Guest guest Posted July 2, 2008 Report Share Posted July 2, 2008 , I want to reassure it is really very easy. My son is bipolar, has panic attacks and severe anxiety. He was terrified. The needles are extremely small. Only 6mm. We now use the 9mm so that it goes in a bit deeper. We also do not use his abdomen because he says it hurts a lot more. I use his love handles on his hips. I also have an agreement with him that I give it to him when he sleeps. He knows it is going to happen but he just goes back to sleep now. I do still have some times where he panics a little bit but we enventually get it in. Lucas had IVIG for 6 years and I think really liked the attention he got with going to the doctors office. This is sooooo low key because you JUST DO IT each week. My son will not let me use emla anymore. He does not like the feeling of the cold and numb and would prefer just getting the poke. My son is 110lbs so is larger but..... we use 30cc per site on his hips and we no longer get any bumps at all. So the swelling is only in the first couple of months and then the tissue begins to stretch and the bumps go away. Sometimes it get a bit red in the beginning and then we now no longer even have that. I do get tired of getting up during the night( early morning) to give it to him. But... that is my problem not his. I think the greatest part of it is the simplicity and low techness of it all. It just allows my son to feel much less tied up in the medical system. Feel free to ask as many question as you have. I would NEVER go back to IVIg unless there were no other choices. Also there are not reactions that I know of. Very different than IV since it absorbs slowly and is much better tolerated. Also another perk is his fatigue has gone away. We never have that 3rd week crash. He has much fewer infections and he just feels better overall. Hope this helps. BARBIE From: rfrench496 <bluemtnfarm@...> Subject: subQ questions Date: Wednesday, July 2, 2008, 6:43 AM Okay, ladies, give it to me. We have loved our home infusion IVIG, but last month was difficult and yesterday was a nightmare. It got to the point yesterday where the back up nurse blew 3 veins and the IV team from our hospital had to come and start his IV. They said his veins were spasming and hard, couldn't advance the IV. It took 4 hrs to get the IV in. Not anxious to do that again. Our immuno said we could try subQ for a month and see if we like it. These are my questions/concerns: 1. Mark is very scared of the " shot " . I am concerned about giving him 2 pokes in the belly every week, versus once a month. I just have no idea which is better for him psychologically. Weekly or one bad day a month? 2. Truly, how bad is the swelling with subQ? Mark is visual and I am afraid a " goose egg " would scare him. If I gave it to him right before bed, by morning it would be gone? Or don't give it before bed because of reaction? Is there anything you can do to reduce swelling/discomfort ? 3. He's a little guy, only 47 lbs. He has some belly fat (I can pinch an inch) but no leg fat, really. Don't you have to rotate the sites? I would really appreciate your feedback. We need to make a decision in the next few days to get it set up for next month, and I just don't know what to do. I don't want to traumatize him like yesterday, but I'm afraid to try something new and further traumatize him. Who said being a mom was easy? They should come with great giant arrows that say " this way! Do this so I turn out right! " . Thanks, mom to Mark 7 CVID Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2008 Report Share Posted July 2, 2008 Hi , sub q has been such a blessing in our house with 3 of us on immunoglobin. I have had to go back to IVIG due to problems (very rare problems). BUT, the girls, 6 and 8 have been on sub q for a little over 2 years now and are great with it. Like IV, there are several choices of meds for Sub q.......there is only one product that is FDA apprived for Sub q (vivaglobin) , but there are many others that can also be used sub q and are in the process of FDA approval. We started on viva, but found issues with the big, red, slow to absorb bumps.....even after a year. We switched to gammunex and have never had bumps and only a small amount of redness. Also, with any procedure, there are many choices of catheter or needle systems to use. It is a matter of choice and finding what you are comfortable with......it is a personal choice. We use minimed catheters. The girls had limited sites with the steel needles as they have very little body fat and we found that they irritated the muslce walls. With the minimeds, you use an introducer needle that comes out immediateley and leaves behind a flexible " straw " . The girls are so much more comfortable just knowing that they have a " straw " and not a needle. At 8, Molly is able to independently do much of her own procedures and we encourage this for both the children....to be involved in their care. They are so funny now.....Molly helps me start my IVs and loves to play nurse. Last night, I had several " procedures " while attached to my IVIG