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A Day in the Life Living with Lipedema
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- Опубликовано: 9 июн 2024
- Sharing a peek into my life living with lipedema.
#lipedema #lipedemaawareness #lipoedema
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Hey babes! I’ll be back with another vlog soon ❤
Thank you for this video.
Hi what was that you were making at the beginning?
Thank you Hannah for sharing your testimony❤️ God bless you for blessing anyone who is watching and they have the same health condition 🙏🏼❤️. I am proud of you beautiful sis staying healthy and moving forward to reach your goals and accomplishments.
Thank you, Hannah! For the video. I try to enjoy my life by ignoring the foolery. Most of all love on myself, and enjoy life. It could be worse.
I’m new here and I think I’m gonna like it here.
Change your diet to whole food plant based veggies and fruits instead of processed foods, you’re health will go in a different and better direction, God bless
SO TRUE
Hannah has 29K subscribers. If all of us send her $1, she would have more than enough for surgery. God bless you Hannah...love you❤
Agreed! I would love to contribute to her surgery if she decides to do it 💕
I would definitely contribute!
Yes good idea❤🙏🏽 I will definitely contribute…
Love this idea if anyone organizes this Id definitely contribute. I hate that health care is so inaccessible!
30k now
I have had Lymphedema for 23 years, I have cried so many tears over the years. It was not until I remembered a song in the church where I grew up, the song is "I want to live so that God can use me anyway and anyhow".
God has given you this platform to educate, inspire, and love yourself. You see God can't use you on the front line if you're not suited up with the whole armor of God.
We can stay in a funk or get out there and start support groups, educate others, and most importantly love each other. I truly love you my sisters and brothers.
Beautifully said! Blessings to you! 💕
She has lipedema not lymphedema
@@RacquelDaigle Believe you me I know the difference. What difference does it make, God has blessed Hannah with a platform that can educate, begin real talk, and explain how the debilitating condition effects your everyday life.
What I feel is the craziness that doctors have stated that they only receive maybe a day of study/rounds with the condition. That is mind boggling.
@@jacquelineparker1133, I pray for healing on your condition
@@user-lk6gv5gy1f Thank you so very much. I pray your health and wellness as well.
I immediately stopped when I read the title. My mom has lymphedema and I empathize with her daily. I diagnosed her with it while I was watching a true life documentary on MTV while I was in high school. Thank God she listened and went to the doctor. She can’t walk long distances, but thank God she isn’t in a wheelchair; she can’t sit in chairs without arms, if they don’t have arms, she has to sit near a wall for it to help her get up. She literally just text me, she never thought her life would change to where she can’t get out of a chair. Thank you for sharing; keep being a light and let’s pray for those who suffer in silo.
She has lipoedema not lymphedema
Lymphedema is the cousin of lipidema
And ppl w/lipodema have nodules & "lipoma's"...Dr. pimple popper removes them all of the time. They are huge fatty nodules.
YOU diagnosed her? That isn’t usually a good idea. Can she go to a doctor?
@@seeleygirl6178she said that she went to a doctor
Second comment, but I have to add this: you’re so soooo pretty 😭💛 the face? The skin? The style? The hair? The personality?
10 out of 10
And I’m so proud of you for fighting for your relationship with God. Life gets hard, and it’s so easy to feel frustrated and confused and even distant as we walk with Him. But He’s right there, patiently waiting for us to embrace Him as we navigate the challenges, and ebbs & flows of life.
Oh my gosh I love how you worded that ❤thank you love
I second everything you just said.
It doesn’t look the way you think it looks. You still have a nice shape even through all of this.
Right thats what im thinking she still looks good
Right! She still looks good, I’m confused🤷🏽♀️
Having a nice shape means absolutely nothing when you’re swollen. My medication swells me up and yeah, I have hips or what but I’m in pain. I understand where she’s coming from. I stopped wearing shorts and dresses. I don’t wear heals and I’m bad days my sneakers don’t fit from the swelling.
