skip to main | skip to sidebar

About me

Dulce
From the AVM SURVIVORS web site: "Arteriovenous malformations (AVMs) are defects of the circulatory system that are generally believed to arise during embryonic or fetal development or soon after birth. Although AVMs can develop in many different sites, those located in the brain or spinal cord can have especially widespread effects on the body". I am currently undergoing embolizations with Dr. Wayne Yakes @ the Swedish Medical Center in Englewood, CO every 8 weeks! Our lives are either planning a procedure, having a procedure or recovering from a procedure! The trick lately seems to be to keep the "bleeds" under control! My husband Mark is also my caregiver! He has become an expert wound care therapist, not to mention all around bundle of being just exactly what I need to get through the day and this ordeal we call an AVM! I recently finished 10 years of Embolizations w/Dr. Yakes and am finally ready for my next stage - Debulking and reconstructive surgery w/Dr. Robinson in CO - he is a dentist and plastic surgeon! Best advice to an avm patient - Stay positive and surround yourself with supportive people! Lots of faith, prayer and love are all crucial too!
View my complete profile

Check out these links!

  • Shalon's blog
  • Shalon's Website

Archivo del blog

  • ► 2014 (3)
    • ► July (1)
    • ► May (1)
    • ► January (1)
  • ► 2013 (12)
    • ► December (1)
    • ► November (1)
    • ► October (1)
    • ► July (3)
    • ► June (2)
    • ► April (1)
    • ► February (2)
    • ► January (1)
  • ► 2012 (24)
    • ► December (2)
    • ► November (2)
    • ► October (2)
    • ► September (3)
    • ► August (4)
    • ► June (2)
    • ► May (2)
    • ► April (2)
    • ► March (1)
    • ► February (1)
    • ► January (3)
  • ► 2011 (24)
    • ► December (1)
    • ► November (1)
    • ► October (2)
    • ► September (1)
    • ► August (1)
    • ► June (2)
    • ► May (1)
    • ► March (4)
    • ► February (5)
    • ► January (6)
  • ► 2010 (30)
    • ► December (3)
    • ► October (1)
    • ► September (3)
    • ► August (7)
    • ► July (2)
    • ► June (3)
    • ► May (4)
    • ► April (1)
    • ► March (3)
    • ► February (1)
    • ► January (2)
  • ► 2009 (47)
    • ► December (6)
    • ► November (1)
    • ► October (4)
    • ► September (2)
    • ► July (5)
    • ► June (2)
    • ► May (3)
    • ► April (5)
    • ► March (6)
    • ► February (7)
    • ► January (6)
  • ▼ 2008 (27)
    • ► December (3)
    • ► November (4)
    • ► October (6)
    • ► September (7)
    • ▼ August (7)
      • Timeline photos!
      • Holy Saba! I named my kid Mackerel!
      • August 29th - New Ear Tube!
      • August 26, 2008
      • Denver 27
      • The beginning of my story...
      • Cyndi's New Blog!

Cyndi's AVM journey

Check out my Pictures at the bottom of the page!

August 26, 2008

Tuesday, August 26, 2008





Hi again!

Just for fun, I thought we would ad some photos of my little Saba! Our family was very involved in the Olympics as you can see!

Our favorite of course was Michael Phelps! Saba made sure she had the right suit, swimcap and goggles! Of course we had to be involved in the gold medal ceremony!

Ok! Back to avm stuff! I am doing great so far! Of course I'm on steroids - I only have 2 days left of them, darn! No more bleeds - which is awesome! Mark has been doing an amazing job keeping my wound area clean and dressed, so it is healing nicely! We're hoping by the time we go back to CO Oct. 6th, 7th and 8th - that the wound area will finally be closed after being so deep! Mark is so patient and takes the time to make sure the area is clean, puts more ointment, layers of dressings and makes sure we have all the supplies necessary! I'm currently trying to get off the Percocet and on to another new med that is not a narcotic! It's knocking me out though - but @ least I am getting some much needed rest! The one good thing is I've lost some weight. W/the meds, I can't drink and sometimes don't have much of an appetite. Right now I do though, w/the steroids! I'm just taking it one day @ a time and doing what I need to survive!
Thank you family and friends for looking in on myself and Shalons web sites! Shalon came along right when I needed that extra boost in dealing w/this avm! She is bringing so many people together that either have avms, or know someone that has one! Her web site is full of good, medical information and she puts a lot of work into it! I'm hoping in the future to make sure she and I meet up again during one of our appointments! Shalon does not stay overnight like I do though - she gets sent home after being in recovery for a while. I've come to like staying overnight because I get excellent care from the nurses @ Swedish and they have become friends! Here I am with a new nurse to me - her name is Gina and she and I bonded over knowing we love to read! She had just finished reading Pillars of the Earth, a recent favorite book of mine!
Please do check back periodically on both our sites, as I'm sure we will do our best to keep you informed on the latest! Thank you for all your prayers and support!

Cyndi Schuman

Posted by Dulce at 4:58 PM  

1 comments:

Anonymous said...

Cyndi you are my hero. I have had AVM in my left hand since I was 14 and it grew at 28 now I am 51. It's time that my thumb be taken off if they can only do that without taking alot more of my hand. I know the pain and all that other stuff, you know. I just wanted you to know I care. Hang TOUGH!!!!! God Bless you and keep you. Your friend Tweet

February 18, 2009 at 1:52 AM  

Post a Comment

Newer Post Older Post Home
Subscribe to: Post Comments (Atom)

Timeline Pics

Blog Design by Gisele Jaquenod