ranging from cuticle care to massaging my feet, to massaging my " cellulite cream " (consisting of a lovely massage with lavender oil) on my arms and face. At first, sub q may feel a bit overwhelming as you get used to it because it is more frequent than IV. But now, for the kids, it is no different than brushing their teeth and we have gotten so used to it that we can get an infusion started, from start to finish, in about 2 minutes......very fast. The kids tuck their pumps into the waistband of the shorts and off we go......they have gone to disneyland while pumping.....to the Orange County marketplace.....to the springs desert preserve gardens....the grocery store.....etc........It is so much better than being glued to an IV pole all day.....feeling " mucky " from the meds (no " muckiness " with subq). Hope that helps. Terri subQ questions Okay, ladies, give it to me. We have loved our home infusion IVIG, but last month was difficult and yesterday was a nightmare. It got to the point yesterday where the back up nurse blew 3 veins and the IV team from our hospital had to come and start his IV. They said his veins were spasming and hard, couldn't advance the IV. It took 4 hrs to get the IV in. Not anxious to do that again. Our immuno said we could try subQ for a month and see if we like it. These are my questions/concerns: 1. Mark is very scared of the " shot " . I am concerned about giving him 2 pokes in the belly every week, versus once a month. I just have no idea which is better for him psychologically. Weekly or one bad day a month? 2. Truly, how bad is the swelling with subQ? Mark is visual and I am afraid a " goose egg " would scare him. If I gave it to him right before bed, by morning it would be gone? Or don't give it before bed because of reaction? Is there anything you can do to reduce swelling/discomfort? 3. He's a little guy, only 47 lbs. He has some belly fat (I can pinch an inch) but no leg fat, really. Don't you have to rotate the sites? I would really appreciate your feedback. We need to make a decision in the next few days to get it set up for next month, and I just don't know what to do. I don't want to traumatize him like yesterday, but I'm afraid to try something new and further traumatize him. Who said being a mom was easy? They should come with great giant arrows that say " this way! Do this so I turn out right! " . Thanks, mom to Mark 7 CVID Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2008 Report Share Posted July 2, 2008 We too are using gammagard and have not problems with site redness or bumping. I think it is less caustic because it is 10% rather than the 16%. We have not ever used Vivoglobin thougth. BARBIE From: Terri Cerda <tcerda@...> Subject: Re: subQ questions Date: Wednesday, July 2, 2008, 10:15 AM Hi , sub q has been such a blessing in our house with 3 of us on immunoglobin. I have had to go back to IVIG due to problems (very rare problems). BUT, the girls, 6 and 8 have been on sub q for a little over 2 years now and are great with it. Like IV, there are several choices of meds for Sub q.......there is only one product that is FDA apprived for Sub q (vivaglobin) , but there are many others that can also be used sub q and are in the process of FDA approval. We started on viva, but found issues with the big, red, slow to absorb bumps.....even after a year. We switched to gammunex and have never had bumps and only a small amount of redness. Also, with any procedure, there are many choices of catheter or needle systems to use. It is a matter of choice and finding what you are comfortable with......it is a personal choice. We use minimed catheters. The girls had limited sites with the steel needles as they have very little body fat and we found that they irritated the muslce walls. With the minimeds, you use an introducer needle that comes out immediateley and leaves behind a flexible " straw " . The girls are so much more comfortable just knowing that they have a " straw " and not a needle. At 8, Molly is able to independently do much of her own procedures and we encourage this for both the children.... to be involved in their care. They are so funny now.....Molly helps me start my IVs and loves to play nurse. Last night, I had several " procedures " while attached to my IVIG ranging from cuticle care to massaging my feet, to massaging my " cellulite cream " (consisting of a lovely massage with lavender oil) on my arms and face. At first, sub q may feel a bit overwhelming as you get used to it because it is more frequent than IV. But now, for the kids, it is no different than brushing their teeth and we have gotten so used to it that we can get an infusion started, from start to finish, in about 2 minutes..... .very fast. The kids tuck their pumps into the waistband of the shorts and off we go......they have gone to disneyland while pumping..... to the Orange County marketplace. ....to the springs desert preserve gardens....the grocery store.....etc. .......It is so much better than being glued to an IV pole all day.....feeling " mucky " from the meds (no " muckiness " with subq). Hope that helps. Terri subQ questions Okay, ladies, give it to me. We have loved our home infusion IVIG, but last month was difficult and yesterday was a nightmare. It got to the point yesterday where the back up nurse blew 3 veins and the IV team from our hospital had to come and start his IV. They said his veins were spasming and hard, couldn't advance the IV. It took 4 hrs to get the IV in. Not anxious to do that again. Our immuno said we could try subQ for a month and see if we like it. These are my questions/concerns: 1. Mark is very scared of the " shot " . I am concerned about giving him 2 pokes in the belly every week, versus once a month. I just have no idea which is better for him psychologically. Weekly or one bad day a month? 