Guest guest Posted September 28, 2004 Report Share Posted September 28, 2004 Hi Laurie, I was just reviewing previous posts to the list in prep for my GI appt tomorrow. I ran across this one, and had a few questions. I wondered, how did you know your electrolytes were out of balance? What were your lab values when they were and what did you do to get it in balance? How much Q10 did you increase to? Did you make this increase specifically to address the dysmotility or was that just a byproduct? Was there some report or study to suggest increasing the Q10 and justifying the increase to your nuero? Thanks, Adam > Adam > > I agree with Alice that the sleep apnea should be addressed and might help> you a great deal. I know from experience that dysmotility can be a painful> and just miserable situation. After more years than I can remember, I> finally got relief by having my neuro increase my CoQ10 to many times what> was originally suggested and by getting my electrolytes in balance. It is> amazing that an imbalance can cause so many things to go wrong. > > I hope you find some answers for your problems. > > laurie > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 28, 2004 Report Share Posted September 28, 2004 Adam For the electrolytes, my interest does the electrolyte panel as part of a person's yearly physical. The values of calcium, potassium, and phosphorus were low. She sent me to a nephrologist who did a combination of blood electrolytes and urine. They were high in the urine and low in the blood, confirming that I am spilling them in my urine. This is not uncommon in mito. He also checked the magnesium which was the lowest. I take supplements for the calcium and magnesium and prescription potassium. So far we are just watching the phosphorus. I have them checked every 3-6 months. I take 240 mg of Q-gel four times a day. My neuro is an MDA clinic director and they had a half day session on CoQ. All the research done on Parkinson's disease showed that there was no decrease in symptoms until the level was over 1200 mg. The clinic directors concluded that they were probably ordering it at too low a dose. The 1200 mg is what they are giving patients with ALS. Since the Q-gel is more bio-available, we decided that this level was worth a try and it really helped. The increase was not to address the dysmotility specifically, but it was what I noticed most. Good luck at your appointment with the GI. laurie > > Reply-To: > Date: Tue, 28 Sep 2004 21:35:05 -0000 > To: > Subject: Laurie..Re: Not better after gallbladder surgery, being > readmitted today. > > Hi Laurie, > > I was just reviewing previous posts to the list in prep for my GI > appt tomorrow. I ran across this one, and had a few questions. I > wondered, how did you know your electrolytes were out of balance? > What were your lab values when they were and what did you do to get > it in balance? How much Q10 did you increase to? Did you make this > increase specifically to address the dysmotility or was that just a > byproduct? Was there some report or study to suggest increasing the > Q10 and justifying the increase to your nuero? > > Thanks, > Adam > > > >> Adam >> >> I agree with Alice that the sleep apnea should be addressed and > might help> you a great deal. I know from experience that dysmotility > can be a painful> and just miserable situation. After more years than > I can remember, I> finally got relief by having my neuro increase my > CoQ10 to many times what> was originally suggested and by getting my > electrolytes in balance. It is> amazing that an imbalance can cause > so many things to go wrong. >> >> I hope you find some answers for your problems. >> >> laurie >> >> > > > > Medical advice, information, opinions, data and statements contained herein > are not necessarily those of the list moderators. The author of this e mail is > entirely responsible for its content. List members are reminded of their > responsibility to evaluate the content of the postings and consult with their > physicians regarding changes in their own treatment. > > Personal attacks are not permitted on the list and anyone who sends one is > automatically moderated or removed depending on the severity of the attack. > > > > Quote Link to comment Share on other sites More sharing options...
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