It’s literally all in my hips, legs and butt.
Praying 🙏🙏🙏🙏❤️❤️❤️❤️
Hannah they have cover ups for swimwear. Just food for thought. They have long pants or even skirts. I don’t want to see you miss out on Summer fun!!🥺
Hey girl! I wear the coverups all day errrday lol I was referencing actually taking that off to get in the ocean/pool. Thank you love for the suggestion ❤
Amazon has a huge selection of swimwear. For religious reasons, I have to wear an ultra modest bathing suit. I got a cute “burkini” there. You don’t have to go that route, but they have swim dresses in different lengths and swim shorts and even swim pants that are very stylish and decently priced.
@@hannaholiviaI bought some rashguard type leggings and long sleeve. It looks like it is for the water with tropical print and I didn’t feel out of place,in the pool, plus SPF, so good. Have fun out there
Maxi dresses are floor length. It may be a better more breathable option for you in spring and summer. Wishing you all the best.❤
Yeah girl I’m gonna have to bust the maxi dresses back out lol❤
Yes, rock some long skirts and maxi dresses...some are beach friendly!😊
Hi beautiful 💕! I’m so glad you shared your experience with Lipedema! I’m older than you, but have experienced this most of my adult life! We are shaped similarly and I use to (still do) have some of the insecurities you have with wearing anything that shows my legs. I use to steer clear of shorts, leggings, knee-length dresses or sandals without straps (using the straps to hide my chubby ankles 😁). I just started wearing leggings in public and I love it. I wore shorts and slides for the first time in a long time last year! Also, I wore a swimsuit without a coverup and got in the water at the beach in the Bahamas, and had a blast! I had to tell myself these people don’t know me and I’ll probably never see them again 🤣! I’m learning to embrace it! It’s definitely a journey! Sending you love, hugs and prayers on your journey!
I’m tryna get like you!! 😆such an inspiration
I remembered awhile back, where you getting your toes did and you broke down crying, and left because you were embarrassed about your feet, I felt your pain that day. I too have lymphedema, it started in middle school, and it does take a mind shift in your whole body. Trust and believe, it gets better with time. I will be 60 next month, and young lady let me tell you, GOD is good! Yes, i a few flare ups every now and then, but i understand now how to control this temple...
Mine started in middle school too and I'm 52. I'm so glad for RUclips and hearing more about it, because I never met someone in person who was dealing with Lymphedema.
I can relate because I go through the exact same and I'm 58
@@Erica-en2qzmeee for 20+ years . We are out here . Lymphedema was barely recognized as a disease, much less for his disabling to your physical and emotional well being
Please note lymphedema and lipodema are different ❤
@@Erica-en2qzHey Erica! I’m 53 my Lymphedema started in middle school too but only in one leg! My left leg got larger in my late 30’s… I only know 1 person like me
You are the face of self-care.!!! You needed to share so that you could feel good about who you as a person. You putting yourself out there so gracefully is a true reflection of your glow up. We didn’t deserve to be this deep in your personal life though I’m sure you have encouraged a many people.
I HAVE THAT AND THIS IS THE FIRST TIME I FOUND SOMEONE THAT CAN RELATE I AM 51 YEARS OLD U HAVED LIVED WITH THIS THE PAST 30 YEARS OF MY LIFE😢
I was just recently diagnosed last year. The pain is the worst. It has definitely affected my life in ways I could have never imagined. The worst part is doctors telling you to just lose weight. If it were that easy, don’t you think I would? I’m so glad you shared your story. I can definitely identify with a lot of the things you shared. ❤
I have it and am 68...I still get up but have a rollater to help me at home and also a walking stick. I cried a lot but am past that now. It is a horrible disease. Someone I get so tired from fighting the pain I just have to lay down. I still drive. It is not fun and I feel so bad for people with leg or feet problems I just start praying for them and they don't even know it. ❤😊
Hi Hannah , there is one called Lipodema and a Lymphoedema. I have Lymphoedema and I go to a Lymphoedema clinic where they wrap my legs nice and firm. I don’t know the cost , but Medicare pays. But look up the difference between these two words , very similar.
