Shalon's AVM Story

Contact Me

I would love to hear from you!
 

My "Blog" -has moved to blogger!

I finally decided that I wanted a real blog instead of this "fake" one. 
 
So all future posts will be at my NEW blogsot http://shalonavm.blogspot.com/ 
 
You can also subscribe to this new blog.  Just scroll to the bottom of the blog page and click where it says "Subscribe to: Posts (Atom)" which will set you up with a "feed" and will allow you to stay in the loop!
 
Goodbye fake blog...you really weren't that cool...
 
Just to clarfiy (as some people were confused.)  This website is still my website, the meat & potatoes (well tofu & potatoes) of my story.  The new blog is now just a "sub-site" of this one as it has better functionality for me, allows you guys to stay in the loop, and even will allow you guys to leave "comments" about individual posts if you wanted.  I don't plan on taking down THIS site or discontinuing updating other pages on this site.  The blog is just in addition to it!

Random places my website pops up!

posted ‎‎Aug 14, 2008 5:43 PM‎‎ by Shalon Whitgob

So Josh had posted my site on his LandCruiser forum a while ago just to chat with his LC friends and such. 
 
Today I was looking for AVM info and found a website affiliated with Stanford called "wellsphere."  I'm not exactly sure what it is, but they have an area called WellMix 360 and it shows trusted sources, web results, blogs & news, etc.  http://stanford.wellsphere.com/wellmix360/arterio-venous-malformation
 
Anyways, Josh's post on Ih8mud comes up under the "blog & news" section.  So that was neat.  Totally random and round about...

Thanks!

posted ‎‎Aug 12, 2008 2:02 PM‎‎ by Shalon Whitgob   [ updated ‎‎Aug 12, 2008 2:09 PM‎‎ ]

Just wanted to say a quick thanks to eveyone who participated in our fundraiser this weekend.  It was a perfect weekend for our goodies.  Not too hot (like it can be in Sacramento in August!) but just warm enough to make our summer time treats hard to resist!  We sold lots of popcorn and snow cones and handed out quite a few "business cards" to help spread the word about my website.  I really appreciate the donations we have also received from both friends and strangers.  It is so wonderful to have so much support!
 
Also, wanted to say a special thanks to Carrie, Jenn, & Danielle for organizing and running this event!  You ladies are the best.  xoxo

A little less scabby today!

posted ‎‎Aug 6, 2008 3:05 PM‎‎ by Shalon Whitgob

So when I got to HBOT today I noticed that the gigantic scab on my face from last months embo, was kinda loose and hanging.  A little nudge and it came off (I promptly threw it on the ground and stomped on it with a "good riddance!")  So now there is a little bit of an ugly scar, but who cares!  It is much better than the wound.  I updated my "Timeline Pics" with a new one from today w/o the scab!
 
Now I just need my lip and my hole to finish healing!  Progress!

Another Facial AVM

posted ‎‎Aug 5, 2008 1:34 PM‎‎ by Shalon Whitgob

I have been emailing for the last few days with a guy who also has a facial AVM.  He has opted for surgery instead of embos.  Him and I have had a friendly debate over the benefits of each treatment and agree that we would make a great "case study" to see how the two options are both similar and different, which is better, and what the long term results are.  So here is the story he sent me detailing the last 32 years for him!
 
I was born 8/9/76 with what appeared to be a port wine stain on my right cheek. My parents were told it was a hemangioma and would go away by the time i was 6 or 7. It didnt. My parents found a surgeon to speak with (Mt. Sinai hosp) and his recommendation was surgery (at this point the term AVM didnt exist). My parents (and i guess myself, i was 6) felt that was a drastic route to take so they sought another opinion, a Dr. Sedak Hilal. He had a new procedure (that i believe he was part of pioneering) called embolization. A non- surgical way to control the growth. So rather than a massive invasive surgery, we could work on it with a non-invasive, less risky, procedure (though still very risky, stroke, etc) I had 2 embolizations at the age of 6 1/2 and 7. Then another at 10 (with minimal improvement in size, it would come down, then pop back up (it was always swollen, even from birth).
 
