Food is meant to nourish our bodies, bring us enjoyment, and is a HUGE part of our lives. When certain foods become potentially life threatening, sometimes anxiety, fear, and avoidance become a daily struggle. Megan remembers what it is like to go into anaphylactic shock! Now that this is her reality yet again, anxiety and fear have taken hold. With a handful of food allergies, from severe to anaphylactic, food can become a scary monster. Add in the mix a predisposition to anxiety already and you end up with a train wreck!! After her diagnosis with EoE which resulted in weight loss, nausea, vomiting, and often feeling sick after eating, the problem intensified. Megan is now getting help through several medications as well as weekly therapy to help her cope and deal with her health conditions. I am extremely grateful for a wonderful therapist who is patient, understanding, and knowledgable about the daily struggles that Megan faces. As a mom I cannot change or take away the health problems but I intend to support, empower, and give Megan the tools she needs to fight.
Tuesday, February 23, 2016
Megan is on a regiment of swallowed Pulmicort to hopefully put into remission her EoE. She will be scoped again in a couple of months to see if her esophagus and stomach look better. That scope will determine which road we will be taking. If her EoE is under control then we are good to go but if her EoE is not better Megan will loose egg. Megan went through Egg Desensitization too. Egg could be contributing to her EoE but at this time we do not know if it is. We have also been told that there is a chance that DIARY may need to be taken out as well. I am really praying that is not the case. Megan already has many dietary limitations due to Celiac Disease and a handful of other food allergies.
Monday, February 1, 2016
Megan has been diagnosed with EoE. She has been dealing with severe GI issues for some time now and last week a scope revealed damage to her esophagus and stomach due to EoE. Biopsy results confirmed EoE. After graduating from peanut desensitization, Megan began having issues with maintaining proper maintenance dosage of daily peanut. Over the years we have had to continually decrease the amount of peanut until we were at 1/2 of a peanut for daily dosing. Maintenance is 8 peanuts. As of today Megan will stop peanut and unfortunately go back to her prior anaphylactic state. Megan has a great deal of anxiety. Life will change again. I will continue to update on how she progresses. At this time Dr. Wasserman is uncertain how long it will take for her body to revert back to her full anaphylactic state. Being that her peanut numbers are still quite high and she was only doing 1/2 of a peanut I am sure it will not be long. Time will tell............
Thursday, March 12, 2015
Megan continues to eat peanuts on a daily basis. For quite some time Megan has not tolerated the whole maintenance dose. She eats 3-4 peanuts a day. If she eats more peanuts she tends to get a bit nauseated and her throat gets itchy for a short time. She HAS NOT had any anaphylactic issues, just minor issues that resolve on their own. Megan still really dislikes peanuts so it does not bother her that she cannot tolerate a lot of peanut. From time to time she will eat a peanut butter and jelly sandwich without issue. Since Megan has other nut allergies she is limited in the peanut area due to cross contamination issues. We stick with peanuts in the shells and tree nut free peanut butter.
Tuesday, December 31, 2013
Megan's peanut desensitization has not been as flawless as her egg desensitization. Off and on Megan has had issues with nausea after her daily dose of peanut. Unlike egg, Megan really does not like the taste of peanut and I really think that is why it has not gone as smooth as egg. But on a positive note, Megan has NOT HAD ONE relapse anaphylactic reaction to peanut since completing her peanut desensitization. Just recently Megan has decided that she likes peanut butter and jelly sandwiches, HUGE SCORE!!! On several occasions she has eaten more than one sandwich. For those like Megan who haven't warmed up to the food desensitized to it is crucial to maintain the 8 peanut a day dosing. For a long stretch Dr. Wasserman was having us decrease her daily maintenance dose due to the nausea and mild mouth itching. Symptoms would always subside and go away within a half hour of dosing. Megan's favorite way to eat her peanuts are with chocolate chips. We don't restrict her in the amount of peanut she eats, rather we just always make sure that she eats the daily required amount. I cannot tell you how grateful we are that Megan's life is not held captive by peanut anymore. Desensitization has definitely changed her/our lives!!!!
Monday, September 10, 2012
Megan is getting back on track and doing fine with peanut again. Since desensitization is fairly new in treating anaphylactic food allergies protocols are constantly having to be evaluated and re-evaluated, changed and tested. Not everyone fits the same mold.
Tuesday, September 4, 2012
What works for one doesn't always work for another. Megan is having some issues with her peanut. She is starting to react to peanut again. It is not severe enough to need EPI but still a reaction. Dr. Wasserman said this has happened in a few cases before post desensitization. They recently changed peanut protocol and said that once daily dosing was enough for the three months following desensitization. For Megan this is not working. She was doing fine on the two doses a day and started having issues only when we went to the one dose a day. Hopefully this is only a hiccup in the road and her body just needs more time with higher doses of peanut before decreasing. Dr. Wasserman said that he felt confident that once Megan gets back up to the 8 peanuts twice a day she will be just fine again. On a positive note, her peanut number did decrease over 50%.