2. Truly, how bad is the swelling with subQ? Mark is visual and I am afraid a " goose egg " would scare him. If I gave it to him right before bed, by morning it would be gone? Or don't give it before bed because of reaction? Is there anything you can do to reduce swelling/discomfort ? 3. He's a little guy, only 47 lbs. He has some belly fat (I can pinch an inch) but no leg fat, really. Don't you have to rotate the sites? I would really appreciate your feedback. We need to make a decision in the next few days to get it set up for next month, and I just don't know what to do. I don't want to traumatize him like yesterday, but I'm afraid to try something new and further traumatize him. Who said being a mom was easy? They should come with great giant arrows that say " this way! Do this so I turn out right! " . Thanks, mom to Mark 7 CVID Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2008 Report Share Posted July 2, 2008 Thanks for all your input. I actually called our infusion company and they do subQ. They are sending me info on it, and so is the company that makes Vivaglobin. I REALLY appreciate your responses since this is just a very difficult decision to make! mom to Mark 7 CVID > From: Terri Cerda <tcerda@...> > Subject: Re: subQ questions > > Date: Wednesday, July 2, 2008, 10:15 AM > > > > > > > > > > > > Hi , > > > > sub q has been such a blessing in our house with 3 of us on immunoglobin. I have had to go back to IVIG due to problems (very rare problems). BUT, the girls, 6 and 8 have been on sub q for a little over 2 years now and are great with it. Like IV, there are several choices of meds for Sub q.......there is only one product that is FDA apprived for Sub q (vivaglobin) , but there are many others that can also be used sub q and are in the process of FDA approval. We started on viva, but found issues with the big, red, slow to absorb bumps.....even after a year. We switched to gammunex and have never had bumps and only a small amount of redness. Also, with any procedure, there are many choices of catheter or needle systems to use. It is a matter of choice and finding what you are comfortable with......it is a personal choice. We use minimed catheters. The girls had limited sites with the steel needles as they have very little body fat and we found > that they irritated the muslce walls. With the minimeds, you use an introducer needle that comes out immediateley and leaves behind a flexible " straw " . The girls are so much more comfortable just knowing that they have a " straw " and not a needle. At 8, Molly is able to independently do much of her own procedures and we encourage this for both the children.... to be involved in their care. They are so funny now.....Molly helps me start my IVs and loves to play nurse. Last night, I had several " procedures " while attached to my IVIG ranging from cuticle care to massaging my feet, to massaging my " cellulite cream " (consisting of a lovely massage with lavender oil) on my arms and face. > > > > At first, sub q may feel a bit overwhelming as you get used to it because it is more frequent than IV. But now, for the kids, it is no different than brushing their teeth and we have gotten so used to it that we can get an infusion started, from start to finish, in about 2 minutes..... .very fast. The kids tuck their pumps into the waistband of the shorts and off we go......they have gone to disneyland while pumping..... to the Orange County marketplace. ....to the springs desert preserve gardens....the grocery store.....etc. .......It is so much better than being glued to an IV pole all day.....feeling " mucky " from the meds (no " muckiness " with subq). > > > > Hope that helps. > > > > Terri > > subQ questions > > > > Okay, ladies, give it to me. We have loved our home infusion IVIG, > > but last month was difficult and yesterday was a nightmare. It got > > to the point yesterday where the back up nurse blew 3 veins and the > > IV team from our hospital had to come and start his IV. They said > > his veins were spasming and hard, couldn't advance the IV. It took 4 > > hrs to get the IV in. Not anxious to do that again. Our immuno said > > we could try subQ for a month and see if we like it. > > > > These are my questions/concerns: > > 1. Mark is very scared of the " shot " . I am concerned about giving > > him 2 pokes in the belly every week, versus once a month. I