Kicks for Conan

There will be a Quad-Cities alumni soccer tournament on Dec. 27-28 to benefit Rock Island girls' soccer coach Conan Dalton, who is battling a recurrence of brain cancer. All proceeds from "Kicks for Conan" will be donated to his family to offset his medical bills.

The event will have a 30-and-over and 30-and-under bracket of alumni teams. There also are sponsorship opportunities for those who want to help.

Dalton was diagnosed with brain cancer in 2008. During his fight, he has encountered two operations. A recent surveillance visit with his oncologist revealed three lesions on his brain, resulting in chemotherapy sessions in Iowa City.

For more information, contact Amy Kent at 309-236-2544 or ankent39@gmail.com.

(From: http://www.qconline.com/sports/high_school_sports/kicks-for-conan-to-benefit-rocky-girls-soccer-coach/article_a9b457d9-7af5-5030-9d99-31eebb7b1f2d.html)

(Correction from Amy: The paper today stated that this event was set to be at the end of October. That date is wrong. The correct date is at the end of December. December 27th and December 28!)

More info . . .

After additional discussions with the doc, Gretta gave me more info.

They didn't start the temodar right away because they wanted to make sure it wouldn't disqualify him for a potential study. It doesn't, so that will start this week and continue for 8 weeks. At that point they will scan again.

Meanwhile, they are still in discussions with other med centers to see what new treatments are emerging for recurrent brain tumors.

Not Good News Monday

Review of the latest MRI revealed that this chemo wasn't working. The tumors were not smaller.

Big hit, but the doctor also said this is not the end. UIHC staff called around for second opinions and has made some suggestions.

Also, these tumors are still small and were found because docs were looking with quarterly MRIs.

Conan is restarting temodar, the chemo he had in 2008 & 2011.

Conan and Gretta are still sorting through the news and looking at options. Continue offering your support as best you can.

Here we go Again

Unfortunately, a scan last week revealed new tumors. They are small -- in fact the two docs talked for awhile to decide if it was 2 or 3 hot spots. The surgeon also reviewed the scans and agreed that chemo should take care of these new trouble spots.

The plan is to run an infusion of irinotecan for chemo, which is new for Conan, and also treat with avastin, which he got in 2011. Next week he'll get the first dose and we'll take it from there. 

We have known all along that the likelihood of recurrence is high, so the scans have continued about every three months. Because of that, these new growths were caught early and will be treated quickly and effectively.  

Happy Birthday Conan!

I am more than a few days late on the HB, but that's because I struggled to find the words for what I wanted to say.

Conan celebrated his 40th birthday earlier this month.  One of the American Cancer Society's slogans in recent years has been about creating a world with more birthdays.  

Here is one more birthday.  It has been close to six years since Conan's initial surgery.  His chemotherapy pill was first approved about 15 years ago.  My father-in-law's brain tumor was discovered before temodar was available.  The best the doctors had in treatments at the time didn't work and he died less than 6 months after his diagnosis.

Because of the hard work of many scientists and doctors, as well as cancer patients willing to take a chance, and people willing to donate money to promote research Conan is with us today. Lately I have been thinking about the perseverance it takes for there to be people, medicines, and machines to treat them. All the doctors, nurses and technicians that he has seen in the last six years all had to spend time, money and great effort to get to a place where they can help others.  Donors have sent millions of dollars so UIHC can build a place to administer treatments and look for new and better treatments. Researchers have spent decades developing safer ways to deliver radiation to tumors and look for new medicines that will be more effective.

So take a moment to be thankful for the birthdays around you. Take moment to mourn the ones that didn't happen. Take time to thank someone you know has helped you or someone else. And take more time to help someone - be it in time, money, or effort - you never know how much you can do until you try.

On the way home!

Gretta worked a full day today and was swinging by the hospital to pick up Conan when I talked to her earlier.

He is having a little trouble walking, so the physical therapist that put him through his paces suggested using a cane for a few days.  Gretta thinks he may still be getting more meds than he needs, but they have a regular checkup at UIHC on Tuesday, so they will bring all the notes and test from Rock Island with them.

I am repeating myself, but things looked so bleak on Tuesday, so for a person's brain to be so attacked and then recover is amazing.

Feeling Good!

Conan says he feels as good as any other day.

