Guest guest Posted October 13, 2003 Report Share Posted October 13, 2003 , I have tried the calcium channel blockers. I could not tolerate the side effects. I had awful headaches,, I mean so bad that I had to take narcotics for the headaches ! ( That was kinda silly ), so I stopped the calcium channel blockers.. I have been quite successful with taking Clidinium. It is an anticholinergic with the old Librax from many years ago mixed with Qurazam which is an antispasmotic. That has given me the best relief. I went to a GI guy in our next town and also to Indy to see Dr. Lehamn. I did not resort to a ERCP. I am an RN and after my one and only surgery ( gallbladder when all of this crap started ), I decided I was not going to have the ERCP unless I was half dead !!!! The Clidinum helps the best, then I do Actigal after my evening meal to help thin the bile. Low fat diet helps and I do acupuncture once a month. Never was a believer in it before, but boy am I now. I also do some different herbs, but mosty if I miss one does of Clidinium I have SOD attack, not pretty. It has kept me out of the ER. If it was not for the Clidinium and the acupuncture, I would be in bad shape. The calcium channel blockers did nothing for me but give me such a throbbing headace that I was misreable. I considered Botox injections but have not had to initiate that avenue yet. I was able to go back to work after the Clidinum was onboard for about one month. I would be lost without it. They use it for IBS as well and I do not have IBS. But I noticed my periods and cramping are so much more tolerable since I started the Clidinum. It is an anticholinergic so my vision gets blurred for about one hour after I take it. No other side effects. When I feel an attack approachin I also take a drink of ice water and that seems to help sometimes. If the attack is too bad then I take Levsin under my tongue. That has been a real life saver. If they ever take Clidinium off of the market,, I got major trouble ! All I know is that I have researched about every avenue of SOD and this is what works for me. I took the best of Chinese medicine and mixed it with some Western medicine and came up with a tolerable treatment plan. It was a long haul and it took me 7 months of trying out all different kinds of meds before I found a mix that made my pain tolerable. That does not mean I don't have bad days, they are just not as bad. Hope this info helps you, Lily from Ohio Calcium Channel Blockers Has any one ever tried Calcium Channel Blockers as a treatment for spasms of the SOD? I have tried Elavil, an anitdipressant, for spasm pain and it did not do a thing. Helped a lot with sleeping though, and that is always a bonus. Thanks, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 16, 2006 Report Share Posted April 16, 2006 Ann-Marie, I am on Atenolol (Tenormin) for my tachycardia. If my memory serves me correctly, that is a beta blocker. Last summer, my neurologist and cardiologist tried switching me over to Verapamil (calcium channel blocker), for both the tachycardia and the headaches. I had to take a low dose so it wouldn't cause dizziness, so it didn't help either situation and I ended up going back on the Atenolol. That is the only thing that has helped me over the past 14 years with the tachycardia and I do not have any adverse side effects from it, but as you know, we are all different! I have been able to get off of it for awhile, but always have to go back on it. I'm sorry I couldn't be of much help. I hope something works for you. Smiles, a Hi guys, I was wondering if any of you are on calcium channel blockers? If so what one are you on? And for what reason are you on the calcium channel blocker? My tachycardia is becoming more of a problem and so is my SOB.My 30 day heart event monitor also showed sinus tachycardia and narrow complex tachycardia. My PCP wants to put me on a calcium channel blocker and has recommended Cardizem CD. I am wondering if it is a safe drug to use if you have a Mitochondrial Disease, does anyone know? And yes I have a confirmed diagnosis of Mitochondrial disease, MELAS variant. Thanks Hugs, Ann-Marie Quote Link to comment Share on other sites More sharing options...
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