just > > have no idea which is better for him psychologically. Weekly or one > > bad day a month? > > > > 2. Truly, how bad is the swelling with subQ? Mark is visual and I > > am afraid a " goose egg " would scare him. If I gave it to him right > > before bed, by morning it would be gone? Or don't give it before bed > > because of reaction? Is there anything you can do to reduce > > swelling/discomfort ? > > > > 3. He's a little guy, only 47 lbs. He has some belly fat (I can > > pinch an inch) but no leg fat, really. Don't you have to rotate the > > sites? > > > > I would really appreciate your feedback. We need to make a decision > > in the next few days to get it set up for next month, and I just > > don't know what to do. I don't want to traumatize him like > > yesterday, but I'm afraid to try something new and further traumatize > > him. Who said being a mom was easy? They should come with great > > giant arrows that say " this way! Do this so I turn out right! " . > > Thanks, mom to Mark 7 CVID > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2008 Report Share Posted July 2, 2008 personally if I had a choice between Vivoglobin and another significant product I would choose the other product mostly due to the subcutaneous irritation that occurs. Just my 2 cents. BARBIE From: rfrench496 <bluemtnfarm@...> Subject: Re: subQ questions Date: Wednesday, July 2, 2008, 5:30 PM Thanks for all your input. I actually called our infusion company and they do subQ. They are sending me info on it, and so is the company that makes Vivaglobin. I REALLY appreciate your responses since this is just a very difficult decision to make! mom to Mark 7 CVID > From: Terri Cerda <tcerda@...> > Subject: Re: subQ questions > groups (DOT) com > Date: Wednesday, July 2, 2008, 10:15 AM > > > > > > > > > > > > Hi , > > > > sub q has been such a blessing in our house with 3 of us on immunoglobin. I have had to go back to IVIG due to problems (very rare problems). BUT, the girls, 6 and 8 have been on sub q for a little over 2 years now and are great with it. Like IV, there are several choices of meds for Sub q.......there is only one product that is FDA apprived for Sub q (vivaglobin) , but there are many others that can also be used sub q and are in the process of FDA approval. We started on viva, but found issues with the big, red, slow to absorb bumps.....even after a year. We switched to gammunex and have never had bumps and only a small amount of redness. Also, with any procedure, there are many choices of catheter or needle systems to use. It is a matter of choice and finding what you are comfortable with......it is a personal choice. We use minimed catheters. The girls had limited sites with the steel needles as they have very little body fat and we found > that they irritated the muslce walls. With the minimeds, you use an introducer needle that comes out immediateley and leaves behind a flexible " straw " . The girls are so much more comfortable just knowing that they have a " straw " and not a needle. At 8, Molly is able to independently do much of her own procedures and we encourage this for both the children.... to be involved in their care. They are so funny now.....Molly helps me start my IVs and loves to play nurse. Last night, I had several " procedures " while attached to my IVIG ranging from cuticle care to massaging my feet, to massaging my " cellulite cream " (consisting of a lovely massage with lavender oil) on my arms and face. > > > > At first, sub q may feel a bit overwhelming as you get used to it because it is more frequent than IV. But now, for the kids, it is no different than brushing their teeth and we have gotten so used to it that we can get an infusion started, from start to finish, in about 2 minutes..... .very fast. The kids tuck their pumps into the waistband of the shorts and off we go......they have gone to disneyland while pumping..... to the Orange County marketplace. ....to the springs desert preserve gardens....the grocery store.....etc. .......It is so much better than being glued to an IV pole all day.....feeling " mucky " from the meds (no " muckiness " with subq). > > > > Hope that helps. > > > > Terri > > subQ questions > > > > Okay, ladies, give it to me. We have loved our home infusion IVIG, > > but last month was difficult and yesterday was a nightmare. It got > > to the point yesterday where the back up nurse blew 3 veins and the > > IV team from our hospital had to come and start his IV. They said > > his veins were spasming and hard, couldn't advance the IV. It took 4 > > hrs to get the IV in. Not anxious to do that again. Our immuno said > > we could try subQ for a month and see if we like it. > > > > These are my questions/concerns: > > 1. Mark is very scared of the " shot " . I am concerned about giving > > him 2 pokes in the belly every week, versus once a month. I just > > have no idea which is better for him psychologically. Weekly or one > > bad day a month? > > > > 2. Truly, how bad is the swelling with subQ? Mark is visual and I > > am afraid a " goose egg " would scare him. If I gave it to him right > > before bed, by morning it would be gone? Or don't give it before bed > > because of reaction? Is there anything you can do to reduce > > swelling/discomfort ? > > > > 3. He's a little guy, only 47 lbs. He has some belly fat (I can > > pinch an inch) but no leg fat, really. Don't you have to rotate the > > sites? > > > > I would really appreciate your feedback. We need to make a decision > > in the next few days to get it set up for next month, and I just > > don't know what to do. I don't want to traumatize him like > > yesterday, but I'm afraid to try something new and further traumatize > > him. Who said being a mom was easy? They should come with great > > giant arrows that say " this way! Do this so I turn out right! " . > > Thanks, mom to Mark 7 CVID > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2008 Report Share Posted July 2, 2008 Hi , We have been using subq for almost a year with our oldest who is almost 9, and for about 9 months with our younger sons who are 6 and 3 (in couple of weeks). We made the change from IVIG at home initially because of 's sudden and serious reactions to the IVIG. Prior to subq, we did IVIG for 6 years. Once we got used to subq, we decided to switch the other two--- for , because it helped alleviate the harsh trough periods he would experience a week before he was due for his IVIG, and for because he had such poor venous access that it was taking several sticks to get his IV started and it was traumatic for all of us. We have loved subq so far. In answer to your specific questions:1. Ben was also very scared at the thought of subq. He requires 4 sites for infusion, so it was hard for him to see that 4 needles once a week would be better than one needle every 3 weeks. But, he was old enough to know he needed the medicine, and his side effects from the IVIG were so bad that we didn't have any other option at the time. We continued to use EMLA to numb the sites, and we have found that they never feel the needle stick. They honestly are more bothered by the tegaderm, and we know other families that use gentler tapes when that is a big issue. For our boys, it's not. Believe it or not, we actually do our littlest, who is almost 3, with no EMLA at all anymore because the cream bothers him more than the needle stick. He gets two sites and he lays right back for me and gives a little whimper and ouch when the stick comes, but that's it! 2. How bad is the swelling with subQ? It can really vary based on the site you choose, how much is infused per site, body shape and probably other reasons too. We infuse all three boys in the legs. is our skinniest and gets 20cc through 4 sites because he barely has an inch to pinch.... so with only 5 cc per site, it's not that noticeable a bump. gets 12cc in 2 sites, but because he has chunky toddler legs, they really pop out (but still not goose eggs... probably about half a centimeter?). gets 36cc in 4 sites so 9 cc per site and you can hardly see the bumps anymore. We've been using the 5mm needles (the tiny ones) for all 3 boys and have just started the longer 9 mm ones for Bejamin since he's put on some weight and was leaking medicine a little because it was no longer deep enough for him. As for giving before bed, we do that all the time, and most times the bumps are gone by morning. I don't think there is any greater reaction risk at that time, and in general subq should have much less side effects and chance of reactiont than IVIG. During the school year we try to infuse on a Saturday afternoon (after soccer or baseball) so that Sunday can be a take it easy day and there is no soreness during the school week to interfere with gym or other activities. The first few times with a new site we found the swelling was worse and very sore (although our youngest has never seemed sore). Sometimes 's sites still get a little sore or itchy (probably because he's so skinny). We always pre-medicate with benadryl and tylenol or ibuprofen. A second dose of the pre-meds can help with soreness, as does a heating pad (not too hot of course) which my boys find relaxing. 3. Our boys are pretty skinny too. We tried the belly with Ben in the beginning beause he had more fat there, but it was not a good spot for him at all-- very painful. We ended up with the legs, and rotate around the legs each week from outer thighs one week, front of thighs the next week, to inner thighs the third week. This works for us. (the skinniest) had the hardest time in the beginning. He initally started with 3 sites, and we found that 4 worked better becuse he didn't have enough room for more in each site and was not only sore, but leaking the medicine. You may need to experiment a little to find which site works best for your son. If it doesn't go perfectly the first time, don't give up Feel free to also visit our family site as there are pictures of our boys infusing (both subq and IVIG). When we switched it really helped Ben to see photos of other kids doing the new treatment before he tried it. http:/foxfamilypidd.bravehost.com/ Good luck, whatever you decide! Hope our experience helps! mom to 3 with