Author Topic: Special prayer request  (Read 10064 times)

free2be

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Special prayer request
« on: August 23, 2010, 07:28:24 pm »
This is off topic, but for my AN rad friends...a request. A dear friend of ours, a 9-year-old adorable, smart, artistic, smart little boy, was just diagnosed with a brain stem brain tumor. He only just started having symptoms, but we just found out it is taking up 85% of the brain stem (no I don't know how that is possible, but that's what I've been told) and is inoperable. Chemo was the only treatment that's been offered and apparently it is not usually effective. I don't know the type of tumor (biopsy is tomorrow). If anyone knows where might specialize in child brain stem tumors...it doesn't sound like the family is being offered much.

In the mean time, prayers, well wishes, miracles, anything would be appreciated. His name is Wylie.

Connie
Diagnosed Nov. 2008 Right AN 7 mm x 9 mm
Incremental MRIs enhancing mass
June 2010 1.4 cm x 0.9 cm extension into the CP angle
Pre-CK Stanford measurements 1.6 X 1.1 cm
9/29/10 - 10/1/10 CK completed with Dr Steven Chang and Soltys, Stanford.
6-month thru three year (8/13) follow ups MRI: stable

Larry

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Re: Special prayer request
« Reply #1 on: August 23, 2010, 07:38:46 pm »
Hi Connie,

This is so sad. I feel for the family and friends. When this happens at all, its not fair but for a kid - words fail me apart from wishing for a miracle.

There is a surgeon in Sydney - Dr Charles Teo at the prince of Wales Hospital in Sydney - details below, who is the only surgeon who will do "last gasp" surgery. He mainly deals with the brain. he is hailed as one of, if not the best surgeon in the country. You could always call him - not a lot to lose i guess.

http://www.neuroendoscopy.info/contactUs.asp

Laz
2.0cm AN removed Nov 2002.
Dr Chang St Vincents, Sydney
Australia. Regrowth discovered
Nov 2005. Watch and wait until 2010 when I had radiotherapy. 20% shrinkage and no change since - You beauty
Chronologer of the PBW
http://www.frappr.com/laz

iluuvpups

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Re: Special prayer request
« Reply #2 on: August 23, 2010, 07:40:07 pm »
I'm so sorry to hear about this.  Makes me very sad.  I will say a prayer.

Here are a few resources that others sent to me that may help:

http://www.braintumor.org/
http://www.dailystrength.org/c/Brain-CNS-Tumors/support-group
http://www.abta.org/

--Carol Ann
« Last Edit: August 23, 2010, 07:48:19 pm by iluuvpups »
Original 1.75cm left-side AN diagnosed Feb 2010
Translab surgery May 27, 2010 with Drs. Kartush and Pieper of MEI
SSD on left side, some facial weakness, tear duct doesn't work
Found I actually had a facial neuroma during translab
Remaining 6mm facial neuroma - watch and wait

leapyrtwins

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Re: Special prayer request
« Reply #3 on: August 23, 2010, 09:33:14 pm »
So sorry to hear this.  Prayers go out to Wylie and his family.

Children's Memorial Hospital in Chicago has a very well-known brain tumor treatment center.

Jan
Retrosig 5/31/07 Drs. Battista & Kazan (Hinsdale, Illinois)
Left AN 3.0 cm (1.5 cm @ diagnosis 6 wks prior) SSD. BAHA implant 3/4/08 (Dr. Battista) Divino 6/4/08  BP100 4/2010 BAHA 5 8/2015

I don't actually "make" trouble..just kind of attract it, fine tune it, and apply it in new and exciting ways

free2be

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Re: Special prayer request UPDATE
« Reply #4 on: August 23, 2010, 10:30:10 pm »
They believe it is a diffuse intrinsic pontine glioma. It seems they are doing a biopsy tomorrow, but from my research that isn't usually necessary or recommended; so, I'm concerned about that. But this is BAD if that's what it is. Definitely need to find the cutting edge docs on this if they can offer any hope. I'm still praying, but my heart is broken.

Connie
Diagnosed Nov. 2008 Right AN 7 mm x 9 mm
Incremental MRIs enhancing mass
June 2010 1.4 cm x 0.9 cm extension into the CP angle
Pre-CK Stanford measurements 1.6 X 1.1 cm
9/29/10 - 10/1/10 CK completed with Dr Steven Chang and Soltys, Stanford.
6-month thru three year (8/13) follow ups MRI: stable

Lizard

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Re: Special prayer request
« Reply #5 on: August 24, 2010, 08:20:38 am »
Connie,
I'm so sorry to hear about your friends son.  Although I do not know any Dr's who specialize in children's brain tumors I can only say if they are not happy with the Dr or Dr's they are currently seeing they should find another and quickly. 
I'll be saying my prayers.
Hang in there,
Liz
Left AN 2.5CM,retrosigmoid 11/2008, second surgery to repair CSF leak. 
Headaches began immediately.  Dr. Ducic occipital nerve resection, December 2011!!!!!

"When you come to the end of your rope, tie a knot and hang on"
-Franklin D. Roosevelt

lori67

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Re: Special prayer request
« Reply #6 on: August 24, 2010, 08:44:33 am »
Lots or prayers for that poor little boy and his family.  I can't imagine going through something like that.

In my opinion, the first place I'd be headed if he was my child would be to St. Jude in Memphis.  They do share all their research and findings with other hospitals, so any of the larger children's hospitals would be able to offer him excellent treatment, I'm sure.

I pray that his family stays strong to help him through this struggle.