Thanks for being so vulnerable. I developed a mild case of this after pregnancy. Some days are better than others. ❤
Same, 4 months postpartum with my 3rd, and my ankles are still swollen.
❤
I did not know that June is Lipedema Awareness Month👀 I am still trying to grasp this part of my life. Thank you.
I didn't know either this my first time I'm hearing this word I've have this problem I'm crying right now this my first time looking at this video I go through my heatlh
Me either 😮 I just learned something new
I didn't know it either
It’s comforting to see someone that looks like Me share this experience. I appreciate you.🌹
Your willingness to open up and share something so personal is huge. It's not easy to be vulnerable. I know you will help people. God bless Hannah.
Hi Hannah, I been watching your content for a while and I too suffer from symptoms of Lipdema. What I have found that is helpful but it's quite a challenge, is giving up dairy products. I found for me that's where majority of my imflammation comes from. I've seen a lot of good results from slowly removing it from my diet and incorpoating more fruits like blueberries and oranges. Reducing my intake of dairy has been a game changer, but it's definitely hard because I love cheese, milk, and yogurt.
I don't comment alot but you're my internet sister (even if u don't know it 😆) You are so courageous and beautiful. The Lord will bless you, Hannah. He doesn't put to shame those who trust in Him. Keep up the amazing work!
Honest to God, your lymphedema is not that noticeable… I pray for your healing, you’re so pretty ❤
Lipedema and lymphadema not the same
Yes I did not think they looked that bad because my legs look just like hers. I’m older and a lot heavier but I’m pretty sure it is starting in my ankles. Bought a vibration plate the other day because I RA and I’m not very mobile..
You have a beautiful spirit. It's not easy dealing with any form of weight gain. I'm over weight with lipedema! I wear what I like. I'm 61 years strong. I dress my age, I have heavy upper arms, that does not stop me from wearing sleeveless tops. I love wearing sandles shoes, and I do. My feet start swelling about 30 years ago. Doctor's could not give me answer to why. Made me so sad. I pray for us all, the universe. Thank you for sharing. I pray I helped someone as well. Many blessing to you all.🙏❤️
I had a life altering injury to my hip 4 years ago. Before that I lived a very healthy lifestyle and exercised every day. One day I hurt my hip while I was exercising and I’ve had chronic pain ever since. I’ve gotten surgery, PT, and nothing has worked. I felt you when you said you felt angry you had to deal with this. I’m still dealing with frustration of it all
So glad I found your channel. I also have lipedema. I think it started during puberty but it stayed at stage 1 for years and was unnoticeable to the naked eye. It wasn't until my last pregnancy that things took a turn for the worse. I'm now between stage 2 and 3. I have so much pain and tenderness. I also have fibromyalgia and just started with perimenopause. It's been tough but I'm not going down without a fight. I'm getting into the gym, going on a inflammatory diet and consulting with a specialist to discuss my treatment options. I'll be following your journey and I wish healing and wellness for you, myself and all my lippy sisters all over the world 💋❤
Thank you for educating me/us 🙌🏾 have a great week Hannah girl ❤
Hello Gorgeous! You will perhaps never know how much you inspire women of all ages. Lipedema is not talked about enough, and so many suffer from it. Thank you for your courage and we love you. 🙏🏽♥️
❤
Hi Hannah! I'll say this, Variety is the Spice of Life. If we all looked, sounded and acted the same, this world would be so boring. For a woman, I have a deeper voice. I spent so long not talking around people afraid of how they would react and would get teased as a kid. I started thanking God for giving me a voice because some people wish they could speak 🗣️. Kudos to you for blocking out negativity and living your life for you.💐 My dad used to tell me that "you will never be able to satisfy people so it's best not to even try".
