I had Lyme Disease about 25 years ago and it went into remission. However it came back about 4-5 years ago. In googling it I found the MLDA and allied. The president directed me to a LLMD (which I had no clue what that meant then). They also sent me a lot of information on LD and answered a lot of questions. I was also given a list of names I could contact for support sand eventually started a support group in my area. I wouldn't be here today if it weren't for the MLDA. They supported me at my lowest points and ow I'm able to give back. They also have an e mail support for those that prefer that way as well as many FB groups on Lyme Disease. It's great getting new info and communicate with someone who understands what I'm going through. I will forever be grateful for this non profit organization
I am a member of the MLDA. I was so appreciative of how much I was able to learn from it's members and especially the board members that I joined the board. I have learned more about Lyme and received so much support from everyone involved in this charity. It is non profit and while so many of the individual board members have Lyme Disease and are therefore often sick, they put a lot of effort into helping others and are a wonderful source of support. They are very involved in all research and extremely knowledgeable in the various treatment options. They advocate on behalf of anyone that needs help. They are very involved in trying to keep the publice aware of what parts of the state of Michigan are at highest risk for places where the disease is showing up the highest. This is not to deter people from going to these parts but so they know to make sure they protect themselves if they are going to be outside in those locations. I can't say thank you enough to the board and all volunteers who are there to listen and help in any way possible.
The MLDA is a wonderful organization with caring and dedicated individuals, who are a great resource for those who need help with anything to do with Lyme Disease and associated confections. We strive to raise awareness through many research campaigns, brochures and much more. All to often we provide support to those in need to many newly diagnosed patients and health professionals seeking additional information. Without the MLDA, many would struggle in knowing where to go for help or information on what Lyme Disease is all about. I'm happy to serve as a board member, in continuing to help educate the public and assist in much of the planning the goes on for the association.
I've had lyme disease now for 18 years but took a year to get diagnosed. I was quite young at the time, 15 years old and my mom was desperate for help. We thank God every day that we came across the MLDA, and the president Linda at the time. She helped us immensely and has helped me to want to give back by joining the board. Without the MLDA, many people would be lost. They are THE best non-profit I know. I don't know where I'd be today without them.
Next month (9-13-2014) will be 21 years with Lyme disease. ( Also had Babesia and Ehrlichia) I would not be here today. if someone from the MLDA did not help me. I was very ill and needed help. The ER Dr. said I would be fine and not to worry. I started volunteering early on. I am the secretary and the person who sends out all the information to those who ask. Over the last 21 years I have sent out tens of
thousands of pieces of literature. We do not charge for any of it. We pay for all the printing and postage ourselves. I am mostly homebound now but still send out information and do what I can.. Through the MLDA I have seen the education of medical personal rise, slowly but surely and it is all through the
hard work of the MLDA.
When I got bit in 1993, there was almost no help from the medical community. I was so sick, most days I didn't know who I was or where I lived. The MLDA helped me in so many ways. When attending support group meetings, then board meetings I found out that they were the only ones interested in getting information to people. iI is hard to function and find information when your brain is swollen. If it wasn't for them, who gave me information to take to my doctor, I am sure I would probably be in a nursing home intead of now being a volunteer and "passing it forward" This is a great organization.
MLDA has been the only hope and only place to turn to for anyone with or anyone who knows someone suffering with Lyme. As a mother with all 3 of my children having Lyme Disease times can be hard. It is because of the MLDA and Linda that we given any direction at all on how to help them to get better! My oldest son was very ill and still after 3 years of treatment is still fighting this disease daily. It is all because of Linda and the MLDA that we were able to even know where to start to even treat him. Our family owes the MLDA everything! The health of your family is the most important thing and the information and support that is given and offered by the MLDA is second to none!
Tell your story here and help others understand this charity It scares me to death to think of where we would be if it had not been for Linda and the MLDA! After seeing dr after dr and had test after test ran on my son to come up with nothing over and over again and to watch him get sicker and sicker, to then be put into contact with Linda and MLDA who gave us hope and direction and support! Linda was able to lead us towards the right direction in getting our son's health back on track and finding out what he was struggling with. We owe our son's health to Linda and the MLDA! The knowledge and the support that has been giving to us by the people behind the MLDA has been so important and needed in our time dealing with this disease. Our journey is far from over but I'm not as scared of the out come knowing that we have Linda and the MLDA helping us with every step forward! Our family thanks them for the bottom of our hearts!
The MLDA and Linda Lobes saved my son's life! He was very sick and getting sicker by the day and after seeing many doctor's and many tests no one could find what was wrong. Linda took the time to talk to me and help us get some answers, directed us to a Dr that was finally able to test my son and help him. That was almost 2 years ago, and still struggling daily with Lyme and Co Infections, my son is at least doing better.
And because of the help and the knowledge I have learned from the MLDA, I was able to see the signs and get my 5 year old son tested before he got very sick and found out he also has Lyme and now is being treated.
If it wasn't for this group my 9 year old son would be at the point now where he could not function, before we got him treated he was getting to the point where he was unable to walk or think. It was the scariest time of my life. My husband and I owe everything to the MLDA, Linda and this group saved my son's life!
The knowlegde that I have learned from the MLDA has helped me, help other people in need also. I have been able to guide people that were sick with some of the same things and get them help along with being able to teach people who don't know anything about Lyme so they can protect themselves and their families.
A great organization with friendly hard working people. They really make a different by giving support and helping educate people about lyme disease.
I have been a board member for some time. I initially attended meetings to have access to lyme information to distribute to my support group. Now it is relatively easy to get information on the computer and through Michagan Lyme Support. I've learned of these sites through the MLDA. The MLDA does a valuable service by getting information out to the public about the disease and its treatment. Linda is always available to answer question and to help people find a doctor to treat them. The MLDA is a valuable resource in our state for getting information out to the public, health departments, and so many more. Without the MLDA,lyme disease would still be in the dark ages.
I have been a Board Member for about 3 years now as I was so frustrated to find out a diagnosis for my "multi symptom illness". I had the help of the MLDA to access a doctor after 16 years, there was a possibilty that I had Lyme. I had the bulleye rash in 1983 following a camping trip to Nashville, Indiana. At the time, I worked for 2 Surreons and they sent me to every Dermatologist in Genesee County. From there, i was sent with my dogs to the Vet for the possibility of "ring worm". Our Vet told me that was out of the question and whatever I had, please don't give it to the dogs as he would have no idea how to treat it. The rash finally went away, but for the next 16 years I had severe arthritis pain, plantar faschitis, right hamstring pain, off and on again acute right sciatica and finally migraine headaches. During this time, my family doctor did blood work testing for Lyme 3-4 times with only "iffy" results. Finaally in 1999, 4 bands came back positive, the second time, for Lyme and I was started on antibiotics. I then was put on a waiting list for a Doctor in Saginaw that treated Lyme. After a couple months, I called MLDA, frustrated and crying as I felt I was at the end of my rope. Through the last 10 + years, I have asked the President of MLDA, Linda, many questions that she has always had an answer for. I have never called without receiving a return call. MLDA helped me get in to see the Doctor in Saginaw and has helped me through many crisises in this period and that is why I went to an annual meeting out of curiosity apprx. 4 years ago. One thing lead to another and I became a Board Member. I do the best I can to help educate the public about Lyme and help out on as many educaational projects as I can. At the present time, my Lyme is in the fibromylgia stage and I tire easily along with the constant pain. Going to the monthly Board meetings gives me the support I need to keep sane. Thank you MLDA Sally Lurvey