Dr. Martin Ross is a crook, dont let all of his knowledge of Lymes disease fool you into thinking that hes the doctor for you. This doctor is only out for your money!! When looking for a doctor to treat you for Lyme you have to really be careful because a lot of them are in it for the money and theyre not in it to help people. I researched every Lyme doctor in the area of Seattle Washington. First you need to make sure that they are a lyme literate doctor. Otherwise they wont know what tests to run, or how to read your tests. They do not teach this in medical school. The doctor has to go to special training. To become a lyme literate doctor so that they are able to help you. This is in addition to their regular medical schooling. Dr Martin Rosss office wanted me to give them $1,300 before they would be even willing to see me. I was literally on my deathbed begging and pleading for help. All they care about is the money not about how sick you are. The doctor that came through for me in the end was Dr. Susan L Marra. Shes reasonably priced and has Bartonella. Her visit average $325.00, the first one is $550.00, but this includes genomics testing. Only 65 doctors in the United States can offer genomics testing. Dr. Marra is very well versed in genomics and uses it as an aid in treating her patients effectively. She understands more than any other doctors, that Ive seen. What the suffering of Lymes disease can be like. She lost her eyesight to Bartonella and was able to gain it back and now she treats others. Dr. Marra saved my life when Dr. Ross wouldnt even take the time of day for me, because I didnt have enough money!! He charges over double what the average Lyme doctor charges. I am currently now on daily IV antibiotics and have been in treatment for over 2 years now. I was so sick and Dr. Mara knew that I needed more than just oral meds. Dr Mara has been practicing Lymes disease for over 20 years and has a lot of connections. Thank goodness for this because she was able to send me to Pacific Frontier Medical in Foster City California. Just to give you an idea here my first visit with the Lyme doctor in California cost me $385.00 vs Dr. Ross $1300.00. To me to charge that much money when somebody is in need is taking advantage of sick people which is absolutely disgusting Dr. Ross!!!!! If youre not rich and you dont have money to pay him he doesnt care about you!!!! I dont consider somebody like this to actually even be a doctor thats why I called him a crook!!! Please stay away from him hell just take your money!!! Go see Dr. Marra!!!!

Marty saved my wifes life. He is an absolute rock star and all around caring, amazing doc. Lyme and all that goes with it is a tricky beast. There is trail and error, but Marry never gave up on her. He is simply the best.

Fantastic first meeting with Dr. Ross! He is was so nice and knowledgeable.Has a great handle on the new and exciting things happening in the Lyme community. Very comfortable with the protocols he prescribed. Super excited about my wellness plan moving forward. Super thankful to finally be diagnosed! Thanks Dr. Ross!

Dr. Ross engages in collaborative care and true informed consent.

Never post reviews but Marty Ross deserves one. Just trying to save someone time. Saw Marty ross for the first time 6 months ago for my 2nd time treating lyme. Got about 70% better the first time treating lyme from a great LLMD who died. years later my symptoms came back and decided to go to Marty Ross because he was in a movie and heard decent reviews about him. Did 1 blood test in 6 months, diagnosed and treated me with a different co infection then what I got tested for years ago, Long story short ended up in the hospital from an allergic reaction to some antibiotics he put me on. Took him 3 days to reply to me on updox telling me to go to the hospital as I was bed ridden broke out in hives liver was insanely inflamed and in pain, and I was puking. Tried many different antibiotics after that and have only gotten worse. In it for the money, not getting any more of mine.

Dr. Ross was the only Doctor listening to me when I needed it the most. He is extremely knowledgeable, compassionate and caring. I am so glad I have him as my doctor.

Great doctor who knows his specialty well and is kind and a good listener while still being directive. He even has a blog about Lyme. I feel confident I am in good hands. Worth the 3 hour drive.

Im not posting under my real name because I dont want potential employers to know I have Lyme disease. I saw Marty during the aughts and he was a very solid MD. I spent 30 years chasing a diagnosis until someone thought to test me for Lyme disease in 2006; I had been told I had lupus, RA, FMS, Etc.- you name it, I had it. Marty was a good and careful diagnostician and practiced solid conventional medicine complimented by some New Age modalities. He did not force the latter on me; he offered and I availed myself of them, largely out of curiosity.Diagnosing Lyme disease or any MSIDS is extremely difficult; the testing technology is over 40 years old, and woefully inadequate. Diagnosis is largely a process of elimination, and anyone who follows Lyme Disease in the news knows that there is significant disagreement between two medical societies about treatment. Any doctor willing to treat long-term Lyme disease is incurring risk and becomes a target for IDSA (Infectious Disease Society of America). Marty belongs to ILADS, the medical society for docs willing to treat Lyme Disease.In my 30 year quest for diagnosis and treatment I saw a ton of docs (probably in excess of 50), learned a lot, already had a science education. I can comfortably say that Marty is a good and careful diagnostician with no agenda other than questing for the true and accurate diagnosis and following the up-to-date protocols for infectious agents. Given that the average infected tick carries 12 infectious agents, this is not childs play.

Marty is one of the best at what he does. And he knows about chronic illness and how to treat them. Ive been seeing him for half a year now and feel better than Ive felt in years.

Carl h.Maybe thats YOUR case. But its insane that the lyme Drs that have treated patients that have been diagnosed with lyme ...are unable to treat them with protocols that have actually worked. Its insane that a person has to hide their true disease when crying in pain and go to ER. To fully understand what Im saying please Google lyme lawsuit Houston texas Lisa Torrey. This controversy on lyme infuriates me beyond words when I have a daughter who screams in pain 24/7 and can not get admitted. She once ran 3 miles a day and was enrolled on nursing school. September of 2016 went hiking in Oregon became very sick. 4 months later she was diagnosed with lyme AND rocky Mountain spotted fever. The dr. Gave her the 21 days of doxy per CDC guidelines OBVIOUSLY their guidelines are BS....she is now bedridden and last month she was tested again for lyme etc...thru lab Corp , Western blot and igenex.....all came back STILL highly active for lyme, rmsf and babesia duncani. Which babesia duncani is found on West coast which naturally makes since whereas thats when she got sick. We are now taking her to Germany due to the fact thats the only place she can be admitted and monitored when have this wicked disease. Its BS pharmaceutical companies tell Drs how to do their jobs. 2 things that completely piss me off is GREEDINESS AND MONEY!!JENIFER LIBYGLASCO KANSAS

Dr Marty Ross misdiagnosed me with Lyme disease. This led to my seeking treatment elsewhere after their office didn’t answer calls or voicemails with problems I had with supplements he sold me. The next doctor I went to after Martys misdiagnosis that mistreated me for lyme disease lost his medical license for four years and is under FDA criminal investigation because of their mistreatment of meDr Marty Ross prescribed me Levaquin, which would not have treated what I really have, but does have serious and life long side effects.I filed a complaint again Marty Ross with the state medical board and they opened an investigation into his misdiagnosis of me.