At the age of 14 or so (when i hit puberty) we saw a large growth in the AVM and decided it was time to explore surgical options. We met with a Dr. Mark Sultan (columbia presbiterian, recomended by Dr. Hilal). And the plan was to operate (nov. 19th, i remember that date well for some reason)...but in the preparation for this i had visited with a neurosurgeon who felt that the AVM was too massive and that any attempt to remove it would be seriously life threatening. So we backed out and I had 6 embolizations in a 9 month period (my 10th grade of H.S). Dr. Hilal also had developed an experimental substance (he called the Hilan Gel) similar to the glue they now use...it worked, but again not for long.
 
At the age of 17 it began to grow again, this time more than ever before. It got to a point of ulcerating the skin and bleeding from the surface (up to this point, unlike you, i had never dealt with bleeding). This scared me, so i sought a dr. that Dr. sultan had said he had trained under in Boston, a Dr. Mulliken. He saw me and said there is only one thing to do. and i quote "Remove that sucker." He at the time had operated on 12 AVM's similar to mine and that was considered alot. He was considered at the time ('95) the worlds leader in this. So we went ahead with the surgery. 2 preop embolizations, and 21 hours of surgery later, I made it. They had to use skin and tissue from my abdomen in whats called a tissue transfer to make up for the loss of pigmented red skin etc.. It looked ok, but one more surgey later, it looked alot better. I had another surgery in '97 then again in 2000.
 
The problem now is regrowth. It continues to want to proliferate itself. So from 2000 to 2004 i left it alone, fed up with it really. It continued to grow. So finally in 2004 i decided to go back tothe dr's i once saw in NY (dr. sultan) and see what if anything new is out there. He sent us to Dr. Alejandro Berenstein (who you should know, the pioneer of the alcohol embolizations, and the absolute best at what he does (endovascular surgeon))...He told us about this amazing doctor, Dr. Waner, who is coming to NY soon. Timing was perfect as I was one of the first patients he treated in NY. He operated in 2004, then i had follow up cosmetic procedures (3 of them) with another surgeon (which didnt work out so great) But am now back with Dr. Waner ( i had my most recent surgery in April, i have one scheduled for october and then, i think thats it. Hopefully. And it looks amazing.

To Blog or not to Blog

posted ‎‎Aug 5, 2008 7:47 AM‎‎ by Shalon Whitgob   [ updated ‎‎Aug 5, 2008 1:41 PM‎‎ ]

So I'm totally annoyed that Google Sites doesn't allow you to have a REAL blog on your site.  I'm thinking of ditching this fake one and just linking to a blogger site.  Plus maybe that will help spread the word a little more, since there would be another place for people to "find" me.
 
I have been talking with a lady in TX, Cyndi, who has a facial AVM and is being treated by Dr Yakes as well.  I bullied her into letting me create a blog for her so that she can post updates about her journey.  Once it is ready to go I will link to it as well for anyone who is interested.

Website is all up to date!

posted ‎‎Aug 2, 2008 10:26 AM‎‎ by Shalon Whitgob

I finally finished updating my trip reports under the "Denver Trips" page.  All of the Medical Mumbo Jumbo took a long time to type up and a lot of spell checking!
 
I also wanted to say thanks to everyone who has signed my guestbook and sent me emails with such wonderful and encouraging words.  I really do appreciate all of the support from family, friends, and strangers (new friends!)  I've also been very welcomed at the new AVM Support Network that I joined.  It is mostly "brainers" and I haven't heard from any "no-brainers" yet but still am excited to have found the website.
 
