Guest guest Posted October 27, 2004 Report Share Posted October 27, 2004 from Dale, Mom to Katy, CVID, age 20 Amy, I'm so glad you are getting some progress. I looked up his web-page and what a cutie! Hope he's feeling better soon. In His service, Dale Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 28, 2004 Report Share Posted October 28, 2004 hey, how is it going? we go for the first IVIG tommorow,,,, wish us luck with finding a vein... food trials failed again... but other than that we are goood. how is nick> and the rest of your family.. ' 3 month check with the immuno Hi all! Well Nick went to the immuno for his 3 months checkup after starting the SubQ. He was not at all pleased since in the three months he has still been sick almost all the time. So Friday they are going to try and give Nick a boost with a IVIG treatment thru the vein and then go back to subQ again. He said tho that they would just see how his veins looked. If they didn't get it Friday they would just keep looking each time he goes in until they are sure they will get the IV started on one poke. Also Nick will be starting rotating phrophlaxic abx. He will do 21 days amoxicillin and then 21 days Septra (if I spelled all the right) He will do this until April. He also put him on some other med, but I can't think of the name and the pharmacy didn't have it in so I will get it tomorrow. I think it was a decongestant of some sort. I hope this does the trick. The immuno's office called last night and heard Nick coughing and the nurse talked to the immuno and called back because they were concerned that it sounded like whooping cough. I called the ER and talked to a nurse there for an hour, she was so nice. She called our ped and he said to just up his flovent an xopenex treatments and he settled down finally at 1 am. That was the first sleep he had gotten in almost 40 hours. We were so glad. Amy, mom to: , 22 months old. CVID, MSPI, GERD, Asthma.. On claritin, flovent, xopenex, and SubQIG every two weeks (Carimune NF) visit Nick's website: http://www3.caringbridge.org/ne/nicholasb/<http://www3.caringbridge.org/ne/nicho\ lasb/><http://www3.caringbridge.org/ne/nicholasb/<http://www3.caringbridge.org/n\ e/nicholasb/>> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 28, 2004 Report Share Posted October 28, 2004 Thanks Kathleen, we are all doing okay. Nick has one heck of a sinus infection and bronchitis again. We will be doing the vein thing tomorrow too. Good luck and we will keep Conan in our thoughts tomorrow. Post an update when you can. Amy ' 3 month check with the immuno Hi all! Well Nick went to the immuno for his 3 months checkup after starting the SubQ. He was not at all pleased since in the three months he has still been sick almost all the time. So Friday they are going to try and give Nick a boost with a IVIG treatment thru the vein and then go back to subQ again. He said tho that they would just see how his veins looked. If they didn't get it Friday they would just keep looking each time he goes in until they are sure they will get the IV started on one poke. Also Nick will be starting rotating phrophlaxic abx. He will do 21 days amoxicillin and then 21 days Septra (if I spelled all the right) He will do this until April. He also put him on some other med, but I can't think of the name and the pharmacy didn't have it in so I will get it tomorrow. I think it was a decongestant of some sort. I hope this does the trick. The immuno's office called last night and heard Nick coughing and the nurse talked to the immuno and called back because they were concerned that it sounded like whooping cough. I called the ER and talked to a nurse there for an hour, she was so nice. She called our ped and he said to just up his flovent an xopenex treatments and he settled down finally at 1 am. That was the first sleep he had gotten in almost 40 hours. We were so glad. Amy, mom to: , 22 months old. CVID, MSPI, GERD, Asthma.. On claritin, flovent, xopenex, and SubQIG every two weeks (Carimune NF) visit Nick's website: http://www3.caringbridge.org/ne/nicholasb/<http://www3.caringbridge.org/ne/nicho\ lasb/><http://www3.caringbridge.org/ne/nicholasb/<http://www3.caringbridge.org/n\ e/nicholasb/>><http://www3.caringbridge.org/ne/nicholasb/<http://www3.caringbrid\ ge.org/ne/nicholasb/><http://www3.caringbridge.org/ne/nicholasb/<http://www3.car\ ingbridge.org/ne/nicholasb/>>> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 29, 2004 Report Share Posted October 29, 2004 hey, IVIG, went well how bout you guys... ' 3 month check with the immuno Hi all! Well Nick went to the immuno for his 3 months checkup after starting the SubQ. He was not at all pleased since in the three months he has still been sick almost all the time. So Friday they are going to try and give Nick a boost with a IVIG treatment thru the vein and then go back to subQ again. He said tho that they would just see how his veins looked. If they didn't get it Friday they would just keep looking each time he goes in until they are sure they will get the IV started on one poke. Also Nick will be starting rotating phrophlaxic abx. He will do 21 days amoxicillin and then 21 days Septra (if I spelled all the right) He will do this until April. He also put him on some other med, but I can't think of the name and the pharmacy didn't have it in so I will get it tomorrow. I think it was a decongestant of some sort. I hope this does the trick. The immuno's office called last night and heard Nick coughing and the nurse talked to the immuno and called back because they were concerned that it sounded like whooping cough. I called the ER and talked to a nurse there for an hour, she was so nice. She called our ped and he said to just up his flovent an xopenex treatments and he settled down finally at 1 am. That was the first sleep he had gotten in almost 40 hours. We were so glad. Amy, mom to: , 22 months old. CVID, MSPI, GERD, Asthma.. On claritin, flovent, xopenex, and SubQIG every two weeks (Carimune NF) visit Nick's website: http://www3.caringbridge.org/ne/nicholasb/<http://www3.caringbridge.org/ne/nicho\ lasb/><http://www3.caringbridge.org/ne/nicholasb/<http://www3.caringbridge.org/n\ e/nicholasb/>><http://www3.caringbridge.org/ne/nicholasb/<http://www3.caringbrid\ ge.org/ne/nicholasb/><http://www3.caringbridge.org/ne/nicholasb/<http://www3.car\ ingbridge.org/ne/nicholasb/>>><http://www3.caringbridge.org/ne/nicholasb/<http:/\ /www3.caringbridge.org/ne/nicholasb/><http://www3.caringbridge.org/ne/nicholasb/\ <http://www3.caringbridge.org/ne/nicholasb/>><http://www3.caringbridge.org/ne/ni\ cholasb/<http://www3.caringbridge.org/ne/nicholasb/><http://www3.caringbridge.or\ g/ne/nicholasb/<http://www3.caringbridge.org/ne/nicholasb/>>>> Quote Link to comment Share on other sites More sharing options...
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