Banding , my waist was wrapped in rubberbands.
Parathesis from waist to toes. IV solumel for 3 days and then weened off with pills.* weeks later, the complete sensation returnned..but I still fear I am a poor night of sleep away from parathesis.
Cognitive issues with memory and concentration, tested (-7) on t.o.v.a. ADHD test. I have ADHD in my family chemistry for sure but as a girl and a coper I found all kinds of tricks to help...but with lesions I couldn't control it..I was a senile 30 yr old.And headaches...better now than preceeding steriod IV treatment.
I had no history of UTI before cognitive issues or my daughter born in 2008. My hubby and I have been together for 10 years with no genital issues. I think it's got something to do with the chronic yeast infections I have had for the last 5 years. I can't figure out how to control them.
Chronic Yeast Infection, It seemed very obvious to me that there was a connection between sugar/ yeast infections and sugar(insulin) resistance) from PCOS before my MS diagnosis. I had read up on threelac to treat systemic issues...my OB just keeps prescribing diflucan..and that can't be good for my liver...
I have been eating so much vegan since my diagnosis and I lost 35 lbs...looking better that ever(silver lining) but I am def still on a journey finding the right dr's and wellness people. A lot of idiots in LA. So I did a 30 day raw vegan cleanse (Dr. Richard Schulze herbdoc.com) and it's just too unrealistic because I can't eat soy or beans per the best bet diet and I def don't want a neuro reation to lunch so I do vegan in the day and a small portion of white meat or fish in the pm
Baclofen , when needed for spasms or banding
Vitamin D omega 800 mg /dy
Currently trying to work in pilates, yoga, and acciupuncture to keep me well.
I go to USC Oct 10th to see a real MS specialist!!!!!!!!!!!!! I couldn't be more excited. My MS is currently considered mild/moderate(mostly because no one gives a shit if your MS symptoms are not currently mobility) and I want to limit this disease in whatever ways possible. It's so random and unpredictable..there is no comfort in my current RRMS diagnosis..it can evolve to Progressive? I respect a FOR NOW ...way of thinking.For now it is incurable...but I do believe that collectively we can make Dr's cure us all!
By coming together in my grief group I grew stronger and I believe I will gain more than a sigle great thing by joining this group of fighters.
stop by the chiropractic treatment forums to learn more about it or just search upper cervical care on any search engine
It is the most frustrating, elusive illness. You're right about family doctors symbolically waving garlic so that it will go away.
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Last post by Anunymouse
Thu Aug 06, 2020 6:33 am