CVID: Ben (almost 9), (6) and (almost 3) http://www.teamhope.info/ http:/foxfamilypidd.bravehost.com/ _________________________________________________________________ Windows Live Hotmail is giving away Zunes. Enter for your chance to win. http://www.windowslive-hotmail.com/ZuneADay/?locale=en-US & ocid=TXT_TAGLM_Mobile_\ Zune_V3 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2008 Report Share Posted July 2, 2008 , thanks for taking the time to give me the info. I am really struggling with this and what to do for him. I really wish he were a little older, so he could have more control over this issue. I hate forcing a change on him, but we are all very concerned about his veins. It's a tough call, I'm afraid. I have to tell you we found your website before and he loves the pics of your boys. He asks to look at their pictures on the computer-- even tonight at bedtime he wanted to see the " picture of the boy getting his medicine like me " . It really helps him and he doesn't feel so alone. Thanks! mom to Mark 7 CVID > > > Hi , > > We have been using subq for almost a year with our oldest who is almost 9, and for about 9 months with our younger sons who are 6 and 3 (in couple of weeks). We made the change from IVIG at home initially because of 's sudden and serious reactions to the IVIG. Prior to subq, we did IVIG for 6 years. Once we got used to subq, we decided to switch the other two--- for , because it helped alleviate the harsh trough periods he would experience a week before he was due for his IVIG, and for because he had such poor venous access that it was taking several sticks to get his IV started and it was traumatic for all of us. We have loved subq so far. > > In answer to your specific questions:1. Ben was also very scared at the thought of subq. He requires 4 sites for infusion, so it was hard for him to see that 4 needles once a week would be better than one needle every 3 weeks. But, he was old enough to know he needed the medicine, and his side effects from the IVIG were so bad that we didn't have any other option at the time. We continued to use EMLA to numb the sites, and we have found that they never feel the needle stick. They honestly are more bothered by the tegaderm, and we know other families that use gentler tapes when that is a big issue. For our boys, it's not. Believe it or not, we actually do our littlest, who is almost 3, with no EMLA at all anymore because the cream bothers him more than the needle stick. He gets two sites and he lays right back for me and gives a little whimper and ouch when the stick comes, but that's it! > 2. How bad is the swelling with subQ? It can really vary based on the site you choose, how much is infused per site, body shape and probably other reasons too. We infuse all three boys in the legs. is our skinniest and gets 20cc through 4 sites because he barely has an inch to pinch.... so with only 5 cc per site, it's not that noticeable a bump. gets 12cc in 2 sites, but because he has chunky toddler legs, they really pop out (but still not goose eggs... probably about half a centimeter?). gets 36cc in 4 sites so 9 cc per site and you can hardly see the bumps anymore. We've been using the 5mm needles (the tiny ones) for all 3 boys and have just started the longer 9 mm ones for Bejamin since he's put on some weight and was leaking medicine a little because it was no longer deep enough for him. > > As for giving before bed, we do that all the time, and most times the bumps are gone by morning. I don't think there is any greater reaction risk at that time, and in general subq should have much less side effects and chance of reactiont than IVIG. During the school year we try to infuse on a Saturday afternoon (after soccer or baseball) so that Sunday can be a take it easy day and there is no soreness during the school week to interfere with gym or other activities. > > The first few times with a new site we found the swelling was worse and very sore (although our youngest has never seemed sore). Sometimes 's sites still get a little sore or itchy (probably because he's so skinny). We always pre-medicate with benadryl and tylenol or ibuprofen. A second dose of the pre-meds can help with soreness, as does a heating pad (not too hot of course) which my boys find relaxing. > 3. Our boys are pretty skinny too. We tried the belly with Ben in the beginning beause he had more fat there, but it was not a good spot for him at all-- very painful. We ended up with the legs, and rotate around the legs each week from outer thighs one week, front of thighs the next week, to inner thighs the third week. This works for us. (the skinniest) had the hardest time in the beginning. He initally started with 3 sites, and we found that 4 worked better becuse he didn't have enough room for more in each site and was not only sore, but leaking the medicine. You may need to experiment a little to find which site works best for your son. If it doesn't go perfectly the first time, don't give up > > Feel free to also visit our family site as there are pictures of our boys infusing (both subq and IVIG). When we