He's a little loopy as they test medication doses and effectiveness, and he will be in the hospital while they decide on the right mix, but for the most part he is back to his old self.

He remembers very little of what happened Tuesday, but we are assuming that because of the trauma his brain has already sustained through 2 surgeries and his 2008 radiation, the fever triggered a seizure.

I didn't expect an outcome this good when mom told me they had called an ambulance to take him to the hospital  -- thank you all for your prayers and messages of hope and encouragement! 

Awake & Eating

I still have a lot of questions, but it looks like Conan's condition is improving. It appears he was having some seizures on both sides of his brain, perhaps initiated by the fever. He will begin taking some extended release seizure medication and hopefully his condition will stabilize.

I'm not sure how long he will remain hospitalized, but they are moving him out of ICU and into a room.

Still No Answers

MRI was done around 4 this afternoon, but it didn't shed any new light on the situation.

Good news is temperature seems to be under control.  (Looks like I forgot to mention that earlier, but he was running a fever of around 102 and it wasn't responding to attempts to reduce it.)

Need Prayer

Tuesday morning, Conan wasn't feeling great, but it didn't seem to be a big deal.  Gretta took Henry to my parents house and she went to work.  She asked them to check on Conan later in the day.

When they called and he didn't answer, they grew concerned and they went to the house.  He was conscious, but not making sense when my parents and his Mom arrived.  (We think he realized something was wrong and he called his Mom.)

He was admitted to the hospital and had a CT scan and a spinal tap last night.  There was no sign of stroke, tumor regrowth or infection with those tests.

He is still mostly unresponsive, but he has spoken some.  He was moving his arm and trying to sit up some this morning.  They wanted to do an MRI, but decided he was moving too much for that and they didn't want to sedate him.

Happy Valentine's Day

Another clean scan on Tuesday, the 14!!!!!!!

He will continue the avastin infusions bi-weekly.  This is the stuff that suppresses blood vessel formation, and tumors need lots of blood vessels to feed them.  Side effect: high blood pressure.  So Conan is now on blood pressure meds. He also a big bad nosebleed a couple of weeks ago.

He also is continuing the temador for an undetermined length of time. Maybe as long as 2 years. This is the chemo, and the doc wants to be sure to kill any stray cancer that may be around. This causes nausea and the anti-nausea drug causes other issues, so more pills.

While everyone is thrilled there has been no regrowth, Conan was hoping to get off the monthly roller coaster that comes with the chemo dose.  So give him your best smiles and remind him you're glad he is here!

Scan today -- Nothing new

Continuing the course:  Chemo pill (temodar) 5 days this week, avastin IV at the hospital today.

Conan's blood pressure is running high (a temporary side affect of the avastin) so he is on blood pressure medication too.

Other than a REALLY long day today (MRI & lab work early this morning, doc running late for afternoon appt, and then still have to wait for IV time), it was a good day.

Check-up good -- continue the course

Monday, Conan had blood work and his second Avastin treatment at UIHC.  That night he started his second set of temodar (5 days, at home).

Blood work came back as expected, white blood count good, platelet count starting to dip a bit as chemo is hard on that mechanism.  All numbers good enough to start the second round of chemo.

The average for this regimen is six months.  And so that's the target they are shooting for now.

Henry started to really crawl the last couple weeks and is providing lots of giggles and love.

Chemo plan

Temodar (in pill form like before) starting now for 5 day cycles once every 4 weeks.  Not sure of the duration yet, but we'll see how things go.

And then in two weeks Conan will also start Avastin.  It will be given via IV once every 2 weeks at UIHC.  This is to interrupt blood supply to the tumor area.  It is used for other types of cancer but it's use for brain tumors is a newer treatment.  Again, not sure of the duration, but docs will monitor his ability to weather the drugs.

All of this feels deflating after being so pleased that the surgery went well, but it's all just part of the climb back to wellness.

Continued Recovery

Recovery is going well.  Conan proved me wrong and put in an appearance at his Soccer Camp on Thursday.

He is still on some meds to help reduce the brain swelling and they have some side effects: most annoying for Conan are weight gain and trouble sleeping.  He will start to taper off those soon though.

Next step will be the chemo plan.

Argus - July 15

Discharge

And here's what's waiting for them!

Eye exam went well.  Conan's vision had already improved some from Saturday.  I think the message they got was "of course you are having trouble seeing, you had people tramping around in your brain 3 days ago."

