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9 mos post op update

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  • #1

    9 mos post op update

    WOW!!!! 9 months have gone by already....It is truly amazing, that the surgery is over and things are back to normal. Megan is doing really well...We go back for x-rays 9 days before her 1 year anniversary. Hoping that all of your kiddos are doing well, and always praying for those of you who are about to go thru it........Hugs Tracy

    Thought I would share Me and Miss Megan on Easter.......

    www.caringbridge.org/visit/megansheppard
    Last edited by MegansMom; 05-02-2006, 09:18 PM. Reason: add something
    Wife to Scott, the most incredible man God put on this earth, Mom to Joshua who is 16 1/2, Megan who is 11 with CP, seizure disorder, sleep apnea, coritcal visual impairment, non mobile, non verbal, and scoliosis, but the GREATEST blessing we could of ever hoped for,who had posterior spinal fusion surgery on July 19th, 2005, fused from neck to bottom and has the titanium union rod wired in place. and Jacob 3yrs.....Can't forget our16 mos old golden lab puppy, Molly.....
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  • #2
    Tracy,

    Time has surely flown by....thanks for sharing the pic of you and Megan. You both look like you're doing well! Take care,

    Renee

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    • #3
      Hi Tracy
      Megan is looking terrific!! Glad to hear everything is going great for you people.
      Hugs
      Lorrie

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      • #4
        Way to Go Megan and mom! Its amazing how time flies. Glad to hear things are going well.
        Carmell
        mom to Kara, idiopathic scoliosis, Blake 19, GERD and Braydon 14, VACTERL, GERD, DGE, VEPTR #137, thoracic insufficiency, rib anomalies, congenital scoliosis, missing coccyx, fatty filum/TC, anal stenosis, horseshoe kidney, dbl ureter in left kidney, ureterocele, kidney reflux, neurogenic bladder, bilateral hip dysplasia, right leg/foot dyplasia, tibial torsion, clubfoot with 8 toes, pes cavus, single umblilical artery, etc. http://carmellb-ivil.tripod.com/myfamily/

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