switched it really helped Ben to see photos of other kids doing the new treatment before he tried it. http:/foxfamilypidd.bravehost.com/ > Good luck, whatever you decide! Hope our experience helps! > mom to 3 with CVID: Ben (almost 9), (6) and (almost 3) > http://www.teamhope.info/ > http:/foxfamilypidd.bravehost.com/ > > > _________________________________________________________________ > Windows Live Hotmail is giving away Zunes. Enter for your chance to win. > http://www.windowslive-hotmail.com/ZuneADay/?locale=en- US & ocid=TXT_TAGLM_Mobile_Zune_V3 > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 3, 2008 Report Share Posted July 3, 2008 My daughter has used sq gamunex and had great results (physically and emotionally). Also, you may want to do a little cost comparison. Last time I checked, viva was more expensive than some of the other products. This is significant for those with a co-pay. mom to CVIDer, 6 years old Re: Re: subQ questions personally if I had a choice between Vivoglobin and another significant product I would choose the other product mostly due to the subcutaneous irritation that occurs. Just my 2 cents. BARBIE Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 3, 2008 Report Share Posted July 3, 2008 I was worried about 2 pokes a week too but its really not a big deal. I actually double dose with Binadryl on infusion night and she sleeps though the whole thing from pokes (numbed with emla) to infusing. Its better for us, she asks that we do it at night and we don't have the trauma or IV sticks which are a nightmare 2 hour drama at least that ends in 5 people holding her town to get the IV in. You'd need to start SCIG 7-10 days after the last IVIG and not next month so don't wait to long because you still need time to get ins auths, orders and supplies shipped too. We infuse very slowly over night, 10ml hr and there's never an egg in the morning, now if we do 30ml hr then yes we get one and dd says it hurts but she's also 7 and a major drama queen. 's also skinny, she's 45 lbs and will only allow me to use her tummy. You just rotate the sites around the area. Given the choice, once a month is nice but with the drama and side effects (flu like symptoms 3 out of 4 weeks plus the 3rd week crash) IV is just not worth it. Plus she seems to have a lot more energy and her IG numbers are staying around 1200 now instead of the 1000 on IV and she doesn't get sick as often. She always seemed to get sick at least 1-2 times a month while on IV but has only been sick 1-2 times in the 9 months or so we've been on SCIG. wow, doesn't seem like its been that long but it has! 7 (6 weeks shy of 8!) CVID Lilly 2 CVID but back in dx stage AGAIN, waiting to draw pnumovax titers in 2 weeks. subQ questions > Okay, ladies, give it to me. We have loved our home infusion IVIG, > but last month was difficult and yesterday was a nightmare. It got > to the point yesterday where the back up nurse blew 3 veins and the > IV team from our hospital had to come and start his IV. They said > his veins were spasming and hard, couldn't advance the IV. It took 4 > hrs to get the IV in. Not anxious to do that again. Our immuno said > we could try subQ for a month and see if we like it. > > These are my questions/concerns: > 1. Mark is very scared of the " shot " . I am concerned about giving Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 5, 2008 Report Share Posted July 5, 2008 Hi , I'm glad the information helped!! We get alot out of everyone else's websites too.... it's great for the boys to know they are not alone. I forgot to mention that we use Vivaglobin in our house, and that the boys all like it much better than the IVIG. They don;t have any major side effects, they enjoy the freedom of choosing when to have it (what time, and being able to go right to bed afterward if they want).... and they like that I can administer it and there is no longer a need for a nurse to come to the house (I think this makes them feel more normal). Best of luck with your decision! , mom to 3 with CVID: Ben (8), (6) and (3 in a week) http://www.teamhope.info/http://foxfamilypidd.bravehost.com/ Posted by: " rfrench496 " bluemtnfarm@... rfrench496 Wed Jul 2, 2008 7:43 pm (PDT) , thanks for taking the time to give me the info. I am really struggling with this and what to do for him. I really wish he were a little older, so he could have more control over this issue. I hate forcing a change on him, but we are all very concerned about his veins. It's a tough call, I'm afraid.I have to tell you we found your website before and he loves the pics of your boys. He asks to look at their pictures on the computer--even tonight at bedtime he wanted to see the " picture of the boy getting his medicine like me " . It really helps him and he doesn't feel so alone. Thanks! mom to Mark 7 CVID _________________________________________________________________ It’s a talkathon – but it’s not just talk. http://www.imtalkathon.com/?source=EML_WLH_Talkathon_JustTalk Quote Link to comment Share on other sites More sharing options...
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