I'm feeling well but still super freaked out about the hole in my face.  It is seriously gross and actually leaks grodiness like saliva, water, or whatever I put in my mouth!  Brushing my teeth is fun cause when I rinse my mouth it comes out my hole...  Ya...  But I'm learning how to keep it to a minimum and seriously trying not to imagine it healing without closing up and leaving a permanent hole in my face!  But normally I don't have that kind of bad luck.  In my family we leave bad luck to my sister Taryn!!!  ha ha ha

Hole in my face!

posted ‎‎Jul 29, 2008 2:52 PM‎‎ by Shalon Whitgob

So ya...the new wound on the side of my face has a hidden bonus! 
 
I actually have a hole going from the inside of my cheek all the way to the outside where the scab is.  Grody!  And it's infected...again.  I'll spare you all the seriously gross details but let's just say that this is not my favorite new manifestation of the AVM.  Otherwise I'm feeling pretty good.  A few bleeds over the weekend, one more concerning than most.  I saw my dermatologist yesterday (I haven't seen her since April) and she was very excited about the change in my face and lip from the embos.  She said she could definately notice the decrease in size and that the coloring was looking better.  So that was great to hear!!!

My first Blog!

posted ‎‎Jul 23, 2008 11:05 PM‎‎ by Shalon Whitgob   [ updated ‎‎Jul 23, 2008 11:24 PM‎‎ ]

So this is my first post for my new "blog."  And the entire point is to tell you all how I am feeling and coping with the AVM and treatment.  I promise that no other updates will be this long!  But as the first post, there is a lot to tell you!
 
I’ll start out by saying that six treatments into this journey with Dr. Yakes, I have realized that I was not prepared for all that this would entail.  I thought I was totally capable of continuing life as normal and doing these treatments as often as my life would permit.  I was going to fit it into my schedule and make it work on my time.  For those of you who know me, you know I’m just a “little” bit of a control freak and perfectionist.  And by little, I really mean a lot.  So even though I knew that once I jumped into and commit to this endeavor that it would impact my life, I really thought I would be able to control how much of an impact it was going to be.  But this AVM has a mind of it’s own lately and has completely humbled me and shown me that I am not the Super Woman that I thought I was, and that control was something I had to accept was not going to be mine.
 
I’m feeling pretty good right now as I type this.  Sure I look like a poster child for domestic abuse and I’m rather afraid to be out in public due to the continuous fear of bleeding, (like at the grocery store the other day...how unsanitary is that?!?!?) but I feel rested and stronger than I have in a long time.  If I had written this only two months ago, it would have been a completely different tone and a completely different story.  May 20th was when things really fell apart for me.  It had been coming on for a while, but that was the day that did me in. 
 
For months I had been in a lot of pain.  The most pain on a continuous basis as I have ever experienced.  I was taking Tylenol like it was candy, knowing that this excess was bad for my kidneys.  But that was the least of my worries and at least something that I could joke about.  I couldn’t sleep and I was run down, seriously.  This was in part due to the pain but also because I was afraid of bleeding in my sleep and not knowing.  See the wound on my lip continued to deteriorate and I began to have bleeds directly from the wound.  My previous bleeds had all been inside my mouth.  As gross as that is, I would wake up at the taste and could take care of the bleed.  But now I was worried that I wouldn’t know.  That I wouldn’t wake up and that I would lose a lot of blood before I was aware.
 
But I soldiered on, cause that is what I do.  I tried not to let it affect me at work and I tried not to really let on with my group (I manage 14 employees) how much pain I was really in and how much this was really wearing me down.  But they could tell, and they were worried.  No amount of parading around in new high heels (really I don't have a shoe problem) was going to distract them from noticing the change in me.  I didn’t want to show my weakness but also was grateful for the genuine concern that I got from them on a daily basis.  I really only shared my struggle with a few people at work, including my girlfriend Janine.  She was the person that helped me through my scary bleeding episodes at work.  And it was her that started trying to convince me that I needed to take some time off from work and focus on my health.  But that would be admitting that I wasn’t capable of doing everything and I just wasn’t ready to admit defeat.
 