However, he hadn't had trouble before and the neurologist wanted to rule out any new problems, so I think they are glad it was checked. (Even though they had to wait a long time and missed lunch!)

Conan is being discharged later today.  They will stay at our special B & B in Iowa City tonight to rest up before returning home tomorrow.

Post-Surgery

Sunday, July 10:
9:00 pm: Conan took a shower this afternoon and put on shorts & a t-shirt instead of a hospital gown -- just one more step towards person and away from patient.
Right now, I'd say his condition is like someone that has a concussion.  He's mostly ok, but everything's not quite normal.  

2:00 pm: Doc was in early today, continued progress. Conan is scheduled for a complete eye exam and review tomorrow; he is having some trouble with his peripheral vision in his right eye.  Cognitive and neuro-motor assessments are not raising any big concerns. A discharge date is not yet set.

And if you didn't see a QC paper this weekend, they ran two short stories about Conan:
Friday Paper
Saturday Follow-Up (There were enough calls on Friday asking how surgery had gone that the reporter called looking for info)
The Friday article said he wanted to be at soccer camp this week;  I don't see that happening, but that's ok.

Saturday, July 9:
9:00 pm: Conan was able to eat something tonight and talked with Gretta more this afternoon.  He also had a short visit from Henry -- father & son enjoyed it!  Still lots of sleep and rest.

1:00 pm: Doc was in -- MRI looks normal too.  Second time around is just more traumatic to the brain, so recovery will take a little more time.  He sounds more like himself this afternoon, but sleep is still the king.

noon:  Conan is still very tired, sleeping more than he is awake.  He has had a CT and an MRI this morning.  The CT results came back normal and we are waiting to hear about the MRI.

He is taking some pain meds, but not a lot.  If you ask him, he says it hurts a little.  He has been out of bed a little bit, but mostly just wants to sleep.

Gretta is feeding Henry now, Conan is sleeping, more later.

Surgery Day

10:00 pm: The nausea continued most of the day and he slept more than he was awake.

2:30 pm: Parents, sisters, & Betsy have been in for short visits.  He is doing well but a little nauseous.

12:30 pm: He is in his room and Gretta & Henry are with him.

10:35 am: Just got a call.  Surgery done, Conan in recovery, responding to commands but pretty groggy.  Gretta will be able to see him in 30 to 40 minutes.
The surgery went as planned.  The tissue that was removed was about marble sized and appears to be all of it.  It will be sent to pathology for further analysis.

7:30 am: Conan just went back for surgery.  They have 7 hours set aside for him today.  Gretta & Conan got to the hospital at 5:30 this morning for his prep stuff.  I will post updates as I get them.

Surgery Scheduled for July 8

Waiting these last three weeks has been very tough, but getting the news they were hoping for was a huge relief.

Surgery will be Friday in Iowa City (time TBD).  The surgeon's plan is to remove the new growth and the remaining 'old' part.  Notes from September 2010 put the dead cell stuff at 5 mm x 5 mm x 5 mm (I looked at my tape measure!); in June 2011 it was 7 mm x 7 mm x 9 mm. This still seems pretty small and so we have hope that the surgeon will be able to execute his plan. (After all this isn't rocket science!)

Conan is expected to be in the hospital until Monday.  In August, he will meet with the oncologist to hear the chemo plan.

If you see Conan around town, ask him for a bracelet.  He is hauling around a box of brain cancer awareness bracelets: No One FIGHTS Alone!  All the support we are receiving from friends and family is appreciated and Conan knows he is not alone.  So continued thanks and appreciation for all your thoughts and prayers.

Cancer Sucks

The Dalton Family (Henry 7 mos.)

Conan's scan today revealed some small changes to the tumor.

The scan today was a standard checkup. As part of the regular checks, he sees both the oncologist and the radiation oncologist. They both recommended having the neurosurgeon review the MRI and Conan will meet with him on July 5 to discuss the best options.  This does feel like a punch in the gut, but the prognosis is still positive.

At first I wanted to stomp my feet and scream and yell, but that doesn't make it better.  This is disappointing and we had gotten use to a 'no change' headline, but we knew this day would probably come. It has been almost two and a half years since any chemo, so I am thankful to have had that long without any changes. Waiting will again be a tough part.  Conan and Gretta are scared, but strong in their resolve to always get the most out of life.