Guest guest Posted June 14, 2010 Report Share Posted June 14, 2010 Oh, boy. Heavy duty drug. What else have you tried to reduce any inflammation? I assume that is the thought behind the use? Curcumin? Can your son tolerate phenols? If so, higher doses of curcumin (in turmeric) might help. Enhansa is the big curcumin product out there now. Fish oil? High doses (1.5+ grams/day) jump started my son's language. Anti-viral therapies? Olive Leaf Extract really helped increase my son's language. Methylation support? Methylguard (Thorne Research) helped increase my son's language beyond single words. This contains mB12, TMG, folate and B6 (P5P). I see he didn't do well with mB12, but my guess is it was the shots? Chelation? DMSA/ALA. Pam > > We are going to use it for improving speech. My son's main issues are expressive language and tip toe walking > Sent from my BlackBerry® wireless device > > Re: [ ] prednisone > > > Hi All, I would like some advice on prednisone. my son is 6 and he has a dx of PDD NOS (lately the MD says he is looking more like speech disorder) he is doing better in all areas, but his speech still very delayed. now his DAN wants to try prednisone for a short time to see if it helps, we have tried many things including MB12, spirolactone, etc he did really bad on them.could any of you share your experience on prednisone? > thanks a lot!Fernanda > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 14, 2010 Report Share Posted June 14, 2010 Pam we have tried all of that including ldn spirolactone galantamina... No effect the only thing it worked was valtrex that helped with his social life Now that my son has been off all supplements he is doing better in language but improving very slowly... Sent from my BlackBerry® wireless device Re: [ ] prednisone > > > Hi All, I would like some advice on prednisone. my son is 6 and he has a dx of PDD NOS (lately the MD says he is looking more like speech disorder) he is doing better in all areas, but his speech still very delayed. now his DAN wants to try prednisone for a short time to see if it helps, we have tried many things including MB12, spirolactone, etc he did really bad on them.could any of you share your experience on prednisone? > thanks a lot!Fernanda > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 14, 2010 Report Share Posted June 14, 2010 Well, we've seen many off-label uses of drugs that have had positive effects. There is no way to predict who will benefit and who will not, so I hope your child is a responder if you choose to try this out. The whole theory behind the use of Prednisone in Autism does make sense to me, just too bad the drug has so many side effects. I see it is used for several months and is tapered down after an initial high dose? Good luck with your decision. Do they advise an MRI prior to starting? What tests are recommended? Has your doc used this before? Pam > > > > We are going to use it for improving speech. My son's main issues are expressive language and tip toe walking > > Sent from my BlackBerry® wireless device > > > > Re: [ ] prednisone > > > > > > Hi All, I would like some advice on prednisone. my son is 6 and he has a dx of PDD NOS (lately the MD says he is looking more like speech disorder) he is doing better in all areas, but his speech still very delayed. now his DAN wants to try prednisone for a short time to see if it helps, we have tried many things including MB12, spirolactone, etc he did really bad on them.could any of you share your experience on prednisone? > > thanks a lot!Fernanda > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 14, 2010 Report Share Posted June 14, 2010 There are other options to try if you are not comfortable with the prednisone to reduce inflammation. You could look up ISOCORT which is a natural adrenal corticol herbal supplement made from sheeps adrenal glands. It is the only natural product that actually has cortisol. It also has aldosterone and has worked quite well for both myself and daughter in attempt to reduce the hydrocortisone we need. The other thing you could add is licorice drops which help to slow the breakdown of cortisol. Increasing either celtic sea salt or himalayan salt will also help. Epsom salt baths also work really well to reduce inflammation. Increasing magnesium intake has also helped reduce my daughter's swelling. I would try all these things before doing the prednisone. Keep in mind the strong adrenal medications will send a negative feedback loop to the HPA (hypothalamic, pituitary and adrenal) axis. Trust me, this is not fun to try and correct and balance. The other thing to know is that 5mg of prednisone is equal to 20mg of the hydrocortisone, so it is easier to go the least possible amount of steroids as possible with the hydrocortisone. In my daugher's case, we had no choice to put her on the steroids. She had a headache every day for 8 months, was dizzy upon standing, immediate car/motion sickness, photosensitivity, intolerant to any stress, irritable, depressed, had constant joint and muscle pain and was only making it to school 1 and 1/2 days per week. The hydrocortisone, florinef and thyroid meds have been a life saver for her. However, I do want to get her