Guest guest Posted August 11, 2003 Report Share Posted August 11, 2003 Hi , I've had similar sinus problems as has my son Sam. We are both IgA deficient. Sam also has an IgG 2 subclass deficiency and I have a polysaccharide antibody deficiency. I have not tried antibiotics in the nebulizer, although for a while, my dr. had me try gamma through the nebulizer. I didn't see any improvement for that. What I have found that works for both me and Sam is a change of antibiotic. I've had many antibiotics that just suppress the infection (I feel much better at those times and wouldn't know that I still am harboring bacteria) and then it comes back as soon as I or Sam goes off them. What we've done is switch to another antibiotic that hits the same spectrum of bugs but is maybe stronger. I don't know if you're serious about moving to Florida, but that's where we live. Spring is not rainy but it rains from June to October almost daily. Good luck with your dilemma, Anne R. (Sam's mom) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 12, 2003 Report Share Posted August 12, 2003 In a message dated 8/12/03 10:05:47 AM Pacific Daylight Time, LLadden@... writes: > Asthma doc placed him on .5 pulmicort, Atrovent, and Albuterol nebulized 2x > daily.. , Thanks for the info!! Sandi--Mom to , age 10. Immune Deficiency, Tetrology of Fallot, Mitral Valve stenosis, chronic sinusitis, chronic ear infections, asthma, severe allergies, GERD, Pulmonary Valve Transplant--July 18. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 12, 2003 Report Share Posted August 12, 2003 > My daughter Sara 4 has/had been battling a sinus infection for 11 > months,she was on Augmentin,it was working just very slowly. > My question is: has anyone tried antibiotics for the nebulizer? I > have read a little bit about this and was wondering if anyone has any > ideas. She takes Zyrtec everyday to keep the allergies under control mom to Sara 4 and Casey 3 both CVID and 5 months bringing up the rear. ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ Hi ! My son Blake had this problem it seemed like for ever(not that he doesn't now). He would be on an antibiotic dfor 21 days only to have it changed to another then another just to have it " NOT " work. I bet we went through every antibiotic created by the time he was 6 yrs. of age. His sinus infections started when he was just 10 mos. of age as we were weaning him of the O2 he required because of his immature lungs due to being born very prematurely. He was found to be allergic to all cephlasporines, penicillins, sulfur clindamycin and red dye. All of this before he was 3 yrs. of age. Soooooo, this left the Dr. very limited as tt what Blake could take. Which for the most part wound up being IV meds(Gent. and Vanc). He had 12 sinus surgeries in a 2 yr. period because they stayed soooo infected and blocked. He was miserable & and almost non functional! When Blake was inpatient when he was 9 yrs. old for severe asthma and Osteomylitis of the Temporal Bone and severe sinus and ear problems(he was in for 12 weeks) the Pulmonologist decided that the usual inhalers were not accomondating Blake and his asthma. She decided to place Blake on Pulmicort respules. The is an inhaled steroid that goes through the nebulizer. He started out on .2.5mg. 2Xdaily. Well he still was getting no relief. He wound up in the hospital with pneumonia and a collasped lung. We stayed there 6 weeks (after only 4 weeks at home from the 12 week stay!!) His pulmicort was then changed to the higher dose of .5mg 2Xdaily. He was still having asthma issues. But the one thing that was NOT noticed until I got to thinking about it and brought it to the Pulmo. and ENT's attention.....Blake had NOT had one bit of sinus problems since starting on the Pulmicort. Since them Blake has had a great decrease in his lung functioning and required O2 for a while at nite until it was reconized that it was not helping,he was placed on Pulmocort .5mg 4Xdaily for the severe bout of asthma. In the past 2 yrs. while being on the Pulmicort via nebulizer with Pediatric mask), Blake has NOT(knock on wood and pray hard it does not change)he has not had one single sinus infection. He gets a little stuffy or runny and does not fiar well in the cold or rain. It may be possible that you could chance it and ask your Doc. to place Sara on the Pulmicort via neb. just to see what does take place. We were told the reason fot the change in sinus activity is because the Pulmicort is inhaled through the mask and most likele to