Guest guest Posted July 19, 2000 Report Share Posted July 19, 2000 Hello everyone!! Well, I've just returned from a 4 day visit to HOT Phoenix, AZ for a travel convention. Let me start out by telling everyone I was SOOO naughty. I ate just about everything. The odd thing about it is, I lost weight too. I went to work out this morning jumped on the scale first and I'm down 3 lb.. I can't believe it. I ate parts of a beef sandwich, pizza, part of a Subway turkey sub, BBQ ribs, some fries and even my ultimate weakness CHOCOLATE. ; o ) **YummY** I am also sorry to report chocolate tastes the same to me. I took my 9 year old son to Phoenix with me for the convention and in my off time he kept me pretty busy. We went to a local water park where I climb lots O stairs to go on the slides. I know 6 weeks ago before I had MGB just walking through the front gate would have been a task for me. I even stripped down to a 1 piece swim suit and felt somewhat comfortable in it. A loose filling size 16 I might add too. WooHoo! I just wanted to tell everyone that is tossing the cruise idea around, that I talked to my Carnival Rep and she conveyed some new things to me that Carnival is doing. I found them to be pretty cool. All of the newer Carnival ships, which includes the *Imagination* the one we are sailing on, will now have. 1) Sushi bars 2) Seattle Coffee Houses 3) Full lobster choices at dinner. 4) A larger selection on cabin food service 5) Crab for meal choices I hope everyone is doing fine. I have been praying for Candi too. I know she is in good hands. Take care all. Best, Joanne Tillman MGB 06/09/00 - 225 Now 07/19/00 - 198 and feeling great! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2006 Report Share Posted May 11, 2006 Hello everyone.... Jody, Mimi, anyone else who remembers me. My daughter, Katera, was on SCD for 18 months quite a while ago (Ummm... let's see... 2003-04). She does not have autism... she actually has a CP diagnosis and epilepsy, and we started SCD to help support seizure control. Things went fairly well for the first six months or so. Seizures came back with a vengeance and we're back on medication now... plus she has a Vagus Nerve Stimulator. Seizure-wise she is pretty stable... still has them now and then (one or two per month), but they are short and easy to control now, without emergency drug intervention. ANYway, I am here because I am considering putting her back on SCD when summer break gets here... because we are seeing some digestive issues and I also need to address some yeast control, I believe. After 27 months of the Ketogenic Diet, followed by 18 months of SCD, I can honestly say I'm not sure I've recovered YET from the burn out! But, I am trying to gear up and get my head in the right place again. I also have another family that I'm going to be coaching as they get started this summer, for their 7-yr-old daughter with autism. hugs to everyone I know.... Patti, mom to Katera (age 9- CP, ACC, microcephaly, severe delays, motor and speech dyspraxia, epilepsy) in Washington state. Quote Link to comment Share on other sites More sharing options...
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