Then May 20th rolled around.  I was actually only working a half day because I was headed down to UCSF to meet with the Chief of Plastics to get an opinion on what to do about my lip!  All of my trips to the dermatologist had not provided any real results and she had finally decided that she just didn’t have the expertise to deal with the AVM aspect of my wound.  But before I could even make it halfway through the day, I had a bleed at work.  And this one was super scary, not to mention embarrassing.  I was talking with a vendor in the lobby and literally had to run away from him as blood started pouring down my face.  I ran to the bathroom but had so much blood on my hands that I couldn’t get the medicine cabinet open to get some gauze.  I busted into our training center where I knew Janine was in a meeting and she ran to help me.  Of course I was able to stop the blood flow, but the bathroom was a mess and we basically had to “quarantine” it until it could be cleaned up.  I was shaken and embarrassed and just unhappy.
 
Josh came to get me, and we headed down to the city to meet with Dr. Hoffman.  Unfortunately my day just got worse as he recommended that in order to close the wound, we do surgery.  He suggested cutting a chunk out of my lip where the wound was, treating some of the AVM tissue in that general area, and then hoping the new wound would heal up.  We talked in length about potentially just going in and cutting out the AVM altogether.  I was honestly devastated.  I didn’t want to do a surgery.  All of my doctors up until that point had warned against trying to surgically remove the mass.  I was worried about the amount of AVM flow in the area and what kind of can of worms would be opened during surgery.  I worried that there was too high a risk for blood loss and damage.  And I couldn’t logically understand how creating a bigger wound than I already had was going to instigate healing.  I was scared and tired and just confused.
 
I took the next day off from work, and the next.  I talked with Dr. Hoffman by email, and I talked with Rhonda, Dr. Yakes PA, over the phone.  I decided that I did not feel like surgery was a good option.  I was scheduled for another trip to Denver the first week of June and decided I would have Dr. Yakes treat my lip specifically and hope that he could reduce the AVM activity, thus restoring some of the normal blood flow to the area and hopefully healing would then be an option.  I also began my search for a Hyperbaric Oxygen facility that would see me.  And as much as I hated to do it, I talked with my boss and with HR about arranging a LOA from work.
 
I felt very guilty about just “ditching” my group out of the blue, but there was no way that I was strong enough physically or mentally to go back to work.  I went to Denver in June, and again in July.  Both treatments focused on my lip.  And I started HBOT (hyperbaric ox) daily M-F.  The bleeding episodes are way down and much less severe than they were.  And the pain is much more manageable.  Some days I’m not in pain at all.  The wound on my lip is still ugly but I am finally convinced that it is healing…slowly.  Unfortunately this last treatment in July created more tissue breakdown on the side of my mouth.  So I now also have crazy, ugly wounds all scabbed up there too.
 
But I’m focusing on me and my health.  I am not worrying about anything else and I think it makes all the difference.  I can feel that I am healthier and better prepared to deal with the non-healing wound and the embolizations.  I can feel that my body is ready to work and fight to get well.  I wanted to be the perfect “sick” person.  I wanted to prove that I was capable of doing everything.  But I wasn’t.  I’m not.  And I know that it doesn’t make me less of a person, or a failure.  In fact, I am more proud of myself now for admitting when I needed to take a break.  For knowing that my health was more important than my Super Woman status.  For finally deciding that “I” was important enough to be my sole focus for now.
 

So I’m feeling good.  I’m not great, and I think I will have some more stumbles along this journey.  But I’m looking down the road to when I defeat this stupid AVM.  To the time when I won’t have to worry about this on a daily basis.  A time when I won’t wake up in a panic when my hair accidentally tickles my face.  A time when people won’t look at my wonderful husband like he must be abusing me!  I’m excited to have there be an end to this.  I know it is a long way down the road, but it’s there.  And I’m holding onto it.

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