I completely understand your journey. I have lymphedema too. I don’t care what people think or say. I wear what I want
Thanks girl...had a tear in my eye lol because you get me and struggle. Thanks for the transparency and bravery because it's not easy putting yourself out there, having to admit you have a condition. Proud of you and keep putting your positivity out into the world and God will continue to bless you.💜
🥰love you Donna girl
You are a WARRIOR with a positive attitude
I’m so sorry for all that you’re going through. I pray your condition gets better. You’re such a beautiful person and life is so short for all of us. I hope you find a way to be more confident while treating your condition . At the end of the day, no one is really paying attention to anyone. And the ppl who are paying attention are weird and you’ll probably never see them again. Im learning each day that we gotta take life as it is and just make the best of it while we’re here ❤.
Hey Hanna .
My husband and I love ❤️ watching your videos here in Tampa,Florida. Thank you for your transparency on you struggle with lipodema. Prayers surround you on your health journey. Thank you for addressing the question b4 we asked 😊my husband and I were curious about the use of compression leggings or socks for fluid retention and circulation. I had to revamp my diet by removing anti inflammation foods ( cheese and gluten-free foods, reduction of sodium) it's hard but I feel so much better.
Sending hugs and love to you
Awesome content
Love how you constructed this video ❤❤❤❤
Hello. I suffering from the swelling of my feet ankles recently. Going to doctor this month to get check why feet and ankles swelling.
Hi Hannah
Continue exercising continue taking those long walks , go to the gymnasium whenever you have time, never feel anxious or embarrassed doing this coz you doing this for yourself. Don’t pay attention to who’s looking at you, focus on your goals and we got your back here. Your motivation is here on RUclips which should keep you moving but not in public,,,, coz you know what, i guarantee you this should you keep doing what I’m telling in the period of 6 months you will see the difference and that will even motivate you more en more every single day. Much love ❤️
I don’t have lipodema but your message of growth and confidence is inspiring. Sending you positivity 🤎
I shared this video with a friend with an older sister with lymphedema. She told me that her sister sees a cardiologist and an endocrinologist as well to deal with high blood pressure and issues with her hormones that affect her lymphedema. She has been on the "Dash" Diet for over ten years; salt is a no-no for her, and also sugar. After watching this, I also researched, and it's tough. ❤ God bless you Olivia!!
How brave are you?! So incredibly insightful. I'm thankful that you shared this part of your life with us. Keep pushing forward. 💕
I eliminated mines; started water fasting 36hrs then eat 24hrs then repeat fast and so on. I eliminated meat and dairy too which cause inflammation for me. Hope that helps.
Depending on insurance, 7500 may max your out of pocket and if you do that at the beginning of the year, then insurance would pay out 100%. Can you get both surgeries in same year? also, hospitals have charity options that may be able to kick in to help with costs. If you don't have insurance now, try to apply for 'obamacare', that may help at least w/ co pays/tests etc costs. hope it works out
I'm glad your video popped up in my feed cause I've been suffering with this for years. It's nice to see someone else who looks like me is talking about lymphedema.
She has lipedema and obesity.
Great video from a young adult lens.
My cousin’s wife suffered really bad from this too. She talked about how in grade school she would stay home some days because of her insecurities in her words because the bottom half of her body was like an elephants legs. She now 49 and states that having a pescatarian diet changed her life.
Now I, myself have always felt like we can eat whatever just in moderation of course but I can also honestly say and witness with my own two eyes that, that diet has changed her entire life and my best friend’s life who suffers from a different disease-lupus. Both ladies look phenomenal.
Lastly I don’t have all the science behind disease but for me eating mostly fish, seafood and chicken has helped with my inflammatory alopecia. Just something I tried during the pandemic and practice this habit for two years just to test it out. Seems to regulate the body’s immune system and lymphatic system. But still eat beef and pork tho. Just every blue moon.