off the hydrocortisone and florinef. This is why I am wanting to chelate her. I am hoping that all she will be left with is her natural desiccated thyroid. Every child is different. What works for one kid may not work for another. This has just been my experience, but may not be your answer. > > > > We are going to use it for improving speech. My son's main issues are expressive language and tip toe walking > > Sent from my BlackBerry® wireless device > > > > Re: [ ] prednisone > > > > > > Hi All, I would like some advice on prednisone. my son is 6 and he has a dx of PDD NOS (lately the MD says he is looking more like speech disorder) he is doing better in all areas, but his speech still very delayed. now his DAN wants to try prednisone for a short time to see if it helps, we have tried many things including MB12, spirolactone, etc he did really bad on them.could any of you share your experience on prednisone? > > thanks a lot!Fernanda > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2010 Report Share Posted June 15, 2010 the MD (DAN) wants to try prednisone for 3 weeks in total, but he told me that after 5 to 7 days we should see great results with language otherwise we should stop. if it works we should do 3 weeks tops, and then he will look for other options. the idea is to confirm the hypothesis that my son has inflamation on his brain and this is what is stopping his language from progressing... From: Pamela H <phaselow@...> Subject: [ ] Re: prednisone Date: Monday, June 14, 2010, 10:28 PM  Well, we've seen many off-label uses of drugs that have had positive effects. There is no way to predict who will benefit and who will not, so I hope your child is a responder if you choose to try this out. The whole theory behind the use of Prednisone in Autism does make sense to me, just too bad the drug has so many side effects. I see it is used for several months and is tapered down after an initial high dose? Good luck with your decision. Do they advise an MRI prior to starting? What tests are recommended? Has your doc used this before? Pam > > > > We are going to use it for improving speech. My son's main issues are expressive language and tip toe walking > > Sent from my BlackBerry® wireless device > > > > Re: [ ] prednisone > > > > > > Hi All, I would like some advice on prednisone. my son is 6 and he has a dx of PDD NOS (lately the MD says he is looking more like speech disorder) he is doing better in all areas, but his speech still very delayed. now his DAN wants to try prednisone for a short time to see if it helps, we have tried many things including MB12, spirolactone, etc he did really bad on them.could any of you share your experience on prednisone? > > thanks a lot!Fernanda > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2010 Report Share Posted June 15, 2010 Well, the 5-7 days is the same as a taper dose pack my MD husband uses for his back flare ups. That is 'safe'... as far as not having those long term negatives. Honestly, with all the other things we try with our kids, I would not back away from that trial period if nothing else had worked. So you did try the high dose curcumin plus the high dose fish oil? How high did you go? How long did you chelate, and how? Your child was vaccinated, I assume? Is this language LOST language or language that never developed? Curious question: have you ever noticed that your child is better with a fever? Less autistic? Just curious. Pam > > > > > > > > We are going to use it for improving speech. My son's main issues are expressive language and tip toe walking > > > > Sent from my BlackBerry® wireless device > > > > > > > > Re: [ ] prednisone > > > > > > > > > > > > Hi All, I would like some advice on prednisone. my son is 6 and he has a dx of PDD NOS (lately the MD says he is looking more like speech disorder) he is doing better in all areas, but his speech still very delayed. now his DAN wants to try prednisone for a short time to see if it helps, we have tried many things including MB12, spirolactone, etc he did really bad on them.could any of you share your experience on prednisone? > > > > thanks a lot!Fernanda > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2010 Report Share Posted June 15, 2010 I am surprised also. Cortisone lowers the body's immune system, making you more susceptible to get/catch an illness. I do not recommend it for speech. My son has severe verbal apraxia (speaks, but apraxic), history of severe asthma and bilateral pulmonary infiltrates, along with immuno- deficiency; he used to be on pulmicort along with his albuterol in his nebulizer. I realized it was making him more sick. We discontinued the pulmicort and now he is much better. He has not had any of his asthma meds in months (six or more); I think he has been healed from a lot of things, including asthma. > > > > Hi All, I would like some advice on prednisone. my son is 6 and he has a dx of PDD NOS (lately the MD says he is looking more like speech disorder) he is doing better in all areas, but his speech still very delayed. now his DAN wants to try prednisone for a short time to see if it helps, we have tried many things including MB12, spirolactone, etc he did really bad on them.could any of you share your experience on prednisone? > > thanks a lot!Fernanda > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 1, 2010 Report Share Posted October 1, 2010 my rheumy said no to take prenisone because it will make the skin problems worse. i always felt better on the prednisone . just don't know what to do anymore. hope you feel better. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 1, 2010 Report Share Posted October 1, 2010 I had to stop it as it caused me to balloon up to 305 lbs from 214.Also, it caused me to suffer a certain amount of irritability. I had to wean off it slowly and am still having trouble losing all the weight. I am now down to 273 and hopefully will be able to lose the rest. Good luck Walt Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 1, 2010 Report Share Posted October 1, 2010 Carmy, I can so relate to what you said. I am on 2.5 mg of pred every other day now. I have never been on super high doses (20 mg for short time) but even at 5 mg I would have anxiety, my first panic attack, emotional variability and even difficulty functioning day to day at times. I am having the same anti-inflammatory results on the 2.5mg every other day as every day. I drink very little coffee, try to stay away from sugar and exercise is essential for me. That is probably the most important thing for my sanity. Getting enough sleep is major for me too. As with anything, a healthy diet: low fat, low sugar, high in fiber, fruits and veggies. Also, plenty of water. Are you on any other meds. They may also be affecting your emotions. You have been through a really rough time and that can, like you said, make things so much worse. Be gentle on yourself, find someone you trust who you can be real with and who will watch out for you. Keep in touch, we are here for you. God bless, Patty Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 1, 2010 Report Share Posted October 1, 2010 I am not on prednosone, but am always very stressed and emotional. I am by nature emotional, but never as bad as now. I lost my husband last year too, and am alone a lot. I was on Humira twice a month, but when Simponi came out my Dr. changed me. It is a once a month injection. I take cymbalta for fibro, and it is supposed to be for depression, but doesn't seem to help. I also take metho, folic Acid, and b vitamins. I have managed to stay in my home for a year and a half, but will soon have to move out, as I can't afford to keep it up, and pay taxes and insurance. Gonna turn it over to my kids and let them take the responsibilities... God never said we'd only see rainbows , that storms would never rage in our lifetime. But, He did promise the reaping of blessings that come with the new morning sunshine. Have a blessed Day, Ann Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 1, 2010 Report Share Posted October 1, 2010 when i take prednisone for flares after a few days i start to become anxious and i get agitated very quickly at things that don't normally bother me. I suffer from depression and PTSD and the prednisone makes those symptoms worse as well. I usually don't take the full course fue to these side effects. Lori in az Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 2, 2010 Report Share Posted October 2, 2010 I can see not taking it because it can cause bone loss but I don't get why he said no to pred because of skin problems. For me it helps keep the psoriasis I do have in check. I don't have much just some on my head but when I'm not taking pred it gets a whole lot worse. I take 5mg of pred daily because if I don't i get an immediate flare which starts on the top of my feet it feels like I slammed them with a sledge hammer. I've tried to cut it back and even alternating 5mg then 2.5 the next and it makes no difference I still get a flare. Celeste Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 2, 2010 Report Share Posted October 2, 2010 Hi Carmy, I have been taking 5 mg of Prednisone for about 5 years, now. I get a bone density scan every year or two and take 1000 mg calcium and Vitamin D. I always try to take my prednisone at sometime between 10:00 AM and Noon - always with food so as to ameliorate the effects of the epinephrine (adrenaline) boost associated with the predisone and to have it early enough in the day so that I can sleep. I like to spend the first few hours of the day prednisone-free so that I can feel emotionally at ease with myself and my surroundings. I work in a position as a teacher of emotionally/behaviourally-challenged teens, so I understand the compounding effects of stress and prednisone on one's emotions. I am forever working to create calmness in my surroundings - for myself as well as my students. Even though I forewarn them that I am very slow to anger and have only truly gotten angry with students but a few times in 20 years, some of my students forget at-times that the fire in my eyes is not anger, but it is the result of my taking prednisone. We work on their learning to listen to my words more than reading my body-language, and i work to relax tension in my body. It has been an interesting learning experience for me to look for peace when my neurons are screaming to fire. The alternative is so much pain that my body is producing it's own epinephrine to get me though each painful moment. And the pain is more exhausting. At 55, I will retire in 4 months; perhaps then I can wean myself down from the 5 mg per day. I never enjoy my prednisone, but it has kept me mobile and my joints from becoming deformed. I eat as healthily as possible - lots of organic veggies, fish and rice. Low portions of sweet, highly refined, animal protein or high high acid foods. Best wishes to you, Brent Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 4, 2010 Report Share Posted October 4, 2010 prednisone... I went from 215 to 245..... 