cfs/ms

Hi Hug and welcome to HealingWell. I'm sorry to hear about your health problems. I see you were tested for MS, but did your doctor test you for autoimmune diseases like lupus? I'm currently being treated for lupus and I flare up prior to having my period and am also really sensitive to the heat. It's just something to keep an eye on, especially if you start to develop more symptoms.

Has your doctor given you anything to treat your symptoms? I hope your doc is able to help to help you start to be able to function better and alleviate some of your symptoms.

Feel free to ask any questions or we are also here for support if you are having a rough time.

Take care and I'm glad you joined

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Diagnosis:  Suspected Lupus 2004; Raynauds 2006; Sjogren's 2006; CFS 1991; Mono 1985

Meds:  Plaquenil 400mg; Tramadol 100mg 3-4x daily; Amitriptyline 10mg; Neurontin 200mg; Steriod Cream and Mouth Rinse for tongue and mouth ulcers; Hydrocodone 5/500 prn for severe pain

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I have had CFS since 1983.....23 years!!  During this time I have had relapses and remissions (remissions for up to 10 years with no symptoms!)  I have had neurological symptoms with my CFS.  The doctors tested for everything under the sun, including MS, lupus, etc.  I have had several MRI's during this time, and they have all been clear.  I have numbness, tingling, as well as visual problems at times during relapses.  These symptoms can come on for 3-4 months, then totally disappear for years.  In the beginning, my symptoms were more chronic, but now they have subsided quite a bit, and only come on very rarely.  I try to take care of myself by getting plenty of rest, and I also do exercise within reason.  Hope this helps ease your mind a little.