Hi, I am writing today about my Lymphedema which I was born with. I am currently going thru Lymphatic therapy which is basically wrapping my leg a certain way so it can encourage my weak lymphatic system to work. It has been helping. I am also using a tactile medical machine for compression which together is helping. My right leg is 3x the size of my left, there is a lot of build up of waste. I am seeing a plastic surgeon who can perform SAPL (Suction Assisted Protein Lyposuction). It is to remove all the waste in my leg. Fingers crossed I will be able to get the procedure soon or I may have to wait another 3 months.
My journey with Lymphedema: Hi, I am writing today about... - LSN
I have it in both my lower limbs I know what I going through mine is not quite as big as ur leg but it horrible I have had it for 22 yrs
I would agree that no matter the size, it is horrible. I hope you are getting the help you need to live some what of a normal life.
Good luck Bettina 88. I hope the treatment is successful. Lymphoedema is a horrible condition to live with. Mine (in my left arm) is a result of cancer treatment. What I miss most is wearing the sort of clothes I'd like to wear and not what the condition dictates.
Thank you, and yes I would agree. Because my leg is so heavy I am limited with shoes and they wear out quite quickly. Are you getting compression therapy on your arm? SAPL also works for that
I wear a made to measure sleeve which really helps. It seems to keep my arm soft. In the beginning I wore an off the shelf sleeve and I think it actually made it worse with hardening areas in the crease of my elbow. I also learned to do compression bandaging and lymphatic massage.
Before lockdown I attended a tripudio class which is gentle exercises that encourages the movement of lymph fluid. It is now being held on zoom and much as I enjoy it it's not the same as it was held in a church that had a coffee morning. We would all meet up before hand to have a chat and tea and home baking then go along to the room where our class was held. I really miss that. Everyone in the class has gone through cancer, but not everyone has lymphoedema. It was like a support group. With your family you feel you have to be brave and not mention how your condition affects you mentally. Their attitude is "well you're alive" which doesn't validate your feelings.
I am glad you have been able to interact with people about your condition. Though I love my family and my friends, they do not understand what I am going through nor do I have a group to interact with others who have the same thing. it's like being an alien. I found the lymphatic massage therapy and wraps are actually softening up my leg. It gives me hope.
I have had secondary lymphoedema in one leg/foot since 2017 as a result of cancer treatment. It is an onerous and potentially horrible condition to live with, and often made worse because it is not well recognised or catered for by the health services - on a global scale. I wish you all the best for your pending treatment.
Hi Benita , I’m so excited for you . Can you share which surgeon is doing your liposuction and country please . I’ve lived with this since I was 13 yrs old and it’s destroyed. My life I badly need to try and find something succesful . My good wishes are with you 🙏
After help from my vascular doctor, I was referred to a plastic surgeon from NYU name Orianna Cohen. She is just lovely and she is making sure I do everything I must before I can have the procedure.
Thanks for your reply . What is the cost of the procedure you are having ?
I honestly do not know yet. I will share the ballpark once I find out. I have tried to look it up but there is no real info on SAPL. I do know there are 2 hospitals in the midwest that perform the procedure but I will have to look it up again.
Good luck Benita88, hope you don't have to wait too long for the SAPL treatment.
Hey Benita, I’d love to hear more of your story, i was also born with lymphoedema. I’m fortunate enough that my condition was finally diagnosed at the age of 2 and I have benefitted from compression stockings ever since. I’m now 25 and my condition has worsened over the later years, I worry about how my condition will progress as I continue to age or have children, I was lucky enough to undergo some genetic testing recently and was found to be the first carrier of the vegf3 gene in my genetic line, how it happened I will probably never know but what I do know is going forward my descendants will have a 50:50 chance of contracting the condition, if you’d be happy to share more of your story I’d love to hear all about it
I would be happy to share more of my life with it, you can ask me anything.
If your condition is getting worse, I suggest you please act on it now by making sure they send you to therapy to learn the lymphatic drainage therapy and I also use a compression machine by Tactile Medical. the 2 together work well together and are giving me results. But this will take a while for me because my leg is rather large, but I get measured every week and there has been a difference. Also I am going to be fitted for a Juxta-fit. This will be easy for me to ware then all ways having to do the wrapping.
Good luck Benita88. Please, please keep us updated on the SAPL result if it is done. However, I was always informed by plastic surgeons that plastic surgery is not valid for lymth (mine is after car accident in early childhood at 6, now I am 44).
Be strong and courageous!
Actually this is simply for debulking but I will still need to wear compression stockings which is fine by me because there is no cure and after that I will see what else can be done. But I will definitely share.
There definitely are surgical options. I’m getting the debulking liposuction at Stanford and then in 9 months a lymph node transfer. I have primary in my right leg which don’t show up until I was 42 (9 years ago). Best of luck to Benita! I’ll be recovering with you in spirit!
I should also stress that my leg did not look like this until the past 10 years. Before that it was hardly noticeable but because I developed a Fibroid, I bled so much that it increased the size of my leg rapidly. My fibroid was 6 pounds and had to be removed but that did not help my leg at all. I recently had a test at the Department of Nuclear Science, it is a Lymphedema test that takes 4 hours. I will explain more in another post. But the result is, not much is going on in my veins. Oh and I am 53.
Yes please keep us posted with further developments on your story, may God do a miracle and heal it completely. I always put my hands on my leg and declare "Live, Live, Live" I command all my veins and other structures to hear the voice of life and live and carry on! God bless you all!
God bless you as well, and that is a great attitude.
Will keep you in my prayers ❤️🙏🏻🙏🏻🙏🏻