Hey, Hannah -
I'm so sorry that you've been having to deal with this condition. But, also so glad that you're able to be open about it, and that you take precautions when going out in public to ensure your comfort level. 👍🏾👍🏾 for self care. 🙏🏾❤️
Thank you love ❤
Hannah, I battled similar insecurities with showing my legs for years as well. Not to hide a lymphedema but due to scars from impetigo infection as a young girl. Like you, I felt summer was not my season & I watched with sadness as all the girls my age wore sundresses, shorts, etc but I had to be creative with my attire, also spending more time than normal deciding what to wear. It’s so funny how we all have something to contend with while thinking others have it made. I just wanted to share with you that this diagnosis is not the sum of you. You are beautiful, inspiring, intelligent and adored by our creator. He made us in His image, so no mistakes were made. Stay positive and keep this fabulous content coming! This is a ministry and you are giving life to the people!❤
Girl you are doing great. Yes no one is looking they have their own stuff going on.
You are such a sweet, positive, beautiful sister. Enjoy and embrace who you are. Life is way to short to please anyone but you.
I knew I had lipedema for years and was finally diagnosed by a vascular surgeon last year. I remember being 16 and my legs and feet swelling and my mom attributing it to my shoes. That was 2006, so we really didnt know what was happening. I wish surgery was more accessible for lipedema.
I too do not wear shorts but I'm hoping to get back to it this year because when I was in my late teens early 20s, I would wear them and not think twice about it. I just got a pair from target this week. Hopefully I will wear them this summer🤞🏾. Best wishes to you as you continue your journey with lipedema. Thank you for bringing light to this condition.
Hannah!!! Thank you for sharing!!! Having chronic illness makes you more compassionate amd empathic to other people. I had to accept the things I "could" do instead of things I "can't do!!!! My situation is that my family "won't" accept my limitations because I was "always" active before having RSD, Crohn's Disease and DDD. God Bless!!!!
I loved this video Hannah. I feel the same. I have Lymphedema. And I always wear extra long skirts and pants. But with me I also can’t wear most shoes because my feet swell so bad. My doctor basically said even if I loose weight without wraps or compression stockings my legs will still swell. Summer I love because I can wear sandals but winter I can’t wear much. It’s a hassle.
Yes girl, boots are a thing of the past 😫…I think I’m slowly embracing summer
I have a problem finding shoes
I'm a sista in advance stage #3 lipedema. I've learned how to trust in and use the word of God to be able to manage this without the resources other cultures seem to have access to. I haven't experienced pain or had to wear my compression in the last two days.
Normally I would have to put on cream for pain, and then compression for pain. God toldme what Ineeded yo do, and Ilistened. What a blessing and a relief from pain. This ismy 2nd no pain day while getting my stepsinon a trampoline. ❤ I don't know how to reach you on Instagram.
Hannah, I’ve smiled through this entire video. Seeing your transparency, vulnerability, and self awareness is amazing! You sharing your journey is so important and adds so much value to the world! Praying your continued success and victory girl!! 🫶🏾
Never have I ever felt like I can relate to somebody else's experience more than I have while watching your video! Thank you for your courage and grace to share your story!! 😇🙏✨
Hey young lady, I thought about you this weekend. I noticed some pain around my ankles and saw they were swollen out of the blue. I researched and found some exercises that helped bring my swelling down. I thought, my goodness I'm sure Hannah is going through way more because that little mount of swelling for me was uncomfortable, and I got new shoes and couldn't try them on my left foot until it went down. My mom had this really bad when she was sick, and I felt for her. You have a plan and sticking to it will be your success. You're determined to keep moving in your assignment in spite of , and that's what God wants while you wait for your healing. I laughed at your comment about what you would be like if you didn't have it. I feel the same about my weight, girl if I was smaller my family would be like "can you please put some clothes on at your big old age" 😀😀😀😀😀😀
I know it took a lot for you to make this video. Thank you for your courage and I’m sure it will help a lot of people.
