Lynn's blog

What to take for depression associated with CFS?

Submitted by Lynn on Mon, 2008-02-11 14:13

I need any information anybody can give me on overcoming depression associated with CFS. I am currently taking 40 mg/ day Nortriptyline, 300 mg/day Wellbutrin, 75 mg/day DHEA. I'm on a lot of anti-oxidants too.

Still experiencing moderate to severe depression. Most days, severe depression. What will help? Anything? Does Vitmain D help? I have to hold down my full time job and the depression (along with the fatigue) is REALLY taxing me and my motivation and could cost me my job if I can't find something to help.

Any thoughts or suggestions would be greatly appreciated.

Thanks, Lynn

 Cpn, Mpn, CFS, CAP - Doxy, Erythromycin, NAC

Restless Legs??? Need answers quick please!

Submitted by Lynn on Sun, 2007-12-02 15:16

Restless legs?? Need answers quick please! I was out last night with my friend when all of a sudden I felt like I was going to have a seizure.  I have felt this way on and off since starting the protocol so I know it's part of the cpn (besides having a hx of these sizures which i now know is Cpn related seizures). Had not had feelings of a seizure in a couple of years before CAP protocol. Anyway, after that I realized that I felt I could not stand up. My legs were so weak and I started having the sensation that ants were crawing inside legs. Haven't had restless leg syndrome since last winter with EBV. And it got really bad last night.

Best day yet! Quick update...

Submitted by Lynn on Tue, 2007-11-27 23:19

Best day yet! Quick update on my health... I'm in 2nd week of NAC 600mg, Doxy 200mg, and Erythromycin 250mg and I actually had a decent day. Had stamina for about 6 full hours of work today and I've been online a while tonight. I was only nauseated once today and was able to knock it out with some good ole' fashion compazine. I've been stuffy for several days and sneezing, but not so bad that I can't deal with it! Much better than the NAC flu!

I'm tiring now, but actually feel like I can say I felt better today than I have since starting CAP. I'm trying not to set myself up by reminding myself that tomorrow is a new day, come what may, and not to get discouraged if this doesn't last.

Dr. Mergian in Memphis TN, anyone seeing him besides me?

Submitted by Lynn on Wed, 2007-11-21 03:11
I heard that some of you may possibly be seeing my doc here in Memphis, so i thought i would check and see?? He's excellent, MD and toxicologist, treating me with CAPi.

If your in my neighborhood and would like to let me know, please do!  If you are trying to find a dr. and you're close enough to Memphis, I would highly recommend him. It may take a while to get in, but it's well worth it.

New kid on the block: Glad to find you!

Submitted by Lynn on Sat, 2007-10-27 20:09

Hello everyone-I'm so glad to find this site and others who understand what I'm going through!  I have suffered for at least 17 years with various illnesses that I now see may all be related to CPn.  My most recent addition to the plethora of illnesses I've experienced is severe tinnitus with 5-10% hearing loss. I recently had to purchase hearing devices, $3000 worth to drown out the ringing noise as it was driving me insane, literally! Finding out about CPn has made me feel like I have found a gold mine, thanks to my doc, (MD and toxicologist) that knows how to think outside the box. Sure has given me renewed hope. I actually found out I had it after my friend was diagnosed with it.  I had referred him to my doc as he had been experiencing CFS and ADD symptoms.