Guest guest Posted April 20, 1999 Report Share Posted April 20, 1999 Capri, so sorry to hear that you and had such a hard time of it. Is he having an endoscopy? What sedation will they use? Macey had one in May of last year and did fairly well. They biopsied for the hpylori and looked at her stomach muscles and a few other stomach things. All that turned up was that she had some stomach muscle damage from her reflux and pneumonia's. Her GI said that might cause intermittent aches and pains. Good luck with your trip. Any chance of heading up the night before? We also have a 2 hr drive ahead of us when we take Macey to Atlanta and we go up the night before and stay at the Mc House that is associated with the hospital. They only charge $10 for the night and provide you with meals. You just have to tidy after yourself. Might be a thought. Driving 2 hrs before having to deal with all of this might prove a bit too stressful. Ursula Holleman Macey's mom (3 yr. old with CVID, asthma, GERD, sinus disease, grade I left kidney reflux, Sensory Integration Disorder) ICQ # 28592349 http://www.icq.com PedPID email list archives http://www.netpage.org/PedPID/_PedPID/ PedPID email list introductions http://www.netpage.org/PedPID/_PedPID/introduction.htm Day of Pain! From: Peacvalley@... had his IVIG today.... One horror story after another..... We used the ELMA with siran wrap on his good arm.... All his veins in that arm floated out.... two were great and collapsed as we tried to hook up to the IV. It took 4 sticks (in his other arm) before we got a good vein. By then, was hysterical, I took him outside after the third stick and he calmed down. We were told to make sure the ELMA is only on for an hour because the veins will constrict. Drink lots of fluids, which we do and pray..... Give me a break, tell me something new. and I prayed together for his veins to flow well and he talks to them on each stick. We finally get him hooked up and the reactions begin.... At a rate of 12 no reaction, go to 24 burning, eases off and then they increase to 36. He yells out and has intense pain in his arm, we back off to 24, apply ice, alternating with heat. Now has only mild burning and a slight headache. Increase again, major pain, back off to 24, mild pain and more head pain. (His bp and temp stayed within range the whole time). Finally, informs the nurse " Don't touch that IVIG, no more increases! It hurts to much. " Guess what, they actually listened. We got to New Orleans at 9 am, IV started at 11 am and finished at 5:20 pm. During this time his immunologist team comes in. (I know it means trouble, for usually only one sees him at a time.) We do an update to the past 4 weeks and they call in a Ped. Gastroenterologist. The Gastroenterologist wants to run a scope down 's throat to his stomach on Monday. He was inclusive as to what he thinks 's pains are. Maybe bacteria but possible bleeding ulcers also. I asked him about the blood test for bacteria and found out that with 's # s he would not have a positive response to it. He hasn't has a response to any of his antibiody/bacteria tests. Dr. , head of the immunology dept., also stated he wanted to monitor more closely and possibly increase his IVIG to 3 times a week. Scary, for I hear of children, including children in our network, being backed off and their talking of increasing during a shortage. I go from hearing for over a year that IVIG isn't available at this time to be here in 7 days to poss. increasing his amount and adding another specialist to his list. What's the deal? Can your #s crash over night? I know these are questions for his Drs. but it's been a lousy day and I need to vent. I hope to get more info on Monday. Maybe some unanswered questions, sometimes the answers are scarier then the questions though. Dr. also agreed that it would be more beneficial for if we could find a Ped. in Long Beach in case of an emergency. Jumping back, on Monday for his test, he has to be hooked up to IV and can't have any fluids after midnight. We have to be there at 6:30 am, leaving the coast at 4:30 am to make it and allow time to find a good vein. Now that I have vented to the max thanks for being there. I'm so tired of people telling me that it could be worse. Their right, but they don't have to watch their child continue to suffer. Pain is pain, and when a child hurts, it breaks a mom's heart. Capri, (mom to , Dx under investigation, PID, etc) ------------------------------------------------------------------------ Start a new hobby. Meet a new friend. http://www.ONElist.com ONElist: The leading provider of free e-mail list services! ------------------------------------------------------------------------ This forum is open to parents and caregivers of children diagnosed with a Primary Immune Deficiency. Opinions or medical advice stated here are the sole responsibility of the poster and should not be taken as professional advice. Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.