Keep us posted.
Lori
Right 3cm AN diagnosed 1/2007.  Translab resection 2/20/07 by Dr. David Kaylie and Dr. Karl Hampf at Baptist Hospital in Nashville.  R side deafness, facial nerve paralysis.  Tarsorraphy and tear duct cauterization 5/2007.  BAHA implant 11/8/07. 7-12 nerve jump 9/26/08.

grega

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Re: Special prayer request
« Reply #7 on: August 24, 2010, 08:50:59 am »
Connie,

Wylie and his family are in my prayers.  

Here are a couple links that might help in your, and the family's, search:
Johns Hopkins:   http://www.hopkinschildrens.org/index.aspx
World-renowned Ben Carson at Hopkins specializes in pediatric surgery:  http://www.youtube.com/watch?v=IuYmhJUeoBE

Suggstion to Wylie's family ..... ask the local docs to tell them where they should seek treatment.  Hopefully they will get answers they so desparately need.

Greg


1.5 cm AN retrosig 11/04.
Drs. Henry Brem & Michael Holliday @ Johns Hopkins, Baltimore
SSD right. Tinnitus big-time, only when thinking of it.
BAHA since 7/20/10 ... really helps w/ hearing, specially after programming in subliminal message: "Hey, don't listen to your tinnitus!"

Jim Scott

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Re: Special prayer request
« Reply #8 on: August 24, 2010, 01:57:49 pm »
Connie ~

This is heartrending but of course little Wylie will be in my prayers.  I will pray for his parents too and that they'll be led to the right doctor to save their son's life, which appears to be in jeopardy. 

Thanks for posting this.  I've moved the thread to the AN community forum where it's more appropriate - and is likely to be seen by more people.

Jim
4.5 cm AN diagnosed 5/06.  Retrosigmoid surgery 6/06.  Follow-up FSR completed 10/06.  Tumor shrinkage & necrosis noted on last MRI.  Life is good. 

Life is not the way it's supposed to be. It's the way it is.  The way we cope with it is what makes the difference.

saralynn143

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Re: Special prayer request
« Reply #9 on: August 24, 2010, 05:32:19 pm »
I am so very sorry to hear this is happening to Wylie. He and his family are in my prayers.

Sara
MVD for hemifacial spasm 6/2/08
left side facial paresis
 12/100 facial function - 7/29/08
 46 - 11/25/08
 53 - 05/12/09
left side SSD approx. 4 weeks
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Rich56

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Re: Special prayer request
« Reply #10 on: August 24, 2010, 09:32:52 pm »
This is so.......sad.

We will keep little Wylie, and his family in our thoughts and prayers.

Rich & Scarlett
SML (Scarlett's) other half, she had - 1.5 cm x 2.5 cm Cystic AN - Right side
Retrosigmoid on 3/18/09 at MGH in Boston, MA. Dr. Barker & Dr. Lee of MGH/MEEI
no facial issues, SSD right side, balance issues to work on.
The AN Calendar is here: http://www.my.calendars.net/AN_Treatments

Soundy

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Re: Special prayer request
« Reply #11 on: August 25, 2010, 05:04:28 am »
This is so sad ... will keep him and his family in thoughts and prayers ...rock in hand as always

wanted to add  that as Lori said St Jude's does wonders with so many children with cancer ...something a friend and her family found out when her nephew was diagnosed with a malignant brain tumor about a year and a half ago

« Last Edit: August 25, 2010, 05:15:35 am by Soundy »
3mm AN discovered Aug 2004
Translab July 2 ,2007
3.2cm x 2.75cm x 3.3cm @ time of surgery

pjb

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Re: Special prayer request
« Reply #12 on: August 25, 2010, 08:52:53 am »
My thoughts and prayers are with him and his family........

Pat


Diagnosed with a 1 cm. AN had Retrosigmoid
Approach surgery July of 2009, several problems after surgery.

free2be

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Re: Special prayer request UPDATE
« Reply #13 on: August 25, 2010, 08:26:31 pm »
Thanks for the replies and prayers. Please keep them coming. Here is an update and a web site to visit him and send him notes. He would love getting some messages from other parts of the country and world. Tell him where you're from. That would be great!

Wylie had surgery/biopsy today and is in recovery and ICU tonight. He has two tumors; one seems to be calcified. They were able to remove about 30% of the other (active) tumor. They will have pathology back on the biopsy on Friday or Monday and know more then what they are dealing with for sure and what options may be available.
 
Please visit Wylie's Wish page below to learn more, keep informed, see pictures of this adorable boy, and learn how you can help. He needs all our prayers.
 
http://www.wylieswish.blogspot.com/


Blessings,
Connie
Diagnosed Nov. 2008 Right AN 7 mm x 9 mm
Incremental MRIs enhancing mass
June 2010 1.4 cm x 0.9 cm extension into the CP angle
Pre-CK Stanford measurements 1.6 X 1.1 cm
9/29/10 - 10/1/10 CK completed with Dr Steven Chang and Soltys, Stanford.
6-month thru three year (8/13) follow ups MRI: stable

free2be

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Re: Special prayer request
« Reply #14 on: August 26, 2010, 09:00:40 am »
Thank you Donnalynn for posting to Wylie's blog. That was very nice and heartwarming and cool!! I think he'll be excited to get messages from around the country and the world. Keep on blogging and praying. Updates on his condition will be posted to his blog as often as possible.

http://www.wylieswish.blogspot.com/

Connie
Diagnosed Nov. 2008 Right AN 7 mm x 9 mm
Incremental MRIs enhancing mass
June 2010 1.4 cm x 0.9 cm extension into the CP angle
Pre-CK Stanford measurements 1.6 X 1.1 cm
9/29/10 - 10/1/10 CK completed with Dr Steven Chang and Soltys, Stanford.
6-month thru three year (8/13) follow ups MRI: stable