enter the sinus passages therefore helping to open them up. Another option that was suggested and it really helped Blake is when we do the Neb. treatments, is to use PEP mask. THe Dr or RT that works with your Pulmo. can explain this. But what it does for Blake is when he uses the PEP mask, and exhales , he actually has only a very tiny hole to release the air. When this happens it teaches him to use the lower airways to exhale. Then as he tries to exhale the meds. will get in the lower airways and plus it seeps in the sinus cavity and is able to " sit " in there and absorb the meds. I hope this helps and you can get the Doc to agree to try Pulmicort (at least once a day). Anything is worth a try to get get relief for your little Pumpkin! S.(mom to Blake S. CVID With Complete T-Cell Dysfunction, Asperger's Syndrome, CAPD, ADHD Sever Asthma & Severe GERD pending surgery in Sept) Blake's website http://www.Caringbridge.org/ca/blake stop by for a visit when you can.....we'd love to have ya!!!! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 12, 2003 Report Share Posted August 12, 2003 I'll join in--my son has sinus infection problems, as well as constant green infectious nose mucus requiring nasal saline flushes and bulb syrine clean out 2x daily.. Everyone thought my son had CF, but sweat test was neg. Asthma doc placed him on .5 pulmicort, Atrovent, and Albuterol nebulized 2x daily.. The atrovent decreases excess mucous production, and my son has not had as severe, or frequent sinus infections as he once had and he does not get the inflammation of the bronchi- that they always think is pneumonia, but not, since being on these treatments. Also, you can increase the dispensation of the atrovent and albuterol neblized down to every 2 hours during particularly bad times. It hs been a lifesaver Mom to 20 month - GERD, CVID, Asthma, Allergies, ?celiac/Schawman Diamond,Failure to Thrive, Ezcema, Chronic Thrush, Chronic Sinus and Ear infections--Also being accessed for multiple Gastro problems Re: Sinus question > My daughter Sara 4 has/had been battling a sinus infection for 11 > months,she was on Augmentin,it was working just very slowly. > My question is: has anyone tried antibiotics for the nebulizer? I > have read a little bit about this and was wondering if anyone has any > ideas. She takes Zyrtec everyday to keep the allergies under control mom to Sara 4 and Casey 3 both CVID and 5 months bringing up the rear. ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ Hi ! My son Blake had this problem it seemed like for ever(not that he doesn't now). He would be on an antibiotic dfor 21 days only to have it changed to another then another just to have it " NOT " work. I bet we went through every antibiotic created by the time he was 6 yrs. of age. His sinus infections started when he was just 10 mos. of age as we were weaning him of the O2 he required because of his immature lungs due to being born very prematurely. He was found to be allergic to all cephlasporines, penicillins, sulfur clindamycin and red dye. All of this before he was 3 yrs. of age. Soooooo, this left the Dr. very limited as tt what Blake could take. Which for the most part wound up being IV meds(Gent. and Vanc). He had 12 sinus surgeries in a 2 yr. period because they stayed soooo infected and blocked. He was miserable & and almost non functional! When Blake was inpatient when he was 9 yrs. old for severe asthma and Osteomylitis of the Temporal Bone and severe sinus and ear problems(he was in for 12 weeks) the Pulmonologist decided that the usual inhalers were not accomondating Blake and his asthma. She decided to place Blake on Pulmicort respules. The is an inhaled steroid that goes through the nebulizer. He started out on .2.5mg. 2Xdaily. Well he still was getting no relief. He wound up in the hospital with pneumonia and a collasped lung. We stayed there 6 weeks (after only 4 weeks at home from the 12 week stay!!) His pulmicort was then changed to the higher dose of .5mg 2Xdaily. He was still having asthma issues. But the one thing that was NOT noticed until I got to thinking about it and brought it to the Pulmo. and ENT's attention.....Blake had NOT had one bit of sinus problems since starting on the Pulmicort. Since them Blake has had a great decrease in his lung functioning and required O2 for a while at nite until it was reconized that it was not helping,he was placed on Pulmocort .5mg 4Xdaily for the severe bout of asthma. In the past 2 yrs. while being on the Pulmicort via nebulizer