2 years after back to 215.. takes a while. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 2, 2010 Report Share Posted November 2, 2010 > > Hello Friends, > I have a worried mom of a 10yr. old who is randomly fainting. Today she was fainting and throwing up and developed hives. The doctor gave her Finnegan and Prednisone based on it being viral. So far she has only taken 1 of the prednisone pills and does not want to give her another after I told her it just suppresses whatever is trying to detox. I don't know if you can just stop after one pill? Would love any feedback about symptoms and drugs, thanks so much, > P.S. I was going to recommend she have a consultation with you BEE. +++Hi , There can be many reasons for fainting which aren't necessarily viral at all! Doctors are jumping to conclusions and dispensing drugs right, left and center more and more these days. Yes, it is okay to stop prednisone after only one pill! All drugs are poisons to us! Hormones like prednisone are particularly harmful because they manipulate the body more easily, forcing it to respond in ways that cause more health issues. I think it is horrible children are given drugs and no advice about eating healthy! I'd be happy to have a consultation with her, however it is a waste of her time and mine if she doesn't read first so she understands how foods are so important for health, etc. - she should read Foods That Damage, Foods That Heal: http://www.healingnaturallybybee.com/articles/heal13.php First, she needs to get her child off of sugars, fruit juice and fruits, pop, soy of any kind, and junk foods. Have her read the success autistic children have had with my candida program, which is amazing and the dramatic changes happened in only 2 weeks: http://www.healingnaturallybybee.com/success/ss80a.php http://www.healingnaturallybybee.com/success/ss80b.php All the best, Bee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 2, 2010 Report Share Posted November 2, 2010 Hi, have you any idea why this may be happening yourself? Has something changed in her diet or enviroment recently? What is her medical history in terms of related symptoms? If she has a mother suffering from candida( I'm assuming that's why you are on the group) then she is bound to also be a sufferer. Very good idea to have a consultation and get her learning about her health. I used to be a fainter as a child myself and now know it was related to detoxing. My 11 year old daughter is recovering beautifully from autism, hyperactivity,life threatening asthma and major league 'allergies'(healing and detox reactions) that required the constant carrying of epipens. If you talk to kids about what is happening to their bodies and how they can take charge themselves they will really get into it! All the best > > Hello Friends, > I have a worried mom of a 10yr. old who is randomly fainting. Today she was fainting and throwing up and developed hives. The doctor gave her Finnegan and Prednisone based on it being viral. So far she has only taken 1 of the prednisone pills and does not want to give her another after I told her it just suppresses whatever is trying to detox. I don't know if you can just stop after one pill? Would love any feedback about symptoms and drugs, thanks so much, > P.S. I was going to recommend she have a consultation with you BEE. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 3, 2010 Report Share Posted November 3, 2010 's message reminded me that I, too, used to faint as a kid. It was because of low blood sugar. I'd eat sugar, get that sugar high, then crash and faint. If that's this child's problem, Bee's diet would fix it. Lilac > > > > Hello Friends, > > I have a worried mom of a 10yr. old who is randomly fainting. Today she was fainting and throwing up and developed hives. The doctor gave her Finnegan and Prednisone based on it being viral. So far she has only taken 1 of the prednisone pills and does not want to give her another after I told her it just suppresses whatever is trying to detox. I don't know if you can just stop after one pill? Would love any feedback about symptoms and drugs, thanks so much, > > P.S. I was going to recommend she have a consultation with you BEE. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2011 Report Share Posted March 4, 2011 I took 1.0mg for 2 weeks, then down to a 1/2 a tablet i am like a new person,it sure worked for me, and no side effects yet,thanks Billie from Tex Quote Link to comment Share on other sites More sharing options...
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