Dropping back down around 90.. Bouncing from 90-93 just sitting =( Getting winded just walking around the house. Going to see Dr. Sindel tomorrow at 3. Say an extra prayer =)
You guys are in my prayers! I am so glad you found me! I love your blog... The port posts were very descriptive. I love my port way better than piccs!!
I hope that Michael's CF visit goes well tomorrow. It sounds like he needs help of SOME type. I only use O2 at night and when I'm exerting myself.
Even if M needs O2 right now, it doesn't mean it's a permanent thing. I went on it for about 2 mos. and then got to go off it again for several mos. I don't have an sat meter (can't remember what they're called!) so they told me to play it safe and just use it those times.
Anyway, I hope M feels better soon. Oh, and I like your Nasty/Positive game!
Im Kellee! An overly compassionate twenty something year old with the world on my shoulders. I am insanely in love with my very bestfriend,husband, and hero *M* a 25 year old cystic fibrosis patient full of crude humor, inapproiate behavior and a heart of gold.
Together we will write this blog to keep up with all our laughs, tears and priceless memories.
M..The apple of my eye, reason for my smile and thief of my ♥ Hes the most handsome, brave, funny, smart and inappropriate person I know. To know and Love M is a blessing! Hes fixer of all broken things, the creator mf my insanity, avid gamer, treatment avoider and the best mac & cheese maker ever but most of all hes my ♥ & HERO!
Yours Truly
K..The face behind this blog. Lover, fixer, peace keeping, treatment fixer, CF nagger, blood sugar checker, destroyed toy picker upper, back scratcher, poo pick up lady, advocate for whats right, fighter for the underdog and last but not least bubble bath queen ;)
Slimer
AKA Destroyer of all things!! Toy eater, drool bucket, snorting beast..This floppy jawed fellow has won me over..Bad gas and all. He smells up my house hes rude, crude and has managed to eat 1/2 of my things but he is by far the coolest dog I have EVER met. His personality is not even something I can describe..hes very much a 5 year old boy in a english bulldogs body!
Make sure you go HERE to support Cystic Fibrosis!!
Michaels Current Medicine List
Zithromax 500 mg. M-W-F Lexapro 10mg BID Plaquin 500mg BID Naproxen 500mg BID Sulfasalazine 500mg BID Previcid 30mg in the A.M. Enalipril 2.5 in the A.M. Uniphyl 500mg at night Vitamin E ADEK Pancrease MT16 10 with meals 7 with snacks Humalog 1 unit per 10 carbs so really ALOT Lantus 37 units at night Albuterol TID Pulmozyme BID 7% TID Advair 2 puffs BID
You guys are in my prayers! I am so glad you found me! I love your blog... The port posts were very descriptive. I love my port way better than piccs!!
ReplyDeleteXo
Somer
Ditto on what Somer said. The CF community is a wonderful thing!!!
ReplyDeleteThanks for visiting my blog today.
ReplyDeleteI hope that Michael's CF visit goes well tomorrow. It sounds like he needs help of SOME type. I only use O2 at night and when I'm exerting myself.
Even if M needs O2 right now, it doesn't mean it's a permanent thing. I went on it for about 2 mos. and then got to go off it again for several mos. I don't have an sat meter (can't remember what they're called!) so they told me to play it safe and just use it those times.
Anyway, I hope M feels better soon. Oh, and I like your Nasty/Positive game!
Praying for M and for you Kellee:(
ReplyDeleteM