with Pediatric mask), Blake has NOT(knock on wood and pray hard it does not change)he has not had one single sinus infection. He gets a little stuffy or runny and does not fiar well in the cold or rain. It may be possible that you could chance it and ask your Doc. to place Sara on the Pulmicort via neb. just to see what does take place. We were told the reason fot the change in sinus activity is because the Pulmicort is inhaled through the mask and most likele to enter the sinus passages therefore helping to open them up. Another option that was suggested and it really helped Blake is when we do the Neb. treatments, is to use PEP mask. THe Dr or RT that works with your Pulmo. can explain this. But what it does for Blake is when he uses the PEP mask, and exhales , he actually has only a very tiny hole to release the air. When this happens it teaches him to use the lower airways to exhale. Then as he tries to exhale the meds. will get in the lower airways and plus it seeps in the sinus cavity and is able to " sit " in there and absorb the meds. I hope this helps and you can get the Doc to agree to try Pulmicort (at least once a day). Anything is worth a try to get get relief for your little Pumpkin! S.(mom to Blake S. CVID With Complete T-Cell Dysfunction, Asperger's Syndrome, CAPD, ADHD Sever Asthma & Severe GERD pending surgery in Sept) Blake's website http://www.Caringbridge.org/ca/blake stop by for a visit when you can.....we'd love to have ya!!!! 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. To unsubscribe -unsubscribegroups (DOT) To search group archives go to: /messages Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 9, 2008 Report Share Posted October 9, 2008 Today, Bretts sinuses are swollen and he is complaining of headaches and it hurting " way behind his eyes " ....so I am assuming he could have a sinus infection. My question is...what is okay for him to take? I have been looking online and I see a LOT of sprays but no real meds except Benadryl...which I given him before but just wondering if anyone has had to deal with this on a regular basis before. He has never had one before and I have only had one in my life, so I am clueless. Should I see if his doc will call in an antibiotic? When I had mine last year, I was really sick and was on several rounds of antibiotics...just thought I would see if anyone had any input. Thanks Kristal- Mom to Brett- SMA II- Almost 9 years old Visit Brett @ www.our-sma-angels.com/brett OR www.caringbridge.org/visit/brettwilson Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 9, 2008 Report Share Posted October 9, 2008 I used to have major sinus trouble, so much I had surgery for it. Now to keep it under control I take mucinex when my head and nose begin to feel stuffy and it goes away. Sometimes if I wait too long to take that (because it smells and tastes disgusting) and it turns into an actual infection, good ol' amoxy takes care of it if I get some right away. I also get a prescription nasal spray, (nasacort or flonase) and that help keep sinuses clear. By the way, musinex works wonders for all kinds of congestion. It is really amazing. ~`*^~`*^~`*^~`*^~`*^~`*^~`*^~`*^~`*^~`*^~`*^~`*^~`*^~`*^~`*^~`*^~`* Proverbs 14:31 He that oppresseth the poor blasphemeth his Maker; but he that is gracious unto the needy honoureth Him. Proverbs 14:31 Qui opprime le pauvre outrage celui qui l'a fait, mais celui qui l'honore use de grâce envers l'indigent. www.compassion.com From: Kristal Koehler <kkoehler47@...> Subject: Sinus Question " SMA Friends " < > Date: Thursday, October 9, 2008, 1:43 PM Today, Bretts sinuses are swollen and he is complaining of headaches and it hurting " way behind his eyes " ....so I am assuming he could have a sinus infection. My question is...what is okay for him to take? I have been looking online and I see a LOT of sprays but no real meds except Benadryl...which I given him before but just wondering if anyone has had to deal with this on a regular basis before. He has never had one before and I have only had one in my life, so I am clueless. Should I see if his doc will call in an antibiotic? When I had mine last year, I was really sick and was on several rounds of antibiotics...just thought I would see if anyone had any input. Thanks Kristal- Mom to Brett- SMA II- Almost 9 years old Visit Brett @ www.our-sma-angels.com/brett OR www.caringbridge.org/visit/brettwilson Quote Link to comment Share on other sites More sharing options...
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