Support Tazana #LYMEALERT

Tazzy Zarn Tazana ABSOLUTE GODDESS




The creatress of a good time no matter what curve ball may be thrown her way. She finds the positive & juices it out of every opportunity. 

  

She makes the most of her situation spiritually in-tuned with her disease fighting body dedicating her every breathe to healing herself with no prevail. 




She gets knocked down again & again by this relentless tick borne disease of Chronic Lyme.




To only come out stronger, wiser with more awareness of her authentic self.




She’s a constant inspirational motivator to everyone who chooses to listen. 




Her mind dances in the realms of explicit truths & wisdoms. 




She’s sure to light up your day with her raw dirty humour. 




She will never miss your birthday making sure she gifts you with something from her heart.




How unfair it is to watch this injustice as an Australian citizen denied by the government for her disease being denied of its existence in our land.... with no financial or medical support the weight of this incurable disease falls onto her & her beloved husbands shoulders.




Tazana has found her undeniable passion and love for sound healing. And has been so strong to push through these hard times, committed to finding her joy and service to humanity. Tazana is an INCREDIBLE healer, with the biggest heart and this support we give will assist Taz to continue on this amazing conquest to shine her light on the world  




We as a community ~ friends ~ sisters & brothers need to come together for those who are helpless! let’s lift their spirits & shine some love back into their hearts.




& May we all receive the good fortune of energy exchange that will follow. 







TAZANA’S JOURNEY (how it all began) 




Tazana and her husband Trent had the world at their feet. They were together for several years before they were married, travelled  and then decided to pack up their life from Northern Beaches Sydney and move to Northern NSW, buy a house, a beautiful puppy and to start a new life together as husband and wife, with the prospect of starting a family of their own.













                                        Fairytale right......



                          *******NEWS FLASH******









On their way down the coast on a camping trip in October 2015 Tazana found one morning that a tick had embedded in the back of her head. They removed it and didn't think much of it, despite her head being painful to touch where the tick was and having a slight groggy feeling they were not overly concerned.




Fatigue, brain fog and a sense of general unwellness of feeling dizzy and nauseous overwhelmed her for the next few months, along with a few other incidents that occurred before the new year that had them questioning what was going on. Thats when things started to really amp up.




2016 started with Tazana having "no zest for life" where she was so overwhelmed with the sense of no reason for being, she would say to her husband "I want to be dead" and was disappointed that she woke up everyday. This was gradually followed by others symptoms like nausea, dizziness, hot flushes, chronic fatigue, insomnia, asthma, muscle weakness, joint pain, carpel tunnel, headaches, brain fog, high anxiety and panic attacks, tingling and digestive problems and that is just to name a few symptoms.




It was in March 2016 that she went to a naturopath and discovered that her NKCD57 (a collection of natural killer cells) in her blood were extremely low. The below healthy range of these cells are strong indicators for 'lyme' or a 'lyme like' illness. She was told that the prospect of starting a family soon, if at all, had diminished as the the bacteria is transferable via the placenta and breastmilk to a baby.




Wanting more information she found a Dr in Brisbane and sent her bloods overseas to ArminLabs, run by Dr Armin Schwarzbach who is a globally renowned expert in vector-borne diseases, & consultant to the Australian Department of Health in regards to tick-borne diseases in Australian laboratories and showed antibodies to multiple tick-borne infections including Borrellia Burgdorferi (lyme disease) and Anaplasma (co infection of lyme).




She had adopted a treatment plan of a well known herbal medicine protocol with IV Ozone therapy, IV infusions, supplements, EXTREME clean eating and detox methods. Aiming to relieve her symptoms as much as possible by following this approach as approved by her Doctor at the time.




She had to scale back her mobile hairdressing business and passion for photography as she physically and mentally could not cope with the toll the infection was having on her and eventually closing down her business. 




She had near no social life except for contact with "other lyme people" she has found via social media and when she does see "normal" people, she calls on all her strength to "perform" like an everyday functional person. She does have good and bad days and her parents have been supporting her by doing day to day chores as well as financially, but sadly those funds have already been exhausted. 




Tazana did improve over time and has come a long way. She did various therepies, took on studies in Sound Healing and is currently trying to build a business helping improve peoples lives. She has had to keep going without the means to afford the upkeep of her basic treatment protocols and therapies or even appointments with health care professionals. With a strong belief of healing and positive mindset it has taken her so far but symptoms have been making a comeback, and noteablity the neurological symptoms making it clear to take immediate action as she cannot function well enough to study or earn a proper living. 




The consequences of medical denial of Lyme disease in Australia are that patients are left untreated. Without treatment they stay sick, get sicker, & many die untimely deaths. 




People with invisible illness may look completely healthy to the outside world, running one day to be completely floored the next. 




She relys on her husband's income and what little savings they have to continue. All treatment is as full cost with no government support as lyme is not recognised as being within Australia.




She is aware also that there are also a popular Clinics overseas that treat Lyme and Cancer which can cost between 30K to 65K, but there is no guarantee on results.




Her predicament is emotionally draining on both her and Trent, the thought of an incurable disease, the prospect of no future family and the day to day deterioration combined is an enormous burden. 




The funds we raise are to contribute to therapies such as HBOT, herbal protocol, appointments with health care professionals along with all their expensive recommendations. Tazana has faith in the healing therapies that have improved her life before but were cut short due to lack of funds and having already spending tens of thousands of dollars. Every case of this disease is different, where what works for one case may not work for another. We also seek to increase the awareness of Lyme disease within Australia.




This would mean so much to me to know that she and her husband will have a little financial support and to some what degree, relieve them of the financial pressures.




Our goals is to help her focus on her recovery to stay positive so that she can smash this invisible illness. 




Your small donation (as little as $10) will go far but of equal importance is for you to forward this post to as many people as possible. 







And hence the purpose of establishing this campaign is to enable Tazana's friends, and friends and associates of those friends to raise money to assist Tazana in her fight to good health







Tazana, goddess of strength, courage, determination and inspiration







THANKYOU SO MUCH FOR YOUR TIME TO READ THIS







From Tazana 




“I try to stay positive about my personal life and may not share much of my struggles here on FB when it comes to Chronic Lyme Disease. I don't want to associate with disease for the sake of healing and I don't like to speak of symtoms or what I don't want to be as part of my brain retraining but I find myself in a position where my strong faith in healing is wearing thin as its become really clear I need further treatment. I need help and support. I would love to get treatment though I have no idea how I will afford this, we are so spent over these years of paying thousands while I haven't been able to work. I been trying so hard to get my feet off the ground doing my studies and setting up a business that aligns with my moral compass and improves lives. Just organising myself to do 4 sound baths in one month is so challenging when your constanly sick. I've now cut down my sessions so I can work on myself. I'm a highly motivated and easily inspired person. I keep dreaming up ideas and makings plans to offer my services and manifesting an epic future. I am constantly getting back on the horse on the daily and this struggle and set backs have been happening for years now and I don't know how much more I can take. I help myself best I can, I push my brain and body into study, I try to offer a service to help others, earn a living, create a future. I've surrended so much and have learnt what its like to give up most things that brings me joy but still find it. I know how to deal with having no control over my life, and being completely grateful, I just do what I can to make a difference and get on with it. Learning how to ask for help is another story and very scary for me to do. They say reach out if one is finding it hard to cope but I don't want to burden others and I tend to avoid incase it may lead to being victim bullied and or denied of my story or feelings. But at the end of the day my life fucking matters so I'm asking for help. And even if thats just you envisioning me having treatment and sending your healing prayers I fully appreciate your love “