiserated with her and then when she spoke to me said:  "Mom, I didn't tell her how many I had had."  Even at age 13, she knew the difference. 

So here is to Lulu and her struggle.  

I'm Stuck....

In a weird difficult and not the most healthy way.  I feel like there is collar around my neck and if I get too far away, I am yanked back.  I reach to the edges of the universe only to be snapped back in with great force.  

I push Meb out as far as she can go and she seems better at free floating than I am.  So, every single day, I try something to free myself from the deep gooey morass of Cancer World.   

List of things to do.  Then one appointment with the Kidney Doctor and I loose my ability to finish the simplest of tasks.  Going to try again.  
Stuff in places it should not be. No apparent reason, waiting for more analysis.  Possible way to help the kidneys be smarter, waiting for the end of Prednison and Siriolimus.  Best medication also lowers blood pressure so they don't really want to give it to her at this point.  Child would be a slug.

So More waiting.  

I am going to do some laundry, my mom is coming to visit and will be going to see Cher with Mary-Elizabeth. Should be a fun week-end. 

Bit More Progress.... Information from Natalie, who is exhausted and headed home for some much deserved and needed sleep.

Lulu is moving all limbs can answer yes.or no questions and was able to tell us she she is in pain working on sedatives and getting her comfortable no change in lungs ventilator down to 50 percent so doctor said going in right direction has blood clot in right arm started blood thinner. .low fever....dad is staying tonight to give me a break. ..get to see my other girls and my bed...Lulu strong from the icu.


No matter how bad it is at the hospital, going home to your own bed is the best medicine...

A bit of information.... heavy duty waiting....

Quick update on Lulu...I know there hasn't been much last couple days and that is because there isn't much to update. She is still on ventilator. Lungs are slowly releasing fluid. She now has a blood clot in her right arm so on blood thinners. Her blood pressure is kind of all over. She is put back under sedation. She does respond with movement when not sedated but still not answering yes and no questions. Many tests being done next couple days. Keep the prayers coming!!! I believe God has received them and has been answering in small ways. We will take it!! 


News from a friend of Lulu's... 

Quiet... sometimes it can be good?

I won't stop posting until Lulu is out of the woods.  It's that sort of "hanging in there" no matter how long or how hard the process.  

We have such a short attention span.  145 minute movies are often deemed "overly long".  Harry Potter is the longest book most kids have read, ever.  We like short, packaged things.  100 calorie brain bursts. 

Cancer is not like that.  It takes a long time to find, it takes a long time to fight, and it takes an even longer time to ever, ever forget.  Oh, that was a silly question.  No forgetting is possible.  It is just another series of events that are seared in your brain.   A Pearl Harbor, John F. Kennedy, 9-11 sort of moment. 

It has been my experience that no news is not a good thing.  It is easy to write about good news, it is hard to write about bad.  For reasons I don't understand, there is a need to package the bad news in such a way as to ease the blow.  Always be positive.  Always figure out something good to say about a situation.  Mad is acceptable, sad is not.  

I promise to post when I have news about Lulu, until then, keep the candles burning.  

So this is how it goes...One thing leads to another...sometimes it seems like an endless cycle.

The quiver and medicine bag are full.  Full of much magic and a variety of potions and spells and noisy machines.(Now the childhood cancer quiver is rather bleak and antiquated but the potions are better than they were.... but those are thoughts for another day. )

Best example would be Meb.  She is on 20 medications.  Of those, only 2 are therapeutic. The rest are for side effect treatment.  

Prednisone and Sirolimus cause lots and lots of side effects and so there is also
Tacrolimus Cream
Bactrim
Valacyclovier
Multiviatims without iron
Omeprozole
Vitamine D
Cetirizine
Levolthyroxine
Lisinopril
Lovaza
Magnesium
Melatonin
Warfrin
Mylanta
Tums
Zofran
Atavan
Hydroxyzine
Scop Patch
Oxycodone
Sunscreene
Cyclobenaprin

Boy the list is so much shorter now.  It used to be 4 pages. 

So Lulu is suffering strictly from side effects.  Her cancer is not doing all of this to her. Her side effects are what is causing all of this havoc.  The cure for cancer is not easy by any sense of the imagination....  Here is the newest on the poor child. 

Lulu had a blood clot in right arm. Went for ct scan to make sure no bleeding on brain..there was not..started blood thinner to get rid of clot.  Her arm is beyond huge ....her blood pressure was running high at midnight but came down at 2am ventilator is on 60...her lungs need to heal for us to come off this...I asked the doctor how long he thought she would be on ventilator and he said he didn't know. We have been in hospital over 3 weeks and day 9 on ventilator....staying strong and fighting another day from ICU...rubbing lulu's head with coconut oil..wiping her eyes. ..lotion on legs and arms..wipe her face ...caress her ear...smell her.....whisper secrets and dirty jokes in her ear...oh my sweet girl you are loved and prayed for by many but I am the lucky one who you call mom...#luvforlulu

The road is feeling like it will never end.

 
  

Ups and hopefully no downs.

Childhood cancer really is rare in the scope of the 300 million or more of us in the U.S.  Some tiny bit of the population.  Sort of like Medulary  Thyroid Cancer.  But once if shows up in your life all of a sudden everyone has it.   You make connections with those that have it, you run into people that have it. It consumes a part of your life.  

Today Meb had an appointment with our lovely Seattle Children's Bone Marrow Doctor.  She is moving to Portland Maine and this was the last time we would be seeing her. By Dr. Pollard.  It was a great appointment, the taper is working, most days. Meb is getting allergies because she is weaning off prednisone.  She has some spots but they have been around less than 24 hours and we are hoping they will subside.

Her kidneys are unhappy but then we have been down that road again.  Hopefully she will not continue to loose kidney function.  Life is good.  

So while I am sitting there I spot a parent that was on and off the floor during Meb's transplant. He is stressed. He is freaked out. Then I saw his son.  He is older than Meb and he is bald again.  Crap... he is back in treatment.  I didn't ask.  There is no way this is a good thing. 

I just can't get away from it.  It haunts me. It terrifies me. It makes me crazy.  It's a slap in the face.  The ability to believe this will ever ever be over eludes me.  By ignoring what goes on around me I can sometimes forget.  But not in a convincing way.  I am just a bundle of freaked out Mom...  

But on the other hand Lulu is responding.  Really responding.  Her story might turn around.   Sounds like her body is fighting. 

Watch out here she comes....Lullu came back from MRI they could not do it because she wouldn't stay still!!!! She opened her eyes and looked at me. She is responding to me...they had me ask her yes or no questions but no response but when I tried to take my hand away so they could get in there she clamped down on my hand and still holding on to mommy...they are ordering ultra sound on right arm where pic line is because it is huge they are afraid of blood clot....but I'm so excited about her moving I'm giddy!! And She Knows My voice...Will Update Later But Celebrate And Dance Because Lulu is Responding And SHE Hear

s us!!!! And we have 11.7 hemo 5k platelets 6100 white blood cells and a 3200 anc.....she is doing it!!!! Still on 70 percent ventilator

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