I watched the beginning 3 times and still don’t see the fuzz coming out your cute fav slippers 😂 💚 thank you for sharing this! 🫶🏽
😂😂😂❤
I love how careful you are with yourself... taking time to use creams , perfumes, nails done, and dressing well ... love it ❤
Love your new found confidence in your 30s Hannah! I never knew much about lipidemia, so thanks for shedding your light on this disease and making it relatable. I’m praying for a cure.
Thanks for sharing. So many of us deal with such a wide variety of health and weight issues, and we spend so much time hiding, but sharing your journey is so freeing and i hope you got a lot out of this.
Have you ever considered having liposuction surgery geared specifically towards lipedema?
I've seen how much it is said to relieve so much pain.
Girl, you are gorgeous inside as well as out.
I feel you Hannah when you said god made you this way. I use to hate certain things about myself, now Ive grown to love it or have the funds for surgery😊
I really appreciate this video. I have autoimmune disease and whilst it’s a “hidden disability“ but the adjustments I have to make to protect myself and not attending some spaces because of my own comfort and risks associated with certain social events can be difficult sometimes. I hope you continue to share your story with us and celebrate each day where you can x
Here to support and I am having same issues with lipodema ! But I’m much older than you! I was adopted no family history for me! I’ve read that lipodema occurs when lymphatic system breaks down! There’s no way I can wear heals anymore! You have good control on this ailment still walking my heels hurt I can’t walk like that! I appreciate you and you sharing
Oh Hannah!!!! You are sooooo beautiful and I am so proud of you! You are brave (even when you don't think so)! Sharing your TRUTH WILL bless someone else. So much education & empathy for others is what's needed for MOST things!! I have never been diagnosed with Lipedema but I think I have it too! I PRAY you continue to talk about this to bring Awareness for those who look like "us"!!
😌thank you love ❤
Thank you so much for sharing this and educating everyone. This is great content we love to see. First I want to say I’m sorry you had to go through this during young adulthood and I’m so happy you’re working to overcome.. but sis…… you are GORGEOUS!!! I’m so glad you shared this and shared pictures of you. It gave me more insight of you as a person. You was and still is FINE girl!!! I know it’s hard to believe that when you’re going through the motion. And your toes are so so cute!!! Keep working on yourself inside and out. And when you’re ready… maybe start wearing your skirts and stuff like that. Slowly but surely.. because you looked so free then. You are a beautiful woman.. don’t let what society or what you think society would say… continue to rob you of your happiness and freedom. Cause baby you a baddie!! You just got to believe that! 😉 ❤
That’s so true girl ❤thank you for that reminder
Thanks for bringing awareness to this condition. Have you looked closer into your diet to eliminate inflammatory foods? Things like dairy, carbs, processed foods, and meat can cause inflammation in the body. I also have a medical condition that causes inflammation and it helps me so wanted to pass this info on to you. Wishing you the best on your healing journey heart❤
I love your vulnerability in this video!! Thank you for feeling safe to share this with us.
I appreciate your transparency and authenticity. Lymphedema or not you are absolutely beautiful
I can relate to everything you are saying. It’s a hard condition to have, because people don’t really understand it. It’s hard to explain my limitations, my pain, my mindset and my insecurities about it. I’m 51 and I have been dealing with it for over half my life. I don’t have anyone that I can talk to about so when I saw your video I had to subscribe.
Thank you.
I have lipodema/Lymphedema. I know this is not easy but most of us try to adjust with life changes. I was always "heavy" but never knew about Lipodema. Like a lot of us I was told I was fat and put on diet pills that never worked. I was very active and held down two jobs being a personal care attendant for yrs. It was brought to me by a vascular doctor I went to see about pain in the back of my legs. When I hit menopause the Lipodema was put into overdrive quickly which brought me to Lymphedema! I have a lymphema pump, get lymphedema massage therapy from a lymphema therapist, wear custom compression capris. I just recently went through a two week liquid diet (its not easy!) to get ready for the gastric sleeve. I recently came into a set back, but will continue with my weight loss journey in a few more months. I brought up the liquid diet I went through cause I noticed while going thru that 14 day diet of plant based protein drinks, sugar free popsicles, low sodium chicken broth, sugar free jello, and nuun tablets in my water for electrolytes my pain in my thighs had dramatically decreased! I lost 22 lbs too. My son noticed a pep in my step. I was overjoyed to sit up front in a car without having great pain and I was able to get out of the sitting position in the car easily. Now that I am back to regular food I see the same swelling and pain. I know I can reset my body and introduce different foods one by one to see which one gives me more pain and eliminate that food. Thank you for your story🙏🏾
Thank you so much for sharing your experience with Lipedema. I struggle with this disease as well. One day I hope to share my experience with others. I’m 52 so it’s a lot more harder for me. BTW, you’re beautiful.
