UVLrx – Let there be light!

Whilst I was in California accessing intravenous antibiotics, I also tried various other alternative treatments. One of which was an 8 week course of UVLrx. This is a new cutting edge treatment for infection and virus load and is getting great results for patients with Chronic Lyme. Ideally it would have been more beneficial for me to have up to 20 treatments of this but due to lack of financial funds it just wasn’t possible.

 

 

This treatment is the first of this type of direct-to-blood intravenous light therapy treatment to be available. For each treatment an intravenous catheter is inserted into a blood vessel in my arm and the Polychromatic light source administers multiple wavelengths into the insertion site for 1 hour per treatment. Other light based treatments only deliver a single wavelength where as this treatment delivers 3, therefore increasing the potential for healing and for destroying unwanted pathagons. The UV light in this treatment is a powerful antimicrobial agent working against blood born pathogens in the body. The additional wavelengths delivered have been proven to repair damaged cells in the body and enhance the immune system.

 

 

Prior to starting this I was slightly skeptical as to how much it would help, but after seeing other patients get such great results I knew I had to give it a go. I can tell you though, I literally noticed the difference after the first treatment, and during sessions 3-5, I actually noticed the difference during the hour of those sessions. My energy levels over all increased and on occasions it was like I had been given a double espresso! I found my mental clarity improved, and with each treatment my brain fog lessened considerably. The brain fog is on-going, but I do feel as a whole it has lessened in severity and my cognitive abilities have improved. I noticed over time, a considerable reduction of inflammation and pain. This was apparent especially in the back of my head and base of skull and neck, which after having encephalitis was a really troublesome area. During sessions 6-8, I felt I did herx much more than previous sessions, and our thoughts on this were that we were reaching infections at a much deeper level. Maybe it was some of those super persistent bugs who thought they were getting off lightly after invading my body!

I had noticed prior to this course of treatment that my tremors were at a high level and the feeling of internal vibrations/jitters was quite intense, and again although this does still exist on a daily basis the intensity of these type of neurological symptoms are greatly reduced. I believe for myself personally that I was responding well to this cutting edge medical technology and had I been able to afford further treatments of this type, that I would have most likely continued to see positive results.

UV light treatment has been used for over 80 years and has been proven to make rapid readjustments to a variety of health conditions. I think it was only a matter of time before a machine of this nature was invented and I hope that with time it can aid many patients in their healing journey. I am really pleased that Gordon Medical Associates have invested in this technology as it is another option which is less toxic to the body than conventional medicine.

As a whole I feel this treatment has reduced both my viral and infection load and I wouldn’t hesitate to recommend this to another patient who is also suffering with chronic levels of pain and inflammation.

Big love, hope and light! Chantelle x

 

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The last chapter of 2014

December seemed to completely fly by. Maybe it was all the distraction from the festive movies on the box and decorating the tree! I have always been a huge Christmas fan, maybe I was an elf in my past life who knows?! In an ideal world I would have been joining in with all the fun in the build up to Xmas, but for the second year running I really just didn’t have the energy for it.

I continued to suffer from an array of symptoms and there just didn’t seem to be any signs of relief from these. I was back on the antibiotics, now that the toxic load had decreased, and was starting back on the meds slow, and steady by building doses up little by little. I know that some of my symptoms were increasing due to the herxheimer reaction (die-off) and others were infections which were still determined to thrive in my body, finding me an ideal host! Really not very idea for me at all! This was a difficult time and I was spending increasing amounts of time lying horizontal and feeling generally weak and nauseous. When I am experiencing such exhaustion and pain, even showering becomes a mammoth task and sometimes that might be all I achieve in a day. Other days I am more able and can walk round the block and cook a meal, it is all just a lottery. I never really know form day to day how I am going to feel.

My Lyme Doctor and her team had put their heads together and came up with the next plan of action. It seemed out of all the infections I have it was currently the Lyme Borrelia bacteria and its partner in crime Babesiosis (Babesia) that were causing me the most problems. Babesia is a protozoan parasite that infects the red blood cells and it is extremely persistent. As it enters the red blood cells it matures and divides and within 1-2 weeks of incubation it starts to cause havoc. One of my first noticeable symptoms of this illness was night sweats, which started sporadically, until eventually occurring up to 4 times a night and were drenching in nature. This then escalated to myalgia, nausea, loss of appetite, air hunger and pressure headaches. Last year the GP also discovered I had developed low Iron levels, yet another common symptom of this co-infection and another daily pill to add to the pile! I sometimes still struggle to comprehend that this tiny tick has transmitted such aggressive infections into my body.  It has definitely been a shock to my system both physically and mentally!

The Morphology of Babesia – Photo Source: http://web.stanford.edu

On a more positive note, over Christmas I made it back to Cornwall to see my Family and some friends too. I was happy to be there in person even if the brain fog was making it difficult to be there in full focus. I spent most of my time in the house but made sure I I was wore my novelty santa jumber. I was able to live through the excitement of the festive period through the eyes of my little Nephew which was magical. I also won’t deny that a hug from my Mum and Dad, sometimes can make things feel a whole lot more bearable, even at the age of 30! I also tried to remember that although I am still stick, This Christmas I was in a slightly better place than the year before and finally in treatment and for that I am grateful.