You got this ❤
@@hannaholivia thank you.
I don't have this condition, but I enjoyed you educating us on it. I'm seeing more of this condition around. I hope you're able to make it a goal in the new few yes to save the. Money and get the surgery
Great video diary. I appreciate your openness. It’s fantastic that you have learned how to manage your lymphedema and are able to educate your audience.
Hannah, you are so brave and such a badass! I pray this video helps others and I’m soo proud of you! This is HUGE 🫶🏾🙏🏾😘 we love you Hannah! Such an informative vlog! I would love to see your progress
😆thank you Toya girl
Bless your itty bitty little heart 💕 I’m an RN and understand your pain.
You hit 30k! ❤❤❤ love that for you
🎉🎉🎉. I love that you’re opening up about your daily struggles! You’re loved 😍 very insightful thanks for sharing
You are such an encouragement! Let no one's stares or perceived comments bother you whatsoever. Stay focused on your journey. God is with you, He never told us we would have perfect lives, He never told us we wouldn't have detours. Praying for your healing, both physically and mentally. Your video will certainly be a blessing for others. 🙌🥰❤️🙏
Your story is amazing. I was diagnosed with lymphedema 19 years ago and it's good to see that you have decided to take control of the disease instead of it taking control of you like it did me am I younger days. Continue your journey with the faith the even when times get tough, you can overcome it.
Those glasses look so good on you!!💕💕💕
Hey Hannah! I thank you for this video 🥰 I struggle with Lipedema also. Like you - I don't wear shorts or short dresses. I have started embracing leggings this year but I used to not wear them. Girl, as far as the beach - I used to be the same way. I thought others would look at me differently but those folks don't know me and I just start embracing being myself. We all got something going on with us - some conditions people can see and some are internal. My doctor has told me about a lipedema machine that he is supposed to be ordering soon (I'm assuming it's like the one you had pictured or similar) but never said anything about a particular surgery - I'm very interested so I can do some research. Thank you sooo much for this vlog!
Sending you love 🫂 you’re such a beautiful person, and I’m grateful to watch your journey in all aspects. 💛
Thank you for being vulnerable for us! You’re so kind Hannah! Sending you so much love 🫶🏾
Praying for you Hannah 💕…. I have lower extremity swelling….knee down numbness swelling…..ankles looking like grapefruit….. I have anxiety and I’m self conscious….. I will wear an ankle length crochet cover up when swimming or at the beach…..you’re young and beautiful don’t hold yourself back worrying about what others think😍
Thank you for sharing this and helping to educate others. I have got lymhedema & arithritis in both legs, everyday is a struggle but i give God thanks for life. With Him by my side i will walk through this.❤❤❤🙏🏾🙏🏾🙏🏾🌹🌹🌹
Hannah have you ever looked into the Lymphatic Society/Clinic in your area?
They can do “drain therapy” on your legs and you should only have to pay your
co-pay depending on what type of insurance you have. My sister friend has been dealing with this for years. It’s only in one of her legs but it was huge. She had Gastric Bypass and lost a ton of weight even in that leg and had debulking surgery and it looks so much better. Also, check to see if you can get State Insurance that would help with the costs a lot. They also sell compression stockings for wide calf legs that are so much cheaper and comfortable that you could really benefit from
Good luck and God bless❤🙏🏽
Mine looks exactly like yours. All the Drs I went to refuse to diagnose it but will tell me to lose weight and it will help with my swelling. Theres days my left ankle and calve are so swollen it feels like my skin is going to burst. I too havent worn shorts out in public since middle school. My view on my legs are that there so hideous I wouldnt want anyone else to have to deal with looking at them, I know that may not be the case but its been a struggle for me for many years.
So happy i found your channel. To know Im not alone helps. I recently started keto and realized so far my swelling has gone down. Lets see what happens.
your video came up in my scroll. I’ve been looking up a lot of videos about swelling and leg pain. Not sure if I have this condition but I’m definitely going to find out but I want to thank you for being brave enough to open up and discuss it. I know how you feel, I’m older than you but having these pains in my legs, have really restricted me now has even caused me to-stop working
Thank you for this video!! Glasses look really nice on you!! ❤
I also have lipidema. I have compression boots but they do not get rid of problem but helps circulation
The weight loss is going to help with the lipedema. Walking is good, but an exercise bike with back support is better for helping to reduce the swelling and fat. All the best wishes!!
Abundant blessings, total healing & restoration 🙏💜. As someone who battles lymphedema & Lipedema.
Life can throw us lemons just do things to make it better ! You are extremely beautiful both inside and out. Don’t let this define you - lots to be grateful for. Wishing you good health on this journey that is inspiring so many. God bless you 🙏🏾
Thank You for sharing Your Story💐. Being different in any way does take so much courage. I appreciate Your words about having determination to fulfill Your purpose. I agree 💯 I have Edema(water retention) which I have had for about 20 years and it does cause swelling "water weight". I really have to remember what You said about not worrying about people's opinion. God's opinion is All that matters...and He Loves Us regardless!!!❣
Thank you for sharing!!! ❤ I’m 41, I have it and have had it my whole life but didn’t know. Anyway girlllaaaa live your life, you’re gorgeous and so is your body. I hate when my ankles swell but I still wear them out and my legs, swimsuits, shorts and all. It’s really simple who go check you boo😘Your beauty outweighs the disease. Remember that!
This was a good video. I have it to in my Arms my thighs and my butt it has not affected my legs or my feet.
For the readers there are two different disease...lymphedema..and lipedema...one is fat deposits one is lymph ...both have some similarities and some different manages...
Honestly..if you did not share you had lipedema i would not know...i underatand though..its about how you feel and i respect that...
One thing i tell my patients dont let a diagnosis have power over you...easier said than done i know...
GOD BLESS
You are beautiful ❤Praying 🙏🏾 for you Sis!😊
Hey Hannah, I’ve heard you mention your Lipedema before but it wasn’t until I watch this video… that I truly understand. I’ve also heard of the disease n read about it but didn’t know anyone personally going thru it. Many blessings to you beautiful, your story reminds me of my sister, who was diagnosed with MS during her second pregnancy. I know those two diseases are vastly different but the drive and resilience you both have is amazing! n I know it’s thru Gods grace that the both of you keep going on. Before my sister was a damn good hairdresser and now she’s had to scale back from it, something she loves to do, I’ve heard her cry bc doing things that normally wouldn’t be an issue is an event and a struggle… but thru it all she’s come a long way and so have you! Just the other day she took my niece for a walk to the end of her block, that was such a chore for her months ago not to mention not being mobile… she also went to the store with her two kids recently, it was with challenges but she made it home safely and that in of itself was a huge win! I say all that to say, keep doing what you’re doing Hannah and let God do his part. ❤ I truly feel you when you said you thank God for having to learn to navigate your disease bc without you don’t know where you’d be…. I’ve often felt that way about things in my life but it made me chuckle 😂 to think of how real this video truly is.
I love hearing about your mindset shift! Once you realize ppl really aren’t thinking about you and ppl really don’t care lol it